Item | Value |
---|---|
geneid | 84985 |
ensemblid | ENSG00000147689.17 |
hgncid | 28210 |
symbol | FAM83A |
name | family with sequence similarity 83 member A |
refseq_nuc | NM_001394396.1 |
refseq_prot | NP_001381325.1 |
ensembl_nuc | ENST00000690554.1 |
ensembl_prot | ENSP00000509471.1 |
mane_status | MANE Select |
chr | chr8 |
start | 123182665 |
end | 123210078 |
strand | + |
ver | v1.2 |
region | chr8:123182665-123210078 |
region5000 | chr8:123177665-123215078 |
regionname0 | FAM83A_chr8_123182665_123210078 |
regionname5000 | FAM83A_chr8_123177665_123215078 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 434 | 290 | 84 | 52 | 107 | 7 | 38 | 78 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
a0002 | 0/0 | 434 | 73 | 2 | 17 | 41 | 7 | 6 | 32 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
a0003 | 0/0 | 434 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
a0004 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
a0005 | 0/0 | 434 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
a0006 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
a0007 | 0/0 | 434 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
a0008 | 0/0 | 434 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | MSRSR others(429): Show |
chr8 | 123177665 | 123215078 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1302 | 288 | 82 | 52 | 107 | 7 | 38 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0001c0004 | 0/0 | 1302 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0002c0002 | 0/0 | 1302 | 73 | 2 | 17 | 41 | 7 | 6 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0003c0003 | 0/0 | 1302 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0004c0006 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0005c0008 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0006c0009 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0007c0007 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 | ||
a0008c0005 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | ATGAG others(1297): Show |
chr8 | 123177665 | 123215078 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3887 | 213 | 39 | 38 | 96 | 4 | 34 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0002 | 0/0 | 3887 | 7 | 0 | 1 | 5 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0003 | 0/0 | 3887 | 27 | 18 | 6 | 0 | 1 | 2 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0004 | 0/0 | 3887 | 18 | 15 | 3 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0005 | 0/0 | 3887 | 4 | 1 | 3 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0006 | 0/0 | 3887 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0007 | 0/0 | 3880 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3875): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0008 | 0/0 | 3887 | 2 | 0 | 0 | 0 | 2 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0009 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0010 | 0/0 | 3887 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0011 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0012 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0013 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0016 | 0/0 | 3887 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0017 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0021 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0001t0023 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0004t0018 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0001c0004t0019 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0002c0002t0001 | 0/0 | 3887 | 21 | 0 | 11 | 8 | 0 | 2 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0002c0002t0002 | 0/0 | 3887 | 49 | 2 | 6 | 31 | 6 | 4 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0002c0002t0014 | 0/0 | 3887 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0002c0002t0020 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0002c0002t0022 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0003c0003t0005 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0003c0003t0009 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0004c0006t0001 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0005c0008t0001 | 0/0 | 3887 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0006c0009t0015 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0007c0007t0001 | 0/0 | 3887 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
a0008c0005t0001 | 0/0 | 3887 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | AGGAG others(3882): Show |
chr8 | 123177665 | 123215078 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 12 | 0 | 0 | 10 | 0 | 2 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0002 | 0/0 | 10 | 6 | 0 | 2 | 0 | 2 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0003 | 0/1 | 8 | 0 | 0 | 2 | 1 | 4 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 8 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0011 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0026 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0005g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0010g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0012g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0013g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0016g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0021g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0001t0023g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0004t0018g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0001c0004t0019g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0006 | 0/0 | 6 | 2 | 1 | 2 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0010 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0014g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0020g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0002c0002t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0003c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0003c0003t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0004c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0005c0008t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0006c0009t0015g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0007c0007t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
a0008c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0183 | EUR | GBR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | GBR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0219 | EUR | FIN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0010 | EUR | FIN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00423 | hp2 | a0004 | c0006 | t0001 | g0090 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00642 | hp2 | a0005 | c0008 | t0001 | g0003 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01099 | hp1 | a0001 | c0001 | t0010 | g0136 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0198 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01515 | hp1 | a0002 | c0002 | t0014 | g0195 | EUR | IBS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0053 | EUR | IBS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0003 | EUR | IBS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0010 | EUR | IBS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0003 | EUR | IBS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0053 | EUR | IBS | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0149 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0130 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02155 | hp2 | a0006 | c0009 | t0015 | g0024 | EAS | CDX | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | CDX | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02257 | hp1 | a0001 | c0004 | t0019 | g0122 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02698 | hp2 | a0007 | c0007 | t0001 | g0074 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03041 | hp1 | a0003 | c0003 | t0005 | g0119 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0207 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0202 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03834 | hp2 | a0001 | c0001 | t0016 | g0174 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04199 | hp1 | a0008 | c0005 | t0001 | g0110 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18522 | hp1 | a0003 | c0003 | t0009 | g0216 | AFR | YRI | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18522 | hp2 | a0001 | c0001 | t0012 | g0027 | AFR | YRI | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18948 | hp2 | a0002 | c0002 | t0022 | g0006 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18950 | hp1 | a0001 | c0001 | t0013 | g0039 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18954 | hp2 | a0001 | c0001 | t0021 | g0210 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18964 | hp1 | a0002 | c0002 | t0020 | g0052 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19001 | hp1 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | LWK | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19043 | hp1 | a0001 | c0001 | t0023 | g0127 | AFR | LWK | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19064 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19081 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | YRI | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | CLM | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02486 | hp2 | a0001 | c0004 | t0018 | g0143 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0134 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0129 | AFR | USA | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | USA | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | LWK | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0003 | REF | REF | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0026 | REF | REF | FAM83A_chr8_123177665_123215078 | FAM83A | chr8 | 123177665 | 123215078 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123182900 | A | G | 1 | a0006 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.44A>G | p.Glu15Gly | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/4 | 236/3887 | 44/1305 | 15/434 | chr8 | 123182900 | |||
chr8:123183124 | G | A | 1 | a0008 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.268G>A | p.Ala90Thr | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/4 | 460/3887 | 268/1305 | 90/434 | chr8 | 123183124 | |||
chr8:123194084 | G | A | 1 | a0002 | 73 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(70): Show |
missense_variant | MODERATE | c.709G>A | p.Ala237Thr | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/4 | 901/3887 | 709/1305 | 237/434 | chr8 | 123194084 | |||
chr8:123207229 | T | G | 1 | a0004 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.846T>G | p.Phe282Leu | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1038/3887 | 846/1305 | 282/434 | chr8 | 123207229 | |||
chr8:123207252 | A | G | 1 | a0005 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.869A>G | p.Tyr290Cys | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1061/3887 | 869/1305 | 290/434 | chr8 | 123207252 | |||
chr8:123207375 | C | T | 1 | a0007 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.992C>T | p.Ser331Phe | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1184/3887 | 992/1305 | 331/434 | chr8 | 123207375 | |||
chr8:123207675 | C | T | 1 | a0003 | 2 | HG03041.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1292C>T | p.Ser431Phe | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1484/3887 | 1292/1305 | 431/434 | chr8 | 123207675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123207436 | G | T | 1 | a0001c0004 | 2 | HG02257.hp1 HG02486.hp2 |
synonymous_variant | LOW | c.1053G>T | p.Ala351Ala | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1245/3887 | 1053/1305 | 351/434 | chr8 | 123207436 | |||
chr8:123207442 | A | G | 1 | a0001c0004 | 2 | HG02257.hp1 HG02486.hp2 |
synonymous_variant | LOW | c.1059A>G | p.Ser353Ser | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1251/3887 | 1059/1305 | 353/434 | chr8 | 123207442 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123182728 | C | T | 6 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0023 others(3): Show |
60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-129C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/4 | chr8 | 123182728 | |||||||
chr8:123182777 | C | T | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0023 others(2): Show |
31 | HG00323.hp1 HG00735.hp2 HG01106.hp1 others(28): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-80C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/4 | chr8 | 123182777 | |||||||
chr8:123182794 | G | C | 6 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(3): Show |
32 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-63G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/4 | 63 | chr8 | 123182794 | ||||||
chr8:123207712 | C | T | 1 | a0001c0001t0008 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*24C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 24 | chr8 | 123207712 | ||||||
chr8:123207860 | C | G | 1 | a0001c0001t0004 | 18 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*172C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 172 | chr8 | 123207860 | ||||||
chr8:123207913 | T | C | 1 | a0002c0002t0020 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*225T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 225 | chr8 | 123207913 | ||||||
chr8:123208004 | C | T | 2 | a0001c0004t0018 a0001c0004t0019 |
2 | HG02257.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*316C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 316 | chr8 | 123208004 | ||||||
chr8:123208210 | T | C | 2 | a0001c0004t0018 a0001c0004t0019 |
2 | HG02257.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*522T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 522 | chr8 | 123208210 | ||||||
chr8:123208273 | C | T | 2 | a0001c0004t0018 a0001c0004t0019 |
2 | HG02257.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*585C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 585 | chr8 | 123208273 | ||||||
chr8:123208274 | G | A | 1 | a0001c0001t0021 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*586G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 586 | chr8 | 123208274 | ||||||
chr8:123208369 | G | T | 2 | a0001c0004t0018 a0001c0004t0019 |
2 | HG02257.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*681G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 681 | chr8 | 123208369 | ||||||
chr8:123208460 | G | C | 1 | a0001c0001t0010 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*772G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 772 | chr8 | 123208460 | ||||||
chr8:123208620 | T | C | 1 | a0001c0001t0011 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 932 | chr8 | 123208620 | ||||||
chr8:123208975 | A | T | 1 | a0001c0004t0018 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1287 | chr8 | 123208975 | ||||||
chr8:123208980 | A | G | 1 | a0001c0004t0018 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1292A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1292 | chr8 | 123208980 | ||||||
chr8:123209024 | G | A | 1 | a0001c0001t0012 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1336G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1336 | chr8 | 123209024 | ||||||
chr8:123209085 | T | C | 2 | a0001c0004t0018 a0001c0004t0019 |
2 | HG02257.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1397T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1397 | chr8 | 123209085 | ||||||
chr8:123209199 | C | T | 1 | a0001c0001t0006 | 5 | HG01884.hp1 HG02055.hp1 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1511C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1511 | chr8 | 123209199 | ||||||
chr8:123209221 | C | A | 1 | a0002c0002t0022 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1533C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1533 | chr8 | 123209221 | ||||||
chr8:123209226 | G | A | 1 | a0001c0001t0013 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1538G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1538 | chr8 | 123209226 | ||||||
chr8:123209323 | ACTGCTCC | A | 1 | a0001c0001t0007 | 3 | NA18977.hp2 NA19001.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1637_*1643delTGCT others(3): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1637 | INFO_REALIGN_3_PRIME | chr8 | 123209323 | |||||
chr8:123209450 | C | T | 1 | a0001c0001t0017 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1762C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1762 | chr8 | 123209450 | ||||||
chr8:123209483 | T | C | 1 | a0002c0002t0014 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1795 | chr8 | 123209483 | ||||||
chr8:123209560 | G | A | 1 | a0006c0009t0015 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1872G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 1872 | chr8 | 123209560 | ||||||
chr8:123209757 | G | A | 2 | a0001c0004t0018 a0001c0004t0019 |
2 | HG02257.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2069G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 2069 | chr8 | 123209757 | ||||||
chr8:123209774 | G | A | 2 | a0001c0004t0018 a0001c0004t0019 |
2 | HG02257.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2086G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 2086 | chr8 | 123209774 | ||||||
chr8:123209809 | G | A | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(2): Show |
25 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2121G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 2121 | chr8 | 123209809 | ||||||
chr8:123209994 | C | T | 1 | a0001c0001t0016 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2306C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 4/4 | 2306 | chr8 | 123209994 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123183342 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0058 |
5 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.480+6G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123183342 | |||||||
chr8:123183395 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.480+59T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123183395 | |||||||
chr8:123183616 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.480+280A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123183616 | |||||||
chr8:123183734 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.480+398T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123183734 | |||||||
chr8:123183788 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.480+452C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123183788 | |||||||
chr8:123183852 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.480+516C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123183852 | |||||||
chr8:123184085 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.480+749C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123184085 | |||||||
chr8:123184154 | C | T | 40 | a0001c0001t0002g0184 a0001c0001t0002g0188 a0001c0001t0002g0189 others(37): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.480+818C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123184154 | |||||||
chr8:123184284 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.480+948G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123184284 | |||||||
chr8:123184303 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480+967G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123184303 | |||||||
chr8:123184398 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.480+1062G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123184398 | |||||||
chr8:123184690 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
82 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.480+1354A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123184690 | |||||||
chr8:123185019 | T | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0012g0027 |
3 | HG03130.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.480+1683T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185019 | |||||||
chr8:123185063 | C | T | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0002c0002t0001g0022 others(4): Show |
11 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.480+1727C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185063 | |||||||
chr8:123185067 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.480+1731G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185067 | |||||||
chr8:123185092 | T | G | 1 | a0001c0001t0006g0028 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.480+1756T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185092 | |||||||
chr8:123185152 | C | T | 2 | a0002c0002t0001g0146 a0002c0002t0001g0147 |
2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.480+1816C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185152 | |||||||
chr8:123185171 | G | T | 3 | a0001c0001t0001g0151 a0002c0002t0001g0022 a0002c0002t0001g0045 |
6 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+1835G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185171 | |||||||
chr8:123185322 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.480+1986A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185322 | |||||||
chr8:123185374 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.480+2038C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185374 | |||||||
chr8:123185440 | C | T | 1 | a0001c0004t0018g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480+2104C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185440 | |||||||
chr8:123185513 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.480+2177C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185513 | |||||||
chr8:123185793 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
232 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.480+2457G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185793 | |||||||
chr8:123185845 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.480+2509C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185845 | |||||||
chr8:123185916 | G | A | 1 | a0003c0003t0009g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.480+2580G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185916 | |||||||
chr8:123185944 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480+2608C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185944 | |||||||
chr8:123185949 | C | A | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.480+2613C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185949 | |||||||
chr8:123185957 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.480+2621A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123185957 | |||||||
chr8:123186022 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.480+2686C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186022 | |||||||
chr8:123186066 | G | A | 2 | a0002c0002t0002g0051 a0002c0002t0002g0183 |
3 | HG00099.hp1 HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.480+2730G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186066 | |||||||
chr8:123186078 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0181 |
3 | HG00673.hp2 HG02083.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.480+2742C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186078 | |||||||
chr8:123186119 | T | C | 15 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0004g0041 others(12): Show |
22 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.480+2783T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186119 | |||||||
chr8:123186173 | G | C | 1 | a0001c0001t0003g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.480+2837G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186173 | |||||||
chr8:123186240 | C | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | HG00140.hp1 HG01175.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2904C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186240 | |||||||
chr8:123186241 | G | A | 1 | a0001c0001t0001g0023 | 3 | HG03017.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.480+2905G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186241 | |||||||
chr8:123186426 | GC | G | 39 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 others(36): Show |
64 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.480+3091delC | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186426 | |||||||
chr8:123186427 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0003g0015 a0001c0001t0003g0021 others(3): Show |
11 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+3091C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186427 | |||||||
chr8:123186433 | C | T | 39 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 others(36): Show |
64 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.480+3097C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186433 | |||||||
chr8:123186506 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.480+3170A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186506 | |||||||
chr8:123186554 | G | A | 1 | a0001c0001t0023g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.480+3218G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186554 | |||||||
chr8:123186604 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.480+3268T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186604 | |||||||
chr8:123186745 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.480+3409G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186745 | |||||||
chr8:123186886 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480+3550G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123186886 | |||||||
chr8:123187083 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.480+3747C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187083 | |||||||
chr8:123187120 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.480+3784G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187120 | |||||||
chr8:123187148 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0176 |
3 | NA18960.hp2 NA18982.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.480+3812A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187148 | |||||||
chr8:123187168 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0003g0142 a0001c0001t0023g0127 |
3 | HG01433.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.480+3832T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187168 | |||||||
chr8:123187200 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
278 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.480+3864G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187200 | |||||||
chr8:123187218 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.480+3882A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187218 | |||||||
chr8:123187402 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.480+4066G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187402 | |||||||
chr8:123187415 | G | A | 12 | a0001c0001t0001g0015 a0001c0001t0003g0015 a0001c0001t0003g0021 others(9): Show |
18 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.480+4079G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187415 | |||||||
chr8:123187422 | C | T | 3 | a0001c0001t0003g0021 a0001c0001t0003g0128 a0001c0001t0009g0129 |
5 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+4086C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187422 | |||||||
chr8:123187467 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.480+4131C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187467 | |||||||
chr8:123187481 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.480+4145G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187481 | |||||||
chr8:123187544 | A | C | 1 | a0002c0002t0002g0212 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.480+4208A>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187544 | |||||||
chr8:123187554 | A | G | 1 | a0001c0001t0016g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.480+4218A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187554 | |||||||
chr8:123187570 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.481-4233A>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187570 | |||||||
chr8:123187787 | C | T | 3 | a0001c0001t0005g0040 a0001c0001t0005g0124 a0001c0001t0005g0125 |
4 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-4016C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187787 | |||||||
chr8:123187788 | G | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0185 a0002c0002t0002g0186 |
8 | NA18953.hp2 NA18955.hp1 NA19007.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-4015G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187788 | |||||||
chr8:123187837 | T | A | 1 | a0001c0001t0003g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.481-3966T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187837 | |||||||
chr8:123187843 | ATTTTTAT others(8): Show |
A | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-3941_481-3927d others(17): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 123187843 | ||||||
chr8:123187923 | C | T | 3 | a0001c0001t0005g0040 a0001c0001t0005g0124 a0001c0001t0005g0125 |
4 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-3880C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187923 | |||||||
chr8:123187924 | G | A | 1 | a0002c0002t0002g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.481-3879G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123187924 | |||||||
chr8:123188043 | A | AT | 50 | a0001c0001t0001g0140 a0001c0001t0002g0184 a0001c0001t0021g0210 others(47): Show |
79 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.481-3749dupT | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 123188043 | ||||||
chr8:123188046 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0058 |
5 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-3757T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188046 | |||||||
chr8:123188080 | G | A | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0218 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-3723G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188080 | |||||||
chr8:123188204 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0038 others(12): Show |
20 | HG00597.hp2 HG00673.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.481-3599C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188204 | |||||||
chr8:123188394 | T | C | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-3409T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188394 | |||||||
chr8:123188459 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.481-3344T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188459 | |||||||
chr8:123188470 | G | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-3333G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188470 | |||||||
chr8:123188539 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0068 |
5 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-3264G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188539 | |||||||
chr8:123188572 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.481-3231C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188572 | |||||||
chr8:123188586 | C | T | 10 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(7): Show |
16 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.481-3217C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188586 | |||||||
chr8:123188629 | G | A | 1 | a0002c0002t0002g0194 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.481-3174G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188629 | |||||||
chr8:123188679 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.481-3124C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188679 | |||||||
chr8:123188684 | A | T | 71 | a0001c0001t0001g0111 a0001c0001t0001g0131 a0001c0001t0001g0132 others(68): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.481-3119A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188684 | |||||||
chr8:123188685 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.481-3118G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188685 | |||||||
chr8:123188735 | G | A | 1 | a0001c0001t0001g0012 | 4 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-3068G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188735 | |||||||
chr8:123188779 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.481-3024G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188779 | |||||||
chr8:123188781 | C | T | 11 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(8): Show |
17 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.481-3022C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188781 | |||||||
chr8:123188990 | C | G | 1 | a0002c0002t0001g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.481-2813C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123188990 | |||||||
chr8:123189015 | T | C | 1 | a0002c0002t0014g0195 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.481-2788T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189015 | |||||||
chr8:123189137 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.481-2666G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189137 | |||||||
chr8:123189268 | C | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-2535C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189268 | |||||||
chr8:123189450 | T | C | 7 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0218 others(4): Show |
8 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-2353T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189450 | |||||||
chr8:123189496 | T | G | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-2307T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189496 | |||||||
chr8:123189612 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.481-2191C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189612 | |||||||
chr8:123189944 | T | C | 70 | a0001c0001t0001g0111 a0001c0001t0001g0131 a0001c0001t0001g0132 others(67): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.481-1859T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189944 | |||||||
chr8:123189996 | G | A | 46 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(43): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.481-1807G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123189996 | |||||||
chr8:123190112 | A | G | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-1691A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190112 | |||||||
chr8:123190284 | C | G | 1 | a0001c0001t0003g0057 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.481-1519C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190284 | |||||||
chr8:123190419 | T | C | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.481-1384T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190419 | |||||||
chr8:123190422 | A | C | 1 | a0001c0001t0004g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.481-1381A>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190422 | |||||||
chr8:123190465 | A | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-1338A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190465 | |||||||
chr8:123190834 | C | G | 1 | a0008c0005t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.481-969C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190834 | |||||||
chr8:123190946 | G | C | 1 | a0001c0001t0002g0193 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.481-857G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190946 | |||||||
chr8:123190963 | A | C | 4 | a0001c0001t0001g0111 a0001c0001t0004g0036 a0001c0001t0004g0123 others(1): Show |
5 | HG01069.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-840A>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190963 | |||||||
chr8:123190975 | C | T | 47 | a0001c0001t0001g0109 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.481-828C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123190975 | |||||||
chr8:123191067 | G | A | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.481-736G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191067 | |||||||
chr8:123191082 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.481-721T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191082 | |||||||
chr8:123191268 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.481-535G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191268 | |||||||
chr8:123191274 | C | T | 46 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(43): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.481-529C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191274 | |||||||
chr8:123191296 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0153 others(1): Show |
7 | HG00738.hp2 HG01358.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-507C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191296 | |||||||
chr8:123191309 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.481-494G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191309 | |||||||
chr8:123191423 | G | A | 46 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(43): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.481-380G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191423 | |||||||
chr8:123191456 | T | C | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481-347T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191456 | |||||||
chr8:123191495 | C | A | 1 | a0001c0001t0003g0219 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.481-308C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191495 | |||||||
chr8:123191571 | T | C | 1 | a0002c0002t0002g0051 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.481-232T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191571 | |||||||
chr8:123191642 | C | G | 1 | a0002c0002t0001g0209 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.481-161C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191642 | |||||||
chr8:123191721 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.481-82C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 1/3 | chr8 | 123191721 | |||||||
chr8:123192011 | C | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.648+41C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192011 | |||||||
chr8:123192054 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.648+84C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192054 | |||||||
chr8:123192064 | T | G | 7 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0218 others(4): Show |
8 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.648+94T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192064 | |||||||
chr8:123192081 | G | A | 1 | a0002c0002t0002g0183 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.648+111G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192081 | |||||||
chr8:123192250 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.648+280G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192250 | |||||||
chr8:123192255 | C | T | 2 | a0003c0003t0005g0119 a0003c0003t0009g0216 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.648+285C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192255 | |||||||
chr8:123192288 | G | T | 1 | a0002c0002t0002g0208 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.648+318G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192288 | |||||||
chr8:123192341 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.648+371A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192341 | |||||||
chr8:123192468 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.648+498C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192468 | |||||||
chr8:123192471 | A | T | 1 | a0001c0001t0003g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.648+501A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192471 | |||||||
chr8:123192590 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0218 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+620A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192590 | |||||||
chr8:123192655 | T | C | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.648+685T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123192655 | |||||||
chr8:123193100 | C | T | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.649-924C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193100 | |||||||
chr8:123193179 | C | T | 1 | a0001c0001t0016g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.649-845C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193179 | |||||||
chr8:123193189 | T | C | 3 | a0001c0001t0005g0040 a0001c0001t0005g0124 a0001c0001t0005g0125 |
4 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-835T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193189 | |||||||
chr8:123193263 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.649-761C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193263 | |||||||
chr8:123193315 | C | A | 1 | a0002c0002t0001g0116 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.649-709C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193315 | |||||||
chr8:123193403 | C | T | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.649-621C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193403 | |||||||
chr8:123193450 | C | CT | 3 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0138 |
7 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-565dupT | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 123193450 | ||||||
chr8:123193450 | CT | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
7 | HG02257.hp1 HG03831.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.649-565delT | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 123193450 | ||||||
chr8:123193635 | G | T | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.649-389G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193635 | |||||||
chr8:123193710 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.649-314G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193710 | |||||||
chr8:123193723 | C | T | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.649-301C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193723 | |||||||
chr8:123193726 | C | T | 46 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(43): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.649-298C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193726 | |||||||
chr8:123193727 | G | A | 2 | a0001c0004t0019g0122 a0007c0007t0001g0074 |
2 | HG02257.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.649-297G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193727 | |||||||
chr8:123193814 | C | G | 1 | a0002c0002t0001g0149 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.649-210C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193814 | |||||||
chr8:123193897 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.649-127C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193897 | |||||||
chr8:123193958 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.649-66C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 2/3 | chr8 | 123193958 | |||||||
chr8:123194154 | C | G | 46 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(43): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
splice_region_variant&intron_variant | LOW | c.773+6C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194154 | |||||||
chr8:123194190 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0106 a0001c0001t0001g0135 |
4 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+42C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194190 | |||||||
chr8:123194272 | C | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+124C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194272 | |||||||
chr8:123194395 | G | A | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.773+247G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194395 | |||||||
chr8:123194420 | C | T | 1 | a0002c0002t0002g0207 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.773+272C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194420 | |||||||
chr8:123194486 | C | CTT | 43 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(40): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.773+352_773+353dup others(2): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123194486 | ||||||
chr8:123194515 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.773+367G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194515 | |||||||
chr8:123194553 | A | G | 1 | a0001c0001t0002g0192 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.773+405A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194553 | |||||||
chr8:123194594 | C | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+446C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194594 | |||||||
chr8:123194640 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0003g0015 a0001c0001t0003g0021 others(2): Show |
10 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.773+492C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194640 | |||||||
chr8:123194782 | C | T | 44 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(41): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.773+634C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194782 | |||||||
chr8:123194785 | G | A | 47 | a0001c0004t0019g0122 a0002c0002t0001g0006 a0002c0002t0001g0022 others(44): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.773+637G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194785 | |||||||
chr8:123194874 | G | A | 1 | a0002c0002t0001g0117 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.773+726G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194874 | |||||||
chr8:123194878 | A | G | 3 | a0001c0004t0019g0122 a0003c0003t0005g0119 a0003c0003t0009g0216 |
3 | HG02257.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.773+730A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194878 | |||||||
chr8:123194885 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0105 others(1): Show |
4 | HG02895.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.773+737A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194885 | |||||||
chr8:123194967 | A | G | 6 | a0001c0001t0005g0040 a0001c0001t0005g0124 a0001c0001t0005g0125 others(3): Show |
7 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.773+819A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194967 | |||||||
chr8:123194994 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.773+846G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123194994 | |||||||
chr8:123195065 | A | G | 3 | a0001c0004t0019g0122 a0003c0003t0005g0119 a0003c0003t0009g0216 |
3 | HG02257.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.773+917A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195065 | |||||||
chr8:123195072 | T | C | 7 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0218 others(4): Show |
8 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.773+924T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195072 | |||||||
chr8:123195275 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.773+1127T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195275 | |||||||
chr8:123195313 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.773+1165G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195313 | |||||||
chr8:123195521 | G | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+1373G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195521 | |||||||
chr8:123195527 | A | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+1379A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195527 | |||||||
chr8:123195791 | A | G | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+1643A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195791 | |||||||
chr8:123195858 | A | G | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+1710A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195858 | |||||||
chr8:123195875 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.773+1727G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195875 | |||||||
chr8:123195905 | A | G | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+1757A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123195905 | |||||||
chr8:123196010 | T | A | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+1862T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196010 | |||||||
chr8:123196043 | G | A | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+1895G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196043 | |||||||
chr8:123196214 | G | T | 1 | a0002c0002t0001g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.773+2066G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196214 | |||||||
chr8:123196223 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.773+2075A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196223 | |||||||
chr8:123196250 | G | A | 1 | a0001c0001t0010g0136 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.773+2102G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196250 | |||||||
chr8:123196267 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.773+2119C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196267 | |||||||
chr8:123196270 | C | G | 2 | a0003c0003t0005g0119 a0003c0003t0009g0216 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.773+2122C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196270 | |||||||
chr8:123196310 | C | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0176 others(1): Show |
6 | HG02132.hp2 HG02155.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.773+2162C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196310 | |||||||
chr8:123196327 | A | G | 1 | a0002c0002t0002g0206 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.773+2179A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196327 | |||||||
chr8:123196499 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.773+2351G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196499 | |||||||
chr8:123196530 | T | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0153 others(1): Show |
7 | HG00738.hp2 HG01358.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.773+2382T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196530 | |||||||
chr8:123196898 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.773+2750C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196898 | |||||||
chr8:123196917 | C | T | 73 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(70): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.773+2769C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196917 | |||||||
chr8:123196945 | G | A | 72 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(69): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.773+2797G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123196945 | |||||||
chr8:123197039 | C | T | 72 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(69): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.773+2891C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197039 | |||||||
chr8:123197097 | T | C | 72 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(69): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.773+2949T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197097 | |||||||
chr8:123197098 | TA | T | 72 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(69): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.773+2951delA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197098 | |||||||
chr8:123197220 | C | T | 1 | a0002c0002t0002g0194 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.773+3072C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197220 | |||||||
chr8:123197221 | G | A | 1 | a0001c0001t0010g0136 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.773+3073G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197221 | |||||||
chr8:123197446 | A | G | 4 | a0001c0001t0005g0040 a0001c0001t0005g0124 a0001c0001t0005g0125 others(1): Show |
5 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.773+3298A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197446 | |||||||
chr8:123197474 | C | T | 2 | a0002c0002t0002g0204 a0002c0002t0002g0205 |
2 | NA18973.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.773+3326C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197474 | |||||||
chr8:123197485 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.773+3337G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197485 | |||||||
chr8:123197555 | T | A | 1 | a0002c0002t0001g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.773+3407T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197555 | |||||||
chr8:123197604 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.773+3456T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197604 | |||||||
chr8:123197645 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.773+3497C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197645 | |||||||
chr8:123197785 | C | T | 3 | a0002c0002t0002g0187 a0002c0002t0002g0203 a0002c0002t0002g0206 |
3 | NA18983.hp1 NA18989.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.773+3637C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197785 | |||||||
chr8:123197869 | C | T | 35 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(32): Show |
56 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.773+3721C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197869 | |||||||
chr8:123197920 | A | G | 15 | a0001c0001t0001g0111 a0001c0001t0003g0142 a0001c0001t0004g0016 others(12): Show |
22 | HG01069.hp2 HG01243.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.773+3772A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197920 | |||||||
chr8:123197990 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.773+3842C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123197990 | |||||||
chr8:123198063 | G | A | 26 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(23): Show |
34 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.773+3915G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198063 | |||||||
chr8:123198086 | G | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0023 others(31): Show |
56 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.773+3938G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198086 | |||||||
chr8:123198179 | G | A | 26 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(23): Show |
34 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.773+4031G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198179 | |||||||
chr8:123198213 | C | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.773+4065C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198213 | |||||||
chr8:123198314 | C | G | 1 | a0001c0001t0001g0222 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.773+4166C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198314 | |||||||
chr8:123198326 | A | G | 62 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(59): Show |
91 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.773+4178A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198326 | |||||||
chr8:123198443 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0006g0130 |
3 | HG02055.hp1 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.773+4295T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198443 | |||||||
chr8:123198773 | G | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0131 others(3): Show |
6 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.773+4625G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198773 | |||||||
chr8:123198825 | C | A | 35 | a0002c0002t0001g0006 a0002c0002t0001g0022 a0002c0002t0001g0044 others(32): Show |
56 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.773+4677C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198825 | |||||||
chr8:123198961 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.773+4813A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123198961 | |||||||
chr8:123199041 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.773+4893C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123199041 | |||||||
chr8:123199181 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0097 others(3): Show |
11 | HG02040.hp1 HG02056.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.773+5033C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123199181 | |||||||
chr8:123199362 | T | C | 1 | a0001c0001t0010g0136 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.773+5214T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123199362 | |||||||
chr8:123199642 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.773+5494G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123199642 | |||||||
chr8:123199818 | A | G | 61 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(58): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.773+5670A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123199818 | |||||||
chr8:123200127 | G | A | 56 | a0001c0001t0001g0111 a0001c0001t0003g0142 a0001c0001t0004g0016 others(53): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.773+5979G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200127 | |||||||
chr8:123200189 | T | TCA | 55 | a0001c0001t0001g0111 a0001c0001t0003g0142 a0001c0001t0004g0016 others(52): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.773+6042_773+6043i others(4): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123200189 | ||||||
chr8:123200229 | G | C | 1 | a0001c0001t0001g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.773+6081G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200229 | |||||||
chr8:123200245 | G | A | 1 | a0002c0002t0002g0196 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.773+6097G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200245 | |||||||
chr8:123200364 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.773+6216C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200364 | |||||||
chr8:123200397 | C | T | 56 | a0001c0001t0001g0111 a0001c0001t0003g0142 a0001c0001t0004g0016 others(53): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.773+6249C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200397 | |||||||
chr8:123200693 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.774-6464C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200693 | |||||||
chr8:123200752 | G | A | 1 | a0001c0001t0023g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.774-6405G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200752 | |||||||
chr8:123200774 | C | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.774-6383C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200774 | |||||||
chr8:123200775 | A | G | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.774-6382A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200775 | |||||||
chr8:123200787 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.774-6370C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200787 | |||||||
chr8:123200799 | C | T | 2 | a0002c0002t0002g0185 a0002c0002t0002g0186 |
2 | NA18955.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.774-6358C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200799 | |||||||
chr8:123200844 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.774-6313A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200844 | |||||||
chr8:123200890 | G | T | 9 | a0001c0001t0001g0111 a0001c0001t0004g0036 a0001c0001t0004g0123 others(6): Show |
11 | HG01069.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.774-6267G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200890 | |||||||
chr8:123200957 | CA | C | 39 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0111 others(36): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.774-6188delA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123200957 | ||||||
chr8:123200960 | A | AAT | 4 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0126 others(1): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.774-6196_774-6195i others(4): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123200960 | ||||||
chr8:123200961 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.774-6196A>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200961 | |||||||
chr8:123200962 | A | ATAT | 3 | a0001c0001t0005g0040 a0001c0001t0005g0125 a0001c0001t0009g0129 |
4 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.774-6195_774-6194i others(5): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200962 | |||||||
chr8:123200962 | A | T | 12 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(9): Show |
18 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.774-6195A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200962 | |||||||
chr8:123200964 | A | T | 16 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(13): Show |
23 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.774-6193A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200964 | |||||||
chr8:123200966 | A | AT | 3 | a0001c0001t0001g0102 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02257.hp2 HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.774-6191_774-6190i others(3): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200966 | |||||||
chr8:123200966 | A | T | 44 | a0001c0001t0001g0034 a0001c0001t0001g0095 a0001c0001t0001g0096 others(41): Show |
65 | HG00099.hp2 HG00438.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.774-6191A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200966 | |||||||
chr8:123200968 | A | AAT | 4 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0085 others(1): Show |
7 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.774-6173_774-6172d others(4): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123200968 | ||||||
chr8:123200968 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(129): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.774-6189A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200968 | |||||||
chr8:123200970 | T | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0046 others(9): Show |
19 | HG00140.hp2 HG00597.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.774-6187T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200970 | |||||||
chr8:123200984 | T | TATATATA others(19): Show |
1 | a0001c0001t0010g0136 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.774-6172_774-6171i others(28): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123200984 | ||||||
chr8:123200988 | C | T | 12 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(9): Show |
18 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.774-6169C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123200988 | |||||||
chr8:123201027 | T | C | 12 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(9): Show |
18 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.774-6130T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201027 | |||||||
chr8:123201393 | G | A | 5 | a0001c0001t0001g0078 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG02027.hp2 HG02165.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-5764G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201393 | |||||||
chr8:123201604 | C | A | 56 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0003g0142 others(53): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.774-5553C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201604 | |||||||
chr8:123201685 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.774-5472A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201685 | |||||||
chr8:123201720 | G | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0106 a0001c0001t0001g0135 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.774-5437G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201720 | |||||||
chr8:123201811 | A | G | 53 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0004g0016 others(50): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.774-5346A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201811 | |||||||
chr8:123201815 | A | T | 2 | a0001c0001t0003g0142 a0001c0001t0010g0136 |
2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.774-5342A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201815 | |||||||
chr8:123201934 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.774-5223C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123201934 | |||||||
chr8:123202104 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0084 others(12): Show |
27 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.774-5053C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202104 | |||||||
chr8:123202147 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.774-5010T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202147 | |||||||
chr8:123202263 | T | C | 1 | a0002c0002t0001g0199 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.774-4894T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202263 | |||||||
chr8:123202267 | C | T | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.774-4890C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202267 | |||||||
chr8:123202332 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.774-4825G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202332 | |||||||
chr8:123202334 | C | T | 39 | a0001c0001t0001g0097 a0001c0001t0005g0040 a0001c0001t0005g0124 others(36): Show |
61 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.774-4823C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202334 | |||||||
chr8:123202389 | A | G | 1 | a0001c0001t0011g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.774-4768A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202389 | |||||||
chr8:123202605 | C | T | 1 | a0001c0001t0023g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.774-4552C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202605 | |||||||
chr8:123202766 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0003g0015 a0001c0001t0003g0021 others(1): Show |
9 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.774-4391C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202766 | |||||||
chr8:123202767 | G | A | 1 | a0002c0002t0002g0197 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.774-4390G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202767 | |||||||
chr8:123202774 | A | G | 2 | a0001c0001t0003g0142 a0001c0001t0010g0136 |
2 | HG01099.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.774-4383A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202774 | |||||||
chr8:123202816 | A | G | 1 | a0001c0001t0001g0023 | 3 | HG03017.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.774-4341A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202816 | |||||||
chr8:123202913 | G | A | 1 | a0001c0001t0009g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.774-4244G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123202913 | |||||||
chr8:123203066 | C | G | 1 | a0002c0002t0002g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.774-4091C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123203066 | |||||||
chr8:123203085 | G | T | 1 | a0003c0003t0005g0119 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.774-4072G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123203085 | |||||||
chr8:123203221 | T | TA | 57 | a0001c0001t0001g0164 a0001c0001t0003g0142 a0001c0001t0004g0016 others(54): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.774-3924dupA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203221 | ||||||
chr8:123203244 | TA | T | 12 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(9): Show |
18 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.774-3909delA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203244 | ||||||
chr8:123203249 | G | T | 12 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(9): Show |
18 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.774-3908G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123203249 | |||||||
chr8:123203271 | A | G | 12 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(9): Show |
18 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.774-3886A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123203271 | |||||||
chr8:123203313 | T | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0182 a0001c0001t0001g0214 others(4): Show |
9 | HG00597.hp2 HG02027.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.774-3844T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123203313 | |||||||
chr8:123203586 | C | CA | 15 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0087 others(12): Show |
15 | HG00735.hp1 HG01168.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.774-3549dupA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203586 | ||||||
chr8:123203586 | C | CAA | 5 | a0001c0001t0005g0040 a0001c0001t0005g0124 a0001c0001t0009g0129 others(2): Show |
6 | HG01169.hp1 HG01192.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.774-3550_774-3549d others(4): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203586 | ||||||
chr8:123203586 | CA | C | 16 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0093 others(13): Show |
18 | HG00438.hp1 HG00438.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.774-3549delA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203586 | ||||||
chr8:123203586 | CAAAA | C | 8 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(5): Show |
14 | HG01891.hp1 HG02486.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.774-3552_774-3549d others(6): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203586 | ||||||
chr8:123203586 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0011 | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.774-3558_774-3549d others(12): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203586 | ||||||
chr8:123203863 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.774-3294A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123203863 | |||||||
chr8:123203871 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.774-3286C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123203871 | |||||||
chr8:123203957 | C | CA | 9 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0101 others(6): Show |
9 | HG00621.hp2 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.774-3183dupA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203957 | ||||||
chr8:123203957 | CA | C | 13 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0041 others(10): Show |
20 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.774-3183delA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203957 | ||||||
chr8:123203978 | CA | C | 18 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
26 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.774-3170delA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123203978 | ||||||
chr8:123204297 | C | G | 1 | a0001c0001t0001g0033 | 2 | HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.774-2860C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204297 | |||||||
chr8:123204315 | G | A | 18 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
26 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.774-2842G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204315 | |||||||
chr8:123204337 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.774-2820T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204337 | |||||||
chr8:123204450 | G | A | 3 | a0001c0001t0004g0041 a0001c0001t0004g0042 a0001c0001t0004g0112 |
5 | HG01891.hp1 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-2707G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204450 | |||||||
chr8:123204479 | T | C | 2 | a0001c0001t0003g0142 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.774-2678T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204479 | |||||||
chr8:123204590 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.774-2567G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204590 | |||||||
chr8:123204598 | T | TA | 18 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
26 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.774-2555dupA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123204598 | ||||||
chr8:123204710 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.774-2447G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204710 | |||||||
chr8:123204747 | C | G | 1 | a0002c0002t0002g0197 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.774-2410C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204747 | |||||||
chr8:123204765 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-2392A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204765 | |||||||
chr8:123204767 | A | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(22): Show |
40 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.774-2390A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123204767 | |||||||
chr8:123205092 | A | ACTCCTTG others(6): Show |
1 | a0001c0001t0002g0193 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.774-2064_774-2063i others(15): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123205092 | ||||||
chr8:123205094 | A | C | 1 | a0001c0001t0002g0193 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.774-2063A>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205094 | |||||||
chr8:123205095 | G | C | 1 | a0001c0001t0002g0193 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.774-2062G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205095 | |||||||
chr8:123205125 | A | T | 1 | a0001c0001t0003g0221 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.774-2032A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205125 | |||||||
chr8:123205153 | T | A | 18 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
26 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.774-2004T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205153 | |||||||
chr8:123205180 | G | A | 1 | a0001c0004t0018g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774-1977G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205180 | |||||||
chr8:123205233 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-1924A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205233 | |||||||
chr8:123205267 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-1890G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205267 | |||||||
chr8:123205298 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.774-1859C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205298 | |||||||
chr8:123205324 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-1833T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205324 | |||||||
chr8:123205331 | A | ATGCAGGC others(10): Show |
1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-1826_774-1825i others(19): Show |
FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205331 | |||||||
chr8:123205332 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-1825A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205332 | |||||||
chr8:123205334 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-1823A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205334 | |||||||
chr8:123205383 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0217 |
4 | HG02055.hp2 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.774-1774G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205383 | |||||||
chr8:123205488 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.774-1669A>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205488 | |||||||
chr8:123205631 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.774-1526C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205631 | |||||||
chr8:123205913 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.774-1244G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205913 | |||||||
chr8:123205919 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.774-1238C>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205919 | |||||||
chr8:123205934 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.774-1223G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205934 | |||||||
chr8:123205971 | T | C | 1 | a0001c0004t0018g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774-1186T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205971 | |||||||
chr8:123205988 | C | A | 1 | a0001c0004t0018g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774-1169C>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123205988 | |||||||
chr8:123206004 | G | C | 1 | a0001c0004t0019g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.774-1153G>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206004 | |||||||
chr8:123206138 | C | CA | 15 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0089 others(12): Show |
20 | HG00597.hp1 HG01243.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.774-1002dupA | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 123206138 | ||||||
chr8:123206247 | T | A | 1 | a0008c0005t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.774-910T>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206247 | |||||||
chr8:123206275 | T | C | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-882T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206275 | |||||||
chr8:123206338 | G | A | 2 | a0001c0001t0003g0057 a0001c0001t0003g0220 |
3 | HG01167.hp1 HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.774-819G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206338 | |||||||
chr8:123206462 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.774-695G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206462 | |||||||
chr8:123206487 | G | T | 1 | a0002c0002t0001g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.774-670G>T | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206487 | |||||||
chr8:123206572 | T | C | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-585T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206572 | |||||||
chr8:123206649 | C | G | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-508C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206649 | |||||||
chr8:123206656 | A | G | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-501A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206656 | |||||||
chr8:123206752 | T | G | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-405T>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206752 | |||||||
chr8:123206755 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.774-402C>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206755 | |||||||
chr8:123206790 | A | G | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-367A>G | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206790 | |||||||
chr8:123206804 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(91): Show |
152 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.774-353T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206804 | |||||||
chr8:123206871 | G | A | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-286G>A | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206871 | |||||||
chr8:123206962 | T | C | 2 | a0001c0004t0018g0143 a0001c0004t0019g0122 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.774-195T>C | FAM83A | ENSG00000147689.17 | transcript | ENST00000690554.1 | protein_coding | 3/3 | chr8 | 123206962 |