Item | Value |
---|---|
geneid | 57102 |
ensemblid | ENSG00000047621.12 |
hgncid | 1184 |
symbol | C12orf4 |
name | chromosome 12 open reading frame 4 |
refseq_nuc | NM_020374.4 |
refseq_prot | NP_065107.1 |
ensembl_nuc | ENST00000261250.8 |
ensembl_prot | ENSP00000261250.3 |
mane_status | MANE Select |
chr | chr12 |
start | 4487735 |
end | 4538469 |
strand | - |
ver | v1.2 |
region | chr12:4487735-4538469 |
region5000 | chr12:4482735-4543469 |
regionname0 | C12orf4_chr12_4487735_4538469 |
regionname5000 | C12orf4_chr12_4482735_4543469 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1656 | 203 | 78 | 35 | 62 | 4 | 22 | C12orf4_chr12_4482735_4543469 | C12orf4 | ATGAA others(1651): Show |
chr12 | 4482735 | 4543469 | ||
a0001c0002 | 0/0 | 1656 | 9 | 8 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | ATGAA others(1651): Show |
chr12 | 4482735 | 4543469 | ||
a0001c0003 | 0/0 | 1656 | 8 | 0 | 6 | 0 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | ATGAA others(1651): Show |
chr12 | 4482735 | 4543469 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3817 | 123 | 37 | 23 | 45 | 3 | 14 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0002 | 0/0 | 3817 | 24 | 6 | 1 | 15 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0003 | 0/0 | 3817 | 15 | 2 | 6 | 1 | 1 | 5 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0004 | 0/0 | 3817 | 11 | 11 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0005 | 0/0 | 3817 | 5 | 4 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0006 | 0/0 | 3817 | 5 | 4 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0007 | 0/0 | 3817 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0009 | 0/1 | 3817 | 3 | 1 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0010 | 0/0 | 3817 | 2 | 1 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0011 | 0/0 | 3820 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3815): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0012 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0013 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0015 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0016 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0017 | 0/0 | 3817 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0018 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0019 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0020 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0001t0021 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0002t0001 | 0/0 | 3817 | 5 | 5 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0002t0008 | 0/0 | 3817 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0002t0014 | 0/0 | 3817 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
a0001c0003t0001 | 0/0 | 3817 | 8 | 0 | 6 | 0 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | AGTGC others(3812): Show |
chr12 | 4482735 | 4543469 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0007g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0009g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0009g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0017g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0019g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0020g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0001t0021g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0002t0014g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0003t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0003t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0158 | EUR | GBR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0089 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01081 | hp1 | a0001 | c0001 | t0009 | g0130 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01261 | hp2 | a0001 | c0001 | t0017 | g0153 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01346 | hp2 | a0001 | c0001 | t0010 | g0169 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01358 | hp1 | a0001 | c0002 | t0014 | g0171 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CDX | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0168 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0050 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02895 | hp1 | a0001 | c0002 | t0008 | g0041 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0049 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0042 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03195 | hp1 | a0001 | c0001 | t0016 | g0148 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0179 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0180 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03540 | hp1 | a0001 | c0001 | t0018 | g0152 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03540 | hp2 | a0001 | c0002 | t0008 | g0172 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0078 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0161 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG04204 | hp1 | a0001 | c0001 | t0021 | g0063 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0091 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18957 | hp1 | a0001 | c0001 | t0019 | g0056 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0133 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA20129 | hp1 | a0001 | c0002 | t0008 | g0170 | AFR | ASW | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03471 | hp1 | a0001 | c0001 | t0020 | g0082 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | USA | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | USA | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0097 | REF | REF | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0111 | REF | REF | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
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 |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4505379 | A | G | 1 | a0001c0002 | 9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.1164T>C | p.Asp388Asp | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/14 | 1250/3817 | 1164/1659 | 388/552 | chr12 | 4505379 | |||
chr12:4518248 | C | T | 1 | a0001c0003 | 8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
synonymous_variant | LOW | c.843G>A | p.Gln281Gln | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/14 | 929/3817 | 843/1659 | 281/552 | chr12 | 4518248 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4487812 | T | C | 2 | a0001c0001t0002 a0001c0001t0019 |
25 | HG01071.hp2 HG02074.hp1 HG02155.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1995A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1995 | chr12 | 4487812 | ||||||
chr12:4487916 | C | A | 1 | a0001c0001t0019 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1891 | chr12 | 4487916 | ||||||
chr12:4488032 | T | C | 1 | a0001c0001t0007 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1775A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1775 | chr12 | 4488032 | ||||||
chr12:4488111 | G | C | 1 | a0001c0001t0020 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1696C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1696 | chr12 | 4488111 | ||||||
chr12:4488163 | A | G | 1 | a0001c0001t0018 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1644 | chr12 | 4488163 | ||||||
chr12:4488307 | T | C | 2 | a0001c0001t0007 a0001c0001t0011 |
6 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1500A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1500 | chr12 | 4488307 | ||||||
chr12:4488315 | A | C | 6 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(3): Show |
24 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1492T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1492 | chr12 | 4488315 | ||||||
chr12:4488465 | C | T | 1 | a0001c0001t0017 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1342G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1342 | chr12 | 4488465 | ||||||
chr12:4488541 | T | C | 1 | a0001c0001t0006 | 5 | HG01192.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1266A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1266 | chr12 | 4488541 | ||||||
chr12:4488579 | G | A | 1 | a0001c0001t0003 | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1228C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1228 | chr12 | 4488579 | ||||||
chr12:4488800 | G | A | 1 | a0001c0001t0007 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1007 | chr12 | 4488800 | ||||||
chr12:4488968 | C | T | 2 | a0001c0001t0004 a0001c0001t0016 |
12 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*839G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 839 | chr12 | 4488968 | ||||||
chr12:4489005 | A | G | 1 | a0001c0001t0005 | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*802T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 802 | chr12 | 4489005 | ||||||
chr12:4489183 | A | G | 1 | a0001c0001t0015 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*624T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 624 | chr12 | 4489183 | ||||||
chr12:4489254 | T | C | 1 | a0001c0001t0010 | 2 | HG01346.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*553A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 553 | chr12 | 4489254 | ||||||
chr12:4489371 | C | T | 2 | a0001c0002t0008 a0001c0002t0014 |
4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*436G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 436 | chr12 | 4489371 | ||||||
chr12:4489401 | A | T | 2 | a0001c0001t0012 a0001c0001t0013 |
2 | HG02809.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*406T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 406 | chr12 | 4489401 | ||||||
chr12:4489403 | G | T | 2 | a0001c0001t0012 a0001c0001t0013 |
2 | HG02809.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*404C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 404 | chr12 | 4489403 | ||||||
chr12:4489585 | G | C | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 222 | chr12 | 4489585 | ||||||
chr12:4538457 | C | CGCA | 1 | a0001c0001t0011 | 2 | HG03453.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75_-74insTGC | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/14 | 2264 | chr12 | 4538457 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4490017 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-118A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 13/13 | chr12 | 4490017 | |||||||
chr12:4490037 | C | T | 1 | a0001c0001t0004g0149 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1567-138G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 13/13 | chr12 | 4490037 | |||||||
chr12:4490386 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1566+136G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 13/13 | chr12 | 4490386 | |||||||
chr12:4490600 | A | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-11T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4490600 | |||||||
chr12:4490766 | T | C | 9 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0175 others(6): Show |
9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1499-177A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4490766 | |||||||
chr12:4490846 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0105 |
2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1499-257T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4490846 | |||||||
chr12:4491156 | CAGAG | C | 3 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0120 |
3 | HG02523.hp2 NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1498+17_1498+20del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4491156 | |||||||
chr12:4491467 | AT | A | 4 | a0001c0002t0008g0041 a0001c0002t0008g0170 a0001c0002t0008g0172 others(1): Show |
4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-234delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491467 | |||||||
chr12:4491468 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(47): Show |
64 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1441-234A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491468 | |||||||
chr12:4491470 | T | A | 4 | a0001c0002t0008g0041 a0001c0002t0008g0170 a0001c0002t0008g0172 others(1): Show |
4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-236A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491470 | |||||||
chr12:4491721 | G | GT | 2 | a0001c0001t0001g0096 a0001c0003t0001g0089 |
2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1441-488dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491721 | |||||||
chr12:4491753 | C | T | 6 | a0001c0001t0015g0042 a0001c0002t0001g0173 a0001c0002t0008g0041 others(3): Show |
6 | HG01358.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-519G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491753 | |||||||
chr12:4491780 | G | A | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1441-546C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491780 | |||||||
chr12:4491780 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1441-546C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491780 | |||||||
chr12:4491853 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1441-619T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491853 | |||||||
chr12:4491902 | G | A | 22 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(19): Show |
30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1441-668C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491902 | |||||||
chr12:4491990 | G | A | 1 | a0001c0001t0009g0133 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1441-756C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491990 | |||||||
chr12:4492326 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1441-1092T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492326 | |||||||
chr12:4492497 | C | G | 7 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(4): Show |
7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1263G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492497 | |||||||
chr12:4492525 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1441-1291G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492525 | |||||||
chr12:4492550 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1441-1316G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492550 | |||||||
chr12:4492609 | C | T | 7 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(4): Show |
7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1375G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492609 | |||||||
chr12:4492610 | C | T | 7 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(4): Show |
7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1376G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492610 | |||||||
chr12:4492716 | T | C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0025 others(13): Show |
19 | HG00558.hp2 HG00621.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1441-1482A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492716 | |||||||
chr12:4492765 | T | C | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1441-1531A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492765 | |||||||
chr12:4492865 | A | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-1631T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492865 | |||||||
chr12:4492972 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0136 |
7 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1738C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492972 | |||||||
chr12:4493034 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1441-1800A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493034 | |||||||
chr12:4493152 | T | C | 1 | a0001c0001t0009g0130 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1441-1918A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493152 | |||||||
chr12:4493298 | A | G | 7 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(4): Show |
7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-2064T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493298 | |||||||
chr12:4493408 | T | C | 7 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(4): Show |
7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-2174A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493408 | |||||||
chr12:4493489 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1441-2255A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493489 | |||||||
chr12:4493555 | G | GTT | 26 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(23): Show |
34 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1441-2323_1441-232 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493555 | |||||||
chr12:4493725 | C | T | 1 | a0001c0001t0006g0078 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1441-2491G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493725 | |||||||
chr12:4493830 | C | T | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0028 others(7): Show |
15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1441-2596G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493830 | |||||||
chr12:4493858 | C | T | 2 | a0001c0001t0011g0179 a0001c0001t0011g0180 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1441-2624G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493858 | |||||||
chr12:4493859 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1441-2625C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493859 | |||||||
chr12:4493890 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0086 a0001c0001t0001g0098 |
3 | HG01952.hp2 HG02004.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1441-2656G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493890 | |||||||
chr12:4493957 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1441-2723T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493957 | |||||||
chr12:4494001 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0132 a0001c0001t0001g0137 others(1): Show |
4 | HG00280.hp2 HG03239.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-2767C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494001 | |||||||
chr12:4494099 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1441-2865A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494099 | |||||||
chr12:4494128 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1441-2894C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494128 | |||||||
chr12:4494132 | C | T | 1 | a0001c0001t0004g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1441-2898G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494132 | |||||||
chr12:4494228 | T | A | 14 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0010g0168 others(11): Show |
14 | HG01346.hp2 HG01358.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1441-2994A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494228 | |||||||
chr12:4494228 | T | TA | 5 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(2): Show |
7 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441-2995dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494228 | |||||||
chr12:4494532 | T | C | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0010 others(14): Show |
23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1441-3298A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494532 | |||||||
chr12:4494546 | C | T | 5 | a0001c0002t0001g0173 a0001c0002t0008g0041 a0001c0002t0008g0170 others(2): Show |
5 | HG01358.hp1 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-3312G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494546 | |||||||
chr12:4494714 | C | T | 9 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0175 others(6): Show |
9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1441-3480G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494714 | |||||||
chr12:4494950 | G | A | 10 | a0001c0001t0015g0042 a0001c0002t0001g0173 a0001c0002t0001g0174 others(7): Show |
10 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1441-3716C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494950 | |||||||
chr12:4495172 | AT | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1441-3939delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495172 | |||||||
chr12:4495413 | A | G | 3 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 |
4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-4179T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495413 | |||||||
chr12:4495466 | T | G | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1441-4232A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495466 | |||||||
chr12:4495512 | C | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1441-4278G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495512 | |||||||
chr12:4495546 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1441-4312C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495546 | |||||||
chr12:4495559 | T | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1441-4325A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495559 | |||||||
chr12:4495750 | C | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+4388G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495750 | |||||||
chr12:4495767 | TATGTGTG others(9): Show |
T | 1 | a0001c0001t0001g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1440+4355_1440+437 others(20): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495767 | |||||||
chr12:4495786 | G | C | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1440+4352C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495786 | |||||||
chr12:4495792 | G | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+4346C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495792 | |||||||
chr12:4495844 | A | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+4294T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495844 | |||||||
chr12:4495852 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+4286T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495852 | |||||||
chr12:4495939 | A | T | 6 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0008g0041 others(3): Show |
6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+4199T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495939 | |||||||
chr12:4496145 | C | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3993G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496145 | |||||||
chr12:4496445 | G | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3693C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496445 | |||||||
chr12:4496589 | A | AAG | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3547_1440+354 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496589 | |||||||
chr12:4496668 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1440+3470G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496668 | |||||||
chr12:4497002 | T | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(18): Show |
29 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1440+3136A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497002 | |||||||
chr12:4497125 | G | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3013C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497125 | |||||||
chr12:4497305 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1440+2833T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497305 | |||||||
chr12:4497322 | G | T | 9 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0175 others(6): Show |
9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+2816C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497322 | |||||||
chr12:4497361 | T | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(19): Show |
30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1440+2777A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497361 | |||||||
chr12:4497490 | C | T | 10 | a0001c0001t0001g0075 a0001c0002t0001g0173 a0001c0002t0001g0174 others(7): Show |
10 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1440+2648G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497490 | |||||||
chr12:4497514 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1440+2624C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497514 | |||||||
chr12:4498135 | T | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+2003A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498135 | |||||||
chr12:4498176 | A | T | 34 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(31): Show |
42 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1440+1962T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498176 | |||||||
chr12:4498221 | T | C | 3 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 |
4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+1917A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498221 | |||||||
chr12:4498380 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0076 |
3 | NA18971.hp2 NA18988.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1440+1758A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498380 | |||||||
chr12:4498530 | G | C | 1 | a0001c0001t0002g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1440+1608C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498530 | |||||||
chr12:4498619 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1440+1519G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498619 | |||||||
chr12:4498765 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1440+1373A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498765 | |||||||
chr12:4498823 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+1315C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498823 | |||||||
chr12:4498844 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1440+1294G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498844 | |||||||
chr12:4498855 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0164 others(4): Show |
9 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+1283T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498855 | |||||||
chr12:4498901 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1440+1237G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498901 | |||||||
chr12:4498937 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1440+1201T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498937 | |||||||
chr12:4498943 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0105 |
2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1440+1195G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498943 | |||||||
chr12:4499159 | C | T | 1 | a0001c0001t0003g0010 | 3 | HG00741.hp1 HG02148.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1440+979G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499159 | |||||||
chr12:4499172 | T | C | 12 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0001t0015g0042 others(9): Show |
12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1440+966A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499172 | |||||||
chr12:4499205 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1440+933T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499205 | |||||||
chr12:4499213 | C | T | 3 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 |
4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+925G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499213 | |||||||
chr12:4499245 | T | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1440+893A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499245 | |||||||
chr12:4499437 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1440+701G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499437 | |||||||
chr12:4499478 | T | C | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1440+660A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499478 | |||||||
chr12:4499670 | T | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+468A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499670 | |||||||
chr12:4499812 | G | C | 6 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0008g0041 others(3): Show |
6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+326C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499812 | |||||||
chr12:4499839 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+299C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499839 | |||||||
chr12:4499950 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1440+188C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499950 | |||||||
chr12:4500098 | A | G | 1 | a0001c0001t0006g0078 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1440+40T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4500098 | |||||||
chr12:4500459 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(48): Show |
65 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.1238-119T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500459 | |||||||
chr12:4500482 | C | T | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1238-142G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500482 | |||||||
chr12:4500545 | A | AT | 6 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0008g0041 others(3): Show |
6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-206dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500545 | |||||||
chr12:4500645 | A | AAATT | 3 | a0001c0001t0001g0009 a0001c0001t0001g0134 a0001c0001t0009g0133 |
5 | HG02896.hp2 HG02897.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-309_1238-306d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500645 | |||||||
chr12:4500651 | A | G | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1238-311T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500651 | |||||||
chr12:4500739 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 |
5 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-399C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500739 | |||||||
chr12:4500777 | C | T | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-437G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500777 | |||||||
chr12:4500858 | G | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-518C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500858 | |||||||
chr12:4500930 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-590G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500930 | |||||||
chr12:4501110 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1238-770T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501110 | |||||||
chr12:4501361 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(11): Show |
18 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1238-1021A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501361 | |||||||
chr12:4501457 | A | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1238-1117T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501457 | |||||||
chr12:4501532 | C | G | 1 | a0001c0002t0008g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1238-1192G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501532 | |||||||
chr12:4501535 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-1195A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501535 | |||||||
chr12:4501570 | A | T | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-1230T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501570 | |||||||
chr12:4501597 | A | G | 1 | a0001c0001t0004g0027 | 2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1238-1257T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501597 | |||||||
chr12:4501818 | C | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-1478G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501818 | |||||||
chr12:4502083 | A | G | 1 | a0001c0001t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1238-1743T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502083 | |||||||
chr12:4502461 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-2121G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502461 | |||||||
chr12:4502776 | C | T | 3 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 |
4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-2436G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502776 | |||||||
chr12:4502997 | A | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0134 others(11): Show |
18 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1237+2309T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502997 | |||||||
chr12:4503241 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1237+2065T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503241 | |||||||
chr12:4503283 | T | A | 1 | a0001c0001t0016g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1237+2023A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503283 | |||||||
chr12:4503447 | AG | A | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1237+1858delC | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503447 | |||||||
chr12:4503496 | CTG | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+1808_1237+180 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503496 | |||||||
chr12:4503659 | C | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+1647G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503659 | |||||||
chr12:4503675 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1237+1631A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503675 | |||||||
chr12:4503695 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237+1611T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503695 | |||||||
chr12:4503777 | C | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+1529G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503777 | |||||||
chr12:4503867 | T | TA | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+1438dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503867 | |||||||
chr12:4503974 | C | T | 1 | a0001c0002t0008g0041 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1237+1332G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503974 | |||||||
chr12:4504127 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1237+1179G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504127 | |||||||
chr12:4504200 | C | G | 3 | a0001c0002t0008g0170 a0001c0002t0008g0172 a0001c0002t0014g0171 |
3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1237+1106G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504200 | |||||||
chr12:4504212 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1237+1094G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504212 | |||||||
chr12:4504286 | A | C | 1 | a0001c0001t0005g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1237+1020T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504286 | |||||||
chr12:4504515 | C | T | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1237+791G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504515 | |||||||
chr12:4504521 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1237+785T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504521 | |||||||
chr12:4504667 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1237+639T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504667 | |||||||
chr12:4504710 | A | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+596T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504710 | |||||||
chr12:4504863 | G | T | 1 | a0001c0003t0001g0090 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1237+443C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504863 | |||||||
chr12:4504962 | G | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1237+344C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504962 | |||||||
chr12:4505417 | A | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-37T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505417 | |||||||
chr12:4505579 | T | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(18): Show |
27 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1163-199A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505579 | |||||||
chr12:4505645 | A | G | 4 | a0001c0002t0008g0041 a0001c0002t0008g0170 a0001c0002t0008g0172 others(1): Show |
4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-265T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505645 | |||||||
chr12:4505770 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1163-390C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505770 | |||||||
chr12:4505829 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1163-449C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505829 | |||||||
chr12:4505870 | C | T | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1163-490G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505870 | |||||||
chr12:4505917 | TC | T | 4 | a0001c0002t0008g0041 a0001c0002t0008g0170 a0001c0002t0008g0172 others(1): Show |
4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-538delG | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505917 | |||||||
chr12:4505942 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1163-562C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505942 | |||||||
chr12:4506020 | T | C | 1 | a0001c0001t0013g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1163-640A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506020 | |||||||
chr12:4506036 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(4): Show |
9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-656C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506036 | |||||||
chr12:4506310 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0043 others(3): Show |
9 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-930C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506310 | |||||||
chr12:4506315 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
188 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1163-935G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506315 | |||||||
chr12:4506569 | A | C | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1163-1189T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506569 | |||||||
chr12:4506770 | T | C | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1163-1390A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506770 | |||||||
chr12:4506889 | C | T | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1163-1509G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506889 | |||||||
chr12:4506923 | A | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-1543T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506923 | |||||||
chr12:4506939 | A | G | 6 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0008g0041 others(3): Show |
6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163-1559T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506939 | |||||||
chr12:4507475 | T | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0094 others(12): Show |
18 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.1163-2095A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507475 | |||||||
chr12:4507476 | C | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1163-2096G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507476 | |||||||
chr12:4507487 | C | T | 5 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-2107G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507487 | |||||||
chr12:4507508 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1163-2128C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507508 | |||||||
chr12:4507524 | A | AT | 31 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(28): Show |
37 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1163-2145dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507524 | |||||||
chr12:4507529 | C | G | 3 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 |
4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-2149G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507529 | |||||||
chr12:4507568 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1163-2188G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507568 | |||||||
chr12:4507642 | C | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-2262G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507642 | |||||||
chr12:4507735 | C | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1163-2355G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507735 | |||||||
chr12:4507937 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1163-2557A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507937 | |||||||
chr12:4507989 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1163-2609A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507989 | |||||||
chr12:4508076 | A | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-2696T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508076 | |||||||
chr12:4508095 | T | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-2715A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508095 | |||||||
chr12:4508526 | CAT | C | 5 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-3148_1163-314 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508526 | |||||||
chr12:4508730 | T | C | 3 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0001t0018g0152 |
3 | HG01346.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1163-3350A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508730 | |||||||
chr12:4508743 | C | CA | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3364dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508743 | |||||||
chr12:4508950 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1163-3570T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508950 | |||||||
chr12:4509028 | G | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(23): Show |
34 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1163-3648C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509028 | |||||||
chr12:4509065 | G | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3685C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509065 | |||||||
chr12:4509081 | C | T | 1 | a0001c0002t0008g0041 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1163-3701G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509081 | |||||||
chr12:4509156 | A | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3776T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509156 | |||||||
chr12:4509180 | T | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3800A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509180 | |||||||
chr12:4509186 | A | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3806T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509186 | |||||||
chr12:4509190 | C | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3810G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509190 | |||||||
chr12:4509191 | C | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3811G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509191 | |||||||
chr12:4509202 | C | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3822G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509202 | |||||||
chr12:4509220 | T | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3840A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509220 | |||||||
chr12:4509226 | A | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3846T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509226 | |||||||
chr12:4509248 | C | T | 3 | a0001c0001t0002g0002 a0001c0001t0002g0055 a0001c0001t0019g0056 |
5 | NA18951.hp2 NA18957.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-3868G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509248 | |||||||
chr12:4509253 | A | C | 13 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0001t0012g0050 others(10): Show |
13 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1163-3873T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509253 | |||||||
chr12:4509292 | C | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3912G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509292 | |||||||
chr12:4509304 | G | A | 5 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-3924C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509304 | |||||||
chr12:4509317 | G | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(32): Show |
43 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.1163-3937C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509317 | |||||||
chr12:4509341 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1163-3961C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509341 | |||||||
chr12:4509341 | G | C | 3 | a0001c0002t0001g0174 a0001c0002t0001g0176 a0001c0002t0001g0177 |
3 | HG02572.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1163-3961C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509341 | |||||||
chr12:4509342 | G | A | 10 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(7): Show |
10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163-3962C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509342 | |||||||
chr12:4509348 | A | C | 1 | a0001c0002t0001g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1163-3968T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509348 | |||||||
chr12:4509368 | G | C | 10 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(7): Show |
10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163-3988C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509368 | |||||||
chr12:4509377 | C | G | 1 | a0001c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1163-3997G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509377 | |||||||
chr12:4509385 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1163-4005G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509385 | |||||||
chr12:4509386 | A | G | 14 | a0001c0001t0001g0043 a0001c0001t0002g0038 a0001c0001t0002g0040 others(11): Show |
14 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1163-4006T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509386 | |||||||
chr12:4509392 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1163-4012G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509392 | |||||||
chr12:4509428 | C | A | 10 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0174 others(7): Show |
10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163-4048G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509428 | |||||||
chr12:4509521 | C | G | 16 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0004g0026 others(13): Show |
18 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1163-4141G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509521 | |||||||
chr12:4509537 | G | A | 2 | a0001c0001t0002g0123 a0001c0002t0001g0176 |
2 | HG02572.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1163-4157C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509537 | |||||||
chr12:4509539 | G | A | 5 | a0001c0001t0001g0110 a0001c0001t0002g0123 a0001c0001t0012g0050 others(2): Show |
5 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1163-4159C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509539 | |||||||
chr12:4509574 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1163-4194T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509574 | |||||||
chr12:4509599 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(49): Show |
66 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.1163-4219G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509599 | |||||||
chr12:4509606 | C | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1163-4226G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509606 | |||||||
chr12:4509625 | C | G | 1 | a0001c0001t0001g0020 | 2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1163-4245G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509625 | |||||||
chr12:4509627 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(64): Show |
84 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1163-4247C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509627 | |||||||
chr12:4509628 | G | C | 3 | a0001c0001t0002g0038 a0001c0001t0017g0153 a0001c0003t0001g0091 |
3 | HG01261.hp2 HG02886.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1163-4248C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509628 | |||||||
chr12:4509635 | T | A | 1 | a0001c0001t0001g0020 | 2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1163-4255A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509635 | |||||||
chr12:4509635 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(64): Show |
83 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.1163-4255A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509635 | |||||||
chr12:4509645 | C | G | 14 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0028 others(11): Show |
20 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1163-4265G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509645 | |||||||
chr12:4509650 | C | G | 10 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0144 others(7): Show |
12 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1163-4270G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509650 | |||||||
chr12:4509653 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1163-4273C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509653 | |||||||
chr12:4509662 | T | C | 1 | a0001c0001t0003g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1163-4282A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509662 | |||||||
chr12:4509667 | A | G | 1 | a0001c0001t0009g0130 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1163-4287T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509667 | |||||||
chr12:4509670 | C | G | 39 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0084 others(36): Show |
47 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1163-4290G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509670 | |||||||
chr12:4509672 | T | C | 39 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0084 others(36): Show |
47 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1163-4292A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509672 | |||||||
chr12:4509714 | A | C | 1 | a0001c0001t0003g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1163-4334T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509714 | |||||||
chr12:4509728 | C | T | 2 | a0001c0001t0003g0160 a0001c0002t0001g0173 |
2 | HG02698.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1163-4348G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509728 | |||||||
chr12:4509734 | A | G | 2 | a0001c0001t0010g0169 a0001c0002t0001g0173 |
2 | HG01346.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1163-4354T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509734 | |||||||
chr12:4509820 | A | C | 1 | a0001c0003t0001g0090 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1163-4440T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509820 | |||||||
chr12:4509832 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1163-4452C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509832 | |||||||
chr12:4509839 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0101 |
3 | HG02132.hp2 NA18983.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1163-4459C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509839 | |||||||
chr12:4509840 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
81 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.1163-4460A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509840 | |||||||
chr12:4509879 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1163-4499A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509879 | |||||||
chr12:4509880 | G | A | 1 | a0001c0001t0012g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1163-4500C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509880 | |||||||
chr12:4509918 | G | GAGA | 3 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0002g0077 |
4 | HG00438.hp2 HG02155.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-4541_1163-453 others(7): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509918 | |||||||
chr12:4509932 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0002g0077 |
4 | HG00438.hp2 HG02155.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-4552G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509932 | |||||||
chr12:4510010 | G | T | 3 | a0001c0002t0008g0170 a0001c0002t0008g0172 a0001c0002t0014g0171 |
3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1163-4630C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510010 | |||||||
chr12:4510147 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1163-4767T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510147 | |||||||
chr12:4510176 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1163-4796T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510176 | |||||||
chr12:4510269 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1163-4889A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510269 | |||||||
chr12:4510369 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1163-4989G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510369 | |||||||
chr12:4510395 | C | T | 1 | a0001c0003t0001g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1163-5015G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510395 | |||||||
chr12:4510414 | G | A | 1 | a0001c0001t0005g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1163-5034C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510414 | |||||||
chr12:4510417 | A | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(15): Show |
22 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1163-5037T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510417 | |||||||
chr12:4510433 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1163-5053G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510433 | |||||||
chr12:4510434 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1163-5054T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510434 | |||||||
chr12:4510446 | G | C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0025 others(13): Show |
19 | HG00621.hp1 HG01952.hp2 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.1163-5066C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510446 | |||||||
chr12:4510652 | G | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-5272C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510652 | |||||||
chr12:4510770 | G | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(4): Show |
9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-5390C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510770 | |||||||
chr12:4510771 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(4): Show |
9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-5391C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510771 | |||||||
chr12:4510773 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(4): Show |
9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-5393T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510773 | |||||||
chr12:4510813 | A | G | 12 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0001t0015g0042 others(9): Show |
12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1163-5433T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510813 | |||||||
chr12:4511017 | T | C | 1 | a0001c0002t0014g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1163-5637A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511017 | |||||||
chr12:4511228 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1162+5833T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511228 | |||||||
chr12:4511344 | CAACAAGG | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+5710_1162+571 others(11): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511344 | |||||||
chr12:4511355 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1162+5706G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511355 | |||||||
chr12:4511356 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162+5705C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511356 | |||||||
chr12:4511580 | G | T | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1162+5481C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511580 | |||||||
chr12:4511594 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0123 |
2 | NA18984.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1162+5467C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511594 | |||||||
chr12:4511662 | G | A | 5 | a0001c0003t0001g0007 a0001c0003t0001g0022 a0001c0003t0001g0089 others(2): Show |
8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+5399C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511662 | |||||||
chr12:4511673 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1162+5388T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511673 | |||||||
chr12:4511727 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1162+5334G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511727 | |||||||
chr12:4511728 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0066 others(2): Show |
7 | HG02615.hp1 HG02886.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162+5333C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511728 | |||||||
chr12:4511728 | G | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(2): Show |
7 | HG01109.hp1 HG02258.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162+5333C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511728 | |||||||
chr12:4511807 | A | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(16): Show |
23 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.1162+5254T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511807 | |||||||
chr12:4511819 | A | C | 1 | a0001c0001t0004g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1162+5242T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511819 | |||||||
chr12:4511845 | C | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1162+5216G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511845 | |||||||
chr12:4511948 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1162+5113C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511948 | |||||||
chr12:4512117 | C | T | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1162+4944G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512117 | |||||||
chr12:4512139 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162+4922C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512139 | |||||||
chr12:4512152 | A | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(8): Show |
13 | HG01109.hp1 HG01358.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1162+4909T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512152 | |||||||
chr12:4512160 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162+4901C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512160 | |||||||
chr12:4512187 | C | G | 1 | a0001c0001t0001g0024 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1162+4874G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512187 | |||||||
chr12:4512218 | T | C | 3 | a0001c0002t0008g0170 a0001c0002t0008g0172 a0001c0002t0014g0171 |
3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1162+4843A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512218 | |||||||
chr12:4512358 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1162+4703C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512358 | |||||||
chr12:4512492 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1162+4569A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512492 | |||||||
chr12:4512543 | T | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+4518A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512543 | |||||||
chr12:4512612 | G | C | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1162+4449C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512612 | |||||||
chr12:4512623 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1162+4438T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512623 | |||||||
chr12:4512897 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1162+4164A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512897 | |||||||
chr12:4512899 | G | C | 5 | a0001c0003t0001g0007 a0001c0003t0001g0022 a0001c0003t0001g0089 others(2): Show |
8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+4162C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512899 | |||||||
chr12:4512944 | T | C | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0010 others(14): Show |
23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1162+4117A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512944 | |||||||
chr12:4512978 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(28): Show |
37 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1162+4083T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512978 | |||||||
chr12:4513097 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1162+3964T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513097 | |||||||
chr12:4513182 | A | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+3879T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513182 | |||||||
chr12:4513235 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1162+3826A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513235 | |||||||
chr12:4513296 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1162+3765G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513296 | |||||||
chr12:4513610 | C | A | 3 | a0001c0002t0008g0170 a0001c0002t0008g0172 a0001c0002t0014g0171 |
3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1162+3451G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513610 | |||||||
chr12:4513615 | A | T | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0028 others(7): Show |
15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1162+3446T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513615 | |||||||
chr12:4513716 | G | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG00280.hp2 HG00558.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1162+3345C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513716 | |||||||
chr12:4513767 | G | A | 4 | a0001c0002t0008g0041 a0001c0002t0008g0170 a0001c0002t0008g0172 others(1): Show |
4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162+3294C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513767 | |||||||
chr12:4513814 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0043 |
4 | HG02630.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+3247G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513814 | |||||||
chr12:4513830 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1162+3231T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513830 | |||||||
chr12:4514001 | A | G | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1162+3060T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514001 | |||||||
chr12:4514087 | C | T | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0028 others(7): Show |
15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1162+2974G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514087 | |||||||
chr12:4514106 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162+2955T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514106 | |||||||
chr12:4514155 | T | C | 1 | a0001c0002t0008g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1162+2906A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514155 | |||||||
chr12:4514215 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1162+2846T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514215 | |||||||
chr12:4514319 | C | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+2742G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514319 | |||||||
chr12:4514349 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1162+2712A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514349 | |||||||
chr12:4514391 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0019g0056 |
4 | NA18951.hp2 NA18957.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+2670T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514391 | |||||||
chr12:4514407 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1162+2654T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514407 | |||||||
chr12:4514522 | T | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+2539A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514522 | |||||||
chr12:4514528 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162+2533T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514528 | |||||||
chr12:4514611 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162+2450A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514611 | |||||||
chr12:4514628 | A | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+2433T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514628 | |||||||
chr12:4514639 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0136 |
4 | HG00099.hp1 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+2422C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514639 | |||||||
chr12:4514924 | CTAAA | C | 6 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0008g0041 others(3): Show |
6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162+2133_1162+213 others(8): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514924 | |||||||
chr12:4515080 | TAATA | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0124 |
2 | HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1162+1977_1162+198 others(8): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515080 | |||||||
chr12:4515216 | C | T | 1 | a0001c0001t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1162+1845G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515216 | |||||||
chr12:4515307 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1162+1754A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515307 | |||||||
chr12:4515339 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1162+1722G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515339 | |||||||
chr12:4515413 | C | T | 10 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0144 others(7): Show |
12 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162+1648G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515413 | |||||||
chr12:4515859 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1162+1202C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515859 | |||||||
chr12:4516109 | C | T | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1162+952G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516109 | |||||||
chr12:4516153 | G | C | 1 | a0001c0001t0002g0040 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1162+908C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516153 | |||||||
chr12:4516281 | A | G | 5 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 others(2): Show |
6 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+780T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516281 | |||||||
chr12:4516552 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1162+509G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516552 | |||||||
chr12:4516670 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(60): Show |
79 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.1162+391G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516670 | |||||||
chr12:4516735 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1162+326T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516735 | |||||||
chr12:4516825 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1162+236A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516825 | |||||||
chr12:4516862 | A | G | 6 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0008g0041 others(3): Show |
6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162+199T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516862 | |||||||
chr12:4516942 | T | TA | 12 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0001t0015g0042 others(9): Show |
12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162+118dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516942 | |||||||
chr12:4516956 | A | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1162+105T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516956 | |||||||
chr12:4516965 | C | T | 5 | a0001c0003t0001g0007 a0001c0003t0001g0022 a0001c0003t0001g0089 others(2): Show |
8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+96G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516965 | |||||||
chr12:4517218 | C | T | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1034-29G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517218 | |||||||
chr12:4517257 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1034-68A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517257 | |||||||
chr12:4517365 | A | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034-176T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517365 | |||||||
chr12:4517470 | C | T | 2 | a0001c0001t0004g0026 a0001c0001t0016g0148 |
3 | HG01891.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1034-281G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517470 | |||||||
chr12:4517558 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034-369G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517558 | |||||||
chr12:4517684 | A | AAAATATA others(9): Show |
1 | a0001c0001t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1033+373_1033+374i others(18): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | |||||||
chr12:4517684 | A | AAT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0073 others(9): Show |
14 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1033+372_1033+373d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | |||||||
chr12:4517684 | A | AATAT | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033+370_1033+373d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | |||||||
chr12:4517684 | A | AATATATA others(15): Show |
1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1033+352_1033+373d others(24): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | |||||||
chr12:4517684 | AAT | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1033+372_1033+373d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | |||||||
chr12:4517706 | T | TATATATA others(13): Show |
1 | a0001c0002t0008g0041 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(22): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | |||||||
chr12:4517706 | T | TATATATA others(17): Show |
1 | a0001c0001t0010g0169 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1033+351_1033+352i others(26): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | |||||||
chr12:4517706 | T | TATATATA others(19): Show |
1 | a0001c0001t0010g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(28): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | |||||||
chr12:4517706 | T | TATATATA others(17): Show |
1 | a0001c0002t0008g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1033+351_1033+352i others(26): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | |||||||
chr12:4517706 | T | TATATATA others(19): Show |
1 | a0001c0002t0014g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(28): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | |||||||
chr12:4517706 | T | TATATATA others(21): Show |
1 | a0001c0002t0008g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(30): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | |||||||
chr12:4517708 | G | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0036 others(7): Show |
14 | HG01109.hp1 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1033+350C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517708 | |||||||
chr12:4517710 | C | CAG | 6 | a0001c0001t0021g0063 a0001c0002t0001g0173 a0001c0002t0001g0174 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+346_1033+347d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | |||||||
chr12:4517710 | C | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0036 others(13): Show |
20 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.1033+348G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | |||||||
chr12:4517710 | CAG | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0043 others(25): Show |
37 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1033+346_1033+347d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | |||||||
chr12:4517710 | CAGAG | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0066 |
2 | HG03704.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1033+344_1033+347d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | |||||||
chr12:4517712 | G | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0036 others(7): Show |
14 | HG01109.hp1 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1033+346C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517712 | |||||||
chr12:4517927 | ATGTT | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(4): Show |
9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1033+127_1033+130d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517927 | |||||||
chr12:4517946 | G | C | 1 | a0001c0001t0005g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1033+112C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517946 | |||||||
chr12:4517955 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1033+103C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517955 | |||||||
chr12:4518036 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1033+22T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4518036 | |||||||
chr12:4518351 | T | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.836-96A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 7/13 | chr12 | 4518351 | |||||||
chr12:4518434 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0002g0070 a0001c0001t0002g0156 |
3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.836-179A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 7/13 | chr12 | 4518434 | |||||||
chr12:4518720 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.835+54T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 7/13 | chr12 | 4518720 | |||||||
chr12:4518914 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.729-34C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4518914 | |||||||
chr12:4518958 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.729-78T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4518958 | |||||||
chr12:4519100 | T | C | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.729-220A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519100 | |||||||
chr12:4519323 | TGAA | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.729-446_729-444del others(3): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519323 | |||||||
chr12:4519483 | C | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.729-603G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519483 | |||||||
chr12:4519484 | G | A | 1 | a0001c0001t0007g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.729-604C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519484 | |||||||
chr12:4519530 | C | T | 1 | a0001c0001t0017g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.729-650G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519530 | |||||||
chr12:4519666 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.729-786C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519666 | |||||||
chr12:4519733 | T | C | 23 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(20): Show |
31 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.729-853A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519733 | |||||||
chr12:4519752 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-872C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519752 | |||||||
chr12:4520136 | C | A | 1 | a0001c0001t0002g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.729-1256G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520136 | |||||||
chr12:4520253 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.729-1373T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520253 | |||||||
chr12:4520557 | A | G | 1 | a0001c0001t0009g0130 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.729-1677T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520557 | |||||||
chr12:4520561 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0076 |
3 | NA18971.hp2 NA18988.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.729-1681T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520561 | |||||||
chr12:4521251 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0083 a0001c0001t0001g0102 |
4 | HG02132.hp1 NA18951.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-2371A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521251 | |||||||
chr12:4521299 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.729-2419G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521299 | |||||||
chr12:4521579 | G | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.729-2699C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521579 | |||||||
chr12:4521655 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.729-2775G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521655 | |||||||
chr12:4521697 | AAAAC | A | 5 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-2821_729-2818d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521697 | |||||||
chr12:4521946 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.729-3066A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521946 | |||||||
chr12:4522055 | A | C | 1 | a0001c0001t0005g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.729-3175T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522055 | |||||||
chr12:4522081 | A | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+3173T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522081 | |||||||
chr12:4522163 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.728+3091G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522163 | |||||||
chr12:4522322 | G | A | 5 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 others(2): Show |
6 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+2932C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522322 | |||||||
chr12:4522570 | C | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0124 |
2 | HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.728+2684G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522570 | |||||||
chr12:4522906 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.728+2348T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522906 | |||||||
chr12:4522959 | A | G | 5 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+2295T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522959 | |||||||
chr12:4522976 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.728+2278T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522976 | |||||||
chr12:4523008 | G | T | 1 | a0001c0001t0005g0031 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.728+2246C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523008 | |||||||
chr12:4523060 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.728+2194T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523060 | |||||||
chr12:4523372 | C | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+1882G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523372 | |||||||
chr12:4523622 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.728+1632G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523622 | |||||||
chr12:4523725 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.728+1529G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523725 | |||||||
chr12:4523801 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.728+1453T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523801 | |||||||
chr12:4523968 | T | A | 1 | a0001c0002t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.728+1286A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523968 | |||||||
chr12:4523968 | T | TA | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.728+1285dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523968 | |||||||
chr12:4523977 | A | G | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.728+1277T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523977 | |||||||
chr12:4524033 | CT | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
7 | HG02922.hp2 NA18953.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+1220delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524033 | |||||||
chr12:4524244 | G | A | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.728+1010C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524244 | |||||||
chr12:4524338 | CAGTA | C | 7 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0031 others(4): Show |
7 | HG01952.hp1 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+912_728+915del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524338 | |||||||
chr12:4524418 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.728+836G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524418 | |||||||
chr12:4524513 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.728+741G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524513 | |||||||
chr12:4524582 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.728+672G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524582 | |||||||
chr12:4524583 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.728+671T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524583 | |||||||
chr12:4525170 | A | G | 1 | a0001c0001t0018g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.728+84T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4525170 | |||||||
chr12:4525217 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.728+37C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4525217 | |||||||
chr12:4525702 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.507-119A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525702 | |||||||
chr12:4525837 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.507-254C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525837 | |||||||
chr12:4525879 | A | G | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0010 others(14): Show |
23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.507-296T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525879 | |||||||
chr12:4525927 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.507-344T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525927 | |||||||
chr12:4526306 | G | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.507-723C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526306 | |||||||
chr12:4526747 | T | G | 18 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0010 others(15): Show |
24 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.507-1164A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526747 | |||||||
chr12:4526841 | CA | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(49): Show |
66 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.507-1259delT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526841 | |||||||
chr12:4526884 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | NA18968.hp1 NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.507-1301T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526884 | |||||||
chr12:4526889 | G | GAT | 2 | a0001c0001t0001g0060 a0001c0001t0001g0075 |
2 | HG02523.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.507-1308_507-1307d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526889 | |||||||
chr12:4526929 | A | G | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0028 others(7): Show |
15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.507-1346T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526929 | |||||||
chr12:4527354 | A | AT | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0010 others(14): Show |
23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.507-1772dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527354 | |||||||
chr12:4527429 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-1846A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527429 | |||||||
chr12:4527505 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507-1922A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527505 | |||||||
chr12:4527589 | TGAAATGG others(4): Show |
T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.507-2017_507-2007d others(13): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527589 | |||||||
chr12:4527627 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.507-2044G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527627 | |||||||
chr12:4527648 | A | T | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0028 others(7): Show |
15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.507-2065T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527648 | |||||||
chr12:4527706 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.507-2123C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527706 | |||||||
chr12:4527725 | T | C | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.507-2142A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527725 | |||||||
chr12:4527912 | G | GA | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0010 others(14): Show |
23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.506+1956dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527912 | |||||||
chr12:4528063 | G | A | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+1806C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528063 | |||||||
chr12:4528094 | A | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+1775T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528094 | |||||||
chr12:4528698 | G | T | 15 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0028 others(12): Show |
21 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.506+1171C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528698 | |||||||
chr12:4528811 | C | CTGTAT | 2 | a0001c0001t0003g0011 a0001c0001t0003g0157 |
4 | HG00735.hp2 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+1053_506+1057d others(7): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528811 | |||||||
chr12:4528818 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.506+1051G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528818 | |||||||
chr12:4528896 | T | TAC | 12 | a0001c0001t0001g0009 a0001c0001t0001g0129 a0001c0001t0001g0131 others(9): Show |
15 | HG01081.hp1 HG01261.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.506+971_506+972dup others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | T | TACAC | 4 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG01346.hp1 HG01891.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+969_506+972dup others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TAC | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(32): Show |
47 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.506+971_506+972del others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TACAC | T | 29 | a0001c0001t0001g0019 a0001c0001t0001g0061 a0001c0001t0001g0064 others(26): Show |
32 | HG00438.hp2 HG00621.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.506+969_506+972del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TACACAC | T | 5 | a0001c0001t0001g0057 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG01952.hp1 HG02280.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+967_506+972del others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TACACACA others(1): Show |
T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0069 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+965_506+972del others(8): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0043 others(6): Show |
14 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+963_506+972del others(10): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TACACACA others(7): Show |
T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(5): Show |
10 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.506+959_506+972del others(14): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TACACACA others(9): Show |
T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+957_506+972del others(16): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528896 | TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.506+945_506+972del others(28): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | |||||||
chr12:4528901 | A | C | 1 | a0001c0001t0005g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.506+968T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528901 | |||||||
chr12:4528903 | A | C | 3 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0035 |
3 | HG02818.hp1 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.506+966T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528903 | |||||||
chr12:4528905 | A | C | 1 | a0001c0001t0005g0031 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.506+964T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528905 | |||||||
chr12:4528907 | A | C | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.506+962T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528907 | |||||||
chr12:4528909 | A | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0043 others(4): Show |
10 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.506+960T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528909 | |||||||
chr12:4528913 | A | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(4): Show |
9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+956T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528913 | |||||||
chr12:4528915 | A | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+954T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528915 | |||||||
chr12:4528916 | C | CAT | 1 | a0001c0001t0001g0018 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.506+952_506+953ins others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528916 | |||||||
chr12:4528917 | A | C | 3 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 |
3 | HG02572.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.506+952T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528917 | |||||||
chr12:4528930 | CACACACA others(3): Show |
C | 1 | a0001c0001t0003g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.506+929_506+938del others(10): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528930 | |||||||
chr12:4528932 | CACACACA | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0002g0115 |
3 | HG01934.hp2 NA19086.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.506+930_506+936del others(7): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528932 | |||||||
chr12:4528936 | CACA | C | 2 | a0001c0001t0002g0121 a0001c0001t0006g0142 |
2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.506+930_506+932del others(3): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528936 | |||||||
chr12:4528936 | CACAA | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0165 a0001c0001t0001g0166 others(9): Show |
18 | HG00735.hp2 HG00741.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.506+929_506+932del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528936 | |||||||
chr12:4528938 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.506+931G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528938 | |||||||
chr12:4528938 | CA | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0106 a0001c0001t0001g0126 |
3 | HG00639.hp1 NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.506+930delT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528938 | |||||||
chr12:4528938 | CAA | C | 6 | a0001c0001t0003g0028 a0001c0001t0003g0161 a0001c0001t0011g0179 others(3): Show |
6 | HG02257.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+929_506+930del others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528938 | |||||||
chr12:4528939 | A | AC | 3 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 |
3 | HG01081.hp2 NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.506+929_506+930ins others(1): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528939 | |||||||
chr12:4528940 | A | C | 4 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 others(1): Show |
5 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+929T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528940 | |||||||
chr12:4528942 | C | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.506+927G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528942 | |||||||
chr12:4528998 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.506+871A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528998 | |||||||
chr12:4529284 | C | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG00621.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.506+585G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529284 | |||||||
chr12:4529329 | C | T | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+540G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529329 | |||||||
chr12:4529466 | G | A | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.506+403C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529466 | |||||||
chr12:4529518 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+351A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529518 | |||||||
chr12:4529575 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.506+294C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529575 | |||||||
chr12:4529687 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.506+182T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529687 | |||||||
chr12:4529736 | A | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.506+133T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529736 | |||||||
chr12:4530132 | C | T | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-82G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530132 | |||||||
chr12:4530138 | T | C | 1 | a0001c0001t0002g0037 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.325-88A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530138 | |||||||
chr12:4530224 | G | GA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(10): Show |
17 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-175dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530224 | |||||||
chr12:4530424 | AT | A | 2 | a0001c0001t0003g0011 a0001c0001t0003g0157 |
4 | HG00735.hp2 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-375delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530424 | |||||||
chr12:4530534 | G | A | 6 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0149 others(3): Show |
8 | HG01891.hp2 HG02109.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-484C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530534 | |||||||
chr12:4530697 | T | C | 1 | a0001c0001t0004g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.325-647A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530697 | |||||||
chr12:4530701 | A | T | 1 | a0001c0001t0021g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.325-651T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530701 | |||||||
chr12:4530704 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.325-654C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530704 | |||||||
chr12:4530797 | C | T | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-747G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530797 | |||||||
chr12:4530856 | G | A | 5 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-806C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530856 | |||||||
chr12:4531042 | T | TAAGAGTA others(342): Show |
1 | a0001c0001t0001g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.325-993_325-992ins others(349): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531042 | |||||||
chr12:4531071 | A | G | 12 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0001t0015g0042 others(9): Show |
12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-1021T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531071 | |||||||
chr12:4531113 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.325-1063G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531113 | |||||||
chr12:4531196 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(19): Show |
30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.325-1146G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531196 | |||||||
chr12:4531449 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.325-1399A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531449 | |||||||
chr12:4531500 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.325-1450T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531500 | |||||||
chr12:4531521 | G | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-1471C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531521 | |||||||
chr12:4531586 | C | T | 1 | a0001c0001t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.325-1536G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531586 | |||||||
chr12:4531896 | G | A | 5 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0033 others(2): Show |
5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-1846C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531896 | |||||||
chr12:4531929 | A | C | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-1879T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531929 | |||||||
chr12:4532085 | A | AT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0043 others(25): Show |
37 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.325-2036dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | |||||||
chr12:4532085 | A | ATT | 7 | a0001c0001t0001g0015 a0001c0001t0005g0031 a0001c0001t0005g0032 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.325-2037_325-2036d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | |||||||
chr12:4532085 | A | T | 3 | a0001c0001t0002g0002 a0001c0001t0002g0055 a0001c0001t0019g0056 |
5 | NA18951.hp2 NA18957.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-2035T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | |||||||
chr12:4532085 | AT | A | 9 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0175 others(6): Show |
9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-2036delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | |||||||
chr12:4532717 | A | AT | 4 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(1): Show |
6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+1439dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532717 | |||||||
chr12:4532726 | T | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1431A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532726 | |||||||
chr12:4532985 | A | G | 2 | a0001c0001t0011g0179 a0001c0001t0011g0180 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324+1172T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532985 | |||||||
chr12:4533018 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(60): Show |
79 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.324+1139C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533018 | |||||||
chr12:4533024 | C | G | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.324+1133G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533024 | |||||||
chr12:4533392 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.324+765G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533392 | |||||||
chr12:4533406 | G | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.324+751C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533406 | |||||||
chr12:4533517 | C | A | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.324+640G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533517 | |||||||
chr12:4533529 | G | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0002g0014 others(4): Show |
9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+628C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533529 | |||||||
chr12:4533933 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.324+224A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533933 | |||||||
chr12:4534102 | T | A | 1 | a0001c0001t0018g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.324+55A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4534102 | |||||||
chr12:4534109 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.324+48G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4534109 | |||||||
chr12:4534513 | C | G | 11 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(8): Show |
11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-211G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534513 | |||||||
chr12:4534591 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.179-289T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534591 | |||||||
chr12:4534871 | ATAAAG | A | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.179-574_179-570del others(5): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534871 | |||||||
chr12:4534897 | T | C | 1 | a0001c0001t0017g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.179-595A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534897 | |||||||
chr12:4535423 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.178+594A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535423 | |||||||
chr12:4535455 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.178+562C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535455 | |||||||
chr12:4535462 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.178+555T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535462 | |||||||
chr12:4535528 | G | A | 1 | a0001c0001t0015g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.178+489C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535528 | |||||||
chr12:4535581 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.178+436A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535581 | |||||||
chr12:4535616 | A | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+401T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535616 | |||||||
chr12:4535713 | C | T | 17 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0003g0010 others(14): Show |
23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+304G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535713 | |||||||
chr12:4535744 | A | C | 1 | a0001c0001t0003g0157 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.178+273T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535744 | |||||||
chr12:4535854 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.178+163T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535854 | |||||||
chr12:4535966 | A | G | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.178+51T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535966 | |||||||
chr12:4535995 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.178+22A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535995 | |||||||
chr12:4536234 | G | A | 22 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0165 others(19): Show |
30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-25-15C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536234 | |||||||
chr12:4536282 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25-63A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536282 | |||||||
chr12:4536612 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-25-393G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536612 | |||||||
chr12:4536785 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-566C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536785 | |||||||
chr12:4536922 | G | T | 2 | a0001c0001t0012g0050 a0001c0001t0013g0049 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-25-703C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536922 | |||||||
chr12:4536980 | C | T | 3 | a0001c0001t0007g0017 a0001c0001t0007g0047 a0001c0001t0007g0048 |
4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-761G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536980 | |||||||
chr12:4537624 | G | A | 5 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0175 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+785C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537624 | |||||||
chr12:4537802 | A | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(28): Show |
37 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.-26+607T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537802 | |||||||
chr12:4537960 | AACTTGTT others(4): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+438_-26+448del others(11): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537960 | |||||||
chr12:4537972 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+437A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537972 | |||||||
chr12:4537974 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+435T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537974 | |||||||
chr12:4537979 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+430T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537979 | |||||||
chr12:4537980 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+429A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537980 | |||||||
chr12:4537987 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+422A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537987 | |||||||
chr12:4537991 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+418G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537991 | |||||||
chr12:4537993 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+416C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537993 | |||||||
chr12:4537994 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+415G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537994 | |||||||
chr12:4538002 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+407T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538002 | |||||||
chr12:4538005 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+404T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538005 | |||||||
chr12:4538013 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+396T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538013 | |||||||
chr12:4538022 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+387A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538022 | |||||||
chr12:4538044 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+365C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538044 | |||||||
chr12:4538049 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+360A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538049 | |||||||
chr12:4538056 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+353T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538056 | |||||||
chr12:4538058 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+351T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538058 | |||||||
chr12:4538062 | G | A | 10 | a0001c0001t0010g0168 a0001c0001t0010g0169 a0001c0002t0001g0173 others(7): Show |
10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+347C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538062 | |||||||
chr12:4538219 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-26+190G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538219 | |||||||
chr12:4538339 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-26+70C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538339 |