Item | Value |
---|---|
geneid | 54765 |
ensemblid | ENSG00000166326.7 |
hgncid | 19016 |
symbol | TRIM44 |
name | tripartite motif containing 44 |
refseq_nuc | NM_017583.6 |
refseq_prot | NP_060053.2 |
ensembl_nuc | ENST00000299413.7 |
ensembl_prot | ENSP00000299413.5 |
mane_status | MANE Select |
chr | chr11 |
start | 35662775 |
end | 35818007 |
strand | + |
ver | v1.2 |
region | chr11:35662775-35818007 |
region5000 | chr11:35657775-35823007 |
regionname0 | TRIM44_chr11_35662775_35818007 |
regionname5000 | TRIM44_chr11_35657775_35823007 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 344 | 390 | 94 | 76 | 173 | 14 | 31 | 132 | TRIM44_chr11_35657775_35823007 | TRIM44 | MASGV others(339): Show |
chr11 | 35657775 | 35823007 |
a0002 | 0/0 | 344 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | MASGV others(339): Show |
chr11 | 35657775 | 35823007 |
a0003 | 0/0 | 344 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | MASGV others(339): Show |
chr11 | 35657775 | 35823007 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1032 | 390 | 94 | 76 | 173 | 14 | 31 | TRIM44_chr11_35657775_35823007 | TRIM44 | ATGGC others(1027): Show |
chr11 | 35657775 | 35823007 | ||
a0002c0002 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | ATGGC others(1027): Show |
chr11 | 35657775 | 35823007 | ||
a0003c0003 | 0/0 | 1032 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | ATGGC others(1027): Show |
chr11 | 35657775 | 35823007 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13000 | 51 | 14 | 5 | 30 | 0 | 2 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0002 | 0/1 | 12997 | 43 | 2 | 15 | 19 | 4 | 2 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0003 | 0/0 | 13001 | 24 | 5 | 2 | 11 | 4 | 2 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0004 | 0/0 | 12999 | 23 | 0 | 11 | 12 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0005 | 0/0 | 13002 | 23 | 0 | 4 | 19 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0006 | 0/0 | 12999 | 13 | 2 | 5 | 5 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0007 | 0/0 | 13001 | 13 | 0 | 2 | 7 | 1 | 3 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0008 | 0/0 | 12998 | 9 | 0 | 4 | 3 | 0 | 2 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12993): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0009 | 0/0 | 13001 | 9 | 9 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0010 | 0/0 | 13001 | 8 | 1 | 1 | 5 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0011 | 0/0 | 13003 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12998): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0012 | 0/0 | 13001 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0013 | 0/0 | 13003 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12998): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0014 | 0/0 | 13000 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0015 | 0/0 | 12999 | 5 | 0 | 1 | 1 | 3 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0016 | 0/0 | 12996 | 5 | 1 | 2 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12991): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0017 | 0/0 | 13001 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0018 | 1/0 | 12994 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0019 | 0/0 | 13001 | 4 | 0 | 3 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0020 | 0/0 | 12995 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12990): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0021 | 0/0 | 12994 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0022 | 0/0 | 13002 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0023 | 0/0 | 13000 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0024 | 0/0 | 13002 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0025 | 0/0 | 13002 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0026 | 0/0 | 13000 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0027 | 0/0 | 13002 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0028 | 0/0 | 12994 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0029 | 0/0 | 12997 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0030 | 0/0 | 13001 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0031 | 0/0 | 13000 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0032 | 0/0 | 13001 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0033 | 0/0 | 13002 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0034 | 0/0 | 13001 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0035 | 0/0 | 13002 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0036 | 0/0 | 13001 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0037 | 0/0 | 13000 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0038 | 0/0 | 13000 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0039 | 0/0 | 12999 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0040 | 0/0 | 13000 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0041 | 0/0 | 13001 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0042 | 0/0 | 13001 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0043 | 0/0 | 13001 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0044 | 0/0 | 13002 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0045 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12999): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0046 | 0/0 | 13000 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0047 | 0/0 | 13000 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0048 | 0/0 | 12999 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0049 | 0/0 | 12999 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0050 | 0/0 | 12999 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0051 | 0/0 | 12999 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0052 | 0/0 | 12999 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0053 | 0/0 | 13001 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0054 | 0/0 | 13001 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0055 | 0/0 | 13000 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0056 | 0/0 | 12998 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12993): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0057 | 0/0 | 12998 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12993): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0058 | 0/0 | 12998 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12993): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0059 | 0/0 | 12998 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12993): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0060 | 0/0 | 12994 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0061 | 0/0 | 12999 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0062 | 0/0 | 13002 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0063 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12998): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0064 | 0/0 | 13002 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0065 | 0/0 | 13001 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0066 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12998): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0067 | 0/0 | 13002 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0068 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12998): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0069 | 0/0 | 13001 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0070 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0071 | 0/0 | 13000 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0072 | 0/0 | 13001 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0073 | 0/0 | 13001 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0074 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0075 | 0/0 | 13000 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0076 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0077 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0078 | 0/0 | 13000 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0079 | 0/0 | 13000 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0080 | 0/0 | 13000 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0081 | 0/0 | 12999 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0082 | 0/0 | 12999 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12994): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0083 | 0/0 | 13001 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0084 | 0/0 | 12995 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12990): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0085 | 0/0 | 12994 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0086 | 0/0 | 12994 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0087 | 0/0 | 12994 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0088 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0089 | 0/0 | 12998 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12993): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0090 | 0/0 | 13001 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0091 | 0/0 | 12997 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0092 | 0/0 | 12997 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0093 | 0/0 | 12997 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0094 | 0/0 | 12997 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0095 | 0/0 | 12997 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0096 | 0/0 | 12997 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0097 | 0/0 | 13002 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0098 | 0/0 | 12996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12991): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0099 | 0/0 | 12996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12991): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0100 | 0/0 | 12994 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0101 | 0/0 | 12997 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12992): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0102 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0103 | 0/0 | 13002 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12997): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0104 | 0/0 | 13001 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0105 | 0/0 | 13001 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0106 | 0/0 | 13000 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0107 | 0/0 | 13000 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0108 | 0/0 | 12995 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12990): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0109 | 0/0 | 13001 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12996): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0110 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0001c0001t0111 | 0/0 | 12994 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12989): Show |
chr11 | 35657775 | 35823007 |
a0002c0002t0001 | 0/0 | 13000 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12995): Show |
chr11 | 35657775 | 35823007 |
a0003c0003t0008 | 0/0 | 12998 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | GGCGG others(12993): Show |
chr11 | 35657775 | 35823007 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0314 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0004g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0008g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0011g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0012g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0012g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0012g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0012g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0012g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0013g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0013g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0014g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0014g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0014g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0015g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0015g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0015g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0015g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0015g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0016g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0016g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0016g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0016g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0016g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0017g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0017g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0017g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0017g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0017g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0018g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0018g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0018g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0018g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0019g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0019g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0019g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0019g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0020g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0020g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0020g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0020g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0021g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0021g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0021g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0022g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0022g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0022g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0023g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0023g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0023g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0024g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0024g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0024g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0025g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0025g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0025g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0026g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0026g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0027g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0027g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0027g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0028g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0028g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0028g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0029g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0029g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0029g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0030g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0030g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0030g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0031g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0031g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0032g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0032g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0033g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0033g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0034g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0034g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0035g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0035g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0036g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0036g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0037g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0037g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0038g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0038g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0039g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0039g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0040g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0040g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0041g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0041g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0042g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0042g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0043g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0043g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0044g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0044g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0045g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0046g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0047g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0048g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0049g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0050g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0051g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0052g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0053g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0054g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0055g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0056g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0057g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0058g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0059g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0060g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0061g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0062g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0063g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0064g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0065g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0066g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0067g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0068g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0069g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0070g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0071g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0072g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0073g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0074g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0075g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0076g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0077g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0078g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0079g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0080g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0081g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0082g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0083g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0084g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0085g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0086g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0087g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0088g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0089g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0090g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0091g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0092g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0093g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0094g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0095g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0096g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0097g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0098g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0099g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0100g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0101g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0102g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0103g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0104g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0105g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0106g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0107g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0108g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0109g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0110g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0001c0001t0111g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
a0003c0003t0008g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0189 | EUR | GBR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00099 | hp2 | a0001 | c0001 | t0015 | g0281 | EUR | GBR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0335 | EUR | FIN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00280 | hp2 | a0001 | c0001 | t0030 | g0197 | EUR | FIN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0222 | EUR | FIN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0359 | EUR | FIN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00423 | hp2 | a0001 | c0001 | t0017 | g0010 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00438 | hp1 | a0001 | c0001 | t0010 | g0184 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00438 | hp2 | a0001 | c0001 | t0104 | g0190 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00544 | hp1 | a0001 | c0001 | t0077 | g0289 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00558 | hp2 | a0001 | c0001 | t0029 | g0290 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00597 | hp1 | a0001 | c0001 | t0043 | g0210 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0363 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00609 | hp2 | a0001 | c0001 | t0029 | g0293 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00621 | hp2 | a0001 | c0001 | t0008 | g0337 | EAS | CHS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00639 | hp1 | a0001 | c0001 | t0075 | g0114 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00639 | hp2 | a0001 | c0001 | t0023 | g0233 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0077 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0089 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00733 | hp2 | a0001 | c0001 | t0008 | g0324 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00738 | hp2 | a0001 | c0001 | t0082 | g0279 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0331 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG00741 | hp2 | a0001 | c0001 | t0030 | g0203 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01069 | hp2 | a0001 | c0001 | t0016 | g0321 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01070 | hp2 | a0001 | c0001 | t0021 | g0366 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01071 | hp1 | a0001 | c0001 | t0021 | g0367 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01081 | hp1 | a0001 | c0001 | t0053 | g0220 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01081 | hp2 | a0001 | c0001 | t0083 | g0159 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01106 | hp2 | a0001 | c0001 | t0031 | g0002 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01109 | hp1 | a0001 | c0001 | t0033 | g0244 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0301 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0083 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01175 | hp1 | a0001 | c0001 | t0022 | g0286 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0240 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01257 | hp1 | a0001 | c0001 | t0027 | g0116 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01257 | hp2 | a0001 | c0001 | t0016 | g0325 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01258 | hp1 | a0001 | c0001 | t0097 | g0221 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01261 | hp1 | a0001 | c0001 | t0015 | g0282 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01261 | hp2 | a0001 | c0001 | t0027 | g0100 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01358 | hp1 | a0001 | c0001 | t0030 | g0202 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01361 | hp1 | a0001 | c0001 | t0095 | g0300 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01496 | hp1 | a0001 | c0001 | t0100 | g0368 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01516 | hp1 | a0001 | c0001 | t0107 | g0200 | EUR | IBS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0140 | EUR | IBS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0139 | EUR | IBS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0302 | EUR | IBS | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01884 | hp1 | a0001 | c0001 | t0028 | g0371 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0111 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01891 | hp1 | a0001 | c0001 | t0086 | g0374 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01891 | hp2 | a0001 | c0001 | t0024 | g0266 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0081 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01934 | hp1 | a0001 | c0001 | t0051 | g0084 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0037 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01943 | hp1 | a0001 | c0001 | t0106 | g0112 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01943 | hp2 | a0001 | c0001 | t0008 | g0288 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01952 | hp2 | a0001 | c0001 | t0047 | g0090 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01975 | hp1 | a0001 | c0001 | t0019 | g0192 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0068 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01978 | hp1 | a0001 | c0001 | t0010 | g0113 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01978 | hp2 | a0001 | c0001 | t0060 | g0069 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0239 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG01993 | hp2 | a0001 | c0001 | t0019 | g0092 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02027 | hp1 | a0001 | c0001 | t0111 | g0001 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02027 | hp2 | a0001 | c0001 | t0010 | g0167 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02040 | hp1 | a0001 | c0001 | t0052 | g0057 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02056 | hp1 | a0001 | c0001 | t0023 | g0229 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02071 | hp1 | a0001 | c0001 | t0022 | g0277 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02071 | hp2 | a0001 | c0001 | t0093 | g0297 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02129 | hp2 | a0001 | c0001 | t0013 | g0031 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02132 | hp2 | a0001 | c0001 | t0017 | g0011 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02135 | hp1 | a0001 | c0001 | t0044 | g0001 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0099 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0157 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0072 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02155 | hp1 | a0001 | c0001 | t0101 | g0292 | EAS | CDX | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02258 | hp1 | a0001 | c0001 | t0079 | g0252 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02280 | hp1 | a0001 | c0001 | t0038 | g0275 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0158 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02293 | hp1 | a0001 | c0001 | t0019 | g0205 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0088 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0349 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PEL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0264 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02602 | hp1 | a0001 | c0001 | t0007 | g0209 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02622 | hp1 | a0001 | c0001 | t0078 | g0242 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02630 | hp2 | a0001 | c0001 | t0039 | g0237 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02647 | hp1 | a0001 | c0001 | t0084 | g0272 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02698 | hp1 | a0001 | c0001 | t0010 | g0146 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02698 | hp2 | a0001 | c0001 | t0059 | g0060 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0097 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02717 | hp2 | a0001 | c0001 | t0034 | g0260 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02723 | hp1 | a0001 | c0001 | t0055 | g0255 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02738 | hp1 | a0003 | c0003 | t0008 | g0361 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0104 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0375 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02895 | hp1 | a0001 | c0001 | t0011 | g0247 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0333 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02896 | hp1 | a0001 | c0001 | t0081 | g0054 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02897 | hp1 | a0001 | c0001 | t0016 | g0332 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0103 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02922 | hp2 | a0001 | c0001 | t0011 | g0154 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0267 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02965 | hp2 | a0001 | c0001 | t0014 | g0120 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02970 | hp1 | a0001 | c0001 | t0036 | g0102 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02970 | hp2 | a0001 | c0001 | t0033 | g0243 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02976 | hp1 | a0001 | c0001 | t0071 | g0096 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02976 | hp2 | a0001 | c0001 | t0073 | g0271 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03041 | hp1 | a0001 | c0001 | t0009 | g0274 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03041 | hp2 | a0001 | c0001 | t0046 | g0235 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0273 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03130 | hp1 | a0001 | c0001 | t0061 | g0254 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03130 | hp2 | a0001 | c0001 | t0009 | g0265 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03139 | hp1 | a0001 | c0001 | t0087 | g0378 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0153 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0270 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03209 | hp2 | a0001 | c0001 | t0072 | g0263 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03225 | hp2 | a0001 | c0001 | t0037 | g0253 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03239 | hp1 | a0001 | c0001 | t0041 | g0212 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03239 | hp2 | a0001 | c0001 | t0096 | g0341 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03453 | hp1 | a0001 | c0001 | t0039 | g0238 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03453 | hp2 | a0001 | c0001 | t0085 | g0376 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03486 | hp1 | a0001 | c0001 | t0045 | g0155 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03486 | hp2 | a0001 | c0001 | t0020 | g0129 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03491 | hp1 | a0001 | c0001 | t0040 | g0012 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03492 | hp1 | a0001 | c0001 | t0040 | g0013 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03492 | hp2 | a0001 | c0001 | t0007 | g0201 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0278 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03516 | hp2 | a0001 | c0001 | t0028 | g0370 | AFR | ESN | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03540 | hp1 | a0001 | c0001 | t0031 | g0236 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03540 | hp2 | a0001 | c0001 | t0028 | g0369 | AFR | GWD | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03579 | hp1 | a0001 | c0001 | t0020 | g0127 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03579 | hp2 | a0001 | c0001 | t0038 | g0276 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03654 | hp1 | a0001 | c0001 | t0019 | g0191 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03654 | hp2 | a0001 | c0001 | t0026 | g0280 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03669 | hp1 | a0001 | c0001 | t0026 | g0006 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03669 | hp2 | a0001 | c0001 | t0022 | g0213 | SAS | PJL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03688 | hp1 | a0001 | c0001 | t0090 | g0342 | SAS | STU | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03688 | hp2 | a0001 | c0001 | t0068 | g0115 | SAS | STU | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03834 | hp2 | a0001 | c0001 | t0026 | g0006 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03927 | hp1 | a0001 | c0001 | t0105 | g0196 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03927 | hp2 | a0001 | c0001 | t0008 | g0346 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03942 | hp1 | a0001 | c0001 | t0089 | g0343 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG04184 | hp1 | a0001 | c0001 | t0008 | g0307 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG04184 | hp2 | a0001 | c0001 | t0041 | g0211 | SAS | BEB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0093 | SAS | STU | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG04199 | hp2 | a0001 | c0001 | t0027 | g0131 | SAS | STU | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG04204 | hp2 | a0001 | c0001 | t0049 | g0080 | SAS | STU | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18522 | hp1 | a0001 | c0001 | t0021 | g0365 | AFR | YRI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18522 | hp2 | a0001 | c0001 | t0034 | g0364 | AFR | YRI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18612 | hp2 | a0001 | c0001 | t0066 | g0049 | EAS | CHB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18747 | hp1 | a0001 | c0001 | t0057 | g0070 | EAS | CHB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18747 | hp2 | a0001 | c0001 | t0099 | g0356 | EAS | CHB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18906 | hp1 | a0001 | c0001 | t0018 | g0373 | AFR | YRI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18906 | hp2 | a0001 | c0001 | t0080 | g0379 | AFR | YRI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18939 | hp2 | a0001 | c0001 | t0044 | g0316 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18941 | hp1 | a0001 | c0001 | t0056 | g0064 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18941 | hp2 | a0001 | c0001 | t0035 | g0021 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18943 | hp1 | a0001 | c0001 | t0008 | g0345 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0380 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18945 | hp2 | a0001 | c0001 | t0076 | g0183 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18946 | hp2 | a0001 | c0001 | t0110 | g0125 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18949 | hp1 | a0001 | c0001 | t0063 | g0048 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18951 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18953 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18954 | hp2 | a0001 | c0001 | t0035 | g0028 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18957 | hp1 | a0001 | c0001 | t0069 | g0025 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18960 | hp2 | a0001 | c0001 | t0094 | g0353 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0207 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18962 | hp2 | a0001 | c0001 | t0091 | g0351 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18963 | hp1 | a0001 | c0001 | t0012 | g0318 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18965 | hp1 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18965 | hp2 | a0001 | c0001 | t0025 | g0026 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18967 | hp1 | a0001 | c0001 | t0010 | g0177 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18968 | hp1 | a0001 | c0001 | t0017 | g0193 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18969 | hp1 | a0001 | c0001 | t0098 | g0344 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18969 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18971 | hp2 | a0001 | c0001 | t0017 | g0199 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18974 | hp2 | a0001 | c0001 | t0029 | g0291 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18978 | hp1 | a0001 | c0001 | t0065 | g0166 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18978 | hp2 | a0001 | c0001 | t0013 | g0041 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18979 | hp1 | a0001 | c0001 | t0008 | g0348 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18990 | hp1 | a0001 | c0001 | t0102 | g0169 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18990 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18998 | hp1 | a0001 | c0001 | t0074 | g0187 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0079 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19000 | hp2 | a0001 | c0001 | t0103 | g0095 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19002 | hp2 | a0001 | c0001 | t0054 | g0234 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19005 | hp1 | a0001 | c0001 | t0016 | g0310 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19009 | hp1 | a0001 | c0001 | t0013 | g0029 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19010 | hp1 | a0001 | c0001 | t0109 | g0194 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19010 | hp2 | a0001 | c0001 | t0010 | g0164 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19030 | hp1 | a0001 | c0001 | t0064 | g0144 | AFR | LWK | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19030 | hp2 | a0001 | c0001 | t0024 | g0269 | AFR | LWK | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19054 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19058 | hp2 | a0001 | c0001 | t0015 | g0245 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19062 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19063 | hp2 | a0001 | c0001 | t0032 | g0217 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19064 | hp2 | a0001 | c0001 | t0043 | g0204 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19065 | hp1 | a0001 | c0001 | t0016 | g0309 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19066 | hp2 | a0001 | c0001 | t0012 | g0319 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19068 | hp1 | a0001 | c0001 | t0017 | g0198 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19068 | hp2 | a0001 | c0001 | t0070 | g0161 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19070 | hp2 | a0001 | c0001 | t0058 | g0078 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19078 | hp1 | a0001 | c0001 | t0013 | g0018 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19079 | hp1 | a0001 | c0001 | t0088 | g0137 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19081 | hp2 | a0001 | c0001 | t0012 | g0317 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19083 | hp1 | a0001 | c0001 | t0012 | g0360 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19083 | hp2 | a0001 | c0001 | t0032 | g0218 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19084 | hp1 | a0001 | c0001 | t0006 | g0075 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19090 | hp2 | a0001 | c0001 | t0025 | g0027 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19091 | hp1 | a0001 | c0001 | t0025 | g0022 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0268 | AFR | YRI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ASW | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20129 | hp2 | a0001 | c0001 | t0020 | g0128 | AFR | ASW | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0315 | EUR | TSI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20752 | hp2 | a0001 | c0001 | t0015 | g0283 | EUR | TSI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20805 | hp1 | a0001 | c0001 | t0015 | g0284 | EUR | TSI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0241 | EUR | TSI | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0195 | SAS | GIH | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20905 | hp2 | a0001 | c0001 | t0092 | g0339 | SAS | GIH | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02109 | hp1 | a0001 | c0001 | t0062 | g0259 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0156 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02486 | hp1 | a0001 | c0001 | t0050 | g0377 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02486 | hp2 | a0001 | c0001 | t0018 | g0372 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02559 | hp1 | a0001 | c0001 | t0108 | g0130 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03471 | hp1 | a0001 | c0001 | t0036 | g0106 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG03471 | hp2 | a0001 | c0001 | t0048 | g0362 | AFR | MSL | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG06807 | hp1 | a0001 | c0001 | t0037 | g0256 | AFR | USA | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
HG06807 | hp2 | a0001 | c0001 | t0042 | g0258 | AFR | USA | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA18955 | hp2 | a0001 | c0001 | t0023 | g0224 | EAS | JPT | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20300 | hp1 | a0001 | c0001 | t0042 | g0261 | AFR | USA | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | USA | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA21309 | hp1 | a0001 | c0001 | t0020 | g0126 | AFR | LWK | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
NA21309 | hp2 | a0001 | c0001 | t0067 | g0262 | AFR | LWK | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0314 | REF | REF | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
homoSapiens | grch38p0 | a0001 | c0001 | t0018 | g0306 | REF | REF | TRIM44_chr11_35657775_35823007 | TRIM44 | chr11 | 35657775 | 35823007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:35663302 | C | A | 1 | a0002 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.191C>A | p.Ser64Tyr | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/5 | 528/12994 | 191/1035 | 64/344 | chr11 | 35663302 | |||
chr11:35726117 | A | G | 1 | a0003 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.941A>G | p.Lys314Arg | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/5 | 1278/12994 | 941/1035 | 314/344 | chr11 | 35726117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:35662792 | C | G | 7 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0043 others(4): Show |
18 | HG00423.hp2 HG00597.hp1 HG02027.hp1 others(15): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-320C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/5 | chr11 | 35662792 | |||||||
chr11:35662798 | G | A | 1 | a0001c0001t0043 | 2 | HG00597.hp1 NA19064.hp2 |
5_prime_UTR_variant | MODIFIER | c.-314G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/5 | 314 | chr11 | 35662798 | ||||||
chr11:35662804 | G | T | 2 | a0001c0001t0020 a0001c0001t0108 |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-308G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/5 | chr11 | 35662804 | |||||||
chr11:35663083 | C | G | 1 | a0001c0001t0042 | 2 | HG06807.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/5 | 29 | chr11 | 35663083 | ||||||
chr11:35806408 | A | G | 16 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0017 others(13): Show |
45 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*23A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 23 | chr11 | 35806408 | ||||||
chr11:35806697 | A | G | 1 | a0001c0001t0102 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 312 | chr11 | 35806697 | ||||||
chr11:35806723 | G | A | 1 | a0001c0001t0042 | 2 | HG06807.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*338G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 338 | chr11 | 35806723 | ||||||
chr11:35806779 | C | T | 1 | a0001c0001t0101 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 394 | chr11 | 35806779 | ||||||
chr11:35806797 | A | G | 1 | a0001c0001t0100 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 412 | chr11 | 35806797 | ||||||
chr11:35807258 | T | C | 1 | a0001c0001t0021 | 3 | HG01070.hp2 HG01071.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*873T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 873 | chr11 | 35807258 | ||||||
chr11:35807453 | C | G | 21 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0012 others(18): Show |
83 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1068C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1068 | chr11 | 35807453 | ||||||
chr11:35807693 | T | C | 2 | a0001c0001t0011 a0001c0001t0045 |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1308T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1308 | chr11 | 35807693 | ||||||
chr11:35807772 | G | T | 1 | a0001c0001t0088 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1387G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1387 | chr11 | 35807772 | ||||||
chr11:35807928 | G | A | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(20): Show |
86 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1543G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1543 | chr11 | 35807928 | ||||||
chr11:35808031 | A | G | 1 | a0001c0001t0108 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1646A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1646 | chr11 | 35808031 | ||||||
chr11:35808194 | G | T | 1 | a0001c0001t0061 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1809G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1809 | chr11 | 35808194 | ||||||
chr11:35808207 | T | TAAAA | 6 | a0001c0001t0023 a0001c0001t0055 a0001c0001t0056 others(3): Show |
8 | HG00639.hp2 HG02056.hp1 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1837_*1840dupAAAA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1841 | INFO_REALIGN_3_PRIME | chr11 | 35808207 | |||||
chr11:35808207 | T | TAAAAA | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(18): Show |
89 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1836_*1840dupAAAA others(1): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1841 | INFO_REALIGN_3_PRIME | chr11 | 35808207 | |||||
chr11:35808207 | T | TAAAAAA | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(36): Show |
153 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*1835_*1840dupAAAA others(2): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1841 | INFO_REALIGN_3_PRIME | chr11 | 35808207 | |||||
chr11:35808207 | T | TAAAAAAA | 27 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(24): Show |
105 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1834_*1840dupAAAA others(3): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1841 | INFO_REALIGN_3_PRIME | chr11 | 35808207 | |||||
chr11:35808207 | T | TAAAAAAA others(1): Show |
8 | a0001c0001t0013 a0001c0001t0033 a0001c0001t0044 others(5): Show |
14 | HG01109.hp1 HG02109.hp1 HG02129.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1833_*1840dupAAAA others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 1841 | INFO_REALIGN_3_PRIME | chr11 | 35808207 | |||||
chr11:35808450 | T | A | 4 | a0001c0001t0033 a0001c0001t0034 a0001c0001t0042 others(1): Show |
7 | HG01109.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2065T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 2065 | chr11 | 35808450 | ||||||
chr11:35808457 | T | G | 2 | a0001c0001t0011 a0001c0001t0045 |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2072T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 2072 | chr11 | 35808457 | ||||||
chr11:35808493 | A | G | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(25): Show |
93 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2108A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 2108 | chr11 | 35808493 | ||||||
chr11:35808704 | G | A | 1 | a0001c0001t0065 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2319G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 2319 | chr11 | 35808704 | ||||||
chr11:35809096 | G | T | 1 | a0001c0001t0025 | 3 | NA18965.hp2 NA19090.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2711G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 2711 | chr11 | 35809096 | ||||||
chr11:35809188 | A | G | 2 | a0001c0001t0020 a0001c0001t0108 |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2803A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 2803 | chr11 | 35809188 | ||||||
chr11:35809630 | T | C | 1 | a0001c0001t0055 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3245T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3245 | chr11 | 35809630 | ||||||
chr11:35809731 | T | C | 7 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(4): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3346T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3346 | chr11 | 35809731 | ||||||
chr11:35809811 | G | A | 1 | a0001c0001t0026 | 3 | HG03654.hp2 HG03669.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3426G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3426 | chr11 | 35809811 | ||||||
chr11:35809876 | C | A | 6 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(3): Show |
34 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3491C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3491 | chr11 | 35809876 | ||||||
chr11:35809881 | C | CCA | 13 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0022 others(10): Show |
48 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3497_*3498insAC | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3498 | INFO_REALIGN_3_PRIME | chr11 | 35809881 | |||||
chr11:35809883 | G | A | 104 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(101): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*3498G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3498 | chr11 | 35809883 | ||||||
chr11:35809946 | G | A | 1 | a0001c0001t0070 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3561G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3561 | chr11 | 35809946 | ||||||
chr11:35810305 | G | T | 1 | a0001c0001t0061 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3920G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3920 | chr11 | 35810305 | ||||||
chr11:35810345 | C | T | 105 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(102): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
3_prime_UTR_variant | MODIFIER | c.*3960C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 3960 | chr11 | 35810345 | ||||||
chr11:35810614 | G | A | 4 | a0001c0001t0014 a0001c0001t0036 a0001c0001t0071 others(1): Show |
9 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4229G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 4229 | chr11 | 35810614 | ||||||
chr11:35810616 | G | A | 1 | a0001c0001t0048 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4231G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 4231 | chr11 | 35810616 | ||||||
chr11:35810689 | A | G | 1 | a0001c0001t0105 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4304A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 4304 | chr11 | 35810689 | ||||||
chr11:35810905 | C | T | 3 | a0001c0001t0037 a0001c0001t0078 a0001c0001t0079 |
4 | HG02258.hp1 HG02622.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4520C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 4520 | chr11 | 35810905 | ||||||
chr11:35811006 | G | T | 1 | a0001c0001t0052 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4621G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 4621 | chr11 | 35811006 | ||||||
chr11:35811264 | A | T | 1 | a0001c0001t0051 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4879A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 4879 | chr11 | 35811264 | ||||||
chr11:35811388 | G | A | 1 | a0001c0001t0032 | 2 | NA19063.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5003G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5003 | chr11 | 35811388 | ||||||
chr11:35811435 | G | GA | 8 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0038 others(5): Show |
19 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5059dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5060 | INFO_REALIGN_3_PRIME | chr11 | 35811435 | |||||
chr11:35811481 | T | C | 1 | a0001c0001t0074 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5096T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5096 | chr11 | 35811481 | ||||||
chr11:35811591 | T | C | 1 | a0001c0001t0039 | 2 | HG02630.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5206T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5206 | chr11 | 35811591 | ||||||
chr11:35812011 | T | G | 1 | a0001c0001t0104 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5626T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5626 | chr11 | 35812011 | ||||||
chr11:35812240 | C | T | 2 | a0001c0001t0020 a0001c0001t0108 |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5855C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5855 | chr11 | 35812240 | ||||||
chr11:35812288 | A | G | 1 | a0001c0001t0054 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5903A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5903 | chr11 | 35812288 | ||||||
chr11:35812298 | G | A | 3 | a0001c0001t0034 a0001c0001t0042 a0001c0001t0062 |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5913G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5913 | chr11 | 35812298 | ||||||
chr11:35812309 | A | C | 1 | a0001c0001t0039 | 2 | HG02630.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5924A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 5924 | chr11 | 35812309 | ||||||
chr11:35812417 | C | T | 1 | a0001c0001t0042 | 2 | HG06807.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6032C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6032 | chr11 | 35812417 | ||||||
chr11:35812554 | A | C | 2 | a0001c0001t0089 a0001c0001t0096 |
2 | HG03239.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6169A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6169 | chr11 | 35812554 | ||||||
chr11:35812588 | G | T | 1 | a0001c0001t0095 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6203G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6203 | chr11 | 35812588 | ||||||
chr11:35812696 | C | A | 2 | a0001c0001t0020 a0001c0001t0108 |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6311C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6311 | chr11 | 35812696 | ||||||
chr11:35812840 | ATCT | A | 15 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0016 others(12): Show |
70 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*6459_*6461delTCT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6459 | INFO_REALIGN_3_PRIME | chr11 | 35812840 | |||||
chr11:35812936 | G | A | 3 | a0001c0001t0034 a0001c0001t0042 a0001c0001t0062 |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6551G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6551 | chr11 | 35812936 | ||||||
chr11:35812964 | G | C | 2 | a0001c0001t0020 a0001c0001t0108 |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6579G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6579 | chr11 | 35812964 | ||||||
chr11:35812996 | C | CT | 2 | a0001c0001t0020 a0001c0001t0108 |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6612dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6613 | INFO_REALIGN_3_PRIME | chr11 | 35812996 | |||||
chr11:35813002 | C | T | 2 | a0001c0001t0094 a0001c0001t0099 |
2 | NA18747.hp2 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6617C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6617 | chr11 | 35813002 | ||||||
chr11:35813199 | C | G | 3 | a0001c0001t0037 a0001c0001t0078 a0001c0001t0079 |
4 | HG02258.hp1 HG02622.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6814C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6814 | chr11 | 35813199 | ||||||
chr11:35813241 | A | G | 1 | a0001c0001t0028 | 3 | HG01884.hp1 HG03516.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6856A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6856 | chr11 | 35813241 | ||||||
chr11:35813378 | A | G | 1 | a0001c0001t0073 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6993A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 6993 | chr11 | 35813378 | ||||||
chr11:35813418 | A | G | 29 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(26): Show |
95 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*7033A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7033 | chr11 | 35813418 | ||||||
chr11:35813633 | T | G | 1 | a0001c0001t0078 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7248T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7248 | chr11 | 35813633 | ||||||
chr11:35813705 | A | T | 1 | a0001c0001t0077 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7320A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7320 | chr11 | 35813705 | ||||||
chr11:35813733 | A | G | 111 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(108): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*7348A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7348 | chr11 | 35813733 | ||||||
chr11:35813898 | A | G | 1 | a0001c0001t0039 | 2 | HG02630.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7513A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7513 | chr11 | 35813898 | ||||||
chr11:35814038 | A | G | 2 | a0001c0001t0011 a0001c0001t0045 |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7653A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7653 | chr11 | 35814038 | ||||||
chr11:35814076 | G | T | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(20): Show |
86 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*7691G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7691 | chr11 | 35814076 | ||||||
chr11:35814091 | C | T | 2 | a0001c0001t0034 a0001c0001t0062 |
3 | HG02109.hp1 HG02717.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7706C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7706 | chr11 | 35814091 | ||||||
chr11:35814114 | A | G | 2 | a0001c0001t0080 a0001c0001t0087 |
2 | HG03139.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7729A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7729 | chr11 | 35814114 | ||||||
chr11:35814158 | C | T | 1 | a0001c0001t0071 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7773C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7773 | chr11 | 35814158 | ||||||
chr11:35814254 | T | G | 1 | a0001c0001t0070 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7869T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7869 | chr11 | 35814254 | ||||||
chr11:35814270 | G | T | 1 | a0001c0001t0086 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7885G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7885 | chr11 | 35814270 | ||||||
chr11:35814341 | G | C | 1 | a0001c0001t0090 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7956G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7956 | chr11 | 35814341 | ||||||
chr11:35814355 | A | C | 1 | a0001c0001t0093 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7970A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 7970 | chr11 | 35814355 | ||||||
chr11:35814431 | T | C | 1 | a0001c0001t0075 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8046T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8046 | chr11 | 35814431 | ||||||
chr11:35814546 | G | A | 1 | a0001c0001t0086 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8161G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8161 | chr11 | 35814546 | ||||||
chr11:35814614 | C | T | 3 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0038 |
14 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8229C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8229 | chr11 | 35814614 | ||||||
chr11:35814705 | G | A | 6 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(3): Show |
34 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*8320G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8320 | chr11 | 35814705 | ||||||
chr11:35814752 | C | T | 1 | a0001c0001t0019 | 4 | HG01975.hp1 HG01993.hp2 HG02293.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8367C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8367 | chr11 | 35814752 | ||||||
chr11:35814760 | T | G | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(25): Show |
93 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*8375T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8375 | chr11 | 35814760 | ||||||
chr11:35814888 | G | A | 1 | a0001c0001t0063 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8503G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8503 | chr11 | 35814888 | ||||||
chr11:35815064 | A | G | 36 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(33): Show |
131 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*8679A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8679 | chr11 | 35815064 | ||||||
chr11:35815179 | T | G | 1 | a0001c0001t0049 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8794T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8794 | chr11 | 35815179 | ||||||
chr11:35815201 | T | C | 35 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(32): Show |
140 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*8816T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8816 | chr11 | 35815201 | ||||||
chr11:35815300 | C | T | 1 | a0001c0001t0058 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8915C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8915 | chr11 | 35815300 | ||||||
chr11:35815339 | G | A | 7 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(4): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*8954G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 8954 | chr11 | 35815339 | ||||||
chr11:35815582 | T | C | 45 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(42): Show |
138 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*9197T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 9197 | chr11 | 35815582 | ||||||
chr11:35815714 | A | G | 4 | a0001c0001t0033 a0001c0001t0034 a0001c0001t0042 others(1): Show |
7 | HG01109.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9329A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 9329 | chr11 | 35815714 | ||||||
chr11:35815868 | A | G | 7 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(4): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*9483A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 9483 | chr11 | 35815868 | ||||||
chr11:35815977 | G | C | 3 | a0001c0001t0089 a0001c0001t0092 a0001c0001t0096 |
3 | HG03239.hp2 HG03942.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9592G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 9592 | chr11 | 35815977 | ||||||
chr11:35816081 | C | T | 1 | a0001c0001t0093 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9696C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 9696 | chr11 | 35816081 | ||||||
chr11:35816197 | A | G | 1 | a0001c0001t0082 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9812A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 9812 | chr11 | 35816197 | ||||||
chr11:35816257 | A | AC | 7 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(4): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*9872_*9873insC | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 9873 | chr11 | 35816257 | ||||||
chr11:35816653 | C | T | 1 | a0001c0001t0079 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10268C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 10268 | chr11 | 35816653 | ||||||
chr11:35816718 | T | G | 2 | a0001c0001t0029 a0001c0001t0101 |
4 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10333T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 10333 | chr11 | 35816718 | ||||||
chr11:35817003 | C | A | 3 | a0001c0001t0034 a0001c0001t0042 a0001c0001t0062 |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10618C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 10618 | chr11 | 35817003 | ||||||
chr11:35817369 | T | C | 6 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0038 others(3): Show |
17 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*10984T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 10984 | chr11 | 35817369 | ||||||
chr11:35817371 | T | G | 6 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(3): Show |
34 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*10986T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 10986 | chr11 | 35817371 | ||||||
chr11:35817414 | G | T | 3 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0038 |
14 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*11029G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 11029 | chr11 | 35817414 | ||||||
chr11:35817677 | C | A | 8 | a0001c0001t0004 a0001c0001t0047 a0001c0001t0049 others(5): Show |
30 | HG00423.hp1 HG00733.hp1 HG01074.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*11292C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 11292 | chr11 | 35817677 | ||||||
chr11:35817791 | A | G | 1 | a0001c0001t0040 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11406A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 11406 | chr11 | 35817791 | ||||||
chr11:35817867 | A | G | 30 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0012 others(27): Show |
91 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*11482A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 5/5 | 11482 | chr11 | 35817867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:35663820 | G | A | 2 | a0001c0001t0017g0010 a0001c0001t0017g0011 |
2 | HG00423.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.669+40G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35663820 | |||||||
chr11:35663923 | A | G | 1 | a0001c0001t0004g0380 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.669+143A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35663923 | |||||||
chr11:35664007 | A | G | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.669+227A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664007 | |||||||
chr11:35664189 | C | T | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.669+409C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664189 | |||||||
chr11:35664211 | G | A | 2 | a0001c0001t0040g0012 a0001c0001t0040g0013 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.669+431G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664211 | |||||||
chr11:35664312 | G | A | 1 | a0001c0001t0004g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.669+532G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664312 | |||||||
chr11:35664420 | C | T | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+640C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664420 | |||||||
chr11:35664760 | A | G | 1 | a0001c0001t0034g0364 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.669+980A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664760 | |||||||
chr11:35664842 | C | T | 1 | a0001c0001t0003g0363 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.669+1062C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664842 | |||||||
chr11:35664847 | A | C | 2 | a0001c0001t0006g0009 a0001c0001t0048g0362 |
3 | HG02622.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.669+1067A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664847 | |||||||
chr11:35664930 | G | A | 302 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(299): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.669+1150G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664930 | |||||||
chr11:35664944 | AAACTTAT others(7): Show |
A | 1 | a0001c0001t0022g0286 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.669+1165_669+1178d others(16): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35664944 | |||||||
chr11:35665044 | A | G | 1 | a0001c0001t0004g0285 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.669+1264A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665044 | |||||||
chr11:35665105 | A | T | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.669+1325A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665105 | |||||||
chr11:35665514 | G | C | 1 | a0001c0001t0002g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.669+1734G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665514 | |||||||
chr11:35665582 | ATCTG | A | 7 | a0001c0001t0015g0281 a0001c0001t0015g0282 a0001c0001t0015g0283 others(4): Show |
8 | HG00099.hp2 HG00738.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.669+1804_669+1807d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35665582 | ||||||
chr11:35665586 | G | GT | 19 | a0001c0001t0002g0007 a0001c0001t0002g0312 a0001c0001t0002g0333 others(16): Show |
19 | HG00280.hp1 HG00323.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.669+1832dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35665586 | ||||||
chr11:35665586 | GT | G | 128 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(125): Show |
130 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.669+1832delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35665586 | ||||||
chr11:35665586 | GTT | G | 97 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0110 others(94): Show |
98 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.669+1831_669+1832d others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35665586 | ||||||
chr11:35665586 | GTTTT | G | 14 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(11): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.669+1829_669+1832d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35665586 | ||||||
chr11:35665588 | T | G | 8 | a0001c0001t0003g0015 a0001c0001t0015g0281 a0001c0001t0015g0282 others(5): Show |
9 | HG00099.hp2 HG00738.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+1808T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665588 | |||||||
chr11:35665591 | T | A | 1 | a0001c0001t0017g0010 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.669+1811T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665591 | |||||||
chr11:35665595 | T | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.669+1815T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665595 | |||||||
chr11:35665597 | T | G | 1 | a0001c0001t0008g0288 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.669+1817T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665597 | |||||||
chr11:35665599 | T | G | 54 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(51): Show |
56 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.669+1819T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665599 | |||||||
chr11:35665600 | T | G | 2 | a0001c0001t0014g0097 a0001c0001t0071g0096 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.669+1820T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665600 | |||||||
chr11:35665601 | T | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0010g0099 others(1): Show |
4 | HG01261.hp2 HG02145.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+1821T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665601 | |||||||
chr11:35665602 | T | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00544.hp1 HG02523.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+1822T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665602 | |||||||
chr11:35665605 | T | G | 31 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.669+1825T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665605 | |||||||
chr11:35665680 | C | T | 1 | a0003c0003t0008g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.669+1900C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665680 | |||||||
chr11:35665852 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00558.hp1 NA19007.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.669+2072T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665852 | |||||||
chr11:35665903 | A | AT | 39 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(36): Show |
39 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.669+2131dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35665903 | ||||||
chr11:35665912 | G | T | 301 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(298): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.669+2132G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35665912 | |||||||
chr11:35666338 | C | G | 1 | a0001c0001t0022g0277 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.669+2558C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35666338 | |||||||
chr11:35666399 | T | A | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.669+2619T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35666399 | |||||||
chr11:35666738 | G | A | 3 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0052g0057 |
3 | HG02040.hp1 NA18959.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.669+2958G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35666738 | |||||||
chr11:35666806 | G | A | 1 | a0001c0001t0082g0279 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.669+3026G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35666806 | |||||||
chr11:35666830 | TG | T | 18 | a0001c0001t0002g0359 a0001c0001t0009g0005 a0001c0001t0009g0264 others(15): Show |
19 | HG00323.hp2 HG01891.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.669+3051delG | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35666830 | |||||||
chr11:35666908 | T | G | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+3128T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35666908 | |||||||
chr11:35667154 | G | C | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.669+3374G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35667154 | |||||||
chr11:35667530 | GCTAA | G | 7 | a0001c0001t0002g0352 a0001c0001t0002g0354 a0001c0001t0002g0355 others(4): Show |
7 | HG02056.hp2 NA18747.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+3754_669+3757d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35667530 | ||||||
chr11:35667589 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.669+3809T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35667589 | |||||||
chr11:35667620 | G | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+3840G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35667620 | |||||||
chr11:35667758 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.669+3978C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35667758 | |||||||
chr11:35667759 | G | A | 1 | a0001c0001t0110g0125 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+3979G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35667759 | |||||||
chr11:35667942 | G | A | 59 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(56): Show |
59 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.669+4162G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35667942 | |||||||
chr11:35667990 | G | A | 1 | a0001c0001t0027g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.669+4210G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35667990 | |||||||
chr11:35668170 | T | C | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+4390T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35668170 | |||||||
chr11:35668344 | T | C | 1 | a0001c0001t0088g0137 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.669+4564T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35668344 | |||||||
chr11:35668427 | T | C | 1 | a0001c0001t0026g0280 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+4647T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35668427 | |||||||
chr11:35668447 | T | C | 4 | a0001c0001t0029g0290 a0001c0001t0029g0291 a0001c0001t0029g0293 others(1): Show |
4 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+4667T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35668447 | |||||||
chr11:35668545 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.669+4765G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35668545 | |||||||
chr11:35668663 | G | T | 7 | a0001c0001t0005g0003 a0001c0001t0005g0045 a0001c0001t0005g0046 others(4): Show |
7 | NA18612.hp2 NA18949.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+4883G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35668663 | |||||||
chr11:35668680 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.669+4900G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35668680 | |||||||
chr11:35669217 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+5437C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35669217 | |||||||
chr11:35669456 | C | CTTTA | 54 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(51): Show |
55 | HG00280.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.669+5709_669+5712d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35669456 | ||||||
chr11:35669456 | C | CTTTATTT others(1): Show |
9 | a0001c0001t0002g0350 a0001c0001t0029g0291 a0001c0001t0037g0256 others(6): Show |
9 | HG01891.hp1 HG02155.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+5705_669+5712d others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35669456 | ||||||
chr11:35669456 | C | CTTTATTT others(5): Show |
1 | a0001c0001t0029g0293 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.669+5701_669+5712d others(14): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35669456 | ||||||
chr11:35669456 | CTTTA | C | 11 | a0001c0001t0001g0053 a0001c0001t0003g0139 a0001c0001t0003g0140 others(8): Show |
11 | HG00738.hp1 HG01516.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+5709_669+5712d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35669456 | ||||||
chr11:35669456 | CTTTATTT others(1): Show |
C | 80 | a0001c0001t0004g0014 a0001c0001t0004g0055 a0001c0001t0004g0056 others(77): Show |
82 | HG00423.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.669+5705_669+5712d others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35669456 | ||||||
chr11:35669617 | A | G | 1 | a0001c0001t0002g0320 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.669+5837A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35669617 | |||||||
chr11:35669626 | C | G | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+5846C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35669626 | |||||||
chr11:35669907 | C | T | 1 | a0001c0001t0007g0004 | 2 | NA18951.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.669+6127C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35669907 | |||||||
chr11:35669966 | C | T | 1 | a0001c0001t0003g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.669+6186C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35669966 | |||||||
chr11:35669979 | A | G | 311 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(308): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.669+6199A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35669979 | |||||||
chr11:35670127 | T | C | 2 | a0001c0001t0003g0141 a0001c0001t0003g0142 |
2 | NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.669+6347T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670127 | |||||||
chr11:35670206 | A | C | 2 | a0001c0001t0007g0239 a0001c0001t0007g0240 |
2 | HG01175.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.669+6426A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670206 | |||||||
chr11:35670281 | C | G | 3 | a0001c0001t0002g0315 a0001c0001t0002g0349 a0001c0001t0002g0359 |
3 | HG00323.hp2 HG02300.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.669+6501C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670281 | |||||||
chr11:35670287 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+6507G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670287 | |||||||
chr11:35670417 | T | A | 1 | a0001c0001t0002g0352 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.669+6637T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670417 | |||||||
chr11:35670633 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.669+6853A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670633 | |||||||
chr11:35670700 | A | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+6920A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670700 | |||||||
chr11:35670873 | G | A | 1 | a0001c0001t0007g0143 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.669+7093G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35670873 | |||||||
chr11:35671063 | T | G | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.669+7283T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35671063 | |||||||
chr11:35671266 | G | T | 1 | a0001c0001t0009g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+7486G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35671266 | |||||||
chr11:35671360 | T | C | 2 | a0001c0001t0005g0016 a0001c0001t0005g0017 |
2 | NA18980.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.669+7580T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35671360 | |||||||
chr11:35671577 | T | C | 24 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(21): Show |
24 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.669+7797T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35671577 | |||||||
chr11:35671693 | AG | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+7916delG | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35671693 | ||||||
chr11:35671889 | A | G | 1 | a0001c0001t0004g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.669+8109A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35671889 | |||||||
chr11:35671918 | T | C | 1 | a0001c0001t0013g0018 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.669+8138T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35671918 | |||||||
chr11:35672483 | A | G | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.669+8703A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672483 | |||||||
chr11:35672593 | G | A | 16 | a0001c0001t0004g0014 a0001c0001t0004g0058 a0001c0001t0004g0059 others(13): Show |
16 | HG00423.hp1 HG01074.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.669+8813G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672593 | |||||||
chr11:35672602 | G | A | 2 | a0001c0001t0037g0253 a0001c0001t0079g0252 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.669+8822G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672602 | |||||||
chr11:35672691 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.669+8911C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672691 | |||||||
chr11:35672711 | G | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+8931G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672711 | |||||||
chr11:35672724 | G | A | 1 | a0001c0001t0064g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.669+8944G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672724 | |||||||
chr11:35672749 | G | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.669+8969G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672749 | |||||||
chr11:35672878 | G | T | 1 | a0001c0001t0011g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.669+9098G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672878 | |||||||
chr11:35672920 | G | A | 7 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+9140G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35672920 | |||||||
chr11:35673075 | A | G | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.669+9295A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35673075 | |||||||
chr11:35673338 | T | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.669+9558T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35673338 | |||||||
chr11:35673482 | A | G | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.669+9702A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35673482 | |||||||
chr11:35673571 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.669+9791A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35673571 | |||||||
chr11:35673761 | C | T | 1 | a0001c0001t0015g0284 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.669+9981C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35673761 | |||||||
chr11:35673783 | C | T | 4 | a0001c0001t0024g0273 a0001c0001t0038g0275 a0001c0001t0038g0276 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+10003C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35673783 | |||||||
chr11:35673865 | T | C | 1 | a0001c0001t0022g0286 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.669+10085T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35673865 | |||||||
chr11:35674032 | A | G | 85 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(82): Show |
87 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.669+10252A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35674032 | |||||||
chr11:35674074 | C | T | 2 | a0001c0001t0031g0236 a0001c0001t0046g0235 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.669+10294C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35674074 | |||||||
chr11:35674139 | A | T | 5 | a0001c0001t0024g0273 a0001c0001t0038g0275 a0001c0001t0038g0276 others(2): Show |
5 | HG02280.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+10359A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35674139 | |||||||
chr11:35674235 | C | CGT | 8 | a0001c0001t0001g0119 a0001c0001t0005g0003 a0001c0001t0005g0045 others(5): Show |
8 | HG00408.hp1 NA18612.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.669+10472_669+1047 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674235 | C | CGTGT | 75 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0189 others(72): Show |
78 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.669+10470_669+1047 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674235 | C | CGTGTGT | 40 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0020 others(37): Show |
40 | HG00735.hp2 HG01109.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.669+10468_669+1047 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674235 | C | CGTGTGTG others(1): Show |
12 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0215 others(9): Show |
12 | HG02486.hp1 HG02572.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+10466_669+1047 others(12): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674235 | C | CGTGTGTG others(3): Show |
20 | a0001c0001t0003g0219 a0001c0001t0003g0251 a0001c0001t0004g0058 others(17): Show |
21 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.669+10464_669+1047 others(14): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674235 | C | CGTGTGTG others(5): Show |
48 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(45): Show |
49 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.669+10462_669+1047 others(16): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674235 | C | CGTGTGTG others(7): Show |
5 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0285 others(2): Show |
5 | HG00639.hp2 HG01074.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+10460_669+1047 others(18): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674235 | C | CGTGTGTG others(9): Show |
1 | a0001c0001t0060g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.669+10458_669+1047 others(20): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35674235 | ||||||
chr11:35674448 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.669+10668G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35674448 | |||||||
chr11:35674563 | G | T | 7 | a0001c0001t0004g0058 a0001c0001t0004g0066 a0001c0001t0004g0067 others(4): Show |
7 | HG01074.hp2 HG01192.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-10696G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35674563 | |||||||
chr11:35674753 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.670-10506G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35674753 | |||||||
chr11:35674848 | A | G | 1 | a0001c0001t0002g0359 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.670-10411A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35674848 | |||||||
chr11:35675127 | C | T | 1 | a0001c0001t0028g0371 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.670-10132C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675127 | |||||||
chr11:35675601 | A | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-9658A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675601 | |||||||
chr11:35675650 | T | A | 1 | a0001c0001t0005g0020 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.670-9609T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675650 | |||||||
chr11:35675720 | C | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.670-9539C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675720 | |||||||
chr11:35675861 | T | C | 1 | a0001c0001t0029g0291 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.670-9398T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675861 | |||||||
chr11:35675886 | G | A | 14 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0019 others(11): Show |
14 | HG02129.hp2 NA18941.hp2 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-9373G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675886 | |||||||
chr11:35675898 | A | G | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-9361A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675898 | |||||||
chr11:35675960 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.670-9299G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675960 | |||||||
chr11:35675960 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.670-9299G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675960 | |||||||
chr11:35675995 | A | G | 1 | a0001c0001t0005g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.670-9264A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35675995 | |||||||
chr11:35676001 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.670-9258G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676001 | |||||||
chr11:35676113 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-9146G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676113 | |||||||
chr11:35676298 | A | G | 42 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(39): Show |
44 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.670-8961A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676298 | |||||||
chr11:35676380 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0014g0103 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.670-8879C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676380 | |||||||
chr11:35676763 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.670-8496C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676763 | |||||||
chr11:35676855 | A | AAG | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.670-8401_670-8400d others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35676855 | ||||||
chr11:35676896 | G | C | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.670-8363G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676896 | |||||||
chr11:35676964 | A | T | 1 | a0001c0001t0005g0019 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.670-8295A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676964 | |||||||
chr11:35676968 | T | G | 1 | a0001c0001t0005g0019 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.670-8291T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676968 | |||||||
chr11:35676969 | G | T | 1 | a0001c0001t0005g0019 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.670-8290G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676969 | |||||||
chr11:35676996 | A | C | 14 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-8263A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35676996 | |||||||
chr11:35677204 | T | C | 1 | a0001c0001t0004g0059 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.670-8055T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677204 | |||||||
chr11:35677315 | G | A | 1 | a0001c0001t0048g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-7944G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677315 | |||||||
chr11:35677337 | C | A | 1 | a0001c0001t0022g0213 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.670-7922C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677337 | |||||||
chr11:35677438 | G | A | 2 | a0001c0001t0010g0113 a0001c0001t0106g0112 |
2 | HG01943.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.670-7821G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677438 | |||||||
chr11:35677515 | T | G | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.670-7744T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677515 | |||||||
chr11:35677532 | G | A | 1 | a0001c0001t0039g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.670-7727G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677532 | |||||||
chr11:35677562 | T | G | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.670-7697T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677562 | |||||||
chr11:35677741 | G | A | 1 | a0001c0001t0059g0060 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.670-7518G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677741 | |||||||
chr11:35677797 | CAGTA | C | 8 | a0001c0001t0015g0281 a0001c0001t0015g0282 a0001c0001t0015g0283 others(5): Show |
9 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.670-7459_670-7456d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35677797 | ||||||
chr11:35677893 | G | A | 1 | a0001c0001t0029g0293 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.670-7366G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677893 | |||||||
chr11:35677931 | T | G | 4 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(1): Show |
4 | HG03486.hp2 HG03579.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-7328T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35677931 | |||||||
chr11:35678345 | A | G | 130 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(127): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.670-6914A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678345 | |||||||
chr11:35678376 | A | G | 1 | a0001c0001t0008g0348 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.670-6883A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678376 | |||||||
chr11:35678379 | G | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG00621.hp1 NA18950.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-6880G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678379 | |||||||
chr11:35678616 | C | T | 1 | a0001c0001t0039g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.670-6643C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678616 | |||||||
chr11:35678826 | C | T | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.670-6433C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678826 | |||||||
chr11:35678847 | A | G | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.670-6412A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678847 | |||||||
chr11:35678956 | G | C | 1 | a0001c0001t0004g0055 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.670-6303G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678956 | |||||||
chr11:35678986 | G | T | 1 | a0001c0001t0028g0370 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.670-6273G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35678986 | |||||||
chr11:35678987 | AT | A | 54 | a0001c0001t0002g0320 a0001c0001t0004g0076 a0001c0001t0005g0003 others(51): Show |
55 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.670-6256delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35678987 | ||||||
chr11:35679146 | T | C | 1 | a0001c0001t0012g0317 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.670-6113T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35679146 | |||||||
chr11:35679180 | G | A | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.670-6079G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35679180 | |||||||
chr11:35679350 | A | G | 1 | a0001c0001t0037g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.670-5909A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35679350 | |||||||
chr11:35679449 | G | A | 24 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(21): Show |
24 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.670-5810G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35679449 | |||||||
chr11:35679688 | A | C | 10 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(7): Show |
11 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.670-5571A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35679688 | |||||||
chr11:35679831 | C | A | 17 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.670-5428C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35679831 | |||||||
chr11:35680445 | G | GT | 19 | a0001c0001t0013g0031 a0001c0001t0018g0372 a0001c0001t0018g0373 others(16): Show |
19 | HG01071.hp1 HG01109.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.670-4803dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35680445 | ||||||
chr11:35680585 | T | C | 1 | a0001c0001t0008g0288 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.670-4674T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35680585 | |||||||
chr11:35680612 | A | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-4647A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35680612 | |||||||
chr11:35680911 | CAG | C | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.670-4347_670-4346d others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35680911 | |||||||
chr11:35681027 | T | A | 1 | a0001c0001t0010g0164 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.670-4232T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35681027 | |||||||
chr11:35681250 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-4009G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35681250 | |||||||
chr11:35681297 | A | T | 1 | a0001c0001t0003g0232 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.670-3962A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35681297 | |||||||
chr11:35681621 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-3638A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35681621 | |||||||
chr11:35681743 | T | C | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.670-3516T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35681743 | |||||||
chr11:35681779 | TG | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0298 a0001c0001t0093g0297 |
4 | HG00408.hp2 HG02071.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-3478delG | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35681779 | ||||||
chr11:35681869 | A | G | 2 | a0001c0001t0026g0006 a0001c0001t0026g0280 |
3 | HG03654.hp2 HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.670-3390A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35681869 | |||||||
chr11:35681952 | C | CT | 8 | a0001c0001t0001g0110 a0001c0001t0001g0163 a0001c0001t0001g0186 others(5): Show |
8 | HG00621.hp1 HG01070.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-3283dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35681952 | ||||||
chr11:35681952 | CT | C | 173 | a0001c0001t0001g0050 a0001c0001t0001g0121 a0001c0001t0001g0122 others(170): Show |
176 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.670-3283delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35681952 | ||||||
chr11:35681952 | CTT | C | 21 | a0001c0001t0003g0139 a0001c0001t0003g0257 a0001c0001t0004g0067 others(18): Show |
21 | HG00099.hp1 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.670-3284_670-3283d others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35681952 | ||||||
chr11:35682013 | C | T | 1 | a0001c0001t0031g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670-3246C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682013 | |||||||
chr11:35682060 | G | A | 20 | a0001c0001t0002g0287 a0001c0001t0002g0299 a0001c0001t0002g0302 others(17): Show |
20 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.670-3199G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682060 | |||||||
chr11:35682084 | G | A | 1 | a0001c0001t0002g0359 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.670-3175G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682084 | |||||||
chr11:35682229 | C | T | 303 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(300): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.670-3030C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682229 | |||||||
chr11:35682451 | C | G | 1 | a0001c0001t0108g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.670-2808C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682451 | |||||||
chr11:35682524 | A | T | 10 | a0001c0001t0007g0143 a0001c0001t0007g0206 a0001c0001t0007g0207 others(7): Show |
10 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.670-2735A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682524 | |||||||
chr11:35682528 | A | T | 1 | a0001c0001t0004g0380 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.670-2731A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682528 | |||||||
chr11:35682716 | G | A | 1 | a0001c0001t0002g0358 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.670-2543G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682716 | |||||||
chr11:35682765 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.670-2494T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682765 | |||||||
chr11:35682768 | T | C | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.670-2491T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682768 | |||||||
chr11:35682783 | G | C | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.670-2476G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682783 | |||||||
chr11:35682894 | T | A | 6 | a0001c0001t0005g0003 a0001c0001t0005g0045 a0001c0001t0005g0046 others(3): Show |
6 | NA18949.hp1 NA18966.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-2365T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682894 | |||||||
chr11:35682975 | G | A | 1 | a0001c0001t0048g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-2284G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682975 | |||||||
chr11:35682998 | A | G | 4 | a0001c0001t0014g0097 a0001c0001t0014g0111 a0001c0001t0014g0120 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-2261A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35682998 | |||||||
chr11:35683096 | G | A | 1 | a0001c0001t0005g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.670-2163G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683096 | |||||||
chr11:35683165 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.670-2094A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683165 | |||||||
chr11:35683238 | G | A | 1 | a0001c0001t0029g0293 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.670-2021G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683238 | |||||||
chr11:35683259 | A | G | 2 | a0001c0001t0002g0312 a0001c0001t0002g0313 |
2 | HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.670-2000A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683259 | |||||||
chr11:35683394 | A | G | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.670-1865A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683394 | |||||||
chr11:35683417 | A | G | 1 | a0001c0001t0058g0078 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.670-1842A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683417 | |||||||
chr11:35683680 | T | C | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.670-1579T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683680 | |||||||
chr11:35683782 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.670-1477G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683782 | |||||||
chr11:35683935 | C | A | 5 | a0001c0001t0015g0281 a0001c0001t0015g0282 a0001c0001t0015g0283 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-1324C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35683935 | |||||||
chr11:35684123 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.670-1136G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35684123 | |||||||
chr11:35684261 | T | TA | 37 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(34): Show |
37 | HG00438.hp2 HG00735.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.670-989dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 35684261 | ||||||
chr11:35684686 | G | T | 381 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(378): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.670-573G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35684686 | |||||||
chr11:35685041 | C | T | 3 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0285 |
3 | HG01074.hp2 HG01192.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.670-218C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35685041 | |||||||
chr11:35685232 | G | C | 33 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0189 others(30): Show |
34 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.670-27G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | 35685232 | |||||||
chr11:35685438 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.747+102A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35685438 | |||||||
chr11:35685750 | G | A | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.747+414G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35685750 | |||||||
chr11:35685812 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+476C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35685812 | |||||||
chr11:35685880 | T | C | 1 | a0001c0001t0048g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.747+544T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35685880 | |||||||
chr11:35686296 | G | T | 27 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(24): Show |
28 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.747+960G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686296 | |||||||
chr11:35686305 | T | G | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.747+969T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686305 | |||||||
chr11:35686330 | C | T | 1 | a0001c0001t0002g0357 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.747+994C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686330 | |||||||
chr11:35686331 | G | A | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+995G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686331 | |||||||
chr11:35686362 | G | GT | 30 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(27): Show |
30 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.747+1031dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35686362 | ||||||
chr11:35686362 | G | GTT | 5 | a0001c0001t0005g0030 a0001c0001t0005g0044 a0001c0001t0013g0029 others(2): Show |
5 | NA18949.hp1 NA18954.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+1030_747+1031d others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35686362 | ||||||
chr11:35686367 | T | TTG | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+1031_747+1032i others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686367 | |||||||
chr11:35686368 | G | T | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.747+1032G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686368 | |||||||
chr11:35686374 | G | T | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.747+1038G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686374 | |||||||
chr11:35686374 | GT | G | 7 | a0001c0001t0001g0165 a0001c0001t0003g0015 a0001c0001t0003g0214 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.747+1052delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35686374 | ||||||
chr11:35686380 | T | G | 4 | a0001c0001t0004g0082 a0001c0001t0004g0083 a0001c0001t0049g0080 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+1044T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686380 | |||||||
chr11:35686588 | G | A | 1 | a0001c0001t0008g0288 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.747+1252G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686588 | |||||||
chr11:35686625 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+1289C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686625 | |||||||
chr11:35686804 | C | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+1468C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686804 | |||||||
chr11:35686926 | G | A | 197 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(194): Show |
200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.747+1590G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35686926 | |||||||
chr11:35687465 | A | C | 1 | a0001c0001t0108g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.747+2129A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35687465 | |||||||
chr11:35687553 | C | A | 1 | a0001c0001t0005g0032 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.747+2217C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35687553 | |||||||
chr11:35687798 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+2462G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35687798 | |||||||
chr11:35687948 | A | G | 2 | a0001c0001t0031g0236 a0001c0001t0046g0235 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.747+2612A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35687948 | |||||||
chr11:35687953 | G | A | 26 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0163 others(23): Show |
26 | HG00597.hp2 HG00621.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.747+2617G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35687953 | |||||||
chr11:35688388 | A | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0010g0113 others(1): Show |
4 | HG00408.hp1 HG01943.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+3052A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35688388 | |||||||
chr11:35688544 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.747+3208T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35688544 | |||||||
chr11:35688670 | A | G | 3 | a0001c0001t0003g0215 a0001c0001t0003g0230 a0001c0001t0054g0234 |
3 | HG02132.hp1 NA19002.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.747+3334A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35688670 | |||||||
chr11:35688709 | G | C | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.747+3373G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35688709 | |||||||
chr11:35688891 | G | C | 1 | a0001c0001t0051g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.747+3555G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35688891 | |||||||
chr11:35689433 | T | C | 1 | a0001c0001t0015g0281 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.747+4097T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35689433 | |||||||
chr11:35689447 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+4111C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35689447 | |||||||
chr11:35689753 | A | T | 22 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(19): Show |
22 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.747+4417A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35689753 | |||||||
chr11:35690417 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+5081A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35690417 | |||||||
chr11:35690481 | T | C | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+5145T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35690481 | |||||||
chr11:35690533 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+5197C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35690533 | |||||||
chr11:35691251 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+5915C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691251 | |||||||
chr11:35691270 | T | C | 2 | a0001c0001t0035g0021 a0001c0001t0035g0028 |
2 | NA18941.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.747+5934T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691270 | |||||||
chr11:35691494 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0010g0146 |
2 | HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.747+6158G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691494 | |||||||
chr11:35691537 | C | T | 1 | a0001c0001t0019g0205 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.747+6201C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691537 | |||||||
chr11:35691539 | T | C | 1 | a0001c0001t0078g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.747+6203T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691539 | |||||||
chr11:35691560 | T | A | 3 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0062g0259 |
3 | HG02109.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.747+6224T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691560 | |||||||
chr11:35691674 | T | C | 2 | a0001c0001t0021g0366 a0001c0001t0021g0367 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.747+6338T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691674 | |||||||
chr11:35691800 | A | G | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.747+6464A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691800 | |||||||
chr11:35691836 | G | A | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+6500G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691836 | |||||||
chr11:35691880 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+6544C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35691880 | |||||||
chr11:35692145 | A | AT | 15 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(12): Show |
15 | HG00597.hp2 HG02083.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.747+6819dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35692145 | ||||||
chr11:35692252 | T | G | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.747+6916T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692252 | |||||||
chr11:35692408 | G | A | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.747+7072G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692408 | |||||||
chr11:35692410 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.747+7074A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692410 | |||||||
chr11:35692414 | C | G | 1 | a0001c0001t0046g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.747+7078C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692414 | |||||||
chr11:35692676 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.747+7340A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692676 | |||||||
chr11:35692699 | C | T | 1 | a0001c0001t0023g0229 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.747+7363C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692699 | |||||||
chr11:35692796 | G | A | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747+7460G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692796 | |||||||
chr11:35692986 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+7650A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35692986 | |||||||
chr11:35693048 | G | T | 1 | a0001c0001t0108g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.747+7712G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35693048 | |||||||
chr11:35693166 | A | G | 1 | a0001c0001t0013g0018 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.747+7830A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35693166 | |||||||
chr11:35693547 | G | C | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+8211G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35693547 | |||||||
chr11:35693740 | T | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+8404T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35693740 | |||||||
chr11:35693888 | G | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+8552G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35693888 | |||||||
chr11:35694036 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0061 |
2 | NA18949.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.747+8700G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694036 | |||||||
chr11:35694357 | A | G | 312 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(309): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.747+9021A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694357 | |||||||
chr11:35694408 | A | G | 1 | a0001c0001t0002g0347 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.747+9072A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694408 | |||||||
chr11:35694519 | C | A | 10 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(7): Show |
11 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.747+9183C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694519 | |||||||
chr11:35694757 | T | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+9421T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694757 | |||||||
chr11:35694807 | A | G | 3 | a0001c0001t0004g0059 a0001c0001t0004g0065 a0001c0001t0056g0064 |
3 | NA18939.hp1 NA18941.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.747+9471A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694807 | |||||||
chr11:35694932 | A | G | 1 | a0001c0001t0003g0228 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.747+9596A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694932 | |||||||
chr11:35694950 | A | G | 1 | a0001c0001t0029g0290 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.747+9614A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694950 | |||||||
chr11:35694977 | T | C | 1 | a0001c0001t0015g0284 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.747+9641T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35694977 | |||||||
chr11:35695491 | G | A | 126 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(123): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.747+10155G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35695491 | |||||||
chr11:35695523 | C | G | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.747+10187C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35695523 | |||||||
chr11:35695889 | CT | C | 104 | a0001c0001t0001g0160 a0001c0001t0003g0015 a0001c0001t0003g0139 others(101): Show |
106 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.747+10569delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35695889 | ||||||
chr11:35696136 | A | AT | 17 | a0001c0001t0002g0295 a0001c0001t0002g0357 a0001c0001t0004g0014 others(14): Show |
17 | HG01952.hp1 HG02040.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.747+10820dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35696136 | ||||||
chr11:35696136 | AT | A | 6 | a0001c0001t0001g0160 a0001c0001t0003g0140 a0001c0001t0007g0209 others(3): Show |
6 | HG01496.hp1 HG01516.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+10820delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35696136 | ||||||
chr11:35696244 | C | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.747+10908C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696244 | |||||||
chr11:35696260 | G | C | 1 | a0001c0001t0031g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.747+10924G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696260 | |||||||
chr11:35696377 | C | T | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+11041C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696377 | |||||||
chr11:35696394 | G | A | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.747+11058G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696394 | |||||||
chr11:35696424 | G | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+11088G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696424 | |||||||
chr11:35696846 | CA | C | 124 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(121): Show |
127 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.747+11521delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35696846 | ||||||
chr11:35696856 | A | C | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.747+11520A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696856 | |||||||
chr11:35696884 | A | T | 7 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0156 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.747+11548A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696884 | |||||||
chr11:35696911 | A | G | 104 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(101): Show |
105 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.747+11575A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696911 | |||||||
chr11:35696961 | A | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+11625A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696961 | |||||||
chr11:35696991 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+11655C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35696991 | |||||||
chr11:35697141 | G | A | 1 | a0001c0001t0065g0166 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.747+11805G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697141 | |||||||
chr11:35697160 | C | T | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.747+11824C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697160 | |||||||
chr11:35697214 | T | TC | 35 | a0001c0001t0001g0094 a0001c0001t0001g0151 a0001c0001t0001g0152 others(32): Show |
35 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.747+11884dupC | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35697214 | ||||||
chr11:35697233 | G | T | 119 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(116): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.747+11897G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697233 | |||||||
chr11:35697234 | C | T | 119 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(116): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.747+11898C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697234 | |||||||
chr11:35697237 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.747+11901C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697237 | |||||||
chr11:35697296 | G | A | 1 | a0001c0001t0075g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.747+11960G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697296 | |||||||
chr11:35697374 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG00621.hp1 NA18950.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.747+12038C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697374 | |||||||
chr11:35697440 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+12104C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697440 | |||||||
chr11:35697458 | T | A | 5 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+12122T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697458 | |||||||
chr11:35697505 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.747+12169A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697505 | |||||||
chr11:35697602 | G | A | 1 | a0001c0001t0034g0364 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747+12266G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697602 | |||||||
chr11:35697700 | G | A | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+12364G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697700 | |||||||
chr11:35697851 | C | T | 336 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(333): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.747+12515C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697851 | |||||||
chr11:35697903 | G | A | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+12567G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697903 | |||||||
chr11:35697906 | A | G | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.747+12570A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697906 | |||||||
chr11:35697916 | G | A | 1 | a0001c0001t0011g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.747+12580G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697916 | |||||||
chr11:35697988 | C | G | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.747+12652C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35697988 | |||||||
chr11:35698043 | T | G | 1 | a0001c0001t0022g0277 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.747+12707T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35698043 | |||||||
chr11:35698139 | C | T | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.747+12803C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35698139 | |||||||
chr11:35698499 | A | G | 312 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(309): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.747+13163A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35698499 | |||||||
chr11:35699008 | G | C | 1 | a0001c0001t0022g0277 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.747+13672G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699008 | |||||||
chr11:35699009 | C | G | 1 | a0001c0001t0022g0277 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.747+13673C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699009 | |||||||
chr11:35699016 | T | C | 1 | a0001c0001t0015g0281 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.747+13680T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699016 | |||||||
chr11:35699083 | T | A | 39 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(36): Show |
39 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.747+13747T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699083 | |||||||
chr11:35699099 | T | A | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13763T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699099 | |||||||
chr11:35699100 | A | T | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13764A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699100 | |||||||
chr11:35699105 | C | T | 2 | a0001c0001t0031g0236 a0001c0001t0046g0235 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.747+13769C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699105 | |||||||
chr11:35699106 | A | G | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13770A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699106 | |||||||
chr11:35699120 | T | C | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13784T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699120 | |||||||
chr11:35699124 | G | T | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13788G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699124 | |||||||
chr11:35699135 | T | A | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13799T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699135 | |||||||
chr11:35699138 | G | A | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13802G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699138 | |||||||
chr11:35699142 | G | A | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13806G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699142 | |||||||
chr11:35699146 | A | C | 38 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(35): Show |
38 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.747+13810A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699146 | |||||||
chr11:35699217 | G | A | 2 | a0001c0001t0006g0009 a0001c0001t0048g0362 |
3 | HG02622.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.747+13881G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699217 | |||||||
chr11:35699639 | G | A | 167 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(164): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.747+14303G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699639 | |||||||
chr11:35699655 | G | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+14319G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699655 | |||||||
chr11:35699702 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14366T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699702 | |||||||
chr11:35699703 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14367G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699703 | |||||||
chr11:35699706 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14370G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699706 | |||||||
chr11:35699708 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14372C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699708 | |||||||
chr11:35699711 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14375C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699711 | |||||||
chr11:35699734 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14398C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699734 | |||||||
chr11:35699735 | C | G | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14399C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699735 | |||||||
chr11:35699739 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14403G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699739 | |||||||
chr11:35699754 | G | T | 2 | a0001c0001t0001g0053 a0001c0001t0081g0054 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.747+14418G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699754 | |||||||
chr11:35699773 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.747+14437A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699773 | |||||||
chr11:35699789 | A | C | 4 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(1): Show |
4 | HG00738.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+14453A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35699789 | |||||||
chr11:35700045 | A | T | 4 | a0001c0001t0014g0097 a0001c0001t0014g0111 a0001c0001t0014g0120 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+14709A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700045 | |||||||
chr11:35700093 | A | G | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+14757A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700093 | |||||||
chr11:35700283 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.747+14947T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700283 | |||||||
chr11:35700313 | A | G | 1 | a0001c0001t0012g0360 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.747+14977A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700313 | |||||||
chr11:35700351 | A | G | 1 | a0001c0001t0049g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.747+15015A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700351 | |||||||
chr11:35700650 | A | G | 1 | a0001c0001t0030g0203 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.747+15314A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700650 | |||||||
chr11:35700740 | G | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+15404G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700740 | |||||||
chr11:35700766 | G | C | 2 | a0001c0001t0053g0220 a0001c0001t0097g0221 |
2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.747+15430G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700766 | |||||||
chr11:35700823 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+15487A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35700823 | |||||||
chr11:35701073 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.747+15737C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701073 | |||||||
chr11:35701214 | T | C | 1 | a0001c0001t0018g0372 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.747+15878T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701214 | |||||||
chr11:35701217 | A | G | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+15881A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701217 | |||||||
chr11:35701273 | C | G | 1 | a0001c0001t0033g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.747+15937C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701273 | |||||||
chr11:35701273 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+15937C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701273 | |||||||
chr11:35701274 | G | A | 1 | a0001c0001t0029g0293 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.747+15938G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701274 | |||||||
chr11:35701278 | C | T | 2 | a0001c0001t0009g0270 a0001c0001t0013g0041 |
2 | HG03195.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.747+15942C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701278 | |||||||
chr11:35701531 | C | A | 1 | a0001c0001t0108g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.747+16195C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701531 | |||||||
chr11:35701597 | C | T | 1 | a0001c0001t0029g0290 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.747+16261C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701597 | |||||||
chr11:35701674 | C | T | 17 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.747+16338C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701674 | |||||||
chr11:35701683 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+16347G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701683 | |||||||
chr11:35701733 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.747+16397G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701733 | |||||||
chr11:35701941 | C | A | 127 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(124): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.747+16605C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35701941 | |||||||
chr11:35702006 | C | A | 14 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+16670C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702006 | |||||||
chr11:35702043 | A | G | 15 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0076 others(12): Show |
15 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.747+16707A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702043 | |||||||
chr11:35702051 | A | G | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747+16715A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702051 | |||||||
chr11:35702065 | G | T | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.747+16729G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702065 | |||||||
chr11:35702073 | T | C | 2 | a0001c0001t0042g0258 a0001c0001t0042g0261 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.747+16737T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702073 | |||||||
chr11:35702182 | A | G | 1 | a0001c0001t0002g0315 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.747+16846A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702182 | |||||||
chr11:35702358 | G | A | 1 | a0003c0003t0008g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.747+17022G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702358 | |||||||
chr11:35702363 | C | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+17027C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702363 | |||||||
chr11:35702468 | G | A | 3 | a0001c0001t0004g0059 a0001c0001t0004g0065 a0001c0001t0056g0064 |
3 | NA18939.hp1 NA18941.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.747+17132G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702468 | |||||||
chr11:35702480 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.747+17144A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702480 | |||||||
chr11:35702614 | G | T | 11 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0076 others(8): Show |
11 | HG00733.hp1 HG01255.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.747+17278G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702614 | |||||||
chr11:35702671 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.747+17335G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702671 | |||||||
chr11:35702754 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.747+17418A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702754 | |||||||
chr11:35702832 | A | C | 1 | a0001c0001t0020g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.747+17496A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702832 | |||||||
chr11:35702832 | A | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+17496A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702832 | |||||||
chr11:35702886 | G | C | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.747+17550G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702886 | |||||||
chr11:35702887 | G | T | 4 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(1): Show |
4 | HG01496.hp1 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+17551G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702887 | |||||||
chr11:35702928 | C | T | 1 | a0001c0001t0039g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.747+17592C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702928 | |||||||
chr11:35702949 | C | T | 7 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0226 others(4): Show |
7 | HG02071.hp1 NA18957.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.747+17613C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35702949 | |||||||
chr11:35703053 | C | T | 1 | a0001c0001t0006g0075 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.747+17717C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703053 | |||||||
chr11:35703062 | C | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+17726C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703062 | |||||||
chr11:35703071 | G | A | 1 | a0001c0001t0002g0354 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.747+17735G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703071 | |||||||
chr11:35703090 | G | A | 3 | a0001c0001t0002g0333 a0001c0001t0002g0334 a0001c0001t0016g0332 |
3 | HG02572.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.747+17754G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703090 | |||||||
chr11:35703122 | G | A | 4 | a0001c0001t0019g0092 a0001c0001t0019g0191 a0001c0001t0019g0192 others(1): Show |
4 | HG01975.hp1 HG01993.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+17786G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703122 | |||||||
chr11:35703214 | C | T | 5 | a0001c0001t0015g0281 a0001c0001t0015g0282 a0001c0001t0015g0283 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+17878C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703214 | |||||||
chr11:35703318 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+17982C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703318 | |||||||
chr11:35703320 | G | C | 303 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(300): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.747+17984G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703320 | |||||||
chr11:35703327 | C | T | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.747+17991C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703327 | |||||||
chr11:35703328 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+17992G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703328 | |||||||
chr11:35703417 | C | T | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747+18081C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703417 | |||||||
chr11:35703585 | G | A | 201 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(198): Show |
205 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.747+18249G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703585 | |||||||
chr11:35703809 | GA | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+18480delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35703809 | ||||||
chr11:35703866 | A | G | 1 | a0001c0001t0016g0310 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.747+18530A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703866 | |||||||
chr11:35703898 | A | G | 1 | a0001c0001t0057g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.747+18562A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35703898 | |||||||
chr11:35704015 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.747+18679A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704015 | |||||||
chr11:35704094 | C | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.747+18758C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704094 | |||||||
chr11:35704103 | C | T | 1 | a0001c0001t0008g0346 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.747+18767C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704103 | |||||||
chr11:35704136 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+18800G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704136 | |||||||
chr11:35704186 | G | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+18850G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704186 | |||||||
chr11:35704277 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.747+18941C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704277 | |||||||
chr11:35704305 | G | T | 4 | a0001c0001t0024g0273 a0001c0001t0038g0275 a0001c0001t0038g0276 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+18969G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704305 | |||||||
chr11:35704405 | A | C | 1 | a0001c0001t0002g0354 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.747+19069A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704405 | |||||||
chr11:35704412 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+19076G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704412 | |||||||
chr11:35704417 | A | G | 3 | a0001c0001t0002g0296 a0001c0001t0016g0309 a0001c0001t0016g0310 |
3 | NA19005.hp1 NA19011.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.747+19081A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704417 | |||||||
chr11:35704561 | T | A | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.747+19225T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704561 | |||||||
chr11:35704574 | T | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+19238T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704574 | |||||||
chr11:35704605 | T | C | 1 | a0001c0001t0068g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.747+19269T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704605 | |||||||
chr11:35704615 | T | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+19279T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704615 | |||||||
chr11:35704724 | C | A | 1 | a0001c0001t0002g0315 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.747+19388C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704724 | |||||||
chr11:35704799 | G | A | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.747+19463G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704799 | |||||||
chr11:35704814 | G | A | 303 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(300): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.747+19478G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704814 | |||||||
chr11:35704835 | C | G | 1 | a0001c0001t0108g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.747+19499C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704835 | |||||||
chr11:35704857 | T | C | 6 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+19521T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704857 | |||||||
chr11:35704867 | A | C | 6 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+19531A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704867 | |||||||
chr11:35704896 | A | T | 11 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0076 others(8): Show |
11 | HG00733.hp1 HG01255.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.747+19560A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704896 | |||||||
chr11:35704911 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.747+19575A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704911 | |||||||
chr11:35704970 | T | C | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+19634T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35704970 | |||||||
chr11:35705023 | C | T | 3 | a0001c0001t0028g0369 a0001c0001t0028g0370 a0001c0001t0028g0371 |
3 | HG01884.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.747+19687C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705023 | |||||||
chr11:35705120 | T | C | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.747+19784T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705120 | |||||||
chr11:35705214 | A | C | 1 | a0001c0001t0004g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.747+19878A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705214 | |||||||
chr11:35705294 | T | C | 202 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(199): Show |
206 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.747+19958T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705294 | |||||||
chr11:35705368 | G | A | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.747+20032G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705368 | |||||||
chr11:35705482 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+20146C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705482 | |||||||
chr11:35705547 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.747+20211A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705547 | |||||||
chr11:35705606 | A | T | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.747+20270A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705606 | |||||||
chr11:35705619 | T | C | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.747+20283T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705619 | |||||||
chr11:35705667 | G | A | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-20257G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705667 | |||||||
chr11:35705676 | A | G | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-20248A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705676 | |||||||
chr11:35705680 | T | C | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-20244T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705680 | |||||||
chr11:35705751 | A | G | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-20173A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705751 | |||||||
chr11:35705781 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-20143A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705781 | |||||||
chr11:35705800 | A | G | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-20124A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705800 | |||||||
chr11:35705828 | T | C | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-20096T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705828 | |||||||
chr11:35705890 | G | GA | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-20033dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35705890 | ||||||
chr11:35705897 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748-20027G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705897 | |||||||
chr11:35705931 | C | T | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19993C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705931 | |||||||
chr11:35705946 | A | C | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19978A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705946 | |||||||
chr11:35705987 | G | A | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19937G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35705987 | |||||||
chr11:35706009 | T | C | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-19915T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706009 | |||||||
chr11:35706031 | G | A | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19893G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706031 | |||||||
chr11:35706060 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-19864T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706060 | |||||||
chr11:35706089 | G | T | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19835G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706089 | |||||||
chr11:35706103 | G | A | 201 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(198): Show |
205 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.748-19821G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706103 | |||||||
chr11:35706111 | T | C | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19813T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706111 | |||||||
chr11:35706140 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.748-19784G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706140 | |||||||
chr11:35706145 | T | A | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19779T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706145 | |||||||
chr11:35706149 | T | C | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19775T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706149 | |||||||
chr11:35706181 | T | C | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19743T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706181 | |||||||
chr11:35706182 | G | A | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19742G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706182 | |||||||
chr11:35706189 | G | A | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19735G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706189 | |||||||
chr11:35706193 | C | T | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19731C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706193 | |||||||
chr11:35706239 | A | G | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19685A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706239 | |||||||
chr11:35706247 | C | A | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19677C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706247 | |||||||
chr11:35706248 | T | G | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19676T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706248 | |||||||
chr11:35706264 | C | T | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19660C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706264 | |||||||
chr11:35706274 | C | T | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-19650C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706274 | |||||||
chr11:35706464 | A | G | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.748-19460A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706464 | |||||||
chr11:35706570 | G | A | 76 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(73): Show |
77 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.748-19354G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706570 | |||||||
chr11:35706575 | G | A | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.748-19349G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706575 | |||||||
chr11:35706611 | C | T | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.748-19313C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706611 | |||||||
chr11:35706714 | C | G | 101 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(98): Show |
102 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.748-19210C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706714 | |||||||
chr11:35706757 | A | C | 1 | a0001c0001t0005g0019 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.748-19167A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706757 | |||||||
chr11:35706805 | C | T | 2 | a0001c0001t0053g0220 a0001c0001t0097g0221 |
2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.748-19119C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706805 | |||||||
chr11:35706847 | T | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-19077T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706847 | |||||||
chr11:35706857 | C | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-19067C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706857 | |||||||
chr11:35706914 | G | A | 1 | a0001c0001t0009g0264 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.748-19010G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706914 | |||||||
chr11:35706917 | A | G | 70 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0122 others(67): Show |
71 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.748-19007A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35706917 | |||||||
chr11:35707099 | C | A | 3 | a0001c0001t0007g0195 a0001c0001t0017g0193 a0001c0001t0109g0194 |
3 | NA18968.hp1 NA19010.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.748-18825C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707099 | |||||||
chr11:35707131 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-18793A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707131 | |||||||
chr11:35707189 | A | G | 2 | a0001c0001t0041g0211 a0001c0001t0041g0212 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.748-18735A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707189 | |||||||
chr11:35707210 | C | T | 33 | a0001c0001t0001g0178 a0001c0001t0007g0004 a0001c0001t0007g0143 others(30): Show |
34 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.748-18714C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707210 | |||||||
chr11:35707286 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.748-18638A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707286 | |||||||
chr11:35707353 | G | C | 1 | a0001c0001t0006g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.748-18571G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707353 | |||||||
chr11:35707362 | C | T | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-18562C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707362 | |||||||
chr11:35707410 | C | T | 1 | a0001c0001t0086g0374 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-18514C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707410 | |||||||
chr11:35707468 | C | T | 1 | a0001c0001t0045g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.748-18456C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707468 | |||||||
chr11:35707564 | G | T | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18360G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707564 | |||||||
chr11:35707568 | T | C | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18356T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707568 | |||||||
chr11:35707572 | T | C | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18352T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707572 | |||||||
chr11:35707575 | T | A | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18349T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707575 | |||||||
chr11:35707583 | G | A | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.748-18341G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707583 | |||||||
chr11:35707586 | A | C | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18338A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707586 | |||||||
chr11:35707590 | G | A | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18334G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707590 | |||||||
chr11:35707590 | G | T | 1 | a0001c0001t0100g0368 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.748-18334G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707590 | |||||||
chr11:35707604 | C | T | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18320C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707604 | |||||||
chr11:35707610 | A | T | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18314A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707610 | |||||||
chr11:35707611 | T | A | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-18313T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707611 | |||||||
chr11:35707627 | T | A | 41 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(38): Show |
43 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.748-18297T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707627 | |||||||
chr11:35707767 | A | G | 3 | a0001c0001t0005g0003 a0001c0001t0005g0047 a0001c0001t0013g0003 |
3 | NA18966.hp1 NA18999.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.748-18157A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35707767 | |||||||
chr11:35708253 | A | G | 1 | a0001c0001t0003g0215 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.748-17671A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708253 | |||||||
chr11:35708329 | C | T | 1 | a0001c0001t0015g0281 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.748-17595C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708329 | |||||||
chr11:35708462 | T | C | 1 | a0001c0001t0105g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.748-17462T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708462 | |||||||
chr11:35708526 | T | TGATAGAC others(325): Show |
5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17368_748-1736 others(336): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35708526 | ||||||
chr11:35708552 | C | G | 1 | a0001c0001t0002g0296 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.748-17372C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708552 | |||||||
chr11:35708583 | T | TA | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17336dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35708583 | ||||||
chr11:35708623 | A | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17301A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708623 | |||||||
chr11:35708626 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17298T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708626 | |||||||
chr11:35708633 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17291T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708633 | |||||||
chr11:35708645 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17279G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708645 | |||||||
chr11:35708646 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17278T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708646 | |||||||
chr11:35708655 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17269G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708655 | |||||||
chr11:35708656 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17268T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708656 | |||||||
chr11:35708660 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17264A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708660 | |||||||
chr11:35708677 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17247T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708677 | |||||||
chr11:35708693 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17231C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708693 | |||||||
chr11:35708726 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-17198G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708726 | |||||||
chr11:35708864 | A | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-17060A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708864 | |||||||
chr11:35708882 | G | A | 1 | a0001c0001t0006g0009 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.748-17042G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708882 | |||||||
chr11:35708896 | A | T | 1 | a0001c0001t0004g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-17028A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708896 | |||||||
chr11:35708943 | C | T | 1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.748-16981C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708943 | |||||||
chr11:35708982 | GC | G | 301 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(298): Show |
307 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(304): Show |
intron_variant | MODIFIER | c.748-16932delC | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35708982 | ||||||
chr11:35708992 | CA | C | 17 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(14): Show |
17 | HG02109.hp1 HG02148.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.748-16923delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35708992 | ||||||
chr11:35708993 | A | C | 42 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(39): Show |
44 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.748-16931A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35708993 | |||||||
chr11:35709087 | A | G | 30 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(27): Show |
30 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-16837A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35709087 | |||||||
chr11:35709269 | C | T | 1 | a0001c0001t0002g0358 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.748-16655C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35709269 | |||||||
chr11:35709419 | G | A | 3 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0062g0259 |
3 | HG02109.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.748-16505G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35709419 | |||||||
chr11:35709428 | C | CA | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02451.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-16489dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35709428 | ||||||
chr11:35709479 | T | G | 1 | a0001c0001t0086g0374 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-16445T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35709479 | |||||||
chr11:35709507 | C | T | 1 | a0001c0001t0042g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.748-16417C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35709507 | |||||||
chr11:35709756 | T | A | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.748-16168T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35709756 | |||||||
chr11:35710129 | G | A | 1 | a0001c0001t0005g0038 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.748-15795G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35710129 | |||||||
chr11:35710252 | T | G | 52 | a0001c0001t0004g0082 a0001c0001t0004g0083 a0001c0001t0004g0086 others(49): Show |
54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.748-15672T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35710252 | |||||||
chr11:35710254 | G | T | 16 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-15670G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35710254 | |||||||
chr11:35710485 | A | ATG | 5 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-15436_748-1543 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35710485 | ||||||
chr11:35710525 | A | G | 311 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(308): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.748-15399A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35710525 | |||||||
chr11:35710570 | T | C | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.748-15354T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35710570 | |||||||
chr11:35711022 | T | C | 4 | a0001c0001t0014g0097 a0001c0001t0014g0111 a0001c0001t0014g0120 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-14902T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711022 | |||||||
chr11:35711048 | A | G | 1 | a0003c0003t0008g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.748-14876A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711048 | |||||||
chr11:35711117 | A | G | 213 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(210): Show |
218 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.748-14807A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711117 | |||||||
chr11:35711249 | G | GT | 6 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-14669dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35711249 | ||||||
chr11:35711327 | G | C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0061 |
2 | NA18949.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.748-14597G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711327 | |||||||
chr11:35711432 | A | G | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-14492A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711432 | |||||||
chr11:35711439 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-14485G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711439 | |||||||
chr11:35711468 | G | GT | 14 | a0001c0001t0001g0135 a0001c0001t0002g0308 a0001c0001t0002g0354 others(11): Show |
14 | HG01358.hp2 HG02027.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.748-14443dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35711468 | ||||||
chr11:35711468 | GT | G | 200 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(197): Show |
205 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.748-14443delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35711468 | ||||||
chr11:35711852 | G | A | 1 | a0001c0001t0084g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.748-14072G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711852 | |||||||
chr11:35711871 | C | T | 128 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(125): Show |
132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.748-14053C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35711871 | |||||||
chr11:35712001 | G | A | 2 | a0001c0001t0041g0211 a0001c0001t0041g0212 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.748-13923G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35712001 | |||||||
chr11:35712014 | G | A | 2 | a0001c0001t0010g0113 a0001c0001t0106g0112 |
2 | HG01943.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.748-13910G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35712014 | |||||||
chr11:35712342 | T | G | 1 | a0001c0001t0002g0355 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.748-13582T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35712342 | |||||||
chr11:35712771 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-13153C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35712771 | |||||||
chr11:35712824 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-13100G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35712824 | |||||||
chr11:35713101 | C | G | 2 | a0001c0001t0006g0074 a0001c0001t0006g0075 |
2 | NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.748-12823C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35713101 | |||||||
chr11:35713353 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-12571C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35713353 | |||||||
chr11:35713362 | A | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-12562A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35713362 | |||||||
chr11:35713502 | C | CT | 153 | a0001c0001t0002g0330 a0001c0001t0003g0015 a0001c0001t0003g0139 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.748-12407dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35713502 | ||||||
chr11:35713502 | C | CTT | 11 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0034g0260 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-12408_748-1240 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35713502 | ||||||
chr11:35713572 | T | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-12352T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35713572 | |||||||
chr11:35713949 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-11975G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35713949 | |||||||
chr11:35714138 | T | G | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.748-11786T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714138 | |||||||
chr11:35714232 | A | G | 1 | a0001c0001t0004g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.748-11692A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714232 | |||||||
chr11:35714662 | A | G | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-11262A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714662 | |||||||
chr11:35714676 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.748-11248T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714676 | |||||||
chr11:35714771 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-11153A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714771 | |||||||
chr11:35714795 | G | A | 1 | a0001c0001t0023g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.748-11129G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714795 | |||||||
chr11:35714805 | G | A | 1 | a0001c0001t0006g0072 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.748-11119G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714805 | |||||||
chr11:35714866 | A | G | 1 | a0001c0001t0011g0247 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.748-11058A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35714866 | |||||||
chr11:35715003 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.748-10921C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715003 | |||||||
chr11:35715010 | T | C | 1 | a0001c0001t0010g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.748-10914T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715010 | |||||||
chr11:35715222 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0002g0320 |
2 | HG02040.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.748-10702G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715222 | |||||||
chr11:35715404 | A | ATG | 94 | a0001c0001t0001g0176 a0001c0001t0001g0180 a0001c0001t0001g0185 others(91): Show |
96 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.748-10495_748-1049 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35715404 | ||||||
chr11:35715404 | A | ATGTG | 4 | a0001c0001t0020g0127 a0001c0001t0020g0128 a0001c0001t0020g0129 others(1): Show |
4 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-10497_748-1049 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35715404 | ||||||
chr11:35715404 | ATG | A | 4 | a0001c0001t0003g0215 a0001c0001t0003g0230 a0001c0001t0020g0126 others(1): Show |
4 | HG02132.hp1 NA19002.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-10495_748-1049 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35715404 | ||||||
chr11:35715425 | T | G | 1 | a0001c0001t0007g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.748-10499T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715425 | |||||||
chr11:35715425 | T | TGG | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-10498_748-1049 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35715425 | ||||||
chr11:35715431 | G | T | 7 | a0001c0001t0002g0340 a0001c0001t0003g0015 a0001c0001t0003g0214 others(4): Show |
7 | HG01255.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-10493G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715431 | |||||||
chr11:35715631 | G | T | 14 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0219 others(11): Show |
14 | HG00609.hp1 HG02015.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-10293G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715631 | |||||||
chr11:35715832 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-10092C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715832 | |||||||
chr11:35715917 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748-10007G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35715917 | |||||||
chr11:35716349 | CA | C | 43 | a0001c0001t0004g0014 a0001c0001t0004g0055 a0001c0001t0004g0056 others(40): Show |
44 | HG00423.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.748-9572delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35716349 | ||||||
chr11:35716459 | A | G | 6 | a0001c0001t0004g0076 a0001c0001t0004g0085 a0001c0001t0004g0086 others(3): Show |
6 | HG00733.hp1 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-9465A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35716459 | |||||||
chr11:35716685 | C | T | 1 | a0001c0001t0030g0202 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.748-9239C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35716685 | |||||||
chr11:35716831 | G | A | 2 | a0001c0001t0026g0006 a0001c0001t0026g0280 |
3 | HG03654.hp2 HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.748-9093G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35716831 | |||||||
chr11:35716947 | T | C | 1 | a0001c0001t0004g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.748-8977T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35716947 | |||||||
chr11:35717027 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.748-8897A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35717027 | |||||||
chr11:35717400 | A | C | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.748-8524A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35717400 | |||||||
chr11:35717427 | G | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-8497G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35717427 | |||||||
chr11:35717605 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-8319A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35717605 | |||||||
chr11:35717733 | G | A | 1 | a0001c0001t0034g0364 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.748-8191G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35717733 | |||||||
chr11:35717887 | C | T | 2 | a0001c0001t0015g0283 a0001c0001t0015g0284 |
2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.748-8037C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35717887 | |||||||
chr11:35718012 | T | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-7912T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718012 | |||||||
chr11:35718016 | T | A | 2 | a0001c0001t0001g0147 a0001c0001t0010g0146 |
2 | HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.748-7908T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718016 | |||||||
chr11:35718077 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.748-7847A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718077 | |||||||
chr11:35718229 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0180 a0001c0001t0001g0185 |
3 | HG02523.hp2 NA18612.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.748-7695C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718229 | |||||||
chr11:35718315 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.748-7609A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718315 | |||||||
chr11:35718367 | T | C | 1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.748-7557T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718367 | |||||||
chr11:35718368 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.748-7556G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718368 | |||||||
chr11:35718379 | C | T | 1 | a0001c0001t0004g0085 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.748-7545C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718379 | |||||||
chr11:35718482 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748-7442A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718482 | |||||||
chr11:35718676 | A | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-7248A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718676 | |||||||
chr11:35718679 | G | A | 381 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(378): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.748-7245G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718679 | |||||||
chr11:35718744 | G | A | 2 | a0001c0001t0004g0062 a0001c0001t0059g0060 |
2 | HG00423.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.748-7180G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718744 | |||||||
chr11:35718845 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-7079C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718845 | |||||||
chr11:35718883 | CT | C | 53 | a0001c0001t0002g0323 a0001c0001t0002g0340 a0001c0001t0003g0139 others(50): Show |
53 | HG00323.hp1 HG00735.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.748-7030delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35718883 | ||||||
chr11:35718883 | CTT | C | 80 | a0001c0001t0002g0294 a0001c0001t0003g0015 a0001c0001t0003g0140 others(77): Show |
82 | HG00423.hp1 HG00609.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.748-7031_748-7030d others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35718883 | ||||||
chr11:35718901 | TTTC | T | 33 | a0001c0001t0002g0298 a0001c0001t0007g0004 a0001c0001t0007g0143 others(30): Show |
34 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.748-7017_748-7015d others(5): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35718901 | ||||||
chr11:35718925 | G | C | 4 | a0001c0001t0004g0059 a0001c0001t0004g0065 a0001c0001t0004g0380 others(1): Show |
4 | NA18939.hp1 NA18941.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-6999G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35718925 | |||||||
chr11:35719101 | A | G | 1 | a0001c0001t0031g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.748-6823A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35719101 | |||||||
chr11:35719221 | C | A | 2 | a0001c0001t0006g0009 a0001c0001t0048g0362 |
3 | HG02622.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.748-6703C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35719221 | |||||||
chr11:35719351 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-6573A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35719351 | |||||||
chr11:35719381 | TAGTG | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-6540_748-6537d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35719381 | ||||||
chr11:35719994 | T | G | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.748-5930T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35719994 | |||||||
chr11:35720003 | A | G | 8 | a0001c0001t0012g0001 a0001c0001t0012g0317 a0001c0001t0012g0318 others(5): Show |
9 | HG02027.hp1 HG02135.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-5921A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720003 | |||||||
chr11:35720155 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-5769C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720155 | |||||||
chr11:35720204 | T | G | 1 | a0001c0001t0006g0073 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.748-5720T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720204 | |||||||
chr11:35720232 | A | C | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-5692A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720232 | |||||||
chr11:35720321 | G | A | 1 | a0001c0001t0004g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.748-5603G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720321 | |||||||
chr11:35720415 | T | C | 16 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(13): Show |
17 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-5509T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720415 | |||||||
chr11:35720416 | C | CT | 16 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(13): Show |
17 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-5496dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35720416 | ||||||
chr11:35720416 | C | T | 1 | a0001c0001t0009g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.748-5508C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720416 | |||||||
chr11:35720430 | C | CT | 38 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(35): Show |
38 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.748-5485dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35720430 | ||||||
chr11:35720518 | A | T | 2 | a0001c0001t0031g0236 a0001c0001t0046g0235 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.748-5406A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720518 | |||||||
chr11:35720607 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.748-5317C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720607 | |||||||
chr11:35720719 | C | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.748-5205C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720719 | |||||||
chr11:35720903 | A | C | 46 | a0001c0001t0001g0094 a0001c0001t0001g0124 a0001c0001t0001g0132 others(43): Show |
47 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.748-5021A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35720903 | |||||||
chr11:35720909 | C | CT | 9 | a0001c0001t0005g0019 a0001c0001t0005g0042 a0001c0001t0010g0164 others(6): Show |
9 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-4999dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35720909 | ||||||
chr11:35720909 | CT | C | 6 | a0001c0001t0001g0118 a0001c0001t0002g0352 a0001c0001t0003g0222 others(3): Show |
6 | HG00323.hp1 HG02559.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.748-4999delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35720909 | ||||||
chr11:35720909 | CTTTTT | C | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-5003_748-4999d others(7): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35720909 | ||||||
chr11:35721255 | A | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-4669A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35721255 | |||||||
chr11:35721498 | C | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.748-4426C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35721498 | |||||||
chr11:35721718 | G | A | 1 | a0001c0001t0063g0048 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.748-4206G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35721718 | |||||||
chr11:35721980 | C | G | 2 | a0001c0001t0002g0355 a0001c0001t0002g0357 |
2 | NA18980.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.748-3944C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35721980 | |||||||
chr11:35722067 | A | G | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.748-3857A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722067 | |||||||
chr11:35722391 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-3533C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722391 | |||||||
chr11:35722454 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00544.hp1 HG02523.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-3470C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722454 | |||||||
chr11:35722459 | T | C | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.748-3465T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722459 | |||||||
chr11:35722495 | T | G | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.748-3429T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722495 | |||||||
chr11:35722532 | G | T | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-3392G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722532 | |||||||
chr11:35722553 | T | A | 3 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0062g0259 |
3 | HG02109.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.748-3371T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722553 | |||||||
chr11:35722745 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-3179G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722745 | |||||||
chr11:35722752 | T | C | 1 | a0001c0001t0027g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.748-3172T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722752 | |||||||
chr11:35722816 | C | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.748-3108C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35722816 | |||||||
chr11:35723000 | T | C | 3 | a0001c0001t0030g0197 a0001c0001t0030g0202 a0001c0001t0030g0203 |
3 | HG00280.hp2 HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.748-2924T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35723000 | |||||||
chr11:35723148 | A | T | 1 | a0001c0001t0014g0097 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.748-2776A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35723148 | |||||||
chr11:35723564 | T | A | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-2360T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35723564 | |||||||
chr11:35723637 | T | C | 1 | a0001c0001t0005g0033 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.748-2287T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35723637 | |||||||
chr11:35723922 | T | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-2002T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35723922 | |||||||
chr11:35724176 | G | A | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-1748G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35724176 | |||||||
chr11:35724216 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00558.hp1 NA19007.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.748-1708A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35724216 | |||||||
chr11:35724426 | A | G | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.748-1498A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35724426 | |||||||
chr11:35724580 | G | A | 1 | a0001c0001t0004g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.748-1344G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35724580 | |||||||
chr11:35724799 | T | C | 1 | a0001c0001t0022g0213 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.748-1125T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35724799 | |||||||
chr11:35724929 | T | G | 7 | a0001c0001t0002g0352 a0001c0001t0002g0354 a0001c0001t0002g0355 others(4): Show |
7 | HG02056.hp2 NA18747.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-995T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35724929 | |||||||
chr11:35725057 | T | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.748-867T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725057 | |||||||
chr11:35725058 | GCACACAC others(3): Show |
G | 1 | a0001c0001t0024g0273 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.748-858_748-849del others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725058 | ||||||
chr11:35725060 | ACACACT | A | 14 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(11): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.748-858_748-853del others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725060 | ||||||
chr11:35725064 | A | ACT | 14 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(11): Show |
14 | HG00408.hp1 HG00639.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-858_748-857dup others(2): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725064 | ||||||
chr11:35725066 | T | TCA | 29 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0148 others(26): Show |
29 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.748-820_748-819dup others(2): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | T | TCACA | 30 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(27): Show |
30 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.748-822_748-819dup others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | T | TCACACA | 3 | a0001c0001t0001g0145 a0001c0001t0001g0180 a0001c0001t0064g0144 |
3 | HG02738.hp2 NA18612.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.748-824_748-819dup others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | T | TCTCA | 5 | a0001c0001t0001g0053 a0001c0001t0001g0101 a0001c0001t0001g0110 others(2): Show |
5 | HG01169.hp1 HG02148.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-857_748-856ins others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | T | TCTCACA | 7 | a0001c0001t0014g0097 a0001c0001t0014g0104 a0001c0001t0014g0111 others(4): Show |
7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-857_748-856ins others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | T | TCTCACAC others(3): Show |
1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.748-857_748-856ins others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | TCA | T | 20 | a0001c0001t0001g0098 a0001c0001t0001g0168 a0001c0001t0001g0173 others(17): Show |
21 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.748-820_748-819del others(2): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | TCACA | T | 19 | a0001c0001t0003g0140 a0001c0001t0003g0216 a0001c0001t0003g0251 others(16): Show |
19 | HG00738.hp1 HG01109.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.748-822_748-819del others(4): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | TCACACA | T | 72 | a0001c0001t0003g0015 a0001c0001t0003g0141 a0001c0001t0003g0142 others(69): Show |
74 | HG00423.hp1 HG00609.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.748-824_748-819del others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | TCACACAC others(1): Show |
T | 77 | a0001c0001t0003g0230 a0001c0001t0005g0003 a0001c0001t0005g0016 others(74): Show |
79 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.748-826_748-819del others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725066 | TCACACAC others(5): Show |
T | 3 | a0001c0001t0005g0040 a0001c0001t0043g0204 a0001c0001t0043g0210 |
3 | HG00597.hp1 NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.748-830_748-819del others(12): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725066 | ||||||
chr11:35725068 | A | T | 7 | a0001c0001t0001g0105 a0001c0001t0010g0099 a0001c0001t0027g0100 others(4): Show |
7 | HG00544.hp1 HG01257.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-856A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725068 | |||||||
chr11:35725070 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.748-854A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725070 | |||||||
chr11:35725074 | A | T | 14 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(11): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.748-850A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725074 | |||||||
chr11:35725076 | A | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.748-848A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725076 | |||||||
chr11:35725078 | A | T | 1 | a0001c0001t0024g0273 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.748-846A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725078 | |||||||
chr11:35725098 | ACACACAC | A | 3 | a0001c0001t0005g0037 a0001c0001t0103g0095 a0001c0001t0110g0125 |
3 | HG01934.hp2 NA18946.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.748-824_748-818del others(7): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 35725098 | ||||||
chr11:35725104 | A | C | 1 | a0001c0001t0014g0097 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.748-820A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725104 | |||||||
chr11:35725304 | A | G | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-620A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725304 | |||||||
chr11:35725624 | C | T | 1 | a0001c0001t0015g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.748-300C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725624 | |||||||
chr11:35725746 | G | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-178G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725746 | |||||||
chr11:35725827 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-97A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725827 | |||||||
chr11:35725868 | C | A | 2 | a0001c0001t0041g0211 a0001c0001t0041g0212 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.748-56C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | chr11 | 35725868 | |||||||
chr11:35726473 | G | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.987+310G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35726473 | |||||||
chr11:35726541 | C | T | 7 | a0001c0001t0002g0352 a0001c0001t0002g0354 a0001c0001t0002g0355 others(4): Show |
7 | HG02056.hp2 NA18747.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+378C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35726541 | |||||||
chr11:35726683 | TA | T | 274 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(271): Show |
281 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.987+535delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 35726683 | ||||||
chr11:35726683 | TAA | T | 79 | a0001c0001t0001g0094 a0001c0001t0001g0124 a0001c0001t0001g0132 others(76): Show |
80 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.987+534_987+535del others(2): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 35726683 | ||||||
chr11:35726861 | T | TA | 40 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(37): Show |
40 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.987+709dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 35726861 | ||||||
chr11:35726897 | C | T | 5 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.987+734C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35726897 | |||||||
chr11:35727107 | G | A | 2 | a0001c0001t0033g0243 a0001c0001t0033g0244 |
2 | HG01109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.987+944G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727107 | |||||||
chr11:35727157 | C | CA | 27 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0002g0295 others(24): Show |
27 | HG00423.hp1 HG00738.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.987+1009dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 35727157 | ||||||
chr11:35727285 | A | G | 13 | a0001c0001t0006g0002 a0001c0001t0006g0071 a0001c0001t0006g0072 others(10): Show |
14 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.987+1122A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727285 | |||||||
chr11:35727297 | G | A | 66 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0122 others(63): Show |
67 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.987+1134G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727297 | |||||||
chr11:35727357 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.987+1194G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727357 | |||||||
chr11:35727522 | A | G | 4 | a0001c0001t0037g0253 a0001c0001t0037g0256 a0001c0001t0078g0242 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987+1359A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727522 | |||||||
chr11:35727648 | C | T | 1 | a0001c0001t0003g0219 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.987+1485C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727648 | |||||||
chr11:35727779 | C | A | 1 | a0001c0001t0002g0308 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.987+1616C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727779 | |||||||
chr11:35727808 | G | A | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.987+1645G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727808 | |||||||
chr11:35727908 | A | G | 1 | a0001c0001t0002g0354 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.987+1745A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35727908 | |||||||
chr11:35728012 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.987+1849G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728012 | |||||||
chr11:35728085 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0043 |
2 | HG00735.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.987+1922G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728085 | |||||||
chr11:35728091 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.987+1928C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728091 | |||||||
chr11:35728092 | G | A | 16 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(13): Show |
16 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.987+1929G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728092 | |||||||
chr11:35728162 | C | G | 87 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(84): Show |
89 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.987+1999C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728162 | |||||||
chr11:35728257 | T | C | 310 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(307): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.987+2094T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728257 | |||||||
chr11:35728362 | CTTTTA | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+2205_987+2209d others(7): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 35728362 | ||||||
chr11:35728500 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.987+2337A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728500 | |||||||
chr11:35728713 | A | G | 1 | a0003c0003t0008g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.987+2550A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728713 | |||||||
chr11:35728758 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.987+2595A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728758 | |||||||
chr11:35728793 | A | G | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+2630A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35728793 | |||||||
chr11:35729120 | A | G | 15 | a0001c0001t0004g0063 a0001c0001t0018g0372 a0001c0001t0018g0373 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.987+2957A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729120 | |||||||
chr11:35729208 | G | A | 4 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(1): Show |
4 | HG03486.hp2 HG03579.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.987+3045G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729208 | |||||||
chr11:35729217 | A | G | 131 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(128): Show |
135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.987+3054A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729217 | |||||||
chr11:35729240 | C | T | 1 | a0001c0001t0002g0329 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.987+3077C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729240 | |||||||
chr11:35729375 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.987+3212C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729375 | |||||||
chr11:35729381 | A | C | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.987+3218A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729381 | |||||||
chr11:35729406 | A | G | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.987+3243A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729406 | |||||||
chr11:35729570 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.987+3407A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729570 | |||||||
chr11:35729878 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.987+3715G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729878 | |||||||
chr11:35729950 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.987+3787A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35729950 | |||||||
chr11:35730055 | G | A | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.987+3892G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730055 | |||||||
chr11:35730062 | T | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.987+3899T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730062 | |||||||
chr11:35730202 | C | T | 1 | a0001c0001t0004g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.987+4039C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730202 | |||||||
chr11:35730231 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.987+4068G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730231 | |||||||
chr11:35730614 | T | A | 1 | a0001c0001t0036g0102 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.987+4451T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730614 | |||||||
chr11:35730698 | T | C | 3 | a0001c0001t0004g0082 a0001c0001t0004g0083 a0001c0001t0049g0080 |
3 | HG01168.hp1 HG01169.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.987+4535T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730698 | |||||||
chr11:35730714 | T | A | 1 | a0001c0001t0004g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.987+4551T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730714 | |||||||
chr11:35730736 | T | A | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.987+4573T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730736 | |||||||
chr11:35730851 | C | CT | 73 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0122 others(70): Show |
74 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.988-4557dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 35730851 | ||||||
chr11:35730851 | CT | C | 17 | a0001c0001t0002g0298 a0001c0001t0005g0023 a0001c0001t0005g0040 others(14): Show |
17 | HG01109.hp1 HG01943.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.988-4557delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 35730851 | ||||||
chr11:35730888 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-4538C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730888 | |||||||
chr11:35730889 | G | A | 42 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(39): Show |
44 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.988-4537G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730889 | |||||||
chr11:35730987 | C | T | 1 | a0001c0001t0007g0201 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.988-4439C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35730987 | |||||||
chr11:35731423 | G | A | 2 | a0001c0001t0037g0253 a0001c0001t0079g0252 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.988-4003G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35731423 | |||||||
chr11:35731442 | A | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.988-3984A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35731442 | |||||||
chr11:35731446 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0043 |
2 | HG00735.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.988-3980T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35731446 | |||||||
chr11:35731926 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-3500G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35731926 | |||||||
chr11:35731953 | C | T | 4 | a0001c0001t0002g0340 a0001c0001t0089g0343 a0001c0001t0092g0339 others(1): Show |
4 | HG01255.hp1 HG03239.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-3473C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35731953 | |||||||
chr11:35731963 | A | G | 99 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(96): Show |
100 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.988-3463A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35731963 | |||||||
chr11:35732186 | T | C | 1 | a0003c0003t0008g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.988-3240T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35732186 | |||||||
chr11:35732269 | G | T | 1 | a0001c0001t0086g0374 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.988-3157G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35732269 | |||||||
chr11:35732386 | G | A | 7 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0226 others(4): Show |
7 | HG02071.hp1 NA18957.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-3040G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35732386 | |||||||
chr11:35732641 | A | G | 40 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(37): Show |
40 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.988-2785A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35732641 | |||||||
chr11:35732828 | G | A | 1 | a0001c0001t0014g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.988-2598G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35732828 | |||||||
chr11:35732916 | A | G | 42 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(39): Show |
44 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.988-2510A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35732916 | |||||||
chr11:35733211 | T | G | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.988-2215T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733211 | |||||||
chr11:35733220 | T | A | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.988-2206T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733220 | |||||||
chr11:35733449 | A | T | 1 | a0001c0001t0109g0194 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.988-1977A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733449 | |||||||
chr11:35733482 | T | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-1944T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733482 | |||||||
chr11:35733563 | C | A | 31 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.988-1863C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733563 | |||||||
chr11:35733566 | A | G | 101 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(98): Show |
102 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.988-1860A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733566 | |||||||
chr11:35733652 | C | T | 1 | a0001c0001t0006g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.988-1774C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733652 | |||||||
chr11:35733759 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0064g0144 |
2 | HG01099.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.988-1667A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733759 | |||||||
chr11:35733794 | G | A | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.988-1632G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35733794 | |||||||
chr11:35734457 | G | A | 5 | a0001c0001t0006g0072 a0001c0001t0006g0073 a0001c0001t0006g0074 others(2): Show |
5 | HG02148.hp1 NA18952.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-969G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35734457 | |||||||
chr11:35734519 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-907G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35734519 | |||||||
chr11:35734840 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.988-586A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35734840 | |||||||
chr11:35734859 | A | G | 1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.988-567A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35734859 | |||||||
chr11:35734891 | C | T | 2 | a0001c0001t0040g0012 a0001c0001t0040g0013 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.988-535C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35734891 | |||||||
chr11:35734905 | G | C | 17 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.988-521G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35734905 | |||||||
chr11:35735089 | G | C | 202 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(199): Show |
206 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.988-337G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35735089 | |||||||
chr11:35735193 | C | T | 1 | a0001c0001t0024g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.988-233C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35735193 | |||||||
chr11:35735269 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-157C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35735269 | |||||||
chr11:35735369 | G | A | 1 | a0001c0001t0008g0307 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.988-57G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | chr11 | 35735369 | |||||||
chr11:35735593 | G | A | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1007+148G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35735593 | |||||||
chr11:35735751 | T | C | 1 | a0001c0001t0039g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1007+306T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35735751 | |||||||
chr11:35735803 | G | T | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1007+358G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35735803 | |||||||
chr11:35736121 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+676G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736121 | |||||||
chr11:35736122 | T | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+677T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736122 | |||||||
chr11:35736356 | A | G | 381 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(378): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.1007+911A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736356 | |||||||
chr11:35736472 | C | T | 1 | a0001c0001t0019g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1007+1027C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736472 | |||||||
chr11:35736592 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1007+1147G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736592 | |||||||
chr11:35736604 | C | T | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1007+1159C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736604 | |||||||
chr11:35736799 | A | G | 3 | a0001c0001t0010g0167 a0001c0001t0065g0166 a0001c0001t0102g0169 |
3 | HG02027.hp2 NA18978.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1007+1354A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736799 | |||||||
chr11:35736975 | C | G | 1 | a0001c0001t0084g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1007+1530C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35736975 | |||||||
chr11:35737077 | T | G | 1 | a0001c0001t0023g0229 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1007+1632T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35737077 | |||||||
chr11:35737384 | C | T | 10 | a0001c0001t0002g0008 a0001c0001t0002g0322 a0001c0001t0002g0336 others(7): Show |
11 | HG00621.hp2 NA18943.hp1 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.1007+1939C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35737384 | |||||||
chr11:35737574 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+2129G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35737574 | |||||||
chr11:35737576 | C | T | 7 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0156 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007+2131C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35737576 | |||||||
chr11:35737785 | G | A | 9 | a0001c0001t0014g0097 a0001c0001t0014g0111 a0001c0001t0014g0120 others(6): Show |
9 | HG01884.hp2 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1007+2340G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35737785 | |||||||
chr11:35737958 | A | C | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+2513A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35737958 | |||||||
chr11:35738176 | C | T | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1007+2731C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738176 | |||||||
chr11:35738213 | G | T | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+2768G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738213 | |||||||
chr11:35738265 | C | T | 1 | a0001c0001t0005g0036 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1007+2820C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738265 | |||||||
chr11:35738321 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+2876C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738321 | |||||||
chr11:35738340 | A | G | 32 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1007+2895A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738340 | |||||||
chr11:35738354 | C | T | 5 | a0001c0001t0014g0103 a0001c0001t0014g0104 a0001c0001t0036g0106 others(2): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+2909C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738354 | |||||||
chr11:35738363 | T | TCTTTA | 64 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(61): Show |
64 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.1007+2921_1007+292 others(9): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35738363 | ||||||
chr11:35738401 | G | A | 43 | a0001c0001t0004g0014 a0001c0001t0004g0055 a0001c0001t0004g0056 others(40): Show |
44 | HG00423.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1007+2956G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738401 | |||||||
chr11:35738411 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+2966G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738411 | |||||||
chr11:35738412 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+2967A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738412 | |||||||
chr11:35738512 | G | T | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+3067G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738512 | |||||||
chr11:35738793 | G | A | 1 | a0001c0001t0022g0286 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1007+3348G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738793 | |||||||
chr11:35738810 | G | T | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+3365G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738810 | |||||||
chr11:35738832 | G | A | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007+3387G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738832 | |||||||
chr11:35738893 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1007+3448C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738893 | |||||||
chr11:35738910 | C | G | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1007+3465C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35738910 | |||||||
chr11:35739191 | A | G | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1007+3746A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35739191 | |||||||
chr11:35739401 | T | A | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1007+3956T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35739401 | |||||||
chr11:35739565 | C | T | 6 | a0001c0001t0007g0189 a0001c0001t0020g0126 a0001c0001t0020g0127 others(3): Show |
6 | HG00099.hp1 HG02559.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007+4120C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35739565 | |||||||
chr11:35740096 | T | TA | 84 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0001g0145 others(81): Show |
84 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1007+4674dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35740096 | ||||||
chr11:35740096 | T | TAA | 6 | a0001c0001t0005g0016 a0001c0001t0005g0019 a0001c0001t0005g0045 others(3): Show |
6 | NA18965.hp2 NA18980.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+4673_1007+467 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35740096 | ||||||
chr11:35740096 | TA | T | 34 | a0001c0001t0002g0330 a0001c0001t0007g0004 a0001c0001t0007g0143 others(31): Show |
35 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.1007+4674delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35740096 | ||||||
chr11:35740119 | A | AC | 10 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(7): Show |
11 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1007+4674_1007+467 others(5): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35740119 | |||||||
chr11:35740142 | A | AT | 14 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0226 others(11): Show |
14 | HG02071.hp1 HG02109.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+4711dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35740142 | ||||||
chr11:35740142 | AT | A | 32 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1007+4711delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35740142 | ||||||
chr11:35740142 | ATT | A | 7 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0156 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007+4710_1007+471 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35740142 | ||||||
chr11:35740506 | T | C | 40 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(37): Show |
40 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1007+5061T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35740506 | |||||||
chr11:35740692 | G | C | 1 | a0001c0001t0003g0226 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1007+5247G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35740692 | |||||||
chr11:35740774 | C | G | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+5329C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35740774 | |||||||
chr11:35740777 | C | T | 1 | a0001c0001t0005g0036 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1007+5332C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35740777 | |||||||
chr11:35740827 | A | C | 1 | a0001c0001t0009g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1007+5382A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35740827 | |||||||
chr11:35740875 | T | G | 2 | a0001c0001t0006g0074 a0001c0001t0006g0075 |
2 | NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1007+5430T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35740875 | |||||||
chr11:35741203 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+5758C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35741203 | |||||||
chr11:35741437 | C | T | 1 | a0001c0001t0090g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1007+5992C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35741437 | |||||||
chr11:35741589 | G | C | 1 | a0001c0001t0014g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1007+6144G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35741589 | |||||||
chr11:35741741 | C | T | 7 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
7 | HG00621.hp1 HG02015.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1007+6296C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35741741 | |||||||
chr11:35741803 | C | T | 1 | a0001c0001t0095g0300 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1007+6358C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35741803 | |||||||
chr11:35741804 | G | A | 2 | a0001c0001t0042g0258 a0001c0001t0042g0261 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1007+6359G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35741804 | |||||||
chr11:35741993 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1007+6548C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35741993 | |||||||
chr11:35742317 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0105 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1007+6872C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742317 | |||||||
chr11:35742368 | G | GAT | 24 | a0001c0001t0004g0014 a0001c0001t0004g0058 a0001c0001t0004g0059 others(21): Show |
25 | HG00423.hp1 HG01891.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.1007+6936_1007+693 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742368 | ||||||
chr11:35742368 | G | GATAT | 4 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0285 others(1): Show |
4 | HG01074.hp2 HG01192.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+6934_1007+693 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742368 | ||||||
chr11:35742437 | A | G | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1007+6992A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742437 | |||||||
chr11:35742442 | A | AAATATAA others(17): Show |
1 | a0001c0001t0039g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1007+7016_1007+703 others(28): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742442 | ||||||
chr11:35742472 | AATT | A | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1007+7030_1007+703 others(7): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742472 | ||||||
chr11:35742491 | TATATAAT others(8): Show |
T | 1 | a0001c0001t0001g0165 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1007+7062_1007+707 others(19): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742491 | ||||||
chr11:35742509 | A | ATAATTAT others(26): Show |
6 | a0001c0001t0002g0350 a0001c0001t0004g0086 a0001c0001t0015g0282 others(3): Show |
6 | HG01261.hp1 HG02300.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007+7150_1007+718 others(37): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742509 | ||||||
chr11:35742526 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1007+7081A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742526 | |||||||
chr11:35742533 | ATAATTAT others(2): Show |
A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+7103_1007+711 others(13): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742533 | ||||||
chr11:35742542 | T | TTAAATA | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1007+7100_1007+710 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742542 | ||||||
chr11:35742600 | T | C | 2 | a0001c0001t0021g0366 a0001c0001t0021g0367 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1007+7155T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742600 | |||||||
chr11:35742627 | T | TTTATATA others(17): Show |
1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1007+7226_1007+724 others(28): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742627 | ||||||
chr11:35742672 | TGTA | T | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1007+7228_1007+723 others(7): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742672 | |||||||
chr11:35742675 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00544.hp1 HG02523.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+7230A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742675 | |||||||
chr11:35742704 | T | A | 1 | a0002c0002t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1007+7259T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742704 | |||||||
chr11:35742734 | A | C | 2 | a0001c0001t0020g0126 a0001c0001t0020g0128 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1007+7289A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742734 | |||||||
chr11:35742773 | TAC | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+7330_1007+733 others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742773 | ||||||
chr11:35742775 | C | T | 196 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(193): Show |
200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1007+7330C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742775 | |||||||
chr11:35742780 | A | C | 1 | a0001c0001t0005g0020 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1007+7335A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742780 | |||||||
chr11:35742792 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1007+7347A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35742792 | |||||||
chr11:35742798 | A | ATAT | 381 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(378): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(386): Show |
intron_variant | MODIFIER | c.1007+7354_1007+735 others(7): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742798 | ||||||
chr11:35742846 | ATAT | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+7406_1007+740 others(7): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35742846 | ||||||
chr11:35743139 | A | G | 4 | a0001c0001t0037g0253 a0001c0001t0037g0256 a0001c0001t0078g0242 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+7694A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35743139 | |||||||
chr11:35743305 | C | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+7860C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35743305 | |||||||
chr11:35743319 | G | A | 59 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(56): Show |
59 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1007+7874G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35743319 | |||||||
chr11:35743325 | C | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+7880C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35743325 | |||||||
chr11:35743586 | G | A | 11 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0076 others(8): Show |
11 | HG00733.hp1 HG01255.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007+8141G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35743586 | |||||||
chr11:35743662 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0008g0324 |
2 | HG00733.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1007+8217G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35743662 | |||||||
chr11:35743881 | T | C | 3 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0062g0259 |
3 | HG02109.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1007+8436T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35743881 | |||||||
chr11:35744649 | C | T | 1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1007+9204C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35744649 | |||||||
chr11:35744874 | T | C | 1 | a0001c0001t0070g0161 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1007+9429T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35744874 | |||||||
chr11:35744937 | A | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+9492A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35744937 | |||||||
chr11:35745165 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+9720G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35745165 | |||||||
chr11:35745322 | T | C | 1 | a0001c0001t0039g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1007+9877T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35745322 | |||||||
chr11:35745678 | G | T | 1 | a0001c0001t0029g0291 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1007+10233G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35745678 | |||||||
chr11:35745944 | A | C | 2 | a0001c0001t0040g0012 a0001c0001t0040g0013 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1007+10499A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35745944 | |||||||
chr11:35745990 | G | C | 3 | a0001c0001t0003g0215 a0001c0001t0003g0230 a0001c0001t0054g0234 |
3 | HG02132.hp1 NA19002.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1007+10545G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35745990 | |||||||
chr11:35746143 | G | A | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1007+10698G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746143 | |||||||
chr11:35746150 | T | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+10705T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746150 | |||||||
chr11:35746436 | G | T | 1 | a0001c0001t0005g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1007+10991G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746436 | |||||||
chr11:35746446 | C | CT | 38 | a0001c0001t0003g0214 a0001c0001t0003g0225 a0001c0001t0003g0228 others(35): Show |
39 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1007+11023dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35746446 | ||||||
chr11:35746446 | C | CTT | 74 | a0001c0001t0001g0117 a0001c0001t0002g0007 a0001c0001t0002g0294 others(71): Show |
75 | HG00280.hp2 HG00408.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.1007+11022_1007+11 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35746446 | ||||||
chr11:35746446 | C | CTTT | 161 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(158): Show |
165 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1007+11021_1007+11 others(9): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35746446 | ||||||
chr11:35746446 | C | CTTTT | 31 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(28): Show |
31 | HG00544.hp2 HG00558.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1007+11020_1007+11 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35746446 | ||||||
chr11:35746610 | C | T | 8 | a0001c0001t0001g0053 a0001c0001t0001g0105 a0001c0001t0020g0126 others(5): Show |
8 | HG02559.hp1 HG02896.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007+11165C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746610 | |||||||
chr11:35746665 | T | A | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007+11220T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746665 | |||||||
chr11:35746711 | G | A | 1 | a0001c0001t0086g0374 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1007+11266G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746711 | |||||||
chr11:35746867 | A | G | 1 | a0001c0001t0035g0021 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1007+11422A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746867 | |||||||
chr11:35746908 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+11463G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35746908 | |||||||
chr11:35747018 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1007+11573A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747018 | |||||||
chr11:35747030 | G | T | 1 | a0001c0001t0029g0291 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1007+11585G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747030 | |||||||
chr11:35747228 | A | G | 1 | a0001c0001t0023g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1007+11783A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747228 | |||||||
chr11:35747242 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1007+11797A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747242 | |||||||
chr11:35747611 | T | G | 1 | a0001c0001t0055g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1007+12166T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747611 | |||||||
chr11:35747637 | TTGTC | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+12195_1007+12 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35747637 | ||||||
chr11:35747687 | G | A | 1 | a0001c0001t0014g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1007+12242G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747687 | |||||||
chr11:35747704 | C | A | 4 | a0001c0001t0009g0265 a0001c0001t0009g0268 a0001c0001t0009g0278 others(1): Show |
4 | HG03130.hp2 HG03516.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+12259C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747704 | |||||||
chr11:35747819 | C | T | 34 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(31): Show |
35 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.1007+12374C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747819 | |||||||
chr11:35747880 | C | T | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1007+12435C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747880 | |||||||
chr11:35747924 | G | C | 1 | a0001c0001t0090g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1007+12479G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747924 | |||||||
chr11:35747943 | C | T | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1007+12498C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35747943 | |||||||
chr11:35748449 | C | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+13004C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35748449 | |||||||
chr11:35748493 | C | G | 2 | a0001c0001t0001g0152 a0001c0001t0064g0144 |
2 | HG01099.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1007+13048C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35748493 | |||||||
chr11:35749324 | T | TAGAAAAT others(328): Show |
1 | a0001c0001t0002g0350 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1007+13893_1007+13 others(341): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35749324 | ||||||
chr11:35749489 | A | C | 1 | a0001c0001t0004g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1007+14044A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35749489 | |||||||
chr11:35750087 | C | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+14642C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750087 | |||||||
chr11:35750263 | A | G | 1 | a0001c0001t0019g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1007+14818A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750263 | |||||||
chr11:35750330 | C | T | 14 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+14885C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750330 | |||||||
chr11:35750403 | T | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+14958T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750403 | |||||||
chr11:35750408 | G | A | 79 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1007+14963G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750408 | |||||||
chr11:35750525 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1007+15080T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750525 | |||||||
chr11:35750591 | G | A | 1 | a0001c0001t0055g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1007+15146G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750591 | |||||||
chr11:35750676 | C | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+15231C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750676 | |||||||
chr11:35750698 | G | A | 36 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(33): Show |
37 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.1007+15253G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750698 | |||||||
chr11:35750888 | G | A | 1 | a0001c0001t0029g0291 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1007+15443G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35750888 | |||||||
chr11:35750971 | TA | T | 66 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0122 others(63): Show |
67 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1007+15532delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35750971 | ||||||
chr11:35751030 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0064g0144 |
2 | HG01099.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1007+15585T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35751030 | |||||||
chr11:35751045 | T | C | 1 | a0001c0001t0010g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1007+15600T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35751045 | |||||||
chr11:35751098 | C | T | 1 | a0001c0001t0004g0380 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1007+15653C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35751098 | |||||||
chr11:35751108 | A | C | 2 | a0001c0001t0023g0224 a0001c0001t0023g0229 |
2 | HG02056.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1007+15663A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35751108 | |||||||
chr11:35751198 | A | C | 1 | a0001c0001t0013g0041 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1007+15753A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35751198 | |||||||
chr11:35751580 | C | T | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+16135C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35751580 | |||||||
chr11:35751647 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1007+16202G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35751647 | |||||||
chr11:35752041 | A | G | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+16596A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35752041 | |||||||
chr11:35752152 | C | CT | 32 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(29): Show |
32 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1007+16718dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35752152 | ||||||
chr11:35752497 | C | T | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1007+17052C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35752497 | |||||||
chr11:35752588 | C | T | 3 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0062g0259 |
3 | HG02109.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1007+17143C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35752588 | |||||||
chr11:35752664 | C | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+17219C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35752664 | |||||||
chr11:35752973 | A | G | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+17528A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35752973 | |||||||
chr11:35752998 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0105 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1007+17553A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35752998 | |||||||
chr11:35753064 | C | G | 168 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(165): Show |
171 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1007+17619C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35753064 | |||||||
chr11:35753205 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1007+17760G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35753205 | |||||||
chr11:35753206 | G | T | 1 | a0001c0001t0029g0290 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1007+17761G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35753206 | |||||||
chr11:35753320 | C | G | 43 | a0001c0001t0004g0014 a0001c0001t0004g0055 a0001c0001t0004g0056 others(40): Show |
44 | HG00423.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1007+17875C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35753320 | |||||||
chr11:35753617 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1007+18172G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35753617 | |||||||
chr11:35753683 | A | T | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+18238A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35753683 | |||||||
chr11:35753782 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0117 a0001c0001t0075g0114 |
3 | HG00639.hp1 HG01169.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1007+18337G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35753782 | |||||||
chr11:35754047 | TAAAAAAA others(7): Show |
T | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1007+18608_1007+18 others(20): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35754047 | ||||||
chr11:35754102 | TACTAA | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+18658_1007+18 others(11): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754102 | |||||||
chr11:35754118 | T | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+18673T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754118 | |||||||
chr11:35754192 | G | T | 380 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(377): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1007+18747G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754192 | |||||||
chr11:35754264 | C | A | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+18819C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754264 | |||||||
chr11:35754265 | A | G | 260 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(257): Show |
265 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1007+18820A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754265 | |||||||
chr11:35754301 | G | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+18856G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754301 | |||||||
chr11:35754377 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1007+18932C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754377 | |||||||
chr11:35754378 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+18933G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754378 | |||||||
chr11:35754457 | C | T | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1007+19012C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754457 | |||||||
chr11:35754475 | G | A | 2 | a0001c0001t0017g0199 a0001c0001t0110g0125 |
2 | NA18946.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1007+19030G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754475 | |||||||
chr11:35754510 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1007+19065T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754510 | |||||||
chr11:35754597 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1007+19152T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754597 | |||||||
chr11:35754598 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1007+19153G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754598 | |||||||
chr11:35754604 | A | G | 1 | a0001c0001t0006g0009 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1007+19159A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754604 | |||||||
chr11:35754654 | C | G | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG02451.hp2 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+19209C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754654 | |||||||
chr11:35754751 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0042g0258 a0001c0001t0064g0144 |
3 | HG01099.hp2 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1007+19306G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754751 | |||||||
chr11:35754803 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+19358C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754803 | |||||||
chr11:35754975 | G | A | 3 | a0001c0001t0003g0215 a0001c0001t0003g0230 a0001c0001t0054g0234 |
3 | HG02132.hp1 NA19002.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1007+19530G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754975 | |||||||
chr11:35754999 | T | C | 1 | a0001c0001t0025g0026 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1007+19554T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35754999 | |||||||
chr11:35755036 | G | A | 2 | a0001c0001t0080g0379 a0001c0001t0087g0378 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1007+19591G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755036 | |||||||
chr11:35755044 | G | A | 79 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1007+19599G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755044 | |||||||
chr11:35755100 | G | A | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.1007+19655G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755100 | |||||||
chr11:35755246 | C | T | 4 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(1): Show |
4 | HG00738.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+19801C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755246 | |||||||
chr11:35755247 | A | G | 4 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(1): Show |
4 | HG00738.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+19802A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755247 | |||||||
chr11:35755257 | A | G | 4 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(1): Show |
4 | HG00738.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+19812A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755257 | |||||||
chr11:35755283 | G | T | 1 | a0001c0001t0012g0360 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1007+19838G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755283 | |||||||
chr11:35755310 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1007+19865G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755310 | |||||||
chr11:35755356 | GT | G | 79 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1007+19918delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35755356 | ||||||
chr11:35755410 | T | C | 4 | a0001c0001t0005g0003 a0001c0001t0005g0045 a0001c0001t0005g0047 others(1): Show |
4 | NA18966.hp1 NA18999.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+19965T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755410 | |||||||
chr11:35755470 | G | T | 294 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1007+20025G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755470 | |||||||
chr11:35755581 | T | C | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1007+20136T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755581 | |||||||
chr11:35755685 | G | A | 7 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0156 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007+20240G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755685 | |||||||
chr11:35755728 | T | G | 4 | a0001c0001t0009g0265 a0001c0001t0009g0268 a0001c0001t0009g0278 others(1): Show |
4 | HG03130.hp2 HG03516.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+20283T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755728 | |||||||
chr11:35755791 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+20346G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755791 | |||||||
chr11:35755798 | A | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+20353A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755798 | |||||||
chr11:35755820 | T | C | 260 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(257): Show |
265 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1007+20375T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755820 | |||||||
chr11:35755823 | G | A | 1 | a0001c0001t0004g0076 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1007+20378G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755823 | |||||||
chr11:35755858 | G | A | 1 | a0001c0001t0002g0322 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1007+20413G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755858 | |||||||
chr11:35755919 | A | T | 2 | a0001c0001t0041g0211 a0001c0001t0041g0212 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1007+20474A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755919 | |||||||
chr11:35755936 | C | T | 3 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0285 |
3 | HG01074.hp2 HG01192.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1007+20491C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755936 | |||||||
chr11:35755985 | T | C | 32 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(29): Show |
33 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1007+20540T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755985 | |||||||
chr11:35755986 | G | A | 32 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(29): Show |
33 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1007+20541G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35755986 | |||||||
chr11:35756090 | T | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+20645T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756090 | |||||||
chr11:35756360 | C | G | 4 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(1): Show |
4 | HG03486.hp2 HG03579.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+20915C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756360 | |||||||
chr11:35756386 | C | G | 2 | a0001c0001t0009g0267 a0001c0001t0009g0270 |
2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1007+20941C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756386 | |||||||
chr11:35756387 | A | G | 2 | a0001c0001t0009g0267 a0001c0001t0009g0270 |
2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1007+20942A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756387 | |||||||
chr11:35756486 | A | T | 1 | a0001c0001t0005g0035 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1007+21041A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756486 | |||||||
chr11:35756499 | A | C | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.1007+21054A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756499 | |||||||
chr11:35756621 | A | G | 2 | a0001c0001t0002g0007 a0001c0001t0093g0297 |
3 | HG00408.hp2 HG02071.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1007+21176A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756621 | |||||||
chr11:35756633 | G | A | 1 | a0001c0001t0088g0137 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1007+21188G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756633 | |||||||
chr11:35756779 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+21334G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756779 | |||||||
chr11:35756796 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+21351G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756796 | |||||||
chr11:35756807 | T | G | 1 | a0001c0001t0063g0048 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1007+21362T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756807 | |||||||
chr11:35756891 | T | A | 1 | a0001c0001t0063g0048 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1007+21446T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756891 | |||||||
chr11:35756932 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1007+21487G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35756932 | |||||||
chr11:35757053 | G | A | 2 | a0001c0001t0002g0350 a0001c0001t0095g0300 |
2 | HG01361.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1007+21608G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757053 | |||||||
chr11:35757236 | C | T | 1 | a0001c0001t0070g0161 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1007+21791C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757236 | |||||||
chr11:35757371 | C | T | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1007+21926C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757371 | |||||||
chr11:35757372 | G | A | 2 | a0001c0001t0015g0283 a0001c0001t0055g0255 |
2 | HG02723.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1007+21927G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757372 | |||||||
chr11:35757552 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+22107G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757552 | |||||||
chr11:35757592 | G | A | 1 | a0001c0001t0005g0017 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1007+22147G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757592 | |||||||
chr11:35757639 | G | A | 40 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1007+22194G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757639 | |||||||
chr11:35757668 | G | A | 3 | a0001c0001t0003g0215 a0001c0001t0003g0230 a0001c0001t0054g0234 |
3 | HG02132.hp1 NA19002.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1007+22223G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757668 | |||||||
chr11:35757805 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+22360G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757805 | |||||||
chr11:35757828 | T | C | 10 | a0001c0001t0005g0020 a0001c0001t0005g0032 a0001c0001t0005g0033 others(7): Show |
10 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1007+22383T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757828 | |||||||
chr11:35757873 | A | G | 42 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(39): Show |
44 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1007+22428A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757873 | |||||||
chr11:35757885 | C | A | 1 | a0001c0001t0003g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1007+22440C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757885 | |||||||
chr11:35757910 | T | G | 32 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1007+22465T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757910 | |||||||
chr11:35757947 | A | G | 41 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(38): Show |
41 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.1007+22502A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35757947 | |||||||
chr11:35758051 | G | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+22606G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758051 | |||||||
chr11:35758148 | T | G | 295 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(292): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1007+22703T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758148 | |||||||
chr11:35758216 | G | C | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1007+22771G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758216 | |||||||
chr11:35758247 | TATGTA | T | 4 | a0001c0001t0002g0340 a0001c0001t0089g0343 a0001c0001t0092g0339 others(1): Show |
4 | HG01255.hp1 HG03239.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+22806_1007+22 others(11): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35758247 | ||||||
chr11:35758391 | G | A | 1 | a0001c0001t0037g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1007+22946G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758391 | |||||||
chr11:35758432 | A | G | 2 | a0001c0001t0007g0189 a0001c0001t0107g0200 |
2 | HG00099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1007+22987A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758432 | |||||||
chr11:35758482 | G | A | 4 | a0001c0001t0024g0273 a0001c0001t0038g0275 a0001c0001t0038g0276 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+23037G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758482 | |||||||
chr11:35758492 | C | T | 1 | a0001c0001t0003g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1007+23047C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758492 | |||||||
chr11:35758682 | TAGGGC | T | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+23241_1007+23 others(11): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35758682 | ||||||
chr11:35758761 | C | G | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1007+23316C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758761 | |||||||
chr11:35758819 | G | A | 16 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(13): Show |
17 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1007+23374G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758819 | |||||||
chr11:35758931 | C | T | 1 | a0001c0001t0002g0327 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1007+23486C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758931 | |||||||
chr11:35758961 | C | T | 2 | a0001c0001t0005g0032 a0001c0001t0005g0037 |
2 | HG01361.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1007+23516C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758961 | |||||||
chr11:35758989 | C | G | 1 | a0001c0001t0078g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1007+23544C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35758989 | |||||||
chr11:35759019 | T | C | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1007+23574T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759019 | |||||||
chr11:35759035 | G | C | 1 | a0001c0001t0014g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1007+23590G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759035 | |||||||
chr11:35759063 | G | T | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1007+23618G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759063 | |||||||
chr11:35759091 | G | A | 1 | a0001c0001t0075g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1007+23646G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759091 | |||||||
chr11:35759191 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1007+23746G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759191 | |||||||
chr11:35759681 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+24236G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759681 | |||||||
chr11:35759692 | T | G | 1 | a0001c0001t0108g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1007+24247T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759692 | |||||||
chr11:35759901 | C | A | 1 | a0001c0001t0010g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1007+24456C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759901 | |||||||
chr11:35759913 | G | T | 1 | a0001c0001t0010g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1007+24468G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759913 | |||||||
chr11:35759916 | G | A | 1 | a0001c0001t0105g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1007+24471G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35759916 | |||||||
chr11:35760161 | G | A | 1 | a0001c0001t0005g0035 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1007+24716G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760161 | |||||||
chr11:35760184 | C | A | 1 | a0001c0001t0055g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1007+24739C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760184 | |||||||
chr11:35760184 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1007+24739C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760184 | |||||||
chr11:35760275 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+24830C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760275 | |||||||
chr11:35760287 | C | T | 2 | a0001c0001t0031g0236 a0001c0001t0046g0235 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1007+24842C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760287 | |||||||
chr11:35760464 | C | T | 4 | a0001c0001t0007g0195 a0001c0001t0007g0209 a0001c0001t0007g0239 others(1): Show |
4 | HG01175.hp2 HG01981.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+25019C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760464 | |||||||
chr11:35760563 | A | G | 1 | a0001c0001t0002g0359 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1007+25118A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760563 | |||||||
chr11:35760622 | C | A | 1 | a0001c0001t0003g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1007+25177C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760622 | |||||||
chr11:35760636 | C | G | 1 | a0001c0001t0073g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1007+25191C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760636 | |||||||
chr11:35760665 | T | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+25220T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760665 | |||||||
chr11:35760734 | A | T | 380 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(377): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1007+25289A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760734 | |||||||
chr11:35760779 | T | C | 2 | a0001c0001t0001g0151 a0002c0002t0001g0150 |
2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1007+25334T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760779 | |||||||
chr11:35760823 | T | G | 70 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0122 others(67): Show |
71 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1007+25378T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760823 | |||||||
chr11:35760848 | A | G | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1007+25403A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35760848 | |||||||
chr11:35761236 | G | C | 6 | a0001c0001t0002g0008 a0001c0001t0002g0322 a0001c0001t0002g0336 others(3): Show |
7 | NA18944.hp1 NA18955.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007+25791G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35761236 | |||||||
chr11:35761362 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+25917A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35761362 | |||||||
chr11:35761388 | G | GCT | 10 | a0001c0001t0001g0098 a0001c0001t0002g0303 a0001c0001t0006g0074 others(7): Show |
10 | HG02129.hp2 HG02145.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1007+25960_1007+25 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761388 | ||||||
chr11:35761388 | G | GCTCT | 4 | a0001c0001t0001g0122 a0001c0001t0001g0165 a0001c0001t0001g0186 others(1): Show |
4 | HG00438.hp1 HG00558.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+25958_1007+25 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761388 | ||||||
chr11:35761401 | C | A | 1 | a0001c0001t0037g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1007+25956C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35761401 | |||||||
chr11:35761401 | C | CTA | 28 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0223 others(25): Show |
28 | HG00423.hp1 HG00733.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1007+25957_1007+25 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761401 | ||||||
chr11:35761403 | C | A | 29 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0223 others(26): Show |
29 | HG00423.hp1 HG00733.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1007+25958C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35761403 | |||||||
chr11:35761403 | C | CTA | 69 | a0001c0001t0002g0352 a0001c0001t0003g0141 a0001c0001t0003g0142 others(66): Show |
72 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1007+25959_1007+25 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761403 | ||||||
chr11:35761405 | C | A | 99 | a0001c0001t0002g0352 a0001c0001t0003g0015 a0001c0001t0003g0141 others(96): Show |
102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1007+25960C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35761405 | |||||||
chr11:35761405 | C | CTA | 190 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(187): Show |
194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1007+25970_1007+25 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761405 | ||||||
chr11:35761405 | C | CTATA | 28 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0148 others(25): Show |
28 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.1007+25968_1007+25 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761405 | ||||||
chr11:35761405 | C | CTCTA | 37 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0123 others(34): Show |
38 | HG00621.hp1 HG00738.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.1007+25961_1007+25 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761405 | ||||||
chr11:35761405 | C | CTG | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+25961_1007+25 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35761405 | ||||||
chr11:35762118 | T | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+26673T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762118 | |||||||
chr11:35762123 | G | A | 1 | a0001c0001t0019g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1007+26678G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762123 | |||||||
chr11:35762204 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1007+26759G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762204 | |||||||
chr11:35762485 | T | C | 1 | a0001c0001t0005g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1007+27040T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762485 | |||||||
chr11:35762491 | C | T | 4 | a0001c0001t0019g0092 a0001c0001t0019g0191 a0001c0001t0019g0192 others(1): Show |
4 | HG01975.hp1 HG01993.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+27046C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762491 | |||||||
chr11:35762543 | T | C | 1 | a0001c0001t0011g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1007+27098T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762543 | |||||||
chr11:35762607 | T | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+27162T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762607 | |||||||
chr11:35762714 | C | A | 1 | a0001c0001t0003g0222 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1007+27269C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762714 | |||||||
chr11:35762736 | T | C | 2 | a0001c0001t0015g0283 a0001c0001t0015g0284 |
2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1007+27291T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762736 | |||||||
chr11:35762759 | G | A | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1007+27314G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35762759 | |||||||
chr11:35762817 | AAACTATT others(15): Show |
A | 1 | a0001c0001t0106g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1007+27386_1007+27 others(28): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35762817 | ||||||
chr11:35763570 | T | G | 5 | a0001c0001t0014g0103 a0001c0001t0014g0104 a0001c0001t0036g0106 others(2): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+28125T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35763570 | |||||||
chr11:35763689 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+28244G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35763689 | |||||||
chr11:35764315 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1007+28870A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764315 | |||||||
chr11:35764451 | T | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+29006T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764451 | |||||||
chr11:35764633 | G | A | 1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1007+29188G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764633 | |||||||
chr11:35764667 | C | A | 8 | a0001c0001t0012g0001 a0001c0001t0012g0317 a0001c0001t0012g0318 others(5): Show |
9 | HG02027.hp1 HG02135.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007+29222C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764667 | |||||||
chr11:35764709 | C | T | 79 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1007+29264C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764709 | |||||||
chr11:35764885 | A | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+29440A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764885 | |||||||
chr11:35764926 | T | A | 1 | a0001c0001t0021g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1007+29481T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764926 | |||||||
chr11:35764927 | A | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1007+29482A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764927 | |||||||
chr11:35764965 | A | G | 50 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(47): Show |
52 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1007+29520A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35764965 | |||||||
chr11:35765032 | C | T | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1007+29587C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765032 | |||||||
chr11:35765046 | T | A | 1 | a0001c0001t0014g0097 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1007+29601T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765046 | |||||||
chr11:35765195 | C | T | 1 | a0001c0001t0008g0331 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1007+29750C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765195 | |||||||
chr11:35765451 | G | A | 1 | a0001c0001t0008g0301 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1007+30006G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765451 | |||||||
chr11:35765750 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+30305T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765750 | |||||||
chr11:35765756 | CATTT | C | 43 | a0001c0001t0004g0014 a0001c0001t0004g0055 a0001c0001t0004g0056 others(40): Show |
44 | HG00423.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1007+30312_1007+30 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765756 | |||||||
chr11:35765793 | A | G | 4 | a0001c0001t0024g0273 a0001c0001t0038g0275 a0001c0001t0038g0276 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+30348A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765793 | |||||||
chr11:35765933 | A | G | 42 | a0001c0001t0003g0231 a0001c0001t0005g0003 a0001c0001t0005g0016 others(39): Show |
42 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(39): Show |
intron_variant | MODIFIER | c.1007+30488A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35765933 | |||||||
chr11:35766262 | C | T | 5 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+30817C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35766262 | |||||||
chr11:35766584 | G | A | 97 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(94): Show |
98 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1007+31139G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35766584 | |||||||
chr11:35766643 | CCT | C | 4 | a0001c0001t0014g0097 a0001c0001t0014g0111 a0001c0001t0014g0120 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+31199_1007+31 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35766643 | |||||||
chr11:35766751 | G | C | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1007+31306G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35766751 | |||||||
chr11:35766863 | G | A | 1 | a0001c0001t0015g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1007+31418G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35766863 | |||||||
chr11:35766942 | T | C | 1 | a0001c0001t0007g0201 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1007+31497T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35766942 | |||||||
chr11:35767018 | T | G | 297 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(294): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1007+31573T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767018 | |||||||
chr11:35767054 | C | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+31609C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767054 | |||||||
chr11:35767222 | T | G | 1 | a0001c0001t0005g0042 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1007+31777T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767222 | |||||||
chr11:35767380 | C | A | 1 | a0001c0001t0005g0043 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1007+31935C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767380 | |||||||
chr11:35767405 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1007+31960C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767405 | |||||||
chr11:35767505 | C | G | 2 | a0001c0001t0043g0204 a0001c0001t0043g0210 |
2 | HG00597.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1007+32060C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767505 | |||||||
chr11:35767545 | G | T | 1 | a0001c0001t0007g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1007+32100G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767545 | |||||||
chr11:35767561 | ATAT | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+32120_1007+32 others(9): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35767561 | ||||||
chr11:35767601 | T | A | 41 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(38): Show |
41 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.1007+32156T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767601 | |||||||
chr11:35767603 | G | GTA | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+32169_1007+32 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35767603 | ||||||
chr11:35767607 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007+32162A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35767607 | |||||||
chr11:35768414 | G | A | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007+32969G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35768414 | |||||||
chr11:35768471 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1007+33026G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35768471 | |||||||
chr11:35768643 | C | T | 2 | a0001c0001t0031g0236 a0001c0001t0046g0235 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1007+33198C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35768643 | |||||||
chr11:35768703 | C | T | 2 | a0001c0001t0002g0311 a0001c0001t0008g0307 |
2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1007+33258C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35768703 | |||||||
chr11:35768800 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1007+33355G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35768800 | |||||||
chr11:35768912 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0248 a0002c0002t0001g0150 |
3 | HG02135.hp2 NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1007+33467G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35768912 | |||||||
chr11:35769041 | C | T | 41 | a0001c0001t0001g0094 a0001c0001t0001g0124 a0001c0001t0001g0151 others(38): Show |
42 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1007+33596C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769041 | |||||||
chr11:35769162 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00544.hp1 HG02523.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+33717C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769162 | |||||||
chr11:35769246 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1007+33801C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769246 | |||||||
chr11:35769509 | TA | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+34065delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769509 | |||||||
chr11:35769701 | C | T | 1 | a0001c0001t0007g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1007+34256C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769701 | |||||||
chr11:35769721 | C | T | 1 | a0001c0001t0005g0023 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1007+34276C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769721 | |||||||
chr11:35769741 | G | C | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1007+34296G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769741 | |||||||
chr11:35769859 | A | G | 4 | a0001c0001t0037g0253 a0001c0001t0037g0256 a0001c0001t0078g0242 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+34414A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35769859 | |||||||
chr11:35770068 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0135 |
3 | HG02451.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007+34623G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35770068 | |||||||
chr11:35770253 | A | G | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.1007+34808A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35770253 | |||||||
chr11:35770404 | G | C | 380 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(377): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1007+34959G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35770404 | |||||||
chr11:35770626 | G | A | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1007+35181G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35770626 | |||||||
chr11:35770638 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1007+35193G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35770638 | |||||||
chr11:35770886 | T | C | 6 | a0001c0001t0005g0003 a0001c0001t0005g0045 a0001c0001t0005g0046 others(3): Show |
6 | NA18949.hp1 NA18966.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+35441T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35770886 | |||||||
chr11:35771008 | A | G | 1 | a0001c0001t0005g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1008-35350A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771008 | |||||||
chr11:35771022 | G | A | 1 | a0001c0001t0007g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1008-35336G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771022 | |||||||
chr11:35771035 | G | A | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-35323G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771035 | |||||||
chr11:35771072 | G | A | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1008-35286G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771072 | |||||||
chr11:35771093 | G | A | 43 | a0001c0001t0001g0094 a0001c0001t0001g0124 a0001c0001t0001g0132 others(40): Show |
44 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1008-35265G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771093 | |||||||
chr11:35771116 | G | T | 1 | a0001c0001t0007g0188 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1008-35242G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771116 | |||||||
chr11:35771175 | T | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-35183T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771175 | |||||||
chr11:35771731 | GA | G | 197 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(194): Show |
202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1008-34613delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35771731 | ||||||
chr11:35771777 | A | G | 2 | a0001c0001t0018g0372 a0001c0001t0100g0368 |
2 | HG01496.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1008-34581A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35771777 | |||||||
chr11:35772255 | G | A | 50 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(47): Show |
52 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1008-34103G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35772255 | |||||||
chr11:35772374 | C | G | 5 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-33984C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35772374 | |||||||
chr11:35772377 | G | C | 3 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0231 |
3 | NA18983.hp1 NA18999.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1008-33981G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35772377 | |||||||
chr11:35772440 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0180 a0001c0001t0001g0185 |
3 | HG02523.hp2 NA18612.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1008-33918A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35772440 | |||||||
chr11:35772531 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1008-33827C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35772531 | |||||||
chr11:35772892 | T | C | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1008-33466T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35772892 | |||||||
chr11:35772970 | G | T | 1 | a0001c0001t0002g0358 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1008-33388G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35772970 | |||||||
chr11:35773098 | C | T | 2 | a0001c0001t0041g0211 a0001c0001t0041g0212 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1008-33260C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773098 | |||||||
chr11:35773276 | C | G | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-33082C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773276 | |||||||
chr11:35773286 | A | T | 380 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(377): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1008-33072A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773286 | |||||||
chr11:35773332 | C | A | 1 | a0001c0001t0004g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1008-33026C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773332 | |||||||
chr11:35773426 | T | A | 2 | a0001c0001t0010g0113 a0001c0001t0106g0112 |
2 | HG01943.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1008-32932T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773426 | |||||||
chr11:35773686 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1008-32672T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773686 | |||||||
chr11:35773697 | T | G | 7 | a0001c0001t0005g0003 a0001c0001t0005g0045 a0001c0001t0005g0046 others(4): Show |
7 | NA18612.hp2 NA18949.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-32661T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773697 | |||||||
chr11:35773713 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-32645C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773713 | |||||||
chr11:35773758 | G | T | 21 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(18): Show |
21 | HG00558.hp1 HG01099.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1008-32600G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773758 | |||||||
chr11:35773796 | A | T | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.1008-32562A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35773796 | |||||||
chr11:35774079 | G | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-32279G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35774079 | |||||||
chr11:35774084 | A | G | 2 | a0001c0001t0050g0377 a0001c0001t0061g0254 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1008-32274A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35774084 | |||||||
chr11:35774131 | G | A | 1 | a0001c0001t0057g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1008-32227G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35774131 | |||||||
chr11:35774145 | CT | C | 9 | a0001c0001t0005g0023 a0001c0001t0005g0030 a0001c0001t0013g0029 others(6): Show |
9 | NA18941.hp2 NA18948.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008-32208delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35774145 | ||||||
chr11:35774396 | A | G | 2 | a0001c0001t0089g0343 a0001c0001t0096g0341 |
2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1008-31962A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35774396 | |||||||
chr11:35774419 | G | A | 1 | a0001c0001t0007g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1008-31939G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35774419 | |||||||
chr11:35774497 | C | T | 10 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(7): Show |
11 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008-31861C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35774497 | |||||||
chr11:35774937 | T | A | 2 | a0001c0001t0006g0074 a0001c0001t0006g0075 |
2 | NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1008-31421T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35774937 | |||||||
chr11:35775028 | G | T | 1 | a0001c0001t0055g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1008-31330G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775028 | |||||||
chr11:35775066 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-31292G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775066 | |||||||
chr11:35775498 | A | G | 3 | a0001c0001t0027g0100 a0001c0001t0027g0116 a0001c0001t0068g0115 |
3 | HG01257.hp1 HG01261.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1008-30860A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775498 | |||||||
chr11:35775499 | G | A | 16 | a0001c0001t0006g0009 a0001c0001t0009g0005 a0001c0001t0009g0264 others(13): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1008-30859G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775499 | |||||||
chr11:35775507 | T | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-30851T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775507 | |||||||
chr11:35775586 | G | A | 32 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(29): Show |
33 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1008-30772G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775586 | |||||||
chr11:35775635 | A | C | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-30723A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775635 | |||||||
chr11:35775784 | G | C | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-30574G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775784 | |||||||
chr11:35775818 | G | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0135 |
3 | HG02451.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1008-30540G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775818 | |||||||
chr11:35775892 | T | C | 1 | a0001c0001t0007g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1008-30466T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775892 | |||||||
chr11:35775899 | G | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0117 a0001c0001t0061g0254 others(1): Show |
4 | HG00639.hp1 HG01169.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-30459G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775899 | |||||||
chr11:35775998 | G | A | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1008-30360G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35775998 | |||||||
chr11:35776047 | A | AC | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.1008-30310dupC | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35776047 | ||||||
chr11:35776057 | T | G | 50 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(47): Show |
52 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1008-30301T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776057 | |||||||
chr11:35776158 | G | A | 1 | a0001c0001t0007g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1008-30200G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776158 | |||||||
chr11:35776368 | C | G | 2 | a0001c0001t0091g0351 a0001c0001t0098g0344 |
2 | NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1008-29990C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776368 | |||||||
chr11:35776424 | AT | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00544.hp1 HG02523.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-29927delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35776424 | ||||||
chr11:35776433 | A | G | 1 | a0001c0001t0102g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1008-29925A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776433 | |||||||
chr11:35776500 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1008-29858G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776500 | |||||||
chr11:35776513 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1008-29845C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776513 | |||||||
chr11:35776581 | C | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-29777C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776581 | |||||||
chr11:35776616 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1008-29742A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776616 | |||||||
chr11:35776716 | A | G | 7 | a0001c0001t0007g0189 a0001c0001t0007g0201 a0001c0001t0019g0092 others(4): Show |
7 | HG00099.hp1 HG01516.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-29642A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776716 | |||||||
chr11:35776826 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1008-29532G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776826 | |||||||
chr11:35776941 | G | C | 1 | a0001c0001t0075g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1008-29417G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776941 | |||||||
chr11:35776943 | T | G | 173 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(170): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1008-29415T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776943 | |||||||
chr11:35776944 | G | A | 10 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0163 others(7): Show |
10 | HG00621.hp1 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1008-29414G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35776944 | |||||||
chr11:35777048 | A | C | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-29310A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777048 | |||||||
chr11:35777154 | A | T | 1 | a0001c0001t0008g0307 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1008-29204A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777154 | |||||||
chr11:35777168 | G | A | 1 | a0001c0001t0013g0041 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1008-29190G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777168 | |||||||
chr11:35777235 | T | G | 2 | a0001c0001t0010g0164 a0001c0001t0010g0177 |
2 | NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1008-29123T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777235 | |||||||
chr11:35777291 | T | G | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1008-29067T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777291 | |||||||
chr11:35777355 | A | G | 12 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1008-29003A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777355 | |||||||
chr11:35777363 | TGGGTCTC others(13): Show |
T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0061 |
2 | NA18949.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1008-28994_1008-28 others(26): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777363 | |||||||
chr11:35777400 | T | A | 32 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1008-28958T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777400 | |||||||
chr11:35777405 | C | T | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1008-28953C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777405 | |||||||
chr11:35777417 | T | C | 1 | a0001c0001t0014g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1008-28941T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777417 | |||||||
chr11:35777474 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0186 |
2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1008-28884G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777474 | |||||||
chr11:35777745 | G | A | 1 | a0001c0001t0029g0290 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1008-28613G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777745 | |||||||
chr11:35777861 | C | T | 1 | a0001c0001t0057g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1008-28497C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777861 | |||||||
chr11:35777912 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1008-28446G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777912 | |||||||
chr11:35777958 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-28400A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35777958 | |||||||
chr11:35778167 | T | C | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1008-28191T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778167 | |||||||
chr11:35778389 | G | A | 1 | a0001c0001t0002g0357 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1008-27969G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778389 | |||||||
chr11:35778405 | C | T | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-27953C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778405 | |||||||
chr11:35778523 | A | G | 1 | a0001c0001t0019g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1008-27835A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778523 | |||||||
chr11:35778528 | A | G | 1 | a0001c0001t0007g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1008-27830A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778528 | |||||||
chr11:35778555 | T | G | 3 | a0001c0001t0002g0296 a0001c0001t0016g0309 a0001c0001t0016g0310 |
3 | NA19005.hp1 NA19011.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1008-27803T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778555 | |||||||
chr11:35778728 | A | G | 42 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(39): Show |
44 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1008-27630A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778728 | |||||||
chr11:35778779 | A | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-27579A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778779 | |||||||
chr11:35778944 | G | A | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1008-27414G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778944 | |||||||
chr11:35778946 | T | C | 1 | a0001c0001t0095g0300 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1008-27412T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35778946 | |||||||
chr11:35779024 | G | A | 7 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(4): Show |
7 | HG00323.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-27334G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779024 | |||||||
chr11:35779203 | C | G | 66 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0122 others(63): Show |
67 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1008-27155C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779203 | |||||||
chr11:35779222 | T | C | 296 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(293): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1008-27136T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779222 | |||||||
chr11:35779251 | C | T | 5 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-27107C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779251 | |||||||
chr11:35779299 | G | A | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-27059G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779299 | |||||||
chr11:35779310 | G | C | 1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1008-27048G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779310 | |||||||
chr11:35779474 | A | G | 10 | a0001c0001t0014g0097 a0001c0001t0014g0103 a0001c0001t0014g0104 others(7): Show |
10 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1008-26884A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779474 | |||||||
chr11:35779509 | G | A | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-26849G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779509 | |||||||
chr11:35779525 | G | A | 1 | a0001c0001t0101g0292 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1008-26833G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779525 | |||||||
chr11:35779577 | A | C | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-26781A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779577 | |||||||
chr11:35779618 | A | C | 1 | a0001c0001t0052g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1008-26740A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779618 | |||||||
chr11:35779873 | A | AT | 220 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(217): Show |
224 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1008-26468dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35779873 | ||||||
chr11:35779873 | A | G | 1 | a0001c0001t0107g0200 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1008-26485A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779873 | |||||||
chr11:35779873 | AT | A | 9 | a0001c0001t0006g0071 a0001c0001t0018g0375 a0001c0001t0034g0260 others(6): Show |
9 | HG02109.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008-26468delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35779873 | ||||||
chr11:35779909 | T | G | 1 | a0001c0001t0047g0090 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1008-26449T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779909 | |||||||
chr11:35779962 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1008-26396G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779962 | |||||||
chr11:35779969 | C | G | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1008-26389C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35779969 | |||||||
chr11:35780050 | G | A | 3 | a0001c0001t0002g0287 a0001c0001t0002g0299 a0001c0001t0002g0305 |
3 | HG00735.hp1 HG01074.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1008-26308G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780050 | |||||||
chr11:35780131 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1008-26227T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780131 | |||||||
chr11:35780181 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-26177G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780181 | |||||||
chr11:35780251 | C | A | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-26107C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780251 | |||||||
chr11:35780340 | G | A | 7 | a0001c0001t0007g0189 a0001c0001t0007g0201 a0001c0001t0019g0092 others(4): Show |
7 | HG00099.hp1 HG01516.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-26018G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780340 | |||||||
chr11:35780383 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1008-25975T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780383 | |||||||
chr11:35780491 | T | C | 296 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(293): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1008-25867T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780491 | |||||||
chr11:35780569 | T | C | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-25789T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780569 | |||||||
chr11:35780573 | A | G | 3 | a0001c0001t0006g0072 a0001c0001t0006g0073 a0001c0001t0058g0078 |
3 | HG02148.hp1 NA18952.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1008-25785A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780573 | |||||||
chr11:35780726 | C | G | 13 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1008-25632C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780726 | |||||||
chr11:35780757 | A | G | 1 | a0001c0001t0006g0072 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1008-25601A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35780757 | |||||||
chr11:35780978 | C | CA | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-25373dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35780978 | ||||||
chr11:35781102 | A | G | 1 | a0001c0001t0087g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1008-25256A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35781102 | |||||||
chr11:35781197 | C | T | 1 | a0001c0001t0004g0061 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1008-25161C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35781197 | |||||||
chr11:35781205 | C | T | 3 | a0001c0001t0007g0206 a0001c0001t0007g0207 a0001c0001t0007g0208 |
3 | NA18948.hp2 NA18962.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1008-25153C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35781205 | |||||||
chr11:35781547 | C | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-24811C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35781547 | |||||||
chr11:35781608 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1008-24750G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35781608 | |||||||
chr11:35781928 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1008-24430A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35781928 | |||||||
chr11:35782187 | G | A | 46 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(43): Show |
46 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.1008-24171G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35782187 | |||||||
chr11:35782391 | T | C | 2 | a0001c0001t0010g0164 a0001c0001t0010g0177 |
2 | NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1008-23967T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35782391 | |||||||
chr11:35782475 | G | A | 1 | a0001c0001t0004g0061 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1008-23883G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35782475 | |||||||
chr11:35782807 | C | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-23551C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35782807 | |||||||
chr11:35782812 | T | C | 3 | a0001c0001t0002g0287 a0001c0001t0002g0299 a0001c0001t0002g0305 |
3 | HG00735.hp1 HG01074.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1008-23546T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35782812 | |||||||
chr11:35782844 | C | A | 295 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(292): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1008-23514C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35782844 | |||||||
chr11:35783076 | A | G | 7 | a0001c0001t0002g0352 a0001c0001t0002g0354 a0001c0001t0002g0355 others(4): Show |
7 | HG02056.hp2 NA18747.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-23282A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783076 | |||||||
chr11:35783137 | C | T | 1 | a0001c0001t0074g0187 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1008-23221C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783137 | |||||||
chr11:35783229 | C | T | 2 | a0001c0001t0010g0164 a0001c0001t0010g0177 |
2 | NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1008-23129C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783229 | |||||||
chr11:35783504 | A | G | 4 | a0001c0001t0024g0273 a0001c0001t0038g0275 a0001c0001t0038g0276 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-22854A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783504 | |||||||
chr11:35783648 | C | T | 1 | a0001c0001t0008g0331 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1008-22710C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783648 | |||||||
chr11:35783721 | G | A | 1 | a0001c0001t0006g0079 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1008-22637G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783721 | |||||||
chr11:35783789 | C | T | 1 | a0001c0001t0090g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1008-22569C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783789 | |||||||
chr11:35783911 | GTCT | G | 3 | a0001c0001t0006g0072 a0001c0001t0006g0073 a0001c0001t0058g0078 |
3 | HG02148.hp1 NA18952.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1008-22443_1008-22 others(9): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35783911 | ||||||
chr11:35783969 | G | A | 3 | a0001c0001t0021g0365 a0001c0001t0021g0366 a0001c0001t0021g0367 |
3 | HG01070.hp2 HG01071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1008-22389G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35783969 | |||||||
chr11:35784112 | C | T | 2 | a0001c0001t0039g0237 a0001c0001t0039g0238 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1008-22246C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784112 | |||||||
chr11:35784203 | A | G | 1 | a0001c0001t0004g0059 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1008-22155A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784203 | |||||||
chr11:35784247 | G | T | 17 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(14): Show |
18 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1008-22111G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784247 | |||||||
chr11:35784490 | G | A | 1 | a0001c0001t0003g0222 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1008-21868G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784490 | |||||||
chr11:35784514 | A | G | 1 | a0001c0001t0108g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1008-21844A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784514 | |||||||
chr11:35784627 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-21731T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784627 | |||||||
chr11:35784647 | C | T | 2 | a0001c0001t0053g0220 a0001c0001t0097g0221 |
2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1008-21711C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784647 | |||||||
chr11:35784864 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-21494G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35784864 | |||||||
chr11:35785050 | A | G | 1 | a0001c0001t0002g0355 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1008-21308A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35785050 | |||||||
chr11:35785137 | A | T | 1 | a0001c0001t0033g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1008-21221A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35785137 | |||||||
chr11:35785233 | A | G | 299 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(296): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1008-21125A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35785233 | |||||||
chr11:35785294 | C | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-21064C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35785294 | |||||||
chr11:35785430 | C | T | 1 | a0001c0001t0004g0285 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1008-20928C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35785430 | |||||||
chr11:35785441 | C | T | 2 | a0001c0001t0031g0236 a0001c0001t0046g0235 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1008-20917C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35785441 | |||||||
chr11:35785931 | A | G | 14 | a0001c0001t0018g0372 a0001c0001t0018g0373 a0001c0001t0018g0375 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008-20427A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35785931 | |||||||
chr11:35786230 | T | G | 1 | a0001c0001t0003g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1008-20128T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786230 | |||||||
chr11:35786300 | A | C | 1 | a0001c0001t0002g0326 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1008-20058A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786300 | |||||||
chr11:35786304 | A | G | 1 | a0001c0001t0017g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1008-20054A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786304 | |||||||
chr11:35786369 | G | A | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-19989G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786369 | |||||||
chr11:35786453 | C | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0077 a0001c0001t0006g0081 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008-19905C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786453 | |||||||
chr11:35786588 | C | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0105 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1008-19770C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786588 | |||||||
chr11:35786614 | C | T | 31 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1008-19744C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786614 | |||||||
chr11:35786654 | A | G | 1 | a0001c0001t0039g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1008-19704A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786654 | |||||||
chr11:35786662 | A | G | 1 | a0001c0001t0002g0349 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1008-19696A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35786662 | |||||||
chr11:35787128 | G | A | 4 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(1): Show |
4 | HG03486.hp2 HG03579.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-19230G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787128 | |||||||
chr11:35787130 | G | A | 2 | a0001c0001t0003g0141 a0001c0001t0003g0142 |
2 | NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1008-19228G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787130 | |||||||
chr11:35787177 | A | G | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1008-19181A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787177 | |||||||
chr11:35787266 | G | T | 2 | a0001c0001t0025g0022 a0001c0001t0025g0027 |
2 | NA19090.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1008-19092G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787266 | |||||||
chr11:35787494 | C | T | 7 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(4): Show |
7 | HG00323.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-18864C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787494 | |||||||
chr11:35787737 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1008-18621G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787737 | |||||||
chr11:35787905 | CT | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-18450delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35787905 | ||||||
chr11:35787963 | C | G | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-18395C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787963 | |||||||
chr11:35787963 | C | T | 9 | a0001c0001t0005g0023 a0001c0001t0005g0030 a0001c0001t0013g0029 others(6): Show |
9 | NA18941.hp2 NA18948.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008-18395C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35787963 | |||||||
chr11:35788082 | C | G | 1 | a0001c0001t0002g0296 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1008-18276C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35788082 | |||||||
chr11:35788094 | A | G | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-18264A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35788094 | |||||||
chr11:35788309 | A | T | 1 | a0001c0001t0002g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1008-18049A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35788309 | |||||||
chr11:35788365 | A | G | 2 | a0001c0001t0021g0366 a0001c0001t0021g0367 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1008-17993A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35788365 | |||||||
chr11:35788473 | G | A | 2 | a0001c0001t0006g0071 a0001c0001t0006g0079 |
2 | NA19000.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1008-17885G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35788473 | |||||||
chr11:35788835 | A | T | 1 | a0001c0001t0049g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1008-17523A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35788835 | |||||||
chr11:35789060 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1008-17298A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789060 | |||||||
chr11:35789167 | G | A | 2 | a0001c0001t0042g0258 a0001c0001t0042g0261 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1008-17191G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789167 | |||||||
chr11:35789275 | G | A | 2 | a0001c0001t0023g0224 a0001c0001t0023g0229 |
2 | HG02056.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1008-17083G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789275 | |||||||
chr11:35789310 | A | C | 4 | a0001c0001t0015g0281 a0001c0001t0015g0283 a0001c0001t0015g0284 others(1): Show |
4 | HG00099.hp2 HG00738.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-17048A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789310 | |||||||
chr11:35789456 | GT | G | 31 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1008-16897delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35789456 | ||||||
chr11:35789475 | ACCTGGGA others(9): Show |
A | 31 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1008-16879_1008-16 others(22): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35789475 | ||||||
chr11:35789508 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1008-16850G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789508 | |||||||
chr11:35789608 | C | T | 7 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(4): Show |
7 | HG00323.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-16750C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789608 | |||||||
chr11:35789654 | A | T | 87 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(84): Show |
89 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1008-16704A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789654 | |||||||
chr11:35789708 | C | T | 2 | a0001c0001t0053g0220 a0001c0001t0097g0221 |
2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1008-16650C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789708 | |||||||
chr11:35789712 | C | T | 1 | a0001c0001t0048g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008-16646C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789712 | |||||||
chr11:35789762 | A | T | 1 | a0001c0001t0105g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1008-16596A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789762 | |||||||
chr11:35789903 | C | T | 2 | a0001c0001t0003g0216 a0001c0001t0008g0345 |
2 | HG03942.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1008-16455C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35789903 | |||||||
chr11:35790114 | A | T | 1 | a0001c0001t0007g0208 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1008-16244A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35790114 | |||||||
chr11:35790419 | C | T | 2 | a0001c0001t0002g0329 a0001c0001t0008g0324 |
2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.1008-15939C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35790419 | |||||||
chr11:35790561 | ATG | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-15793_1008-15 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35790561 | ||||||
chr11:35790696 | A | G | 5 | a0001c0001t0003g0015 a0001c0001t0003g0214 a0001c0001t0003g0249 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-15662A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35790696 | |||||||
chr11:35790701 | A | C | 34 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(31): Show |
35 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.1008-15657A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35790701 | |||||||
chr11:35790821 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0248 |
2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1008-15537C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35790821 | |||||||
chr11:35790961 | T | C | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-15397T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35790961 | |||||||
chr11:35791226 | C | T | 368 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(365): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.1008-15132C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791226 | |||||||
chr11:35791295 | G | A | 2 | a0001c0001t0006g0074 a0001c0001t0006g0075 |
2 | NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1008-15063G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791295 | |||||||
chr11:35791329 | G | A | 4 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(1): Show |
4 | HG00738.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008-15029G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791329 | |||||||
chr11:35791371 | A | G | 1 | a0003c0003t0008g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1008-14987A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791371 | |||||||
chr11:35791419 | G | C | 1 | a0001c0001t0036g0102 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1008-14939G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791419 | |||||||
chr11:35791648 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-14710G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791648 | |||||||
chr11:35791681 | C | T | 1 | a0001c0001t0055g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1008-14677C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791681 | |||||||
chr11:35791965 | C | T | 1 | a0001c0001t0023g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1008-14393C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791965 | |||||||
chr11:35791980 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1008-14378G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791980 | |||||||
chr11:35791989 | A | G | 2 | a0001c0001t0010g0246 a0001c0001t0015g0245 |
2 | NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1008-14369A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35791989 | |||||||
chr11:35792023 | A | G | 3 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0062g0259 |
3 | HG02109.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1008-14335A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792023 | |||||||
chr11:35792072 | T | TAC | 13 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(10): Show |
14 | HG02280.hp1 HG02451.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008-14247_1008-14 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACAAC others(2): Show |
6 | a0001c0001t0003g0232 a0001c0001t0003g0241 a0001c0001t0022g0213 others(3): Show |
6 | HG01081.hp1 HG01081.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008-14281_1008-14 others(15): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACAAC others(4): Show |
13 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0215 others(10): Show |
13 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1008-14281_1008-14 others(17): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACAAC others(6): Show |
10 | a0001c0001t0003g0223 a0001c0001t0003g0225 a0001c0001t0003g0226 others(7): Show |
10 | HG00609.hp1 HG01258.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1008-14281_1008-14 others(19): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACAAC others(8): Show |
10 | a0001c0001t0003g0015 a0001c0001t0003g0141 a0001c0001t0003g0142 others(7): Show |
10 | HG02056.hp1 HG02071.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1008-14281_1008-14 others(21): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACAC | 3 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 |
3 | HG03579.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1008-14251_1008-14 others(12): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACACA others(3): Show |
3 | a0001c0001t0042g0258 a0001c0001t0042g0261 a0001c0001t0072g0263 |
3 | HG03209.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1008-14255_1008-14 others(16): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACACA others(5): Show |
1 | a0001c0001t0067g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1008-14257_1008-14 others(18): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACACA others(9): Show |
2 | a0001c0001t0034g0364 a0001c0001t0062g0259 |
2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1008-14261_1008-14 others(22): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | T | TACACACA others(11): Show |
1 | a0001c0001t0034g0260 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1008-14263_1008-14 others(24): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | TAC | T | 8 | a0001c0001t0021g0365 a0001c0001t0021g0366 a0001c0001t0021g0367 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008-14247_1008-14 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | TACACACA others(3): Show |
T | 64 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0122 others(61): Show |
65 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1008-14255_1008-14 others(16): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | TACACACA others(5): Show |
T | 1 | a0001c0001t0076g0183 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1008-14257_1008-14 others(18): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | TACACACA others(7): Show |
T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-14259_1008-14 others(20): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1008-14261_1008-14 others(22): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792072 | TACACACA others(13): Show |
T | 70 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(67): Show |
72 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1008-14265_1008-14 others(26): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792072 | ||||||
chr11:35792103 | ACACACAC others(3): Show |
A | 16 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(13): Show |
16 | HG00544.hp1 HG00639.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008-14253_1008-14 others(16): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792103 | ||||||
chr11:35792105 | ACACACAC others(1): Show |
A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG00408.hp1 HG01943.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-14251_1008-14 others(14): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792105 | ||||||
chr11:35792107 | ACACACT | A | 8 | a0001c0001t0014g0097 a0001c0001t0014g0103 a0001c0001t0014g0104 others(5): Show |
8 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008-14249_1008-14 others(12): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792107 | ||||||
chr11:35792111 | A | ACACACAC others(28): Show |
1 | a0001c0001t0007g0208 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(41): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(39): Show |
1 | a0001c0001t0057g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(52): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(35): Show |
1 | a0001c0001t0058g0078 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(48): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(29): Show |
6 | a0001c0001t0004g0065 a0001c0001t0006g0072 a0001c0001t0006g0077 others(3): Show |
6 | HG00642.hp1 HG01106.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(42): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(31): Show |
1 | a0001c0001t0004g0061 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(44): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(25): Show |
1 | a0001c0001t0004g0056 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(38): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(27): Show |
2 | a0001c0001t0006g0002 a0001c0001t0050g0377 |
3 | HG01069.hp1 HG01071.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(40): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(31): Show |
1 | a0001c0001t0004g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(44): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(23): Show |
1 | a0001c0001t0004g0285 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(36): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(25): Show |
2 | a0001c0001t0007g0206 a0001c0001t0052g0057 |
2 | HG02040.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(38): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(21): Show |
1 | a0001c0001t0048g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(34): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(23): Show |
8 | a0001c0001t0004g0059 a0001c0001t0004g0083 a0001c0001t0004g0086 others(5): Show |
8 | HG01169.hp2 HG01255.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(36): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(21): Show |
8 | a0001c0001t0004g0076 a0001c0001t0004g0082 a0001c0001t0004g0085 others(5): Show |
8 | HG01168.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(34): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(23): Show |
2 | a0001c0001t0004g0014 a0001c0001t0004g0055 |
2 | NA18949.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(36): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(19): Show |
5 | a0001c0001t0004g0062 a0001c0001t0006g0073 a0001c0001t0006g0074 others(2): Show |
5 | HG00423.hp1 HG02622.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(32): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(21): Show |
6 | a0001c0001t0004g0089 a0001c0001t0012g0001 a0001c0001t0017g0199 others(3): Show |
6 | HG00733.hp1 HG01952.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(34): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(15): Show |
2 | a0001c0001t0004g0067 a0001c0001t0004g0068 |
2 | HG01074.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(28): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(17): Show |
4 | a0001c0001t0033g0243 a0001c0001t0049g0080 a0001c0001t0051g0084 others(1): Show |
4 | HG01934.hp1 HG02258.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(30): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(19): Show |
5 | a0001c0001t0007g0209 a0001c0001t0043g0204 a0001c0001t0043g0210 others(2): Show |
5 | HG00597.hp1 HG01516.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(32): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(21): Show |
1 | a0001c0001t0012g0317 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(34): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(15): Show |
1 | a0001c0001t0004g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(28): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(17): Show |
4 | a0001c0001t0012g0001 a0001c0001t0017g0010 a0001c0001t0017g0193 others(1): Show |
4 | HG00423.hp2 HG01358.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(30): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(13): Show |
1 | a0001c0001t0033g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(26): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(15): Show |
10 | a0001c0001t0007g0143 a0001c0001t0007g0201 a0001c0001t0007g0239 others(7): Show |
10 | HG00741.hp2 HG01981.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(28): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(9): Show |
1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(22): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(13): Show |
9 | a0001c0001t0007g0004 a0001c0001t0007g0188 a0001c0001t0007g0189 others(6): Show |
10 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(26): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(9): Show |
3 | a0001c0001t0004g0058 a0001c0001t0004g0066 a0001c0001t0004g0091 |
3 | HG02083.hp1 NA19004.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(22): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(11): Show |
2 | a0001c0001t0012g0318 a0001c0001t0019g0205 |
2 | HG02293.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(24): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(9): Show |
3 | a0001c0001t0019g0092 a0001c0001t0019g0191 a0001c0001t0019g0192 |
3 | HG01975.hp1 HG01993.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1008-14246_1008-14 others(22): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACAC others(7): Show |
1 | a0001c0001t0039g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(20): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACACACTC others(7): Show |
1 | a0001c0001t0039g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1008-14246_1008-14 others(20): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | ACTCT | 17 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0216 others(14): Show |
17 | HG00323.hp1 HG00738.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1008-14241_1008-14 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792111 | ||||||
chr11:35792111 | A | T | 61 | a0001c0001t0001g0133 a0001c0001t0002g0304 a0001c0001t0003g0015 others(58): Show |
61 | HG00609.hp1 HG00639.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1008-14247A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792111 | |||||||
chr11:35792113 | T | A | 19 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(16): Show |
20 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1008-14245T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792113 | |||||||
chr11:35792115 | T | A | 7 | a0001c0001t0024g0273 a0001c0001t0038g0275 a0001c0001t0038g0276 others(4): Show |
7 | HG02280.hp1 HG02647.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-14243T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792115 | |||||||
chr11:35792131 | A | ATTCC | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-14226_1008-14 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35792131 | ||||||
chr11:35792371 | T | G | 130 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(127): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1008-13987T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792371 | |||||||
chr11:35792475 | C | T | 1 | a0001c0001t0066g0049 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1008-13883C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792475 | |||||||
chr11:35792684 | G | T | 1 | a0001c0001t0012g0318 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1008-13674G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792684 | |||||||
chr11:35792739 | C | G | 1 | a0003c0003t0008g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1008-13619C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792739 | |||||||
chr11:35792874 | T | G | 1 | a0001c0001t0012g0318 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1008-13484T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35792874 | |||||||
chr11:35793161 | A | C | 1 | a0001c0001t0012g0318 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1008-13197A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793161 | |||||||
chr11:35793168 | G | GA | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1008-13177dupA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35793168 | ||||||
chr11:35793180 | AAG | A | 26 | a0001c0001t0014g0097 a0001c0001t0014g0103 a0001c0001t0014g0104 others(23): Show |
26 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1008-13176_1008-13 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35793180 | ||||||
chr11:35793181 | AG | A | 197 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(194): Show |
201 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1008-13176delG | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793181 | |||||||
chr11:35793182 | G | A | 148 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0173 others(145): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1008-13176G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793182 | |||||||
chr11:35793208 | TA | T | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008-13144delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35793208 | ||||||
chr11:35793213 | A | T | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008-13145A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793213 | |||||||
chr11:35793350 | A | C | 368 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(365): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.1008-13008A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793350 | |||||||
chr11:35793428 | G | A | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-12930G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793428 | |||||||
chr11:35793439 | C | T | 3 | a0001c0001t0003g0215 a0001c0001t0003g0230 a0001c0001t0054g0234 |
3 | HG02132.hp1 NA19002.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1008-12919C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793439 | |||||||
chr11:35793847 | A | G | 87 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(84): Show |
89 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1008-12511A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793847 | |||||||
chr11:35793883 | A | T | 9 | a0001c0001t0014g0097 a0001c0001t0014g0103 a0001c0001t0014g0104 others(6): Show |
9 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008-12475A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35793883 | |||||||
chr11:35794039 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0010g0099 |
2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1008-12319A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794039 | |||||||
chr11:35794114 | C | T | 1 | a0001c0001t0092g0339 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1008-12244C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794114 | |||||||
chr11:35794217 | C | A | 1 | a0001c0001t0012g0318 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1008-12141C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794217 | |||||||
chr11:35794222 | C | T | 168 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(165): Show |
171 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1008-12136C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794222 | |||||||
chr11:35794234 | G | T | 1 | a0001c0001t0012g0318 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1008-12124G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794234 | |||||||
chr11:35794237 | C | T | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-12121C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794237 | |||||||
chr11:35794461 | A | G | 1 | a0001c0001t0002g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1008-11897A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794461 | |||||||
chr11:35794517 | C | G | 1 | a0001c0001t0003g0363 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1008-11841C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794517 | |||||||
chr11:35794715 | T | C | 1 | a0001c0001t0101g0292 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1008-11643T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794715 | |||||||
chr11:35794794 | T | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02145.hp1 HG02615.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008-11564T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35794794 | |||||||
chr11:35795007 | A | G | 1 | a0001c0001t0084g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1008-11351A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795007 | |||||||
chr11:35795056 | C | T | 5 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0042g0258 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008-11302C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795056 | |||||||
chr11:35795145 | A | C | 1 | a0001c0001t0002g0315 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1008-11213A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795145 | |||||||
chr11:35795168 | G | A | 1 | a0001c0001t0004g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1008-11190G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795168 | |||||||
chr11:35795283 | A | G | 1 | a0001c0001t0039g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1008-11075A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795283 | |||||||
chr11:35795480 | A | G | 7 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0034g0260 others(4): Show |
7 | HG01109.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-10878A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795480 | |||||||
chr11:35795597 | T | A | 1 | a0001c0001t0048g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008-10761T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795597 | |||||||
chr11:35795694 | G | GT | 7 | a0001c0001t0007g0208 a0001c0001t0025g0026 a0001c0001t0034g0260 others(4): Show |
7 | HG02109.hp1 HG02717.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-10655dupT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35795694 | ||||||
chr11:35795822 | C | G | 7 | a0001c0001t0002g0352 a0001c0001t0002g0354 a0001c0001t0002g0355 others(4): Show |
7 | HG02056.hp2 NA18747.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-10536C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795822 | |||||||
chr11:35795863 | A | G | 1 | a0001c0001t0009g0264 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1008-10495A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795863 | |||||||
chr11:35795884 | T | C | 369 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(366): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1008-10474T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35795884 | |||||||
chr11:35796007 | C | T | 1 | a0001c0001t0019g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1008-10351C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796007 | |||||||
chr11:35796030 | C | A | 1 | a0001c0001t0004g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1008-10328C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796030 | |||||||
chr11:35796106 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1008-10252A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796106 | |||||||
chr11:35796138 | G | C | 1 | a0001c0001t0008g0324 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1008-10220G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796138 | |||||||
chr11:35796228 | G | A | 22 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(19): Show |
22 | HG00558.hp1 HG01099.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1008-10130G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796228 | |||||||
chr11:35796251 | CCTCG | C | 71 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(68): Show |
73 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1008-10096_1008-10 others(10): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35796251 | ||||||
chr11:35796255 | G | A | 4 | a0001c0001t0006g0081 a0001c0001t0007g0004 a0001c0001t0007g0188 others(1): Show |
5 | HG00438.hp2 HG01928.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-10103G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796255 | |||||||
chr11:35796258 | C | T | 1 | a0001c0001t0017g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1008-10100C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796258 | |||||||
chr11:35796444 | T | C | 79 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0287 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1008-9914T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796444 | |||||||
chr11:35796535 | G | C | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-9823G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796535 | |||||||
chr11:35796919 | C | T | 1 | a0001c0001t0009g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1008-9439C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35796919 | |||||||
chr11:35797060 | T | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-9298T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35797060 | |||||||
chr11:35797089 | G | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-9269G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35797089 | |||||||
chr11:35797120 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0181 |
2 | NA19005.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1008-9238T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35797120 | |||||||
chr11:35797132 | AAAAC | A | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-9222_1008-921 others(8): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35797132 | ||||||
chr11:35797552 | T | C | 1 | a0001c0001t0002g0340 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1008-8806T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35797552 | |||||||
chr11:35797576 | T | C | 6 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0253 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008-8782T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35797576 | |||||||
chr11:35797874 | T | C | 2 | a0001c0001t0006g0009 a0001c0001t0048g0362 |
3 | HG02622.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1008-8484T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35797874 | |||||||
chr11:35797930 | A | T | 1 | a0001c0001t0004g0285 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1008-8428A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35797930 | |||||||
chr11:35798059 | G | T | 1 | a0001c0001t0002g0338 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1008-8299G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798059 | |||||||
chr11:35798101 | G | C | 178 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(175): Show |
182 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1008-8257G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798101 | |||||||
chr11:35798102 | A | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-8256A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798102 | |||||||
chr11:35798105 | G | A | 16 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(13): Show |
17 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1008-8253G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798105 | |||||||
chr11:35798268 | C | G | 4 | a0001c0001t0037g0253 a0001c0001t0037g0256 a0001c0001t0078g0242 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-8090C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798268 | |||||||
chr11:35798326 | A | G | 7 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0034g0260 others(4): Show |
7 | HG01109.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-8032A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798326 | |||||||
chr11:35798345 | A | G | 180 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(177): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1008-8013A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798345 | |||||||
chr11:35798540 | A | C | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-7818A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798540 | |||||||
chr11:35798557 | G | A | 2 | a0001c0001t0067g0262 a0001c0001t0072g0263 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1008-7801G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798557 | |||||||
chr11:35798789 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0010g0146 |
2 | HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1008-7569A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798789 | |||||||
chr11:35798913 | G | T | 1 | a0001c0001t0003g0228 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1008-7445G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35798913 | |||||||
chr11:35799165 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1008-7193G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35799165 | |||||||
chr11:35799212 | C | A | 1 | a0001c0001t0008g0331 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1008-7146C>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35799212 | |||||||
chr11:35799316 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1008-7042C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35799316 | |||||||
chr11:35799853 | A | C | 369 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(366): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1008-6505A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35799853 | |||||||
chr11:35800062 | C | T | 3 | a0001c0001t0002g0296 a0001c0001t0016g0309 a0001c0001t0016g0310 |
3 | NA19005.hp1 NA19011.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1008-6296C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35800062 | |||||||
chr11:35800068 | CT | C | 370 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(367): Show |
378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.1008-6287delT | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35800068 | ||||||
chr11:35800086 | C | T | 7 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0037g0253 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-6272C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35800086 | |||||||
chr11:35800114 | T | C | 136 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(133): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1008-6244T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35800114 | |||||||
chr11:35800232 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1008-6126C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35800232 | |||||||
chr11:35800471 | T | C | 94 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(91): Show |
96 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1008-5887T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35800471 | |||||||
chr11:35800483 | T | C | 92 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(89): Show |
94 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1008-5875T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35800483 | |||||||
chr11:35800718 | T | C | 92 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(89): Show |
94 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1008-5640T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35800718 | |||||||
chr11:35801129 | G | A | 1 | a0001c0001t0010g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1008-5229G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801129 | |||||||
chr11:35801197 | T | C | 1 | a0001c0001t0002g0340 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1008-5161T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801197 | |||||||
chr11:35801202 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1008-5156A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801202 | |||||||
chr11:35801302 | C | T | 2 | a0001c0001t0006g0074 a0001c0001t0006g0075 |
2 | NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1008-5056C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801302 | |||||||
chr11:35801375 | T | C | 1 | a0001c0001t0004g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1008-4983T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801375 | |||||||
chr11:35801484 | T | A | 1 | a0001c0001t0048g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008-4874T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801484 | |||||||
chr11:35801593 | A | G | 18 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0219 others(15): Show |
18 | HG00609.hp1 HG01257.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1008-4765A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801593 | |||||||
chr11:35801960 | C | T | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1008-4398C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35801960 | |||||||
chr11:35802003 | G | GAGTTTTT others(1137): Show |
2 | a0001c0001t0034g0260 a0001c0001t0034g0364 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1008-4348_1008-434 others(1148): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35802003 | ||||||
chr11:35802003 | G | GAGTTTTT others(1138): Show |
1 | a0001c0001t0062g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1008-4348_1008-434 others(1149): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35802003 | ||||||
chr11:35802055 | T | G | 1 | a0001c0001t0003g0225 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1008-4303T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802055 | |||||||
chr11:35802092 | G | A | 33 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(30): Show |
33 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1008-4266G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802092 | |||||||
chr11:35802103 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1008-4255T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802103 | |||||||
chr11:35802268 | C | T | 161 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(158): Show |
164 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1008-4090C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802268 | |||||||
chr11:35802281 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0010g0099 |
2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1008-4077T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802281 | |||||||
chr11:35802487 | T | G | 5 | a0001c0001t0006g0002 a0001c0001t0006g0077 a0001c0001t0006g0081 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008-3871T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802487 | |||||||
chr11:35802495 | A | G | 1 | a0001c0001t0061g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1008-3863A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802495 | |||||||
chr11:35802549 | T | G | 1 | a0001c0001t0085g0376 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1008-3809T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802549 | |||||||
chr11:35802610 | A | G | 128 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(125): Show |
130 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.1008-3748A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802610 | |||||||
chr11:35802765 | G | T | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-3593G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35802765 | |||||||
chr11:35803081 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-3277A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803081 | |||||||
chr11:35803241 | C | T | 368 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(365): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.1008-3117C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803241 | |||||||
chr11:35803272 | T | A | 3 | a0001c0001t0014g0097 a0001c0001t0014g0111 a0001c0001t0071g0096 |
3 | HG01884.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1008-3086T>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803272 | |||||||
chr11:35803272 | TA | T | 91 | a0001c0001t0001g0117 a0001c0001t0001g0160 a0001c0001t0002g0007 others(88): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1008-3069delA | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35803272 | ||||||
chr11:35803362 | G | A | 38 | a0001c0001t0007g0004 a0001c0001t0007g0143 a0001c0001t0007g0188 others(35): Show |
39 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.1008-2996G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803362 | |||||||
chr11:35803502 | A | C | 4 | a0001c0001t0014g0097 a0001c0001t0014g0111 a0001c0001t0014g0120 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-2856A>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803502 | |||||||
chr11:35803505 | C | T | 4 | a0001c0001t0033g0243 a0001c0001t0033g0244 a0001c0001t0037g0256 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-2853C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803505 | |||||||
chr11:35803668 | C | T | 1 | a0001c0001t0050g0377 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1008-2690C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803668 | |||||||
chr11:35803814 | G | A | 1 | a0001c0001t0005g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1008-2544G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803814 | |||||||
chr11:35803820 | G | A | 1 | a0001c0001t0006g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1008-2538G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803820 | |||||||
chr11:35803871 | A | G | 305 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(302): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1008-2487A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803871 | |||||||
chr11:35803974 | A | G | 369 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(366): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1008-2384A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803974 | |||||||
chr11:35803999 | A | G | 7 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0037g0253 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-2359A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35803999 | |||||||
chr11:35804182 | A | G | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-2176A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35804182 | |||||||
chr11:35804224 | C | G | 1 | a0001c0001t0005g0042 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1008-2134C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35804224 | |||||||
chr11:35804226 | C | G | 369 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(366): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1008-2132C>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35804226 | |||||||
chr11:35804299 | A | G | 48 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(45): Show |
48 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(45): Show |
intron_variant | MODIFIER | c.1008-2059A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35804299 | |||||||
chr11:35804300 | T | G | 1 | a0001c0001t0008g0337 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1008-2058T>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35804300 | |||||||
chr11:35804442 | C | CTGTATAC others(3): Show |
1 | a0001c0001t0027g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1008-1914_1008-190 others(14): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35804442 | ||||||
chr11:35804691 | G | A | 7 | a0001c0001t0034g0260 a0001c0001t0034g0364 a0001c0001t0037g0253 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-1667G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35804691 | |||||||
chr11:35805059 | A | G | 1 | a0001c0001t0027g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1008-1299A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805059 | |||||||
chr11:35805125 | T | C | 2 | a0001c0001t0053g0220 a0001c0001t0097g0221 |
2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1008-1233T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805125 | |||||||
chr11:35805186 | G | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1008-1172G>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805186 | |||||||
chr11:35805194 | A | T | 1 | a0001c0001t0010g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1008-1164A>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805194 | |||||||
chr11:35805196 | T | C | 136 | a0001c0001t0003g0015 a0001c0001t0003g0139 a0001c0001t0003g0140 others(133): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1008-1162T>C | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805196 | |||||||
chr11:35805437 | C | T | 10 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(7): Show |
11 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008-921C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805437 | |||||||
chr11:35805634 | C | T | 1 | a0001c0001t0008g0288 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1008-724C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805634 | |||||||
chr11:35805752 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1008-606G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805752 | |||||||
chr11:35805801 | T | TAGAG | 15 | a0001c0001t0009g0005 a0001c0001t0009g0264 a0001c0001t0009g0265 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008-555_1008-552d others(6): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 35805801 | ||||||
chr11:35805815 | G | A | 36 | a0001c0001t0005g0003 a0001c0001t0005g0016 a0001c0001t0005g0017 others(33): Show |
36 | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008-543G>A | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805815 | |||||||
chr11:35805958 | A | G | 5 | a0001c0001t0020g0126 a0001c0001t0020g0127 a0001c0001t0020g0128 others(2): Show |
5 | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-400A>G | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35805958 | |||||||
chr11:35806075 | C | T | 1 | a0001c0001t0004g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1008-283C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35806075 | |||||||
chr11:35806203 | C | T | 1 | a0001c0001t0005g0039 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1008-155C>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35806203 | |||||||
chr11:35806260 | G | T | 1 | a0001c0001t0013g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1008-98G>T | TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | 35806260 |