Item | Value |
---|---|
geneid | 10094 |
ensemblid | ENSG00000111229.16 |
hgncid | 706 |
symbol | ARPC3 |
name | actin related protein 2/3 complex subunit 3 |
refseq_nuc | NM_001278556.2 |
refseq_prot | NP_001265485.1 |
ensembl_nuc | ENST00000228825.12 |
ensembl_prot | ENSP00000228825.7 |
mane_status | MANE Select |
chr | chr12 |
start | 110434823 |
end | 110450337 |
strand | - |
ver | v1.2 |
region | chr12:110434823-110450337 |
region5000 | chr12:110429823-110455337 |
regionname0 | ARPC3_chr12_110434823_110450337 |
regionname5000 | ARPC3_chr12_110429823_110455337 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 178 | 333 | 88 | 68 | 124 | 15 | 36 | 94 | ARPC3_chr12_110429823_110455337 | ARPC3 | MPAYH others(173): Show |
chr12 | 110429823 | 110455337 |
a0002 | 0/0 | 127 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | MPAYH others(122): Show |
chr12 | 110429823 | 110455337 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 534 | 333 | 88 | 68 | 124 | 15 | 36 | ARPC3_chr12_110429823_110455337 | ARPC3 | ATGCC others(529): Show |
chr12 | 110429823 | 110455337 | ||
a0002c0002 | 0/0 | 542 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | ATGCC others(537): Show |
chr12 | 110429823 | 110455337 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 946 | 317 | 82 | 60 | 123 | 15 | 35 | ARPC3_chr12_110429823_110455337 | ARPC3 | GCCCA others(941): Show |
chr12 | 110429823 | 110455337 |
a0001c0001t0002 | 0/0 | 946 | 6 | 6 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | GCCCA others(941): Show |
chr12 | 110429823 | 110455337 |
a0001c0001t0003 | 0/0 | 946 | 6 | 0 | 6 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | GCTCA others(941): Show |
chr12 | 110429823 | 110455337 |
a0001c0001t0004 | 0/0 | 946 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | GCCCA others(941): Show |
chr12 | 110429823 | 110455337 |
a0001c0001t0005 | 0/0 | 946 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | GCCCA others(941): Show |
chr12 | 110429823 | 110455337 |
a0001c0001t0006 | 0/0 | 946 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | GCCCA others(941): Show |
chr12 | 110429823 | 110455337 |
a0002c0002t0001 | 0/0 | 954 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | GCCCA others(949): Show |
chr12 | 110429823 | 110455337 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 1 | 4 | 0 | 6 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0002 | 0/0 | 10 | 0 | 5 | 3 | 0 | 2 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0003 | 0/0 | 8 | 1 | 1 | 5 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0013 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0032 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0141 | EUR | GBR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | FIN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0217 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0172 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | USA | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0032 | REF | REF | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0076 | REF | REF | ARPC3_chr12_110429823_110455337 | ARPC3 | chr12 | 110429823 | 110455337 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110436172 | G | GGGGGGTC others(5): Show |
1 | a0002 | 1 | HG00099.hp1 | conservative_inframe_insertion | MODERATE | c.411_412insGAGGGGAC others(4): Show |
p.Arg137_Gln138insGl others(10): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 488/946 | 411/537 | 137/178 | chr12 | 110436172 | |||
chr12:110436177 | A | C | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.407T>G | p.Leu136Arg | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 484/946 | 407/537 | 136/178 | chr12 | 110436177 | |||
chr12:110436178 | G | C | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.406C>G | p.Leu136Val | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 483/946 | 406/537 | 136/178 | chr12 | 110436178 | |||
chr12:110436180 | T | C | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.404A>G | p.Gln135Arg | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 481/946 | 404/537 | 135/178 | chr12 | 110436180 | |||
chr12:110436186 | A | C | 1 | a0002 | 1 | HG00099.hp1 | stop_gained | HIGH | c.398T>G | p.Leu133* | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 475/946 | 398/537 | 133/178 | chr12 | 110436186 | |||
chr12:110436187 | A | T | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.397T>A | p.Leu133Ile | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 474/946 | 397/537 | 133/178 | chr12 | 110436187 | |||
chr12:110436190 | A | T | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.394T>A | p.Tyr132Asn | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 471/946 | 394/537 | 132/178 | chr12 | 110436190 | |||
chr12:110436192 | G | T | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.392C>A | p.Ala131Asp | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 469/946 | 392/537 | 131/178 | chr12 | 110436192 | |||
chr12:110436193 | C | T | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.391G>A | p.Ala131Thr | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 468/946 | 391/537 | 131/178 | chr12 | 110436193 | |||
chr12:110436194 | T | G | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.390A>C | p.Arg130Ser | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 467/946 | 390/537 | 130/178 | chr12 | 110436194 | |||
chr12:110436200 | CACTTCTA others(6): Show |
C | 1 | a0002 | 1 | HG00099.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.380-9_383delCTGTTT others(7): Show |
p.Glu127fs | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 460/946 | 380/537 | 127/178 | chr12 | 110436200 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110436188 | A | G | 1 | a0002c0002 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.396T>C | p.Tyr132Tyr | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/7 | 473/946 | 396/537 | 132/178 | chr12 | 110436188 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110435018 | G | C | 1 | a0001c0001t0006 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 7/7 | 137 | chr12 | 110435018 | ||||||
chr12:110435059 | T | G | 1 | a0001c0001t0002 | 6 | HG01884.hp2 HG02257.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*96A>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 7/7 | 96 | chr12 | 110435059 | ||||||
chr12:110435062 | A | G | 1 | a0001c0001t0005 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 7/7 | 93 | chr12 | 110435062 | ||||||
chr12:110450290 | G | A | 1 | a0001c0001t0004 | 2 | HG00738.hp2 HG01069.hp1 |
5_prime_UTR_variant | MODIFIER | c.-30C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/7 | 30 | chr12 | 110450290 | ||||||
chr12:110450335 | G | A | 1 | a0001c0001t0003 | 6 | HG01192.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-75C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/7 | 75 | chr12 | 110450335 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110435299 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.475-82T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435299 | |||||||
chr12:110435322 | C | CT | 13 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
14 | HG00597.hp1 HG01261.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-106dupA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435322 | |||||||
chr12:110435322 | CT | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0097 others(6): Show |
13 | HG01167.hp1 HG01167.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.475-106delA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435322 | |||||||
chr12:110435446 | T | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(35): Show |
47 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.475-229A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435446 | |||||||
chr12:110435538 | G | A | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.475-321C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435538 | |||||||
chr12:110435609 | C | T | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.475-392G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435609 | |||||||
chr12:110435726 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.474+384G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435726 | |||||||
chr12:110435835 | A | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0120 others(3): Show |
10 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+275T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 6/6 | chr12 | 110435835 | |||||||
chr12:110436214 | A | T | 1 | a0002c0002t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.380-10T>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436214 | |||||||
chr12:110436217 | A | G | 1 | a0002c0002t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.380-13T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436217 | |||||||
chr12:110436220 | T | G | 1 | a0002c0002t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.380-16A>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436220 | |||||||
chr12:110436223 | A | T | 1 | a0002c0002t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.380-19T>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436223 | |||||||
chr12:110436225 | A | C | 1 | a0002c0002t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.380-21T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436225 | |||||||
chr12:110436268 | C | G | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.380-64G>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436268 | |||||||
chr12:110436305 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.380-101A>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436305 | |||||||
chr12:110436375 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.380-171A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436375 | |||||||
chr12:110436382 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.379+175G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 5/6 | chr12 | 110436382 | |||||||
chr12:110436687 | G | GA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0056 others(9): Show |
15 | HG01081.hp2 HG01123.hp1 HG01943.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.253-5dupT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436687 | |||||||
chr12:110436687 | G | GAA | 18 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0033 others(15): Show |
25 | HG00423.hp1 HG00423.hp2 HG01243.hp2 others(22): Show |
splice_region_variant&intron_variant | LOW | c.253-6_253-5dupTT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436687 | |||||||
chr12:110436687 | G | GAAA | 15 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0081 others(12): Show |
18 | HG00323.hp2 HG01175.hp1 HG01361.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.253-7_253-5dupTTT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436687 | |||||||
chr12:110436687 | G | GAAAA | 8 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.253-8_253-5dupTTTT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436687 | |||||||
chr12:110436695 | A | AAAT | 5 | a0001c0001t0001g0074 a0001c0001t0001g0090 a0001c0001t0001g0095 others(2): Show |
5 | HG01258.hp1 HG02165.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-13_253-12insAT others(1): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436695 | |||||||
chr12:110436695 | AAT | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0113 a0001c0001t0001g0125 others(2): Show |
6 | HG02148.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-14_253-13delAT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436695 | |||||||
chr12:110436695 | AATAT | A | 11 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0043 others(8): Show |
14 | HG00735.hp2 HG00741.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.253-16_253-13delAT others(2): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436695 | |||||||
chr12:110436696 | AT | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(10): Show |
16 | HG00597.hp2 HG00621.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-14delA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436696 | |||||||
chr12:110436696 | ATAT | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(24): Show |
44 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.253-16_253-14delAT others(1): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436696 | |||||||
chr12:110436697 | T | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.253-14A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436697 | |||||||
chr12:110436699 | T | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(41): Show |
51 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.253-16A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436699 | |||||||
chr12:110436701 | T | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(37): Show |
61 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.253-18A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436701 | |||||||
chr12:110436703 | T | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0085 a0001c0001t0001g0122 others(3): Show |
6 | HG01099.hp2 HG01346.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-20A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436703 | |||||||
chr12:110436705 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-22A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436705 | |||||||
chr12:110436707 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-24A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436707 | |||||||
chr12:110436707 | TATATAC | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0144 others(2): Show |
8 | HG00323.hp1 HG00733.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-30_253-25delGT others(4): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436707 | |||||||
chr12:110436707 | TATATACA others(1): Show |
T | 13 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0111 others(10): Show |
15 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.253-32_253-25delGT others(6): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436707 | |||||||
chr12:110436707 | TATATACA others(5): Show |
T | 1 | a0001c0001t0001g0035 | 2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.253-36_253-25delGT others(10): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436707 | |||||||
chr12:110436709 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0041 others(11): Show |
16 | HG01891.hp1 HG02717.hp2 HG02965.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-26A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436709 | |||||||
chr12:110436709 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.253-27_253-26insGT others(8): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436709 | |||||||
chr12:110436711 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(46): Show |
53 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.253-28A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | T | TACAC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0031 others(3): Show |
6 | HG01515.hp1 HG02683.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-32_253-29dupGT others(2): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | T | TACACAC | 4 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0093 others(1): Show |
5 | HG01943.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-34_253-29dupGT others(4): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0097 |
4 | HG02809.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-36_253-29dupGT others(6): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | T | TACACACA others(5): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0082 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.253-40_253-29dupGT others(10): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | T | TATACACA others(3): Show |
1 | a0001c0001t0001g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.253-29_253-28insGT others(8): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | TAC | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(25): Show |
38 | HG00609.hp2 HG00733.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.253-30_253-29delGT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | TACAC | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG00280.hp2 HG00738.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-32_253-29delGT others(2): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | TACACAC | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0130 others(2): Show |
5 | HG01069.hp1 HG03486.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-34_253-29delGT others(4): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436711 | TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.253-44_253-29delGT others(14): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436711 | |||||||
chr12:110436713 | C | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(38): Show |
59 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.253-30G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436713 | |||||||
chr12:110436715 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0096 others(6): Show |
11 | HG01074.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.253-32G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436715 | |||||||
chr12:110436717 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0100 a0001c0001t0001g0104 others(2): Show |
5 | HG00738.hp2 HG01099.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-34G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436717 | |||||||
chr12:110436719 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0004g0217 a0001c0001t0004g0218 |
3 | HG00738.hp2 HG01069.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.253-36G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436719 | |||||||
chr12:110436721 | C | T | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.253-38G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436721 | |||||||
chr12:110436741 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.253-58G>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436741 | |||||||
chr12:110436753 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0038 others(11): Show |
24 | HG00423.hp1 HG00423.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.253-70G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436753 | |||||||
chr12:110436755 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.253-72A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436755 | |||||||
chr12:110436755 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.253-72A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436755 | |||||||
chr12:110436756 | A | ATT | 5 | a0001c0001t0001g0022 a0001c0001t0001g0161 a0001c0001t0001g0183 others(2): Show |
7 | HG02165.hp2 NA18959.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-75_253-74dupAA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436756 | |||||||
chr12:110436756 | A | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0038 others(12): Show |
25 | HG00423.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.253-73T>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436756 | |||||||
chr12:110436778 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0179 a0001c0001t0001g0210 |
4 | HG01109.hp1 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-95A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436778 | |||||||
chr12:110436879 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0094 |
3 | HG02055.hp2 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.253-196T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436879 | |||||||
chr12:110436916 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.252+168A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 4/6 | chr12 | 110436916 | |||||||
chr12:110437266 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184-114G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110437266 | |||||||
chr12:110437644 | A | G | 1 | a0001c0001t0001g0018 | 3 | HG02258.hp2 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.184-492T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110437644 | |||||||
chr12:110437966 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.184-814C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110437966 | |||||||
chr12:110438132 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0094 |
3 | HG02055.hp2 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.184-980G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438132 | |||||||
chr12:110438204 | C | G | 50 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(47): Show |
62 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.184-1052G>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438204 | |||||||
chr12:110438300 | T | TA | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(22): Show |
37 | HG00423.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.184-1149dupT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438300 | |||||||
chr12:110438328 | G | A | 8 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0132 others(5): Show |
10 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.184-1176C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438328 | |||||||
chr12:110438351 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.184-1199T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438351 | |||||||
chr12:110438491 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0137 a0001c0001t0001g0143 |
3 | HG02129.hp1 NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.184-1339A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438491 | |||||||
chr12:110438523 | C | T | 36 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(33): Show |
45 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.184-1371G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438523 | |||||||
chr12:110438581 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.184-1429C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438581 | |||||||
chr12:110438651 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184-1499T>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438651 | |||||||
chr12:110438652 | T | TA | 3 | a0001c0001t0001g0096 a0001c0001t0001g0104 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.184-1501_184-1500i others(3): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438652 | |||||||
chr12:110438653 | T | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(35): Show |
47 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.184-1501A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438653 | |||||||
chr12:110438654 | T | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0104 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.184-1502A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438654 | |||||||
chr12:110438655 | T | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(30): Show |
42 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.184-1503A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438655 | |||||||
chr12:110438656 | T | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0104 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.184-1504A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438656 | |||||||
chr12:110438657 | T | A | 28 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(25): Show |
37 | HG00323.hp2 HG01167.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.184-1505A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438657 | |||||||
chr12:110438780 | A | G | 36 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(33): Show |
45 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.183+1532T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438780 | |||||||
chr12:110438886 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.183+1426C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110438886 | |||||||
chr12:110439054 | C | T | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.183+1258G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439054 | |||||||
chr12:110439232 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0198 |
2 | HG01099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.183+1080G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439232 | |||||||
chr12:110439415 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0094 |
3 | HG02055.hp2 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.183+897A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439415 | |||||||
chr12:110439553 | C | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0097 others(8): Show |
15 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.183+759G>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439553 | |||||||
chr12:110439554 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.183+758G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439554 | |||||||
chr12:110439555 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.183+757C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439555 | |||||||
chr12:110439607 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.183+705G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439607 | |||||||
chr12:110439662 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.183+650C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439662 | |||||||
chr12:110439700 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0097 others(8): Show |
15 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.183+612C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439700 | |||||||
chr12:110439877 | A | G | 36 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(33): Show |
45 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.183+435T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110439877 | |||||||
chr12:110440193 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0073 a0001c0001t0003g0222 |
3 | HG00597.hp1 HG01975.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.183+119G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110440193 | |||||||
chr12:110440194 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+118C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 3/6 | chr12 | 110440194 | |||||||
chr12:110440399 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.107-11G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110440399 | |||||||
chr12:110440789 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0102 others(3): Show |
10 | HG01167.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-401C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110440789 | |||||||
chr12:110440903 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.107-515G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110440903 | |||||||
chr12:110440983 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107-595A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110440983 | |||||||
chr12:110441133 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0058 |
4 | HG03491.hp2 HG03492.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-745C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441133 | |||||||
chr12:110441219 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107-831C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441219 | |||||||
chr12:110441308 | T | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(33): Show |
45 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.107-920A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441308 | |||||||
chr12:110441353 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107-965C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441353 | |||||||
chr12:110441421 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.107-1033T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441421 | |||||||
chr12:110441421 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.107-1033T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441421 | |||||||
chr12:110441454 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.107-1066C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441454 | |||||||
chr12:110441638 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.107-1250G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441638 | |||||||
chr12:110441847 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0148 a0001c0001t0001g0189 |
3 | HG00323.hp1 HG02258.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.107-1459T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441847 | |||||||
chr12:110441861 | C | T | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.107-1473G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441861 | |||||||
chr12:110441900 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107-1512G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441900 | |||||||
chr12:110441916 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0050 |
3 | HG03491.hp2 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.107-1528G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110441916 | |||||||
chr12:110442026 | T | C | 113 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(110): Show |
152 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.107-1638A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442026 | |||||||
chr12:110442032 | C | CA | 11 | a0001c0001t0001g0025 a0001c0001t0001g0071 a0001c0001t0001g0073 others(8): Show |
12 | HG00597.hp1 HG00738.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.107-1645dupT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442032 | |||||||
chr12:110442163 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(35): Show |
47 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-1775T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442163 | |||||||
chr12:110442330 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(17): Show |
32 | HG00423.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.107-1942C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442330 | |||||||
chr12:110442337 | G | A | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.107-1949C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442337 | |||||||
chr12:110442465 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.107-2077C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442465 | |||||||
chr12:110442634 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0125 a0001c0001t0001g0213 |
4 | HG02717.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-2246A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442634 | |||||||
chr12:110442808 | G | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0087 others(5): Show |
11 | HG00323.hp2 HG01175.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-2420C>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110442808 | |||||||
chr12:110443029 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.106+2423A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110443029 | |||||||
chr12:110443141 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0167 others(1): Show |
8 | HG01168.hp2 HG01169.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+2311A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110443141 | |||||||
chr12:110443416 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0193 |
3 | HG01069.hp2 HG01071.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.106+2036C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110443416 | |||||||
chr12:110443505 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.106+1947G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110443505 | |||||||
chr12:110443832 | C | T | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.106+1620G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110443832 | |||||||
chr12:110443969 | G | GT | 40 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(37): Show |
50 | HG00280.hp2 HG00323.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.106+1482dupA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110443969 | |||||||
chr12:110443969 | GT | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(35): Show |
47 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.106+1482delA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110443969 | |||||||
chr12:110444130 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+1322G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444130 | |||||||
chr12:110444139 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0171 |
3 | HG00741.hp1 HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.106+1313C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444139 | |||||||
chr12:110444181 | C | G | 50 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(47): Show |
62 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.106+1271G>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444181 | |||||||
chr12:110444215 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.106+1237G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444215 | |||||||
chr12:110444223 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+1229C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444223 | |||||||
chr12:110444279 | GA | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0096 a0001c0001t0001g0104 others(2): Show |
5 | HG01099.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+1172delT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444279 | |||||||
chr12:110444287 | A | AT | 8 | a0001c0001t0001g0052 a0001c0001t0001g0123 a0001c0001t0001g0147 others(5): Show |
8 | HG01934.hp1 HG02027.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+1164dupA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444287 | |||||||
chr12:110444287 | AT | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(31): Show |
43 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.106+1164delA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444287 | |||||||
chr12:110444288 | T | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0136 |
2 | HG03579.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.106+1164A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444288 | |||||||
chr12:110444289 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.106+1163A>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444289 | |||||||
chr12:110444358 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106+1094G>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444358 | |||||||
chr12:110444493 | C | T | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.106+959G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444493 | |||||||
chr12:110444781 | A | C | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.106+671T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444781 | |||||||
chr12:110444819 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.106+633G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444819 | |||||||
chr12:110444939 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.106+513C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444939 | |||||||
chr12:110444947 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.106+505A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444947 | |||||||
chr12:110444988 | C | T | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0192 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+464G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 2/6 | chr12 | 110444988 | |||||||
chr12:110445684 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.7-133G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445684 | |||||||
chr12:110445696 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7-145T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445696 | |||||||
chr12:110445828 | A | G | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.7-277T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445828 | |||||||
chr12:110445830 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.7-279C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445830 | |||||||
chr12:110445852 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.7-301G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445852 | |||||||
chr12:110445921 | C | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
9 | HG01081.hp2 HG01943.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-370G>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445921 | |||||||
chr12:110445970 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7-419C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445970 | |||||||
chr12:110445991 | C | A | 36 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(33): Show |
47 | HG00280.hp2 HG00323.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.7-440G>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445991 | |||||||
chr12:110445994 | T | C | 50 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(47): Show |
62 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.7-443A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110445994 | |||||||
chr12:110446008 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0083 others(7): Show |
13 | HG00735.hp1 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.7-457G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446008 | |||||||
chr12:110446159 | CT | C | 8 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0095 others(5): Show |
8 | HG00099.hp2 HG01069.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-609delA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446159 | |||||||
chr12:110446290 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7-739G>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446290 | |||||||
chr12:110446297 | A | AT | 42 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(39): Show |
51 | HG00323.hp2 HG00597.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-747dupA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446297 | |||||||
chr12:110446457 | CCAGCTAA others(20): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.7-933_7-907delTCTC others(23): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446457 | |||||||
chr12:110446502 | C | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(35): Show |
47 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.7-951G>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446502 | |||||||
chr12:110446575 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(35): Show |
47 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.7-1024T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446575 | |||||||
chr12:110446611 | A | AT | 13 | a0001c0001t0001g0029 a0001c0001t0001g0070 a0001c0001t0001g0083 others(10): Show |
14 | HG00735.hp1 HG01099.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-1061dupA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446611 | |||||||
chr12:110446631 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0198 |
2 | HG01099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.7-1080G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446631 | |||||||
chr12:110446712 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.7-1161C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446712 | |||||||
chr12:110446858 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-1307G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446858 | |||||||
chr12:110446902 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.7-1351G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446902 | |||||||
chr12:110446936 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0026 others(3): Show |
10 | NA18941.hp2 NA18942.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-1385G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110446936 | |||||||
chr12:110447149 | G | T | 1 | a0001c0001t0005g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7-1598C>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447149 | |||||||
chr12:110447374 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7-1823G>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447374 | |||||||
chr12:110447441 | G | A | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0192 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-1890C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447441 | |||||||
chr12:110447512 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7-1961G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447512 | |||||||
chr12:110447531 | T | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(33): Show |
45 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.7-1980A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447531 | |||||||
chr12:110447582 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.7-2031C>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447582 | |||||||
chr12:110447703 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.7-2152C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447703 | |||||||
chr12:110447807 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7-2256T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447807 | |||||||
chr12:110447886 | C | CT | 57 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0017 others(54): Show |
71 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.7-2336dupA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447886 | |||||||
chr12:110447886 | C | CTT | 6 | a0001c0001t0001g0070 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG01175.hp2 HG01361.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-2337_7-2336dupAA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447886 | |||||||
chr12:110447886 | CTTTTTT | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
9 | HG01081.hp2 HG01943.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-2341_7-2336delAA others(4): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447886 | |||||||
chr12:110447886 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG01891.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.7-2347_7-2336delAA others(10): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447886 | |||||||
chr12:110447887 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.7-2336A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110447887 | |||||||
chr12:110448231 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6+2024T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448231 | |||||||
chr12:110448399 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6+1856C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448399 | |||||||
chr12:110448652 | C | CA | 41 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(38): Show |
50 | HG00323.hp2 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+1602dupT | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448652 | |||||||
chr12:110448735 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.6+1520G>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448735 | |||||||
chr12:110448737 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6+1518A>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448737 | |||||||
chr12:110448778 | C | CG | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(60): Show |
99 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.6+1476dupC | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448778 | |||||||
chr12:110448778 | C | CGG | 36 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(33): Show |
57 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.6+1475_6+1476dupCC | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448778 | |||||||
chr12:110448778 | CG | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0079 others(12): Show |
18 | HG01081.hp2 HG01099.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.6+1476delC | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448778 | |||||||
chr12:110448788 | G | T | 1 | a0001c0001t0001g0106 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.6+1467C>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448788 | |||||||
chr12:110448790 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6+1465C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448790 | |||||||
chr12:110448790 | G | GC | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(9): Show |
17 | HG01884.hp1 HG01884.hp2 HG02698.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+1464_6+1465insG | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448790 | |||||||
chr12:110448793 | T | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0091 others(10): Show |
17 | HG01175.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.6+1462A>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448793 | |||||||
chr12:110448793 | TG | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0198 others(5): Show |
8 | HG01167.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+1461delC | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448793 | |||||||
chr12:110448794 | G | GT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
11 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6+1460_6+1461insA | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448794 | |||||||
chr12:110448794 | G | T | 20 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0031 others(17): Show |
24 | HG00323.hp2 HG01099.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.6+1461C>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448794 | |||||||
chr12:110448838 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6+1417G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448838 | |||||||
chr12:110448948 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.6+1307C>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448948 | |||||||
chr12:110448977 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6+1278A>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110448977 | |||||||
chr12:110449126 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6+1129A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449126 | |||||||
chr12:110449416 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+839C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449416 | |||||||
chr12:110449418 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+837A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449418 | |||||||
chr12:110449420 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+835C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449420 | |||||||
chr12:110449421 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+834C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449421 | |||||||
chr12:110449429 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+826C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449429 | |||||||
chr12:110449431 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+824C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449431 | |||||||
chr12:110449433 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+822C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449433 | |||||||
chr12:110449435 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+820C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449435 | |||||||
chr12:110449438 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+817A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449438 | |||||||
chr12:110449439 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+816C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449439 | |||||||
chr12:110449440 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+815A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449440 | |||||||
chr12:110449443 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+812A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449443 | |||||||
chr12:110449445 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+810A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449445 | |||||||
chr12:110449447 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+808T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449447 | |||||||
chr12:110449448 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+807C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449448 | |||||||
chr12:110449450 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+805A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449450 | |||||||
chr12:110449451 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+804T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449451 | |||||||
chr12:110449454 | CGGGAGGC others(52): Show |
C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+742_6+800delCTCG others(55): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449454 | |||||||
chr12:110449484 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6+771G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449484 | |||||||
chr12:110449515 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+740A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449515 | |||||||
chr12:110449517 | G | A | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+738C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449517 | |||||||
chr12:110449520 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+735A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449520 | |||||||
chr12:110449522 | A | ACCCCCCC others(55): Show |
1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+732_6+733insGGGG others(58): Show |
ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449522 | |||||||
chr12:110449524 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+731A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449524 | |||||||
chr12:110449525 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+730C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449525 | |||||||
chr12:110449529 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+726A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449529 | |||||||
chr12:110449533 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+722C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449533 | |||||||
chr12:110449537 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+718C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449537 | |||||||
chr12:110449538 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+717C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449538 | |||||||
chr12:110449539 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+716C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449539 | |||||||
chr12:110449541 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+714C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449541 | |||||||
chr12:110449542 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+713T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449542 | |||||||
chr12:110449544 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+711T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449544 | |||||||
chr12:110449545 | G | A | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+710C>T | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449545 | |||||||
chr12:110449547 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+708T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449547 | |||||||
chr12:110449549 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+706C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449549 | |||||||
chr12:110449551 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+704C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449551 | |||||||
chr12:110449552 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+703T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449552 | |||||||
chr12:110449554 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+701A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449554 | |||||||
chr12:110449564 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0083 a0001c0001t0001g0084 |
4 | HG00735.hp1 HG02735.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+691T>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449564 | |||||||
chr12:110449713 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 |
6 | HG01943.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+542G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449713 | |||||||
chr12:110449723 | T | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.6+532A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449723 | |||||||
chr12:110449958 | T | G | 1 | a0001c0001t0004g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6+297A>C | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110449958 | |||||||
chr12:110450003 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+252T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450003 | |||||||
chr12:110450005 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+250C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450005 | |||||||
chr12:110450005 | G | GGA | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.6+248_6+249dupTC | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450005 | |||||||
chr12:110450006 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+249C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450006 | |||||||
chr12:110450007 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+248T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450007 | |||||||
chr12:110450008 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+247C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450008 | |||||||
chr12:110450009 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+246T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450009 | |||||||
chr12:110450010 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+245C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450010 | |||||||
chr12:110450011 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+244T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450011 | |||||||
chr12:110450012 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+243C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450012 | |||||||
chr12:110450013 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+242T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450013 | |||||||
chr12:110450014 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+241T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450014 | |||||||
chr12:110450015 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+240T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450015 | |||||||
chr12:110450016 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+239T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450016 | |||||||
chr12:110450017 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+238C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450017 | |||||||
chr12:110450018 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+237C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450018 | |||||||
chr12:110450019 | G | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+236C>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450019 | |||||||
chr12:110450022 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+233A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450022 | |||||||
chr12:110450025 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+230A>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450025 | |||||||
chr12:110450027 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+228T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450027 | |||||||
chr12:110450029 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+226T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450029 | |||||||
chr12:110450031 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.6+224T>G | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450031 | |||||||
chr12:110450047 | C | T | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.6+208G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450047 | |||||||
chr12:110450135 | C | T | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.6+120G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450135 | |||||||
chr12:110450167 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6+88G>A | ARPC3 | ENSG00000111229.16 | transcript | ENST00000228825.12 | protein_coding | 1/6 | chr12 | 110450167 |