Item | Value |
---|---|
geneid | 25852 |
ensemblid | ENSG00000114098.18 |
hgncid | 24999 |
symbol | ARMC8 |
name | armadillo repeat containing 8 |
refseq_nuc | NM_001363941.2 |
refseq_prot | NP_001350870.1 |
ensembl_nuc | ENST00000469044.6 |
ensembl_prot | ENSP00000419413.1 |
mane_status | MANE Select |
chr | chr3 |
start | 138187301 |
end | 138298373 |
strand | + |
ver | v1.2 |
region | chr3:138187301-138298373 |
region5000 | chr3:138182301-138303373 |
regionname0 | ARMC8_chr3_138187301_138298373 |
regionname5000 | ARMC8_chr3_138182301_138303373 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 673 | 245 | 86 | 49 | 68 | 10 | 30 | 58 | ARMC8_chr3_138182301_138303373 | ARMC8 | MACLL others(668): Show |
chr3 | 138182301 | 138303373 |
a0002 | 0/0 | 673 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | MACLL others(668): Show |
chr3 | 138182301 | 138303373 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2019 | 244 | 85 | 49 | 68 | 10 | 30 | ARMC8_chr3_138182301_138303373 | ARMC8 | ATGGC others(2014): Show |
chr3 | 138182301 | 138303373 | ||
a0001c0003 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | ATGGC others(2014): Show |
chr3 | 138182301 | 138303373 | ||
a0002c0002 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | ATGGC others(2014): Show |
chr3 | 138182301 | 138303373 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4757 | 206 | 69 | 39 | 63 | 10 | 23 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0002 | 0/0 | 4757 | 22 | 6 | 7 | 2 | 0 | 7 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0003 | 0/0 | 4758 | 8 | 6 | 2 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4753): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0004 | 0/0 | 4757 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0005 | 0/0 | 4758 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4753): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0006 | 0/0 | 4758 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4753): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0007 | 0/0 | 4757 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0008 | 0/0 | 4757 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0009 | 0/0 | 4757 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0001c0001t0010 | 0/0 | 4757 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0001c0003t0001 | 0/0 | 4757 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
a0002c0002t0001 | 0/0 | 4757 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | GCTTC others(4752): Show |
chr3 | 138182301 | 138303373 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0001t0010g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0154 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02165 | hp2 | a0001 | c0001 | t0007 | g0028 | EAS | CDX | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | GIH | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | GIH | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0090 | REF | REF | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0164 | REF | REF | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138274488 | A | G | 1 | a0002 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1669A>G | p.Met557Val | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/22 | 1923/4757 | 1669/2022 | 557/673 | chr3 | 138274488 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138223640 | A | G | 1 | a0001c0003 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.342A>G | p.Leu114Leu | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/22 | 596/4757 | 342/2022 | 114/673 | chr3 | 138223640 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138187428 | G | A | 1 | a0001c0001t0005 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/22 | 127 | chr3 | 138187428 | ||||||
chr3:138296178 | G | T | 1 | a0001c0001t0010 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 286 | chr3 | 138296178 | ||||||
chr3:138296246 | A | G | 1 | a0001c0001t0009 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 354 | chr3 | 138296246 | ||||||
chr3:138296347 | T | C | 1 | a0001c0001t0002 | 22 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*455T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 455 | chr3 | 138296347 | ||||||
chr3:138296551 | G | GA | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 |
10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*668dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 669 | INFO_REALIGN_3_PRIME | chr3 | 138296551 | |||||
chr3:138297381 | G | C | 1 | a0001c0001t0004 | 2 | HG00558.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1489G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1489 | chr3 | 138297381 | ||||||
chr3:138297563 | T | G | 1 | a0001c0001t0007 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1671 | chr3 | 138297563 | ||||||
chr3:138297686 | C | T | 2 | a0001c0001t0003 a0001c0001t0005 |
9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1794C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1794 | chr3 | 138297686 | ||||||
chr3:138297700 | C | T | 1 | a0001c0001t0008 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1808C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1808 | chr3 | 138297700 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138187643 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+44T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187643 | |||||||
chr3:138187690 | A | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.45+91A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187690 | |||||||
chr3:138187696 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.45+97C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187696 | |||||||
chr3:138187719 | T | C | 1 | a0001c0001t0007g0028 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.45+120T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187719 | |||||||
chr3:138187813 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.45+214C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187813 | |||||||
chr3:138188058 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0006g0029 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+459T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188058 | |||||||
chr3:138188173 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.45+574C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188173 | |||||||
chr3:138188246 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+647C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188246 | |||||||
chr3:138188383 | T | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+784T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188383 | |||||||
chr3:138188384 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.45+785T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188384 | |||||||
chr3:138188391 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45+792T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188391 | |||||||
chr3:138188392 | T | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(26): Show |
29 | HG00323.hp1 HG01123.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.45+793T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188392 | |||||||
chr3:138188392 | T | TA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG02080.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+800dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138188392 | ||||||
chr3:138188392 | T | TAA | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+799_45+800dupAA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138188392 | ||||||
chr3:138188393 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.45+794A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188393 | |||||||
chr3:138188656 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG00738.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.45+1057G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188656 | |||||||
chr3:138188720 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+1121A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188720 | |||||||
chr3:138189104 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(25): Show |
29 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.45+1505T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189104 | |||||||
chr3:138189251 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.45+1652G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189251 | |||||||
chr3:138189432 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.45+1833T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189432 | |||||||
chr3:138189657 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+2058T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189657 | |||||||
chr3:138189735 | G | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.45+2136G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189735 | |||||||
chr3:138189977 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.45+2378C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189977 | |||||||
chr3:138190054 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.45+2455C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190054 | |||||||
chr3:138190229 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.45+2630A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190229 | |||||||
chr3:138190281 | C | CT | 10 | a0001c0001t0001g0065 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
10 | HG00735.hp2 HG01169.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+2704dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | ||||||
chr3:138190281 | CT | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(14): Show |
17 | HG00323.hp2 HG01070.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+2704delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | ||||||
chr3:138190281 | CTT | C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(7): Show |
11 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+2703_45+2704del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | ||||||
chr3:138190281 | CTTT | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+2702_45+2704del others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | ||||||
chr3:138190281 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.45+2695_45+2704del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | ||||||
chr3:138190428 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+2829A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190428 | |||||||
chr3:138190466 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+2867T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190466 | |||||||
chr3:138190622 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3023C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190622 | |||||||
chr3:138190738 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.45+3139G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190738 | |||||||
chr3:138191052 | C | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3453C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191052 | |||||||
chr3:138191083 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.45+3484G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191083 | |||||||
chr3:138191555 | T | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+3956T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191555 | |||||||
chr3:138191831 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.45+4232G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191831 | |||||||
chr3:138191887 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+4288C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191887 | |||||||
chr3:138191920 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.45+4321G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191920 | |||||||
chr3:138192275 | C | CT | 19 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0062 others(16): Show |
20 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+4696dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138192275 | ||||||
chr3:138192300 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | NA18980.hp1 NA18986.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4701C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192300 | |||||||
chr3:138192314 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.45+4715G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192314 | |||||||
chr3:138192342 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+4743A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192342 | |||||||
chr3:138192476 | A | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+4877A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192476 | |||||||
chr3:138192529 | G | A | 1 | a0001c0001t0006g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+4930G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192529 | |||||||
chr3:138192723 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0229 |
3 | HG02647.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+5124C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192723 | |||||||
chr3:138192845 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+5246C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192845 | |||||||
chr3:138192909 | C | G | 1 | a0001c0001t0001g0219 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.45+5310C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192909 | |||||||
chr3:138192935 | G | A | 20 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0040 others(17): Show |
20 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+5336G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192935 | |||||||
chr3:138193260 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+5661C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193260 | |||||||
chr3:138193375 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.45+5776C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193375 | |||||||
chr3:138193415 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+5816C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193415 | |||||||
chr3:138193528 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+5929A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193528 | |||||||
chr3:138193555 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.45+5956C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193555 | |||||||
chr3:138193671 | A | C | 2 | a0001c0001t0001g0041 a0001c0001t0009g0047 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.45+6072A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193671 | |||||||
chr3:138193692 | C | A | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG01123.hp1 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+6093C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193692 | |||||||
chr3:138193952 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.45+6353T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193952 | |||||||
chr3:138194046 | C | CT | 35 | a0001c0001t0001g0018 a0001c0001t0001g0060 a0001c0001t0001g0078 others(32): Show |
35 | HG00735.hp2 HG01074.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.45+6461dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194046 | ||||||
chr3:138194046 | C | CTT | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
8 | HG01123.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+6460_45+6461dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194046 | ||||||
chr3:138194073 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.45+6474C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194073 | |||||||
chr3:138194186 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(11): Show |
15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+6587G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194186 | |||||||
chr3:138194194 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.45+6595T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194194 | |||||||
chr3:138194293 | GCGGCCTC others(105): Show |
G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18986.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.45+6698_45+6809del | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194293 | ||||||
chr3:138194341 | C | CT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(30): Show |
33 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.45+6760dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194341 | ||||||
chr3:138194409 | G | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+6810G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194409 | |||||||
chr3:138194573 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.45+6974C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194573 | |||||||
chr3:138194644 | AT | A | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0001 others(5): Show |
9 | HG01169.hp2 HG01884.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+7058delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194644 | ||||||
chr3:138194929 | T | C | 4 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG01109.hp2 HG03017.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+7330T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194929 | |||||||
chr3:138195161 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA19012.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.45+7562C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195161 | |||||||
chr3:138195373 | T | C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+7774T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195373 | |||||||
chr3:138195451 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+7852T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195451 | |||||||
chr3:138195859 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.45+8260A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195859 | |||||||
chr3:138195872 | A | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+8273A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195872 | |||||||
chr3:138196097 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.45+8498G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196097 | |||||||
chr3:138196188 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45+8589T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196188 | |||||||
chr3:138196362 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8763C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196362 | |||||||
chr3:138196659 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.45+9060A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196659 | |||||||
chr3:138196736 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.45+9137G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196736 | |||||||
chr3:138196763 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.45+9164A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196763 | |||||||
chr3:138196832 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+9233A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196832 | |||||||
chr3:138196875 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.45+9276A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196875 | |||||||
chr3:138196923 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9324G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196923 | |||||||
chr3:138197163 | C | G | 7 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0083 others(4): Show |
7 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+9564C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138197163 | |||||||
chr3:138197361 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.45+9762T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138197361 | |||||||
chr3:138197476 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+9877A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138197476 | |||||||
chr3:138198197 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.45+10598A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198197 | |||||||
chr3:138198341 | A | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+10742A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198341 | |||||||
chr3:138198377 | A | T | 1 | a0002c0002t0001g0063 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.45+10778A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198377 | |||||||
chr3:138198399 | G | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+10800G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198399 | |||||||
chr3:138198493 | T | TTTA | 10 | a0001c0001t0001g0065 a0001c0001t0001g0160 a0001c0001t0001g0180 others(7): Show |
10 | HG01106.hp1 HG02109.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+10924_45+10926d others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | ||||||
chr3:138198493 | TTTA | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG00408.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+10924_45+10926d others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | ||||||
chr3:138198493 | TTTATTA | T | 140 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(137): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.45+10921_45+10926d others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | ||||||
chr3:138198493 | TTTATTAT others(5): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+10915_45+10926d others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | ||||||
chr3:138198523 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+10924A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198523 | |||||||
chr3:138198526 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.45+10927T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198526 | |||||||
chr3:138198600 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+11001C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198600 | |||||||
chr3:138198607 | G | A | 65 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(62): Show |
65 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.45+11008G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198607 | |||||||
chr3:138198655 | G | A | 1 | a0001c0001t0004g0102 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.45+11056G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198655 | |||||||
chr3:138199024 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.46-10793A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199024 | |||||||
chr3:138199151 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.46-10666A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199151 | |||||||
chr3:138199374 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-10443T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199374 | |||||||
chr3:138199614 | T | G | 1 | a0001c0001t0002g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.46-10203T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199614 | |||||||
chr3:138199682 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.46-10135A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199682 | |||||||
chr3:138199794 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-10023A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199794 | |||||||
chr3:138199818 | T | A | 1 | a0001c0001t0002g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.46-9999T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199818 | |||||||
chr3:138200323 | G | GTTTACTT others(17): Show |
27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-9491_46-9490ins others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200323 | ||||||
chr3:138200433 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-9384A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200433 | |||||||
chr3:138200457 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.46-9360T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200457 | |||||||
chr3:138200503 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.46-9314A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200503 | |||||||
chr3:138200602 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-9215A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200602 | |||||||
chr3:138200737 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-9080C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200737 | |||||||
chr3:138200904 | C | CT | 19 | a0001c0001t0001g0037 a0001c0001t0001g0074 a0001c0001t0001g0088 others(16): Show |
19 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-8887dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | ||||||
chr3:138200904 | CT | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
88 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.46-8887delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | ||||||
chr3:138200904 | CTT | C | 10 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0048 others(7): Show |
10 | HG00140.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-8888_46-8887del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | ||||||
chr3:138200904 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.46-8898_46-8887del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | ||||||
chr3:138200932 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-8885A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200932 | |||||||
chr3:138200974 | G | A | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG01433.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.46-8843G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200974 | |||||||
chr3:138201008 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.46-8809G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201008 | |||||||
chr3:138201222 | A | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.46-8595A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201222 | |||||||
chr3:138201293 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.46-8524C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201293 | |||||||
chr3:138201436 | C | CT | 16 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0074 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-8340dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | C | CTTT | 8 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0001c0001t0001g0198 others(5): Show |
8 | HG00408.hp2 HG01169.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-8342_46-8340dup others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | C | CTTTT | 7 | a0001c0001t0001g0175 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG01074.hp1 HG01106.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8343_46-8340dup others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | C | CTTTTT | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG01515.hp2 HG02683.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-8344_46-8340dup others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0210 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.46-8354_46-8340dup others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0213 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.46-8355_46-8340dup others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.46-8357_46-8340dup others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTT | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0041 others(11): Show |
14 | HG00323.hp1 HG01123.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.46-8344_46-8340del others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0042 others(7): Show |
10 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-8347_46-8340del others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(2): Show |
C | 36 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0050 others(33): Show |
36 | HG00558.hp1 HG00741.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.46-8348_46-8340del others(9): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(3): Show |
C | 62 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.46-8349_46-8340del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0144 a0001c0001t0002g0076 |
3 | HG01069.hp2 HG01070.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.46-8350_46-8340del others(11): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0194 a0001c0001t0001g0233 a0001c0001t0002g0093 others(2): Show |
5 | HG00735.hp2 HG03017.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-8352_46-8340del others(13): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0190 a0001c0001t0001g0193 |
3 | NA18747.hp2 NA18941.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.46-8353_46-8340del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.46-8354_46-8340del others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.46-8356_46-8340del others(17): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-8357_46-8340del others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG00738.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.46-8358_46-8340del others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001g0048 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.46-8360_46-8340del others(21): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-8361_46-8340del others(22): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.46-8362_46-8340del others(23): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.46-8364_46-8340del others(25): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201436 | CTTTTTTT others(23): Show |
C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.46-8369_46-8340del others(30): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | ||||||
chr3:138201739 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.46-8078G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201739 | |||||||
chr3:138201748 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.46-8069T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201748 | |||||||
chr3:138202160 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0002g0153 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46-7657A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202160 | |||||||
chr3:138202187 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-7630C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202187 | |||||||
chr3:138202225 | T | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(11): Show |
15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-7592T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202225 | |||||||
chr3:138202496 | CTT | C | 3 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG01167.hp1 HG01169.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.46-7319_46-7318del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138202496 | ||||||
chr3:138202513 | A | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-7304A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202513 | |||||||
chr3:138202549 | A | G | 33 | a0001c0001t0001g0060 a0001c0001t0001g0078 a0001c0001t0001g0173 others(30): Show |
33 | HG00408.hp2 HG00735.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.46-7268A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202549 | |||||||
chr3:138203371 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6446G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203371 | |||||||
chr3:138203547 | A | G | 2 | a0001c0001t0001g0030 a0001c0003t0001g0031 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.46-6270A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203547 | |||||||
chr3:138203675 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-6142T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203675 | |||||||
chr3:138203979 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.46-5838C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203979 | |||||||
chr3:138204032 | A | G | 1 | a0001c0001t0003g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.46-5785A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204032 | |||||||
chr3:138204331 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.46-5486A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204331 | |||||||
chr3:138204344 | C | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.46-5473C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204344 | |||||||
chr3:138204396 | T | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-5421T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204396 | |||||||
chr3:138204399 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.46-5418G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204399 | |||||||
chr3:138204442 | A | G | 1 | a0001c0001t0007g0028 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.46-5375A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204442 | |||||||
chr3:138205060 | C | CT | 37 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0051 others(34): Show |
38 | HG00140.hp2 HG00558.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.46-4731dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | ||||||
chr3:138205060 | C | CTT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(4): Show |
7 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-4732_46-4731dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | ||||||
chr3:138205060 | C | CTTT | 7 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0023 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-4733_46-4731dup others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | ||||||
chr3:138205060 | CT | C | 8 | a0001c0001t0001g0032 a0001c0001t0001g0122 a0001c0001t0001g0132 others(5): Show |
8 | HG01069.hp1 HG01433.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-4731delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | ||||||
chr3:138205060 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-4741_46-4731del others(11): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | ||||||
chr3:138205060 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-4742_46-4731del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | ||||||
chr3:138205213 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.46-4604T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205213 | |||||||
chr3:138205328 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.46-4489C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205328 | |||||||
chr3:138205340 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0135 |
2 | NA18977.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.46-4477C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205340 | |||||||
chr3:138205937 | C | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0190 a0001c0001t0001g0193 others(1): Show |
4 | NA18747.hp2 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-3880C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205937 | |||||||
chr3:138206332 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.46-3485A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206332 | |||||||
chr3:138206390 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.46-3427G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206390 | |||||||
chr3:138206452 | G | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3365G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206452 | |||||||
chr3:138206553 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.46-3264G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206553 | |||||||
chr3:138206720 | G | A | 64 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0081 others(61): Show |
64 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.46-3097G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206720 | |||||||
chr3:138206753 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-3064A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206753 | |||||||
chr3:138206873 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG00735.hp1 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2944G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206873 | |||||||
chr3:138206999 | G | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG01891.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-2818G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206999 | |||||||
chr3:138207100 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.46-2717T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207100 | |||||||
chr3:138207214 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-2603C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207214 | |||||||
chr3:138207515 | A | G | 1 | a0001c0001t0006g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46-2302A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207515 | |||||||
chr3:138207559 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.46-2258A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207559 | |||||||
chr3:138207564 | G | A | 19 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0040 others(16): Show |
19 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-2253G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207564 | |||||||
chr3:138207794 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.46-2023C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207794 | |||||||
chr3:138207960 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-1857A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207960 | |||||||
chr3:138208088 | G | GT | 90 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0048 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.46-1716dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138208088 | ||||||
chr3:138208088 | GT | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
11 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-1716delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138208088 | ||||||
chr3:138208099 | T | G | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
13 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-1718T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208099 | |||||||
chr3:138208099 | T | TG | 9 | a0001c0001t0001g0051 a0001c0001t0001g0091 a0001c0001t0001g0092 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-1718_46-1717ins others(1): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208099 | |||||||
chr3:138208101 | TG | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02723.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-1715delG | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208101 | |||||||
chr3:138208102 | G | T | 3 | a0001c0001t0001g0041 a0001c0001t0002g0156 a0001c0001t0009g0047 |
3 | HG02615.hp1 HG02965.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.46-1715G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208102 | |||||||
chr3:138208158 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0144 |
2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.46-1659G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208158 | |||||||
chr3:138208264 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.46-1553A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208264 | |||||||
chr3:138208454 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA19012.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.46-1363G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208454 | |||||||
chr3:138208669 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.46-1148C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208669 | |||||||
chr3:138208731 | T | A | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.46-1086T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208731 | |||||||
chr3:138208807 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.46-1010T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208807 | |||||||
chr3:138209461 | A | G | 1 | a0001c0001t0004g0104 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.46-356A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138209461 | |||||||
chr3:138209530 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0125 |
3 | HG01070.hp1 HG01071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.46-287A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138209530 | |||||||
chr3:138210653 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.122+760G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138210653 | |||||||
chr3:138210805 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.122+912C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138210805 | |||||||
chr3:138210984 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.122+1091G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138210984 | |||||||
chr3:138211503 | T | G | 101 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0049 others(98): Show |
101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.122+1610T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138211503 | |||||||
chr3:138211512 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+1619T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138211512 | |||||||
chr3:138211546 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+1653A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138211546 | |||||||
chr3:138212047 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+2154G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212047 | |||||||
chr3:138212082 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122+2189G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212082 | |||||||
chr3:138212308 | C | CT | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+2433dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138212308 | ||||||
chr3:138212308 | CT | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG01167.hp1 HG01515.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.122+2433delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138212308 | ||||||
chr3:138212434 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+2541C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212434 | |||||||
chr3:138212500 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+2607G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212500 | |||||||
chr3:138212573 | C | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.122+2680C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212573 | |||||||
chr3:138212597 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.122+2704G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212597 | |||||||
chr3:138212732 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+2839A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212732 | |||||||
chr3:138212979 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.122+3086G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212979 | |||||||
chr3:138213173 | A | G | 9 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0088 others(6): Show |
9 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+3280A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213173 | |||||||
chr3:138213196 | A | G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+3303A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213196 | |||||||
chr3:138213219 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.122+3326G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213219 | |||||||
chr3:138213667 | A | G | 64 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0081 others(61): Show |
64 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.122+3774A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213667 | |||||||
chr3:138213844 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+3951C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213844 | |||||||
chr3:138214151 | G | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+4258G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214151 | |||||||
chr3:138214159 | T | TA | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+4281dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138214159 | ||||||
chr3:138214180 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+4287G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214180 | |||||||
chr3:138214301 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122+4408C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214301 | |||||||
chr3:138214514 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.122+4621G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214514 | |||||||
chr3:138214702 | G | A | 74 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0049 others(71): Show |
74 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.122+4809G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214702 | |||||||
chr3:138214810 | T | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(19): Show |
23 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+4917T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214810 | |||||||
chr3:138215120 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.122+5227A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138215120 | |||||||
chr3:138215842 | GTTTA | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+5972_122+5975d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138215842 | ||||||
chr3:138216045 | A | AT | 7 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0194 others(4): Show |
7 | HG01243.hp1 HG03098.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-5859dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138216045 | ||||||
chr3:138216045 | AT | A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0041 others(11): Show |
14 | HG01069.hp1 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-5859delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138216045 | ||||||
chr3:138216138 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-5788C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216138 | |||||||
chr3:138216293 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0001g0198 |
3 | NA18957.hp1 NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.123-5633A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216293 | |||||||
chr3:138216397 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.123-5529G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216397 | |||||||
chr3:138216579 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.123-5347A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216579 | |||||||
chr3:138216625 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123-5301T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216625 | |||||||
chr3:138216811 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.123-5115C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216811 | |||||||
chr3:138216939 | A | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0132 a0001c0001t0004g0102 others(1): Show |
4 | HG00558.hp1 NA18747.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-4987A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216939 | |||||||
chr3:138216963 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.123-4963T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216963 | |||||||
chr3:138217212 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-4714C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138217212 | |||||||
chr3:138217329 | A | T | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.123-4597A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138217329 | |||||||
chr3:138217401 | C | CT | 5 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG01123.hp1 HG01515.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-4510dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138217401 | ||||||
chr3:138217688 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.123-4238C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138217688 | |||||||
chr3:138217759 | GCTTA | G | 32 | a0001c0001t0001g0060 a0001c0001t0001g0078 a0001c0001t0001g0173 others(29): Show |
32 | HG00408.hp2 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.123-4162_123-4159d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138217759 | ||||||
chr3:138218227 | A | AC | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.123-3699_123-3698i others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218227 | |||||||
chr3:138218234 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.123-3692G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218234 | |||||||
chr3:138218541 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-3385C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218541 | |||||||
chr3:138218554 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.123-3372T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218554 | |||||||
chr3:138219419 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.123-2507G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219419 | |||||||
chr3:138219426 | T | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.123-2500T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219426 | |||||||
chr3:138219548 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123-2378A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219548 | |||||||
chr3:138219674 | A | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-2252A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219674 | |||||||
chr3:138219726 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-2200C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219726 | |||||||
chr3:138219737 | T | C | 2 | a0001c0001t0001g0055 a0002c0002t0001g0063 |
2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.123-2189T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219737 | |||||||
chr3:138219799 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.123-2127A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219799 | |||||||
chr3:138219941 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-1985C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219941 | |||||||
chr3:138220029 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.123-1897A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220029 | |||||||
chr3:138220159 | T | A | 1 | a0001c0001t0001g0241 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.123-1767T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220159 | |||||||
chr3:138220693 | C | CT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-1219dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138220693 | ||||||
chr3:138220808 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123-1118G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220808 | |||||||
chr3:138220979 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.123-947C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220979 | |||||||
chr3:138221278 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG02615.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-648T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221278 | |||||||
chr3:138221293 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.123-633A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221293 | |||||||
chr3:138221311 | A | G | 64 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0081 others(61): Show |
64 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.123-615A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221311 | |||||||
chr3:138221482 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.123-444G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221482 | |||||||
chr3:138222093 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.194+96G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222093 | |||||||
chr3:138222119 | T | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(11): Show |
15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.194+122T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222119 | |||||||
chr3:138222254 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.194+257C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222254 | |||||||
chr3:138222335 | G | A | 1 | a0001c0001t0006g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.194+338G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222335 | |||||||
chr3:138222467 | TAGGAAGT others(27): Show |
T | 1 | a0001c0001t0001g0219 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.194+473_194+506del others(34): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 138222467 | ||||||
chr3:138222508 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.194+511C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222508 | |||||||
chr3:138222802 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.195-587A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222802 | |||||||
chr3:138223127 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-262A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138223127 | |||||||
chr3:138223174 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.195-215T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138223174 | |||||||
chr3:138223284 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195-105C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138223284 | |||||||
chr3:138223573 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(11): Show |
15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.337+42C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 4/21 | chr3 | 138223573 | |||||||
chr3:138223937 | G | A | 20 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0040 others(17): Show |
20 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.435+204G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138223937 | |||||||
chr3:138223957 | C | CT | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(11): Show |
14 | HG02055.hp1 HG02280.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.435+243dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138223957 | ||||||
chr3:138223957 | CT | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0079 others(3): Show |
6 | HG01069.hp1 HG01069.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+243delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138223957 | ||||||
chr3:138223959 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.435+226T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138223959 | |||||||
chr3:138224019 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.435+286C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224019 | |||||||
chr3:138224049 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.435+316T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224049 | |||||||
chr3:138224614 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.435+881G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224614 | |||||||
chr3:138224676 | A | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+943A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224676 | |||||||
chr3:138224951 | A | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1218A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224951 | |||||||
chr3:138225109 | C | CT | 122 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0040 others(119): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.435+1395dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138225109 | ||||||
chr3:138225109 | C | CTT | 6 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0217 others(3): Show |
6 | HG00741.hp2 HG01256.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+1394_435+1395d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138225109 | ||||||
chr3:138225109 | CT | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(17): Show |
20 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.435+1395delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138225109 | ||||||
chr3:138225148 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0086 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.435+1415C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225148 | |||||||
chr3:138225150 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435+1417G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225150 | |||||||
chr3:138225157 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.435+1424G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225157 | |||||||
chr3:138225176 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.435+1443C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225176 | |||||||
chr3:138225310 | C | T | 3 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 |
3 | HG03017.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.435+1577C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225310 | |||||||
chr3:138225330 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.435+1597G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225330 | |||||||
chr3:138225407 | G | A | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.435+1674G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225407 | |||||||
chr3:138225436 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.435+1703A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225436 | |||||||
chr3:138225574 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.435+1841A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225574 | |||||||
chr3:138225620 | C | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1887C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225620 | |||||||
chr3:138225755 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.435+2022A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225755 | |||||||
chr3:138226083 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0135 |
2 | NA18977.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.435+2350C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226083 | |||||||
chr3:138226216 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0126 others(5): Show |
8 | HG01123.hp2 HG01175.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.435+2483G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226216 | |||||||
chr3:138226264 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+2531G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226264 | |||||||
chr3:138226272 | G | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+2539G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226272 | |||||||
chr3:138226350 | C | T | 31 | a0001c0001t0001g0060 a0001c0001t0001g0078 a0001c0001t0001g0174 others(28): Show |
31 | HG00408.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.436-2568C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226350 | |||||||
chr3:138226470 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.436-2448G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226470 | |||||||
chr3:138226914 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-2004T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226914 | |||||||
chr3:138227133 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.436-1785T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227133 | |||||||
chr3:138227377 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.436-1541A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227377 | |||||||
chr3:138227670 | A | G | 1 | a0001c0001t0007g0028 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.436-1248A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227670 | |||||||
chr3:138227991 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.436-927G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227991 | |||||||
chr3:138228207 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0086 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.436-711T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228207 | |||||||
chr3:138228213 | G | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.436-705G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228213 | |||||||
chr3:138228317 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0109 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.436-601C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228317 | |||||||
chr3:138228324 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0133 |
2 | NA18957.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.436-594G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228324 | |||||||
chr3:138228573 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-345G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228573 | |||||||
chr3:138228580 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.436-338G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228580 | |||||||
chr3:138228653 | A | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0160 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.436-265A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228653 | |||||||
chr3:138228713 | G | A | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.436-205G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228713 | |||||||
chr3:138229132 | GTGTATAT others(11): Show |
G | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.528+124_528+141del others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229132 | ||||||
chr3:138229132 | GTGTATAT others(15): Show |
G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+124_528+145del others(22): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229132 | ||||||
chr3:138229134 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.528+124G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229134 | |||||||
chr3:138229134 | G | GTA | 5 | a0001c0001t0001g0035 a0001c0001t0001g0078 a0001c0001t0001g0176 others(2): Show |
5 | HG02109.hp1 HG02300.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+172_528+173dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | G | GTATA | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0208 |
3 | HG02896.hp1 HG02897.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.528+170_528+173dup others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.528+162_528+173dup others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.528+160_528+173dup others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTA | G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0170 others(5): Show |
8 | HG00323.hp1 HG00735.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+172_528+173del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATA | G | 8 | a0001c0001t0001g0158 a0001c0001t0001g0190 a0001c0001t0001g0192 others(5): Show |
8 | HG01243.hp2 HG01978.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+170_528+173del others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATA | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0166 a0001c0001t0001g0169 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+168_528+173del others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(1): Show |
G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG03195.hp1 NA18965.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.528+166_528+173del others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(3): Show |
G | 5 | a0001c0001t0001g0165 a0001c0001t0001g0218 a0001c0001t0001g0234 others(2): Show |
5 | HG01169.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+164_528+173del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(5): Show |
G | 4 | a0001c0001t0001g0080 a0001c0001t0001g0147 a0001c0001t0001g0179 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+162_528+173del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(7): Show |
G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0232 |
2 | HG01256.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.528+160_528+173del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(9): Show |
G | 8 | a0001c0001t0001g0032 a0001c0001t0001g0113 a0001c0001t0001g0114 others(5): Show |
8 | HG01123.hp2 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+158_528+173del others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(17): Show |
G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0178 |
2 | HG03195.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.528+150_528+173del others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.528+148_528+173del others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229134 | GTATATAT others(21): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.528+146_528+173del others(28): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | ||||||
chr3:138229136 | A | G | 2 | a0001c0001t0002g0177 a0001c0001t0010g0154 |
2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.528+126A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229136 | |||||||
chr3:138229138 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0010g0154 |
2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.528+128A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229138 | |||||||
chr3:138229144 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.528+143_528+144ins others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229144 | ||||||
chr3:138229144 | ATATATAT others(33): Show |
A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.528+140_528+179del others(40): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229144 | ||||||
chr3:138229145 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528+150_528+151ins others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229145 | ||||||
chr3:138229147 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.528+150_528+151ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229147 | ||||||
chr3:138229147 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.528+152_528+153ins others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229147 | ||||||
chr3:138229149 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+150_528+151ins others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229149 | ||||||
chr3:138229150 | ATATATAT others(27): Show |
A | 2 | a0001c0001t0001g0041 a0001c0001t0009g0047 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.528+146_528+179del others(34): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229150 | ||||||
chr3:138229156 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.528+146A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229156 | |||||||
chr3:138229158 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.528+154_528+179del others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229158 | ||||||
chr3:138229160 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0187 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.528+156_528+179del others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229160 | ||||||
chr3:138229164 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA19085.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.528+160_528+179del others(20): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229164 | ||||||
chr3:138229165 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+155T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229165 | |||||||
chr3:138229166 | A | G | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
11 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.528+156A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229166 | |||||||
chr3:138229166 | ATATATAT others(11): Show |
A | 28 | a0001c0001t0001g0039 a0001c0001t0001g0051 a0001c0001t0001g0052 others(25): Show |
28 | HG00140.hp1 HG00408.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.528+162_528+179del others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229166 | ||||||
chr3:138229167 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528+157T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229167 | |||||||
chr3:138229168 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+158A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229168 | |||||||
chr3:138229168 | ATATATAT others(9): Show |
A | 15 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0001g0105 others(12): Show |
15 | HG01071.hp1 HG01071.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+164_528+179del others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229168 | ||||||
chr3:138229169 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0087 |
2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.528+159T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229169 | |||||||
chr3:138229170 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.528+160A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229170 | |||||||
chr3:138229170 | ATATATAT others(7): Show |
A | 16 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0111 others(13): Show |
16 | HG01069.hp1 HG01074.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.528+166_528+179del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229170 | ||||||
chr3:138229171 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+161T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229171 | |||||||
chr3:138229172 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0003g0008 a0001c0001t0003g0009 |
3 | HG01167.hp1 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.528+162A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229172 | |||||||
chr3:138229172 | ATATATAT others(5): Show |
A | 12 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0075 others(9): Show |
12 | HG00323.hp2 HG00558.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.528+168_528+179del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229172 | ||||||
chr3:138229174 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.528+164A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229174 | |||||||
chr3:138229174 | ATATATAT others(3): Show |
A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
13 | HG00558.hp2 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+170_528+179del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229174 | ||||||
chr3:138229174 | ATATATAT others(9): Show |
A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0037 |
3 | HG02559.hp1 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.528+170_528+185del others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229174 | ||||||
chr3:138229177 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG02630.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.528+167T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229177 | |||||||
chr3:138229178 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.528+173_528+174ins others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0229 a0001c0001t0003g0001 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.528+173_528+174ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0074 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.528+173_528+174ins others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0221 |
2 | HG03130.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.528+173_528+174ins others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.528+173_528+174ins others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0163 a0001c0001t0001g0173 a0001c0001t0001g0207 others(2): Show |
5 | HG01884.hp1 HG02683.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+173_528+174ins others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATATATGT others(11): Show |
1 | a0001c0001t0001g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.528+180_528+197dup others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | ATGTATAT others(7): Show |
1 | a0001c0001t0002g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.528+169_528+170ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229178 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0061 others(4): Show |
7 | HG01175.hp1 HG02896.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.528+168A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229178 | |||||||
chr3:138229178 | ATATATG | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(12): Show |
15 | HG00140.hp2 HG00738.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+192_528+197del others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | ||||||
chr3:138229180 | A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | ||||||
chr3:138229180 | A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | ||||||
chr3:138229180 | ATATG | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0001g0107 others(4): Show |
7 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+174_528+177del others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | ||||||
chr3:138229180 | ATATGTAT others(3): Show |
A | 2 | a0001c0001t0001g0160 a0001c0001t0008g0036 |
2 | HG02257.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.528+174_528+183del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | ||||||
chr3:138229182 | ATG | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG00408.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.528+174_528+175del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229182 | ||||||
chr3:138229184 | G | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.528+174G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229184 | |||||||
chr3:138229184 | GTATATGT others(7): Show |
G | 1 | a0001c0001t0001g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.528+178_528+191del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229184 | ||||||
chr3:138229190 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0040 others(7): Show |
11 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.528+180G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229190 | |||||||
chr3:138229198 | A | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.528+188A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229198 | |||||||
chr3:138229214 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
8 | HG01123.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+204T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229214 | |||||||
chr3:138229216 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.528+206T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229216 | |||||||
chr3:138229295 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.528+285A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229295 | |||||||
chr3:138229336 | CT | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+341delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229336 | ||||||
chr3:138229359 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528+349C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229359 | |||||||
chr3:138229402 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+392G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229402 | |||||||
chr3:138229407 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+397G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229407 | |||||||
chr3:138229638 | T | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.528+628T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229638 | |||||||
chr3:138229886 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.528+876A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229886 | |||||||
chr3:138230155 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.528+1145A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230155 | |||||||
chr3:138230179 | C | A | 1 | a0001c0001t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.528+1169C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230179 | |||||||
chr3:138230187 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.528+1177C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230187 | |||||||
chr3:138230209 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.528+1199G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230209 | |||||||
chr3:138230371 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.528+1361C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230371 | |||||||
chr3:138230610 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.528+1600C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230610 | |||||||
chr3:138231309 | GATTT | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(10): Show |
13 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+2302_528+2305d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231309 | ||||||
chr3:138231334 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.528+2324A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138231334 | |||||||
chr3:138231411 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.528+2401A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138231411 | |||||||
chr3:138231788 | GA | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(12): Show |
15 | HG01123.hp2 HG01175.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.528+2788delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231788 | ||||||
chr3:138231789 | A | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0169 |
2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.528+2779A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138231789 | |||||||
chr3:138231961 | C | CT | 156 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0038 others(153): Show |
156 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.528+2978dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | ||||||
chr3:138231961 | C | CTT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
55 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.528+2977_528+2978d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | ||||||
chr3:138231961 | C | CTTT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0032 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+2976_528+2978d others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | ||||||
chr3:138231961 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.528+2966_528+2978d others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | ||||||
chr3:138232026 | A | G | 20 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0001g0144 others(17): Show |
20 | HG00323.hp2 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.529-3008A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232026 | |||||||
chr3:138232154 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.529-2880T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232154 | |||||||
chr3:138232252 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02735.hp1 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.529-2782A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232252 | |||||||
chr3:138232352 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-2682T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232352 | |||||||
chr3:138232484 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.529-2550A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232484 | |||||||
chr3:138232659 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.529-2375T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232659 | |||||||
chr3:138232703 | A | T | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.529-2331A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232703 | |||||||
chr3:138232902 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.529-2132G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232902 | |||||||
chr3:138232982 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529-2052A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232982 | |||||||
chr3:138232983 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529-2051A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232983 | |||||||
chr3:138233035 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529-1999A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233035 | |||||||
chr3:138233052 | C | CG | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-1981dupG | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138233052 | ||||||
chr3:138233473 | T | A | 105 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0049 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.529-1561T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233473 | |||||||
chr3:138233553 | AAG | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0003g0001 others(6): Show |
10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.529-1475_529-1474d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138233553 | ||||||
chr3:138233677 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.529-1357C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233677 | |||||||
chr3:138233826 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG00735.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.529-1208C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233826 | |||||||
chr3:138234036 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.529-998A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234036 | |||||||
chr3:138234154 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529-880A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234154 | |||||||
chr3:138234463 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-571G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234463 | |||||||
chr3:138234565 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.529-469T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234565 | |||||||
chr3:138234642 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.529-392G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234642 | |||||||
chr3:138234794 | T | G | 1 | a0001c0001t0005g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.529-240T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234794 | |||||||
chr3:138234989 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.529-45G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234989 | |||||||
chr3:138235272 | TA | T | 11 | a0001c0001t0001g0048 a0001c0001t0001g0112 a0001c0001t0001g0119 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.609+173delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138235272 | ||||||
chr3:138235651 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.609+537T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138235651 | |||||||
chr3:138235798 | C | CT | 69 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
70 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.609+709dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138235798 | ||||||
chr3:138235798 | C | CTT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0084 others(5): Show |
8 | HG01346.hp2 HG01433.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+708_609+709dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138235798 | ||||||
chr3:138235891 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.609+777C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138235891 | |||||||
chr3:138236133 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.609+1019A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236133 | |||||||
chr3:138236213 | A | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0160 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.610-1096A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236213 | |||||||
chr3:138236287 | C | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-1022C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236287 | |||||||
chr3:138236342 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.610-967T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236342 | |||||||
chr3:138236394 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.610-915C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236394 | |||||||
chr3:138236735 | T | TA | 7 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-560dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138236735 | ||||||
chr3:138237035 | A | G | 15 | a0001c0001t0001g0060 a0001c0001t0001g0175 a0001c0001t0001g0190 others(12): Show |
15 | NA18747.hp2 NA18941.hp1 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.610-274A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138237035 | |||||||
chr3:138237087 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.610-222T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138237087 | |||||||
chr3:138237839 | C | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+267C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138237839 | |||||||
chr3:138238067 | G | GT | 7 | a0001c0001t0001g0070 a0001c0001t0001g0110 a0001c0001t0001g0121 others(4): Show |
7 | HG01255.hp1 HG01255.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.776+511dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr3 | 138238067 | ||||||
chr3:138238084 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.776+512C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238084 | |||||||
chr3:138238085 | T | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(21): Show |
25 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.776+513T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238085 | |||||||
chr3:138238085 | T | TG | 3 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0020 |
3 | HG02258.hp2 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.776+513_776+514ins others(1): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238085 | |||||||
chr3:138238137 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.776+565G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238137 | |||||||
chr3:138238183 | T | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.776+611T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238183 | |||||||
chr3:138238184 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+612C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238184 | |||||||
chr3:138238316 | C | T | 2 | a0001c0001t0001g0055 a0002c0002t0001g0063 |
2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.776+744C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238316 | |||||||
chr3:138238378 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.776+806T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238378 | |||||||
chr3:138238714 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777-754G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238714 | |||||||
chr3:138239310 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0003t0001g0031 |
3 | HG02280.hp1 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.777-158G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138239310 | |||||||
chr3:138239596 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.837+68C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138239596 | |||||||
chr3:138239730 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(22): Show |
26 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.837+202G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138239730 | |||||||
chr3:138240352 | T | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0182 |
3 | HG02965.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.837+824T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240352 | |||||||
chr3:138240686 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.838-1097C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240686 | |||||||
chr3:138240720 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(15): Show |
19 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.838-1063A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240720 | |||||||
chr3:138240815 | G | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-968G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240815 | |||||||
chr3:138240815 | G | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.838-968G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240815 | |||||||
chr3:138241183 | A | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.838-600A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138241183 | |||||||
chr3:138241407 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0003t0001g0031 |
3 | HG02280.hp1 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.838-376G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138241407 | |||||||
chr3:138241758 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.838-25A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138241758 | |||||||
chr3:138242061 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | NA18980.hp1 NA18986.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+78T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242061 | |||||||
chr3:138242097 | T | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
27 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1038+114T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242097 | |||||||
chr3:138242128 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1038+145G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242128 | |||||||
chr3:138242226 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+243A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242226 | |||||||
chr3:138242426 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1038+443C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242426 | |||||||
chr3:138243118 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1038+1135A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243118 | |||||||
chr3:138243123 | C | A | 1 | a0001c0001t0002g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1038+1140C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243123 | |||||||
chr3:138243135 | A | C | 66 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(63): Show |
66 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1038+1152A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243135 | |||||||
chr3:138243378 | C | T | 9 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0083 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038+1395C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243378 | |||||||
chr3:138243575 | G | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1039-1513G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243575 | |||||||
chr3:138243838 | G | T | 1 | a0001c0001t0006g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1039-1250G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243838 | |||||||
chr3:138244190 | A | G | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1039-898A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244190 | |||||||
chr3:138244212 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1039-876A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244212 | |||||||
chr3:138244343 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039-745T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244343 | |||||||
chr3:138244479 | C | T | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1039-609C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244479 | |||||||
chr3:138244569 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1039-519C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244569 | |||||||
chr3:138244745 | G | C | 97 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0049 others(94): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1039-343G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244745 | |||||||
chr3:138244785 | T | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-303T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244785 | |||||||
chr3:138245077 | T | A | 1 | a0001c0001t0007g0028 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1039-11T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138245077 | |||||||
chr3:138245421 | T | G | 9 | a0001c0001t0001g0053 a0001c0001t0001g0073 a0001c0001t0001g0074 others(6): Show |
9 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1134+238T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138245421 | |||||||
chr3:138245862 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+679C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138245862 | |||||||
chr3:138245882 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1134+699C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138245882 | |||||||
chr3:138246029 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1134+846A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138246029 | |||||||
chr3:138246126 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0135 |
2 | NA18977.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1134+943G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138246126 | |||||||
chr3:138246405 | T | TA | 7 | a0001c0001t0001g0055 a0001c0001t0001g0077 a0001c0001t0001g0159 others(4): Show |
7 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1134+1223dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138246405 | ||||||
chr3:138246426 | T | TTGACGCC others(63): Show |
1 | a0001c0001t0001g0187 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1134+1244_1134+131 others(74): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138246426 | ||||||
chr3:138246706 | C | CTAT | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
27 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1134+1524_1134+152 others(7): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138246706 | ||||||
chr3:138246807 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1134+1624G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138246807 | |||||||
chr3:138247043 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1134+1860A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247043 | |||||||
chr3:138247056 | G | C | 1 | a0001c0001t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1134+1873G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247056 | |||||||
chr3:138247089 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1134+1906G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247089 | |||||||
chr3:138247353 | C | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
19 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134+2170C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247353 | |||||||
chr3:138247377 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1134+2194A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247377 | |||||||
chr3:138247483 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1134+2300A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247483 | |||||||
chr3:138247530 | A | G | 9 | a0001c0001t0001g0039 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
9 | HG02080.hp2 HG02300.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1134+2347A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247530 | |||||||
chr3:138247804 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1134+2621T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247804 | |||||||
chr3:138248001 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1134+2818G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248001 | |||||||
chr3:138248186 | G | A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+3003G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248186 | |||||||
chr3:138248337 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1134+3154C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248337 | |||||||
chr3:138248370 | G | GT | 4 | a0001c0001t0001g0048 a0001c0001t0001g0120 a0001c0001t0001g0130 others(1): Show |
4 | HG01884.hp2 HG03704.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+3188dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138248370 | ||||||
chr3:138248434 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1134+3251G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248434 | |||||||
chr3:138248962 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+3779G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248962 | |||||||
chr3:138249037 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0182 |
3 | HG02965.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+3854G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249037 | |||||||
chr3:138249706 | T | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+4523T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249706 | |||||||
chr3:138249774 | A | G | 1 | a0001c0003t0001g0031 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1134+4591A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249774 | |||||||
chr3:138249926 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1134+4743C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249926 | |||||||
chr3:138250111 | T | A | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG01433.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1134+4928T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250111 | |||||||
chr3:138250270 | T | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
19 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134+5087T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250270 | |||||||
chr3:138250485 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1134+5302A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250485 | |||||||
chr3:138250692 | G | T | 10 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0088 others(7): Show |
10 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1134+5509G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250692 | |||||||
chr3:138250763 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1134+5580A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250763 | |||||||
chr3:138250764 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0008g0036 |
2 | HG00735.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1134+5581T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250764 | |||||||
chr3:138250766 | T | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+5583T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250766 | |||||||
chr3:138250887 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1134+5704C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250887 | |||||||
chr3:138251109 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1134+5926C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138251109 | |||||||
chr3:138251233 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1134+6050T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138251233 | |||||||
chr3:138252065 | G | A | 100 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0049 others(97): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1134+6882G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252065 | |||||||
chr3:138252405 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0190 |
2 | NA18747.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1134+7222A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252405 | |||||||
chr3:138252452 | C | CT | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
28 | HG01106.hp1 HG01433.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1134+7288dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252452 | ||||||
chr3:138252461 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1134+7278T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252461 | |||||||
chr3:138252492 | C | T | 1 | a0001c0001t0008g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1134+7309C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252492 | |||||||
chr3:138252493 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+7310G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252493 | |||||||
chr3:138252494 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1134+7311C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252494 | |||||||
chr3:138252719 | G | A | 5 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+7536G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252719 | |||||||
chr3:138252746 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1134+7563G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252746 | |||||||
chr3:138252746 | G | GCC | 22 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(19): Show |
22 | HG01069.hp2 HG01123.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1134+7578_1134+757 others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCC | 41 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0038 others(38): Show |
41 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.1134+7577_1134+757 others(7): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCC | 48 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0044 others(45): Show |
48 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1134+7576_1134+757 others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCCC | 40 | a0001c0001t0001g0032 a0001c0001t0001g0059 a0001c0001t0001g0069 others(37): Show |
40 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.1134+7575_1134+757 others(9): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCCCC | 24 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(21): Show |
24 | HG00738.hp2 HG00741.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1134+7574_1134+757 others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCCCCC | 16 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0103 others(13): Show |
16 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.1134+7573_1134+757 others(11): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCCCCC others(3): Show |
1 | a0001c0001t0001g0136 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1134+7570_1134+757 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCCCCC others(5): Show |
1 | a0001c0001t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1134+7568_1134+757 others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCCCCC others(6): Show |
1 | a0001c0001t0001g0052 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1134+7567_1134+757 others(17): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | G | GCCCCCCC others(8): Show |
1 | a0001c0001t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1134+7565_1134+757 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | GCC | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
19 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134+7578_1134+757 others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252746 | GCCCCCCC others(4): Show |
G | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1134+7569_1134+757 others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | ||||||
chr3:138252757 | C | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(9): Show |
13 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1134+7574C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252757 | |||||||
chr3:138252763 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1134+7580A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252763 | |||||||
chr3:138252808 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1134+7625C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252808 | |||||||
chr3:138253075 | C | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(22): Show |
26 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1134+7892C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253075 | |||||||
chr3:138253148 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1134+7965C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253148 | |||||||
chr3:138253474 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1134+8291A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253474 | |||||||
chr3:138253706 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+8523A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253706 | |||||||
chr3:138254047 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1134+8864C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254047 | |||||||
chr3:138254151 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1134+8968A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254151 | |||||||
chr3:138254336 | T | C | 26 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(23): Show |
26 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1134+9153T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254336 | |||||||
chr3:138254414 | C | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0182 |
3 | HG02965.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+9231C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254414 | |||||||
chr3:138254538 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-9201A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254538 | |||||||
chr3:138254731 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1135-9008G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254731 | |||||||
chr3:138254792 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-8947T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254792 | |||||||
chr3:138255189 | CTGTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1135-8532_1135-851 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255189 | ||||||
chr3:138255191 | G | GT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-8534dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255191 | ||||||
chr3:138255191 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0001g0222 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1135-8534_1135-851 others(20): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255191 | ||||||
chr3:138255200 | T | TG | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-8539_1135-853 others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255200 | |||||||
chr3:138255201 | T | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1135-8538T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255201 | |||||||
chr3:138255202 | T | G | 20 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(17): Show |
21 | HG01099.hp1 HG01109.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1135-8537T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255202 | |||||||
chr3:138255203 | T | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-8536T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255203 | |||||||
chr3:138255206 | G | GT | 22 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
23 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1135-8519dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255206 | ||||||
chr3:138255206 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1135-8533G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255206 | |||||||
chr3:138255209 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-8530T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255209 | |||||||
chr3:138255210 | T | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-8529T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255210 | |||||||
chr3:138255211 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-8528T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255211 | |||||||
chr3:138255212 | T | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0210 |
3 | HG02055.hp1 HG03579.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1135-8527T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255212 | |||||||
chr3:138255213 | T | G | 1 | a0001c0001t0002g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1135-8526T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255213 | |||||||
chr3:138255214 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1135-8525T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255214 | |||||||
chr3:138255215 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-8524T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255215 | |||||||
chr3:138255265 | T | C | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1135-8474T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255265 | |||||||
chr3:138255414 | G | A | 1 | a0001c0001t0006g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1135-8325G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255414 | |||||||
chr3:138255492 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0125 |
3 | HG01070.hp1 HG01071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1135-8247G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255492 | |||||||
chr3:138255707 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1135-8032C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255707 | |||||||
chr3:138255721 | T | G | 1 | a0001c0001t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1135-8018T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255721 | |||||||
chr3:138255817 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1135-7922T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255817 | |||||||
chr3:138255911 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1135-7828C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255911 | |||||||
chr3:138255946 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-7793A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255946 | |||||||
chr3:138256186 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1135-7553A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256186 | |||||||
chr3:138256206 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0217 |
3 | HG00741.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1135-7533C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256206 | |||||||
chr3:138256353 | T | C | 1 | a0001c0001t0002g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1135-7386T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256353 | |||||||
chr3:138256399 | C | CTCCTT | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-7339_1135-733 others(9): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256399 | ||||||
chr3:138256401 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1135-7338T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256401 | |||||||
chr3:138256402 | C | CT | 26 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0049 others(23): Show |
26 | HG01175.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1135-7312dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | ||||||
chr3:138256402 | C | CTTT | 7 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
8 | HG01884.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135-7314_1135-731 others(7): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | ||||||
chr3:138256402 | C | CTTTT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG02723.hp1 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-7315_1135-731 others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | ||||||
chr3:138256402 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0083 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135-7321_1135-731 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | ||||||
chr3:138256402 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1135-7322_1135-731 others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | ||||||
chr3:138256402 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
6 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-7337C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256402 | |||||||
chr3:138256402 | CT | C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0121 a0001c0001t0001g0165 others(2): Show |
5 | HG01516.hp1 HG02897.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-7312delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | ||||||
chr3:138256402 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0241 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1135-7321_1135-731 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | ||||||
chr3:138256457 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG01433.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1135-7282C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256457 | |||||||
chr3:138256701 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1135-7038C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256701 | |||||||
chr3:138256702 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1135-7037G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256702 | |||||||
chr3:138256777 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1135-6962T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256777 | |||||||
chr3:138256835 | G | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(9): Show |
13 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1135-6904G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256835 | |||||||
chr3:138257088 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1135-6651A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138257088 | |||||||
chr3:138257424 | A | G | 1 | a0001c0001t0006g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1135-6315A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138257424 | |||||||
chr3:138257731 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1135-6008A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138257731 | |||||||
chr3:138258057 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-5682C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258057 | |||||||
chr3:138258176 | C | G | 2 | a0001c0001t0003g0006 a0001c0001t0003g0007 |
2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1135-5563C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258176 | |||||||
chr3:138258477 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1135-5262T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258477 | |||||||
chr3:138258636 | GATCCTGT others(6): Show |
G | 1 | a0001c0001t0001g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1135-5101_1135-508 others(17): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138258636 | ||||||
chr3:138258680 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1135-5059A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258680 | |||||||
chr3:138258747 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1135-4992C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258747 | |||||||
chr3:138258834 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1135-4905A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258834 | |||||||
chr3:138259011 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1135-4728A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259011 | |||||||
chr3:138259012 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1135-4727C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259012 | |||||||
chr3:138259191 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1135-4548T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259191 | |||||||
chr3:138259370 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1135-4369G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259370 | |||||||
chr3:138259473 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1135-4266A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259473 | |||||||
chr3:138259493 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1135-4246A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259493 | |||||||
chr3:138259644 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1135-4095T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259644 | |||||||
chr3:138259671 | A | G | 15 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0001g0144 others(12): Show |
15 | HG00323.hp2 HG00408.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1135-4068A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259671 | |||||||
chr3:138260165 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1135-3574C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260165 | |||||||
chr3:138260240 | G | A | 5 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-3499G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260240 | |||||||
chr3:138260252 | A | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(16): Show |
20 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1135-3487A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260252 | |||||||
chr3:138260365 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1135-3374T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260365 | |||||||
chr3:138261023 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1135-2716G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261023 | |||||||
chr3:138261379 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1135-2360A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261379 | |||||||
chr3:138261677 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1135-2062A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261677 | |||||||
chr3:138261897 | A | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
7 | HG02080.hp2 HG02300.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1135-1842A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261897 | |||||||
chr3:138262090 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-1649T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262090 | |||||||
chr3:138262551 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-1188C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262551 | |||||||
chr3:138262597 | TA | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0039 others(15): Show |
18 | HG01069.hp1 HG01257.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1135-1126delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138262597 | ||||||
chr3:138262614 | T | A | 15 | a0001c0001t0001g0077 a0001c0001t0001g0159 a0001c0001t0001g0160 others(12): Show |
15 | HG01433.hp2 HG02080.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1135-1125T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262614 | |||||||
chr3:138262683 | T | TA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(16): Show |
20 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1135-1045dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138262683 | ||||||
chr3:138262706 | A | G | 10 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0088 others(7): Show |
10 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-1033A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262706 | |||||||
chr3:138262776 | T | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-963T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262776 | |||||||
chr3:138262984 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-755T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262984 | |||||||
chr3:138263015 | CT | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-723delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138263015 | |||||||
chr3:138263319 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1135-420G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138263319 | |||||||
chr3:138263876 | T | G | 108 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0049 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1217+55T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 13/21 | chr3 | 138263876 | |||||||
chr3:138263972 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1217+151G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 13/21 | chr3 | 138263972 | |||||||
chr3:138264412 | CT | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1299+225delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 138264412 | ||||||
chr3:138264412 | CTT | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(30): Show |
34 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1299+224_1299+225d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 138264412 | ||||||
chr3:138264445 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0062 |
3 | HG03130.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1299+233A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264445 | |||||||
chr3:138264459 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1299+247A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264459 | |||||||
chr3:138264489 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1299+277G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264489 | |||||||
chr3:138264499 | A | G | 5 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1299+287A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264499 | |||||||
chr3:138264513 | C | T | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1299+301C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264513 | |||||||
chr3:138264520 | A | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+308A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264520 | |||||||
chr3:138264577 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1299+365G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264577 | |||||||
chr3:138264607 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1299+395G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264607 | |||||||
chr3:138264623 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+411T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264623 | |||||||
chr3:138264754 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1299+542C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264754 | |||||||
chr3:138264757 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+545A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264757 | |||||||
chr3:138264768 | C | A | 1 | a0001c0001t0002g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1299+556C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264768 | |||||||
chr3:138264769 | T | C | 1 | a0001c0001t0002g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1299+557T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264769 | |||||||
chr3:138264770 | ATTTGTTT others(47): Show |
A | 1 | a0001c0001t0002g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1299+559_1299+612d others(56): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264770 | |||||||
chr3:138264894 | AT | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
20 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1299+698delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 138264894 | ||||||
chr3:138264946 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1299+734A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264946 | |||||||
chr3:138264958 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1299+746C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264958 | |||||||
chr3:138265084 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1299+872A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265084 | |||||||
chr3:138265093 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1299+881C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265093 | |||||||
chr3:138265105 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1299+893C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265105 | |||||||
chr3:138265151 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0014 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1299+939C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265151 | |||||||
chr3:138265293 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1299+1081A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265293 | |||||||
chr3:138265414 | A | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
11 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1299+1202A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265414 | |||||||
chr3:138265730 | G | C | 1 | a0001c0001t0006g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1300-1425G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265730 | |||||||
chr3:138265740 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1300-1415A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265740 | |||||||
chr3:138265832 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-1323T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265832 | |||||||
chr3:138265892 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0062 |
3 | HG03130.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1300-1263C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265892 | |||||||
chr3:138266010 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1300-1145T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266010 | |||||||
chr3:138266037 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1300-1118A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266037 | |||||||
chr3:138266259 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1300-896A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266259 | |||||||
chr3:138266295 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
11 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1300-860C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266295 | |||||||
chr3:138266489 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1300-666A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266489 | |||||||
chr3:138266527 | C | A | 2 | a0001c0001t0001g0030 a0001c0003t0001g0031 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1300-628C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266527 | |||||||
chr3:138266542 | A | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-613A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266542 | |||||||
chr3:138266666 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1300-489C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266666 | |||||||
chr3:138266966 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-189G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266966 | |||||||
chr3:138267151 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
splice_region_variant&intron_variant | LOW | c.1300-4A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138267151 | |||||||
chr3:138267376 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1386+135G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138267376 | |||||||
chr3:138267970 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1386+729C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138267970 | |||||||
chr3:138268169 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1386+928G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138268169 | |||||||
chr3:138268677 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1387-1363G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138268677 | |||||||
chr3:138268951 | T | A | 1 | a0001c0001t0002g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1387-1089T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138268951 | |||||||
chr3:138269035 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0144 |
2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1387-1005A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269035 | |||||||
chr3:138269120 | C | T | 5 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387-920C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269120 | |||||||
chr3:138269138 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1387-902A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269138 | |||||||
chr3:138269228 | T | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0046 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1387-812T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269228 | |||||||
chr3:138269487 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1387-553G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269487 | |||||||
chr3:138269724 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1387-316C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269724 | |||||||
chr3:138269798 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1387-242G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269798 | |||||||
chr3:138269820 | C | CT | 140 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1387-202dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 138269820 | ||||||
chr3:138269820 | C | CTT | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387-203_1387-202d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 138269820 | ||||||
chr3:138270314 | G | A | 17 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0066 others(14): Show |
17 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1479+182G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270314 | |||||||
chr3:138270452 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1479+320A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270452 | |||||||
chr3:138270514 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0147 others(1): Show |
4 | NA18965.hp1 NA18984.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+382C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270514 | |||||||
chr3:138270636 | T | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0182 |
3 | HG01891.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1479+504T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270636 | |||||||
chr3:138271121 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1479+989T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271121 | |||||||
chr3:138271139 | T | C | 2 | a0001c0001t0003g0064 a0001c0001t0006g0029 |
2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1479+1007T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271139 | |||||||
chr3:138271283 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1479+1151T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271283 | |||||||
chr3:138271719 | A | G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480-1248A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271719 | |||||||
chr3:138271798 | C | CT | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-1154dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | ||||||
chr3:138271798 | C | CTTTCTTT others(8): Show |
1 | a0001c0001t0003g0008 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1480-1166_1480-116 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | ||||||
chr3:138271798 | C | CTTTCTTT others(9): Show |
6 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(3): Show |
7 | HG01167.hp1 HG01884.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1480-1166_1480-116 others(20): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | ||||||
chr3:138271798 | C | CTTTCTTT others(10): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG02723.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1166_1480-116 others(21): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | ||||||
chr3:138271798 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1480-1168_1480-115 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | ||||||
chr3:138271798 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1480-1154_1480-115 others(21): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | ||||||
chr3:138271799 | T | C | 1 | a0001c0001t0007g0028 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1480-1168T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271799 | |||||||
chr3:138271909 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1480-1058C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271909 | |||||||
chr3:138271950 | C | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0159 a0001c0001t0001g0163 others(1): Show |
4 | HG02080.hp1 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1017C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271950 | |||||||
chr3:138272249 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1480-718C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138272249 | |||||||
chr3:138272408 | T | TAAGACAT others(313): Show |
1 | a0001c0001t0001g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1480-548_1480-547i others(322): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138272408 | ||||||
chr3:138272479 | T | TA | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1480-487dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138272479 | ||||||
chr3:138272523 | C | T | 2 | a0001c0001t0001g0030 a0001c0003t0001g0031 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1480-444C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138272523 | |||||||
chr3:138272912 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1480-55T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138272912 | |||||||
chr3:138273188 | G | C | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1629+72G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273188 | |||||||
chr3:138273278 | G | A | 11 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0088 others(8): Show |
11 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1629+162G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273278 | |||||||
chr3:138273369 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0046 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1629+253G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273369 | |||||||
chr3:138273821 | C | CT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG02723.hp1 HG03098.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1630-615dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138273821 | ||||||
chr3:138273909 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1630-540C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273909 | |||||||
chr3:138273962 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630-487G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273962 | |||||||
chr3:138273972 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630-477A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273972 | |||||||
chr3:138274103 | C | T | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630-346C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274103 | |||||||
chr3:138274196 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1630-253T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274196 | |||||||
chr3:138274232 | CAT | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
10 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1630-216_1630-215d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274232 | |||||||
chr3:138274233 | A | ATG | 28 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
28 | HG00408.hp2 HG00735.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1630-190_1630-189d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | ||||||
chr3:138274233 | A | ATGTG | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0166 |
3 | HG01109.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1630-192_1630-189d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | ||||||
chr3:138274233 | A | ATGTGTG | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1630-194_1630-189d others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | ||||||
chr3:138274233 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1630-198_1630-189d others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | ||||||
chr3:138274233 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1630-200_1630-189d others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | ||||||
chr3:138274233 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1630-216A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274233 | |||||||
chr3:138274233 | ATG | A | 27 | a0001c0001t0001g0055 a0001c0001t0001g0071 a0001c0001t0001g0072 others(24): Show |
28 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1630-190_1630-189d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | ||||||
chr3:138274233 | ATGTG | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG01978.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1630-192_1630-189d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | ||||||
chr3:138274747 | C | G | 73 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0049 others(70): Show |
73 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1725+203C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274747 | |||||||
chr3:138274757 | G | T | 1 | a0001c0001t0002g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1725+213G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274757 | |||||||
chr3:138274871 | A | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1725+327A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274871 | |||||||
chr3:138274898 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1725+354G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274898 | |||||||
chr3:138274924 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0106 others(3): Show |
6 | NA18947.hp2 NA18949.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+380C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274924 | |||||||
chr3:138275001 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1725+457C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275001 | |||||||
chr3:138275168 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+624C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275168 | |||||||
chr3:138275195 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1725+651A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275195 | |||||||
chr3:138275267 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1725+723C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275267 | |||||||
chr3:138275403 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1725+859C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275403 | |||||||
chr3:138275477 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1725+933T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275477 | |||||||
chr3:138275505 | T | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
169 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.1725+961T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275505 | |||||||
chr3:138275617 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1725+1073C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275617 | |||||||
chr3:138276153 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1725+1609C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276153 | |||||||
chr3:138276175 | T | C | 27 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1725+1631T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276175 | |||||||
chr3:138276188 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0133 |
2 | NA18957.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1725+1644G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276188 | |||||||
chr3:138276208 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1725+1664G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276208 | |||||||
chr3:138276235 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(8): Show |
12 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1725+1691C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276235 | |||||||
chr3:138276419 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1725+1875C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276419 | |||||||
chr3:138276658 | CA | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+2115delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276658 | |||||||
chr3:138277037 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1725+2493G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277037 | |||||||
chr3:138277064 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1725+2520C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277064 | |||||||
chr3:138277085 | G | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0106 others(3): Show |
6 | NA18947.hp2 NA18949.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+2541G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277085 | |||||||
chr3:138277100 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1725+2556C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277100 | |||||||
chr3:138277206 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1725+2662G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277206 | |||||||
chr3:138277430 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1725+2886C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277430 | |||||||
chr3:138277618 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0092 |
3 | NA18949.hp1 NA18969.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1725+3074A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277618 | |||||||
chr3:138277622 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1725+3078T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277622 | |||||||
chr3:138277785 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1725+3241C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277785 | |||||||
chr3:138277892 | CATATAAT others(3): Show |
C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0037 |
2 | HG00735.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1725+3353_1725+336 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138277892 | ||||||
chr3:138278102 | T | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG01167.hp1 HG01169.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1725+3558T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278102 | |||||||
chr3:138278223 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1725+3679G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278223 | |||||||
chr3:138278397 | G | A | 24 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1725+3853G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278397 | |||||||
chr3:138278456 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+3912A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278456 | |||||||
chr3:138278503 | C | CA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+3970dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138278503 | ||||||
chr3:138278654 | G | A | 2 | a0001c0001t0001g0055 a0002c0002t0001g0063 |
2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1725+4110G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278654 | |||||||
chr3:138278900 | G | T | 12 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0147 others(9): Show |
12 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1725+4356G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278900 | |||||||
chr3:138278945 | A | G | 17 | a0001c0001t0001g0055 a0001c0001t0001g0071 a0001c0001t0001g0077 others(14): Show |
17 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1725+4401A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278945 | |||||||
chr3:138278993 | C | T | 143 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(140): Show |
143 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1725+4449C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278993 | |||||||
chr3:138279010 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+4466A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279010 | |||||||
chr3:138279204 | G | GT | 4 | a0001c0001t0001g0191 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | NA18963.hp2 NA18977.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+4665dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138279204 | ||||||
chr3:138279400 | T | G | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1725+4856T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279400 | |||||||
chr3:138279616 | A | G | 9 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(6): Show |
10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726-4815A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279616 | |||||||
chr3:138279675 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1726-4756G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279675 | |||||||
chr3:138279918 | T | C | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1726-4513T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279918 | |||||||
chr3:138279923 | G | A | 2 | a0001c0001t0001g0030 a0001c0003t0001g0031 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1726-4508G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279923 | |||||||
chr3:138279972 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1726-4459C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279972 | |||||||
chr3:138280051 | G | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0062 |
3 | HG03130.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1726-4380G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280051 | |||||||
chr3:138280184 | A | C | 1 | a0001c0001t0007g0028 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1726-4247A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280184 | |||||||
chr3:138280244 | GCAAAGAA others(20): Show |
G | 16 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0088 others(13): Show |
16 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1726-4160_1726-413 others(31): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138280244 | ||||||
chr3:138280422 | A | G | 17 | a0001c0001t0001g0055 a0001c0001t0001g0071 a0001c0001t0001g0077 others(14): Show |
17 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1726-4009A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280422 | |||||||
chr3:138280497 | C | CT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0235 others(2): Show |
5 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-3920dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138280497 | ||||||
chr3:138280522 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1726-3909C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280522 | |||||||
chr3:138280685 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1726-3746G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280685 | |||||||
chr3:138280738 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1726-3693C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280738 | |||||||
chr3:138280926 | C | G | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1726-3505C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280926 | |||||||
chr3:138281170 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1726-3261G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281170 | |||||||
chr3:138281217 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1726-3214G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281217 | |||||||
chr3:138281219 | T | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0078 others(1): Show |
4 | HG02258.hp2 HG02300.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-3212T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281219 | |||||||
chr3:138281298 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1726-3133C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281298 | |||||||
chr3:138281364 | C | T | 8 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1726-3067C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281364 | |||||||
chr3:138281586 | G | A | 1 | a0001c0001t0008g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1726-2845G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281586 | |||||||
chr3:138281813 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-2618G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281813 | |||||||
chr3:138281860 | A | G | 9 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(6): Show |
10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726-2571A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281860 | |||||||
chr3:138281884 | A | C | 4 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG01109.hp2 HG03017.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-2547A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281884 | |||||||
chr3:138282253 | T | G | 1 | a0001c0001t0007g0028 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1726-2178T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282253 | |||||||
chr3:138282635 | C | CA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(8): Show |
12 | HG00738.hp1 HG01884.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-1776dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138282635 | ||||||
chr3:138282635 | CA | C | 7 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0140 others(4): Show |
7 | HG01069.hp2 HG01255.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1726-1776delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138282635 | ||||||
chr3:138282711 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1726-1720A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282711 | |||||||
chr3:138282832 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1726-1599T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282832 | |||||||
chr3:138282992 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1726-1439C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282992 | |||||||
chr3:138283005 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0182 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1726-1426G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283005 | |||||||
chr3:138283222 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1726-1209A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283222 | |||||||
chr3:138283345 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1726-1086C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283345 | |||||||
chr3:138283455 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1726-976T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283455 | |||||||
chr3:138283581 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-850C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283581 | |||||||
chr3:138284164 | A | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-267A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138284164 | |||||||
chr3:138284549 | C | T | 6 | a0001c0001t0001g0080 a0001c0001t0002g0093 a0001c0001t0002g0094 others(3): Show |
6 | HG01109.hp2 HG03017.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+23C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284549 | |||||||
chr3:138284673 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1821+147T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284673 | |||||||
chr3:138284683 | GA | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1821+164delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 138284683 | ||||||
chr3:138284684 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0130 |
2 | HG01884.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1821+158A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284684 | |||||||
chr3:138284838 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1821+312T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284838 | |||||||
chr3:138285827 | G | A | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1821+1301G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138285827 | |||||||
chr3:138286089 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1821+1563G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286089 | |||||||
chr3:138286090 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1821+1564C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286090 | |||||||
chr3:138286187 | C | T | 5 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 others(2): Show |
5 | HG01109.hp2 HG03017.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821+1661C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286187 | |||||||
chr3:138286191 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
27 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1821+1665T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286191 | |||||||
chr3:138286194 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0122 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1821+1668C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286194 | |||||||
chr3:138286237 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1821+1711C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286237 | |||||||
chr3:138286240 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.1821+1714A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286240 | |||||||
chr3:138286284 | G | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1821+1758G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286284 | |||||||
chr3:138286446 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1821+1920A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286446 | |||||||
chr3:138286738 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1821+2212A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286738 | |||||||
chr3:138286822 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1822-2226T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286822 | |||||||
chr3:138287035 | C | G | 11 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0088 others(8): Show |
11 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1822-2013C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287035 | |||||||
chr3:138287080 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0109 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1822-1968A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287080 | |||||||
chr3:138287798 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1822-1250T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287798 | |||||||
chr3:138287823 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1822-1225C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287823 | |||||||
chr3:138288196 | G | A | 21 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0066 others(18): Show |
21 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1822-852G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288196 | |||||||
chr3:138288402 | C | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-646C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288402 | |||||||
chr3:138288635 | C | CT | 5 | a0001c0001t0001g0058 a0001c0001t0001g0092 a0001c0001t0001g0185 others(2): Show |
5 | HG01106.hp1 HG01255.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-392dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 138288635 | ||||||
chr3:138288635 | CT | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
85 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1822-392delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 138288635 | ||||||
chr3:138288740 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1822-308C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288740 | |||||||
chr3:138288914 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1822-134G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288914 | |||||||
chr3:138289298 | T | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
173 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.1894+178T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289298 | |||||||
chr3:138289824 | C | G | 7 | a0001c0001t0001g0055 a0001c0001t0002g0093 a0001c0001t0002g0094 others(4): Show |
7 | HG00323.hp1 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1894+704C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289824 | |||||||
chr3:138289900 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1895-646G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289900 | |||||||
chr3:138289979 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1895-567A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289979 | |||||||
chr3:138290203 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1895-343G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138290203 | |||||||
chr3:138290342 | A | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(19): Show |
23 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1895-204A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138290342 | |||||||
chr3:138290463 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0116 |
2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1895-83G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138290463 | |||||||
chr3:138290803 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1988+164G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138290803 | |||||||
chr3:138290813 | A | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(19): Show |
23 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1988+174A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138290813 | |||||||
chr3:138291129 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1988+490A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291129 | |||||||
chr3:138291301 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0125 |
3 | HG01070.hp1 HG01071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1988+662C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291301 | |||||||
chr3:138291616 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1988+977A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291616 | |||||||
chr3:138291642 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1988+1003G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291642 | |||||||
chr3:138292063 | G | A | 1 | a0001c0001t0010g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1988+1424G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292063 | |||||||
chr3:138292291 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1988+1652C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292291 | |||||||
chr3:138292320 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1988+1681G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292320 | |||||||
chr3:138292656 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1988+2017G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292656 | |||||||
chr3:138292785 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1988+2146C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292785 | |||||||
chr3:138293014 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1988+2375C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293014 | |||||||
chr3:138293199 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+2560G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293199 | |||||||
chr3:138293307 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1989-2552C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293307 | |||||||
chr3:138293310 | G | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0137 a0001c0001t0004g0102 others(1): Show |
4 | HG00558.hp1 HG02165.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989-2549G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293310 | |||||||
chr3:138293488 | G | C | 13 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0076 others(10): Show |
13 | HG00408.hp1 HG01070.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1989-2371G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293488 | |||||||
chr3:138293802 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1989-2057C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293802 | |||||||
chr3:138294088 | A | G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1989-1771A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294088 | |||||||
chr3:138294223 | G | T | 1 | a0001c0001t0002g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1989-1636G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294223 | |||||||
chr3:138294355 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
176 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.1989-1504T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294355 | |||||||
chr3:138294651 | C | T | 8 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1989-1208C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294651 | |||||||
chr3:138294766 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989-1093T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294766 | |||||||
chr3:138294902 | C | CT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1989-944dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr3 | 138294902 | ||||||
chr3:138295098 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1989-761C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295098 | |||||||
chr3:138295331 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1989-528A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295331 | |||||||
chr3:138295425 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1989-434G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295425 | |||||||
chr3:138295692 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989-167C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295692 |