Item | Value |
---|---|
geneid | 10138 |
ensemblid | ENSG00000015153.15 |
hgncid | 17363 |
symbol | YAF2 |
name | YY1 associated factor 2 |
refseq_nuc | NM_005748.6 |
refseq_prot | NP_005739.2 |
ensembl_nuc | ENST00000534854.7 |
ensembl_prot | ENSP00000439256.2 |
mane_status | MANE Select |
chr | chr12 |
start | 42157104 |
end | 42238248 |
strand | - |
ver | v1.2 |
region | chr12:42157104-42238248 |
region5000 | chr12:42152104-42243248 |
regionname0 | YAF2_chr12_42157104_42238248 |
regionname5000 | YAF2_chr12_42152104_42243248 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 540 | 231 | 57 | 46 | 98 | 8 | 20 | YAF2_chr12_42152104_42243248 | YAF2 | ATGGG others(535): Show |
chr12 | 42152104 | 42243248 | ||
a0001c0002 | 0/0 | 540 | 136 | 24 | 22 | 70 | 4 | 16 | YAF2_chr12_42152104_42243248 | YAF2 | ATGGG others(535): Show |
chr12 | 42152104 | 42243248 | ||
a0001c0003 | 0/0 | 540 | 5 | 5 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATGGG others(535): Show |
chr12 | 42152104 | 42243248 | ||
a0001c0004 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATGGG others(535): Show |
chr12 | 42152104 | 42243248 | ||
a0001c0005 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATGGG others(535): Show |
chr12 | 42152104 | 42243248 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4096 | 151 | 32 | 34 | 67 | 8 | 8 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0002 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0003 | 0/0 | 4098 | 29 | 6 | 6 | 16 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0004 | 0/0 | 4096 | 16 | 0 | 1 | 11 | 0 | 4 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0006 | 0/0 | 4088 | 7 | 0 | 0 | 0 | 0 | 7 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4083): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0008 | 0/0 | 4098 | 3 | 2 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0009 | 0/0 | 4096 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0010 | 0/0 | 4096 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0011 | 0/0 | 4098 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0012 | 0/0 | 4098 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0013 | 0/0 | 4096 | 2 | 0 | 2 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0015 | 0/0 | 4096 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0017 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4099): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0018 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4099): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0019 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0020 | 0/0 | 4096 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0023 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0025 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0026 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0027 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0028 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0029 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0030 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0032 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0001t0033 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0002t0002 | 0/0 | 4096 | 117 | 24 | 11 | 64 | 3 | 15 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0002t0005 | 0/0 | 4096 | 10 | 0 | 9 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0002t0007 | 0/0 | 4096 | 6 | 0 | 2 | 4 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0002t0022 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4093): Show |
chr12 | 42152104 | 42243248 |
a0001c0002t0024 | 0/0 | 4096 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0002t0031 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0003t0001 | 0/0 | 4096 | 3 | 3 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0003t0014 | 0/0 | 4096 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
a0001c0004t0016 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4099): Show |
chr12 | 42152104 | 42243248 |
a0001c0005t0021 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | ATTAT others(4091): Show |
chr12 | 42152104 | 42243248 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0010g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0013g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0013g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0015g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0017g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0018g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0019g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0020g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0023g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0025g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0026g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0027g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0028g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0029g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0030g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0032g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0033g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0022g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0024g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0031g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0014g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0014g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0004t0016g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0005t0021g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0319 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0234 | EUR | FIN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | FIN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00408 | hp2 | a0001 | c0001 | t0023 | g0068 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0325 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0292 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00639 | hp2 | a0001 | c0001 | t0008 | g0057 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00642 | hp1 | a0001 | c0002 | t0005 | g0342 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00733 | hp2 | a0001 | c0002 | t0005 | g0340 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00738 | hp2 | a0001 | c0002 | t0005 | g0341 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01069 | hp1 | a0001 | c0001 | t0013 | g0102 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01069 | hp2 | a0001 | c0002 | t0005 | g0339 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01070 | hp2 | a0001 | c0002 | t0005 | g0335 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0336 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01071 | hp2 | a0001 | c0001 | t0013 | g0111 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0280 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01243 | hp2 | a0001 | c0002 | t0005 | g0281 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0288 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0320 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01358 | hp2 | a0001 | c0001 | t0020 | g0187 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0321 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0273 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0333 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0094 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0322 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01952 | hp2 | a0001 | c0001 | t0015 | g0034 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01975 | hp1 | a0001 | c0002 | t0007 | g0278 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0308 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0309 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0315 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02071 | hp1 | a0001 | c0002 | t0007 | g0293 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0344 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0313 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0311 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0130 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0303 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0332 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02280 | hp2 | a0001 | c0001 | t0028 | g0092 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02293 | hp2 | a0001 | c0002 | t0007 | g0267 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02300 | hp1 | a0001 | c0002 | t0005 | g0337 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0246 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0277 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0244 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0318 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02717 | hp1 | a0001 | c0004 | t0016 | g0122 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0093 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0324 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0330 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0101 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02809 | hp2 | a0001 | c0001 | t0027 | g0090 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0331 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02897 | hp1 | a0001 | c0001 | t0030 | g0123 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02922 | hp1 | a0001 | c0001 | t0033 | g0154 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0099 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0268 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0260 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0223 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0259 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0346 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03209 | hp1 | a0001 | c0001 | t0025 | g0362 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0328 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03225 | hp1 | a0001 | c0003 | t0014 | g0363 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0221 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0272 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03453 | hp1 | a0001 | c0001 | t0017 | g0125 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0121 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0224 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0274 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0245 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03579 | hp2 | a0001 | c0001 | t0032 | g0141 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0225 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0251 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0349 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0103 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0301 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0119 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0343 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03927 | hp1 | a0001 | c0002 | t0024 | g0228 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0087 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0326 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0104 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0329 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0226 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0347 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0220 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0350 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0348 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0222 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18948 | hp1 | a0001 | c0002 | t0022 | g0249 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18995 | hp2 | a0001 | c0002 | t0007 | g0265 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19002 | hp2 | a0001 | c0002 | t0031 | g0302 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19003 | hp1 | a0001 | c0001 | t0026 | g0143 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0327 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19030 | hp2 | a0001 | c0001 | t0018 | g0124 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19043 | hp2 | a0001 | c0001 | t0029 | g0091 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19055 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19066 | hp1 | a0001 | c0002 | t0007 | g0279 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19066 | hp2 | a0001 | c0001 | t0019 | g0195 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19088 | hp2 | a0001 | c0002 | t0007 | g0263 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ASW | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0307 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20805 | hp1 | a0001 | c0002 | t0005 | g0338 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02486 | hp1 | a0001 | c0003 | t0014 | g0364 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02486 | hp2 | a0001 | c0005 | t0021 | g0352 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0100 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0258 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA21309 | hp1 | a0001 | c0001 | t0010 | g0098 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0075 | REF | REF | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0054 | REF | REF | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42160664 | A | G | 1 | a0001c0003 | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.468T>C | p.Asp156Asp | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 536/4096 | 468/543 | 156/180 | chr12 | 42160664 | |||
chr12:42160688 | G | A | 1 | a0001c0004 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.444C>T | p.His148His | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 512/4096 | 444/543 | 148/180 | chr12 | 42160688 | |||
chr12:42160703 | A | G | 2 | a0001c0002 a0001c0005 |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
synonymous_variant | LOW | c.429T>C | p.Ala143Ala | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 497/4096 | 429/543 | 143/180 | chr12 | 42160703 | |||
chr12:42237721 | C | A | 1 | a0001c0005 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.30G>T | p.Pro10Pro | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/4 | 98/4096 | 30/543 | 10/180 | chr12 | 42237721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42157219 | T | C | 2 | a0001c0001t0013 a0001c0001t0020 |
3 | HG01069.hp1 HG01071.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3370A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3370 | chr12 | 42157219 | ||||||
chr12:42157298 | T | A | 3 | a0001c0001t0003 a0001c0001t0026 a0001c0001t0033 |
31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3291A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3291 | chr12 | 42157298 | ||||||
chr12:42157455 | C | G | 1 | a0001c0002t0007 | 6 | HG01975.hp1 HG02071.hp1 HG02293.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3134G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3134 | chr12 | 42157455 | ||||||
chr12:42157490 | G | C | 1 | a0001c0001t0011 | 2 | HG01891.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3099C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3099 | chr12 | 42157490 | ||||||
chr12:42157543 | G | A | 1 | a0001c0001t0009 | 2 | HG02922.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3046C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3046 | chr12 | 42157543 | ||||||
chr12:42157571 | G | A | 1 | a0001c0001t0026 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3018C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3018 | chr12 | 42157571 | ||||||
chr12:42157606 | A | G | 1 | a0001c0001t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2983T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2983 | chr12 | 42157606 | ||||||
chr12:42157621 | A | C | 1 | a0001c0001t0019 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2968T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2968 | chr12 | 42157621 | ||||||
chr12:42157657 | A | G | 1 | a0001c0002t0024 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2932T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2932 | chr12 | 42157657 | ||||||
chr12:42157677 | G | C | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 others(5): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*2912C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2912 | chr12 | 42157677 | ||||||
chr12:42157779 | C | CAT | 9 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 others(6): Show |
41 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2808_*2809dupAT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2809 | chr12 | 42157779 | ||||||
chr12:42157779 | C | CATATATA others(1): Show |
3 | a0001c0001t0017 a0001c0001t0018 a0001c0004t0016 |
3 | HG02717.hp1 HG03453.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2802_*2809dupATAT others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2809 | chr12 | 42157779 | ||||||
chr12:42157917 | G | A | 1 | a0001c0001t0010 | 2 | HG02809.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2672C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2672 | chr12 | 42157917 | ||||||
chr12:42158044 | G | A | 2 | a0001c0002t0005 a0001c0005t0021 |
11 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2545C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2545 | chr12 | 42158044 | ||||||
chr12:42158096 | C | G | 1 | a0001c0001t0027 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2493G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2493 | chr12 | 42158096 | ||||||
chr12:42158390 | ATATTTTT others(1): Show |
A | 1 | a0001c0001t0006 | 7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2191_*2198delCAAA others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2191 | chr12 | 42158390 | ||||||
chr12:42158392 | A | C | 1 | a0001c0001t0001 | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2197T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2197 | chr12 | 42158392 | ||||||
chr12:42158462 | A | T | 1 | a0001c0005t0021 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2127T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2127 | chr12 | 42158462 | ||||||
chr12:42158489 | C | T | 5 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0028 others(2): Show |
6 | HG01891.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2100G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2100 | chr12 | 42158489 | ||||||
chr12:42158495 | G | C | 9 | a0001c0001t0002 a0001c0001t0023 a0001c0002t0002 others(6): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2094C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2094 | chr12 | 42158495 | ||||||
chr12:42158620 | G | A | 1 | a0001c0001t0025 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1969C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1969 | chr12 | 42158620 | ||||||
chr12:42158657 | T | C | 3 | a0001c0001t0003 a0001c0001t0026 a0001c0001t0033 |
31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1932A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1932 | chr12 | 42158657 | ||||||
chr12:42158710 | G | C | 4 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0028 others(1): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1879C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1879 | chr12 | 42158710 | ||||||
chr12:42158787 | G | C | 1 | a0001c0001t0030 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1802C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1802 | chr12 | 42158787 | ||||||
chr12:42158865 | T | A | 1 | a0001c0001t0030 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1724A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1724 | chr12 | 42158865 | ||||||
chr12:42158922 | T | A | 1 | a0001c0002t0031 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1667A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1667 | chr12 | 42158922 | ||||||
chr12:42159005 | T | G | 1 | a0001c0001t0012 | 2 | HG02258.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1584A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1584 | chr12 | 42159005 | ||||||
chr12:42159417 | T | C | 2 | a0001c0001t0004 a0001c0001t0013 |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1172A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1172 | chr12 | 42159417 | ||||||
chr12:42159889 | T | C | 1 | a0001c0001t0032 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*700A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 700 | chr12 | 42159889 | ||||||
chr12:42159928 | T | A | 1 | a0001c0001t0033 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 661 | chr12 | 42159928 | ||||||
chr12:42160245 | A | C | 1 | a0001c0001t0015 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 344 | chr12 | 42160245 | ||||||
chr12:42238185 | T | C | 1 | a0001c0003t0014 | 2 | HG02486.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-5A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 1/4 | 5 | chr12 | 42238185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42160870 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.306-44G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42160870 | |||||||
chr12:42160937 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.306-111C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42160937 | |||||||
chr12:42160993 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.306-167T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42160993 | |||||||
chr12:42161041 | CTG | C | 133 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.306-217_306-216del others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161041 | |||||||
chr12:42161369 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+244G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161369 | |||||||
chr12:42161415 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG01243.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.305+198G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161415 | |||||||
chr12:42161546 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+67C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161546 | |||||||
chr12:42161805 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.153-40G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42161805 | |||||||
chr12:42161928 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-163C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42161928 | |||||||
chr12:42162200 | T | G | 1 | a0001c0002t0002g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153-435A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162200 | |||||||
chr12:42162306 | G | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-541C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162306 | |||||||
chr12:42162755 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.153-990G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162755 | |||||||
chr12:42162788 | T | C | 1 | a0001c0002t0002g0334 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.153-1023A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162788 | |||||||
chr12:42162800 | C | G | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-1035G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162800 | |||||||
chr12:42162899 | T | G | 1 | a0001c0001t0004g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.153-1134A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162899 | |||||||
chr12:42163069 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-1304C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163069 | |||||||
chr12:42163138 | T | G | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-1373A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163138 | |||||||
chr12:42163533 | T | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-1768A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163533 | |||||||
chr12:42163656 | T | C | 1 | a0001c0002t0002g0297 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.153-1891A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163656 | |||||||
chr12:42163779 | G | C | 5 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-2014C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163779 | |||||||
chr12:42163787 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-2022T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163787 | |||||||
chr12:42163916 | T | C | 7 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0129 others(4): Show |
7 | HG02630.hp2 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-2151A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163916 | |||||||
chr12:42164050 | C | T | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-2285G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164050 | |||||||
chr12:42164120 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.153-2355A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164120 | |||||||
chr12:42164201 | T | C | 134 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(131): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-2436A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164201 | |||||||
chr12:42164270 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-2505A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164270 | |||||||
chr12:42164384 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.153-2619A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164384 | |||||||
chr12:42164408 | A | G | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-2643T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164408 | |||||||
chr12:42164538 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-2773C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164538 | |||||||
chr12:42164595 | T | A | 30 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(27): Show |
31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.153-2830A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164595 | |||||||
chr12:42164721 | A | G | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-2956T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164721 | |||||||
chr12:42164749 | C | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG01496.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-2984G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164749 | |||||||
chr12:42164802 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.153-3037C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164802 | |||||||
chr12:42164819 | C | T | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-3054G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164819 | |||||||
chr12:42164846 | G | T | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-3081C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164846 | |||||||
chr12:42164859 | C | G | 16 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(13): Show |
16 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-3094G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164859 | |||||||
chr12:42164921 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-3156T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164921 | |||||||
chr12:42164941 | C | T | 1 | a0001c0001t0028g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-3176G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164941 | |||||||
chr12:42165061 | C | CA | 11 | a0001c0001t0001g0067 a0001c0001t0001g0097 a0001c0001t0001g0196 others(8): Show |
11 | HG00408.hp2 HG01433.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-3297dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165061 | |||||||
chr12:42165061 | CA | C | 7 | a0001c0001t0001g0081 a0001c0001t0011g0093 a0001c0001t0011g0094 others(4): Show |
7 | HG00438.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-3297delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165061 | |||||||
chr12:42165073 | A | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-3308T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165073 | |||||||
chr12:42165076 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.153-3311T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165076 | |||||||
chr12:42165180 | C | T | 4 | a0001c0001t0009g0099 a0001c0001t0009g0100 a0001c0001t0010g0098 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-3415G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165180 | |||||||
chr12:42165187 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.153-3422C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165187 | |||||||
chr12:42165322 | A | G | 11 | a0001c0002t0002g0089 a0001c0002t0002g0163 a0001c0002t0002g0170 others(8): Show |
11 | HG00621.hp1 HG02129.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-3557T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165322 | |||||||
chr12:42165349 | G | A | 30 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(27): Show |
31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.153-3584C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165349 | |||||||
chr12:42165434 | C | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-3669G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165434 | |||||||
chr12:42165452 | G | GGTTTTT | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0006g0221 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-3693_153-3688d others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165452 | |||||||
chr12:42165502 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3737G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165502 | |||||||
chr12:42165503 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0353 others(9): Show |
13 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.153-3738C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165503 | |||||||
chr12:42165503 | G | T | 3 | a0001c0002t0002g0251 a0001c0002t0002g0348 a0001c0002t0002g0350 |
3 | HG03669.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.153-3738C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165503 | |||||||
chr12:42165624 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3859G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165624 | |||||||
chr12:42165661 | C | T | 5 | a0001c0002t0002g0258 a0001c0002t0002g0259 a0001c0002t0002g0260 others(2): Show |
5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3896G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165661 | |||||||
chr12:42165723 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3958T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165723 | |||||||
chr12:42165773 | G | GT | 39 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0033 others(36): Show |
40 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.153-4009dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165773 | |||||||
chr12:42165773 | GT | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
94 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.153-4009delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165773 | |||||||
chr12:42165773 | GTTTT | G | 63 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(60): Show |
67 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.153-4012_153-4009d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165773 | |||||||
chr12:42165884 | A | ATATC | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-4123_153-4120d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165884 | |||||||
chr12:42165902 | A | ATCTATCT others(25): Show |
3 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 |
3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-4138_153-4137i others(34): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165902 | |||||||
chr12:42165902 | A | ATCTATCT others(21): Show |
2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-4138_153-4137i others(30): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165902 | |||||||
chr12:42165957 | A | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-4192T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165957 | |||||||
chr12:42165974 | G | A | 4 | a0001c0001t0001g0353 a0001c0001t0001g0359 a0001c0001t0001g0360 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-4209C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165974 | |||||||
chr12:42166067 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.153-4302A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166067 | |||||||
chr12:42166137 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(11): Show |
15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-4372C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166137 | |||||||
chr12:42166146 | C | T | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-4381G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166146 | |||||||
chr12:42166166 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.153-4401C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166166 | |||||||
chr12:42166182 | G | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-4417C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166182 | |||||||
chr12:42166205 | G | A | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-4440C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166205 | |||||||
chr12:42166207 | C | T | 14 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(11): Show |
15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-4442G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166207 | |||||||
chr12:42166338 | T | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | NA18747.hp2 NA18956.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-4573A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166338 | |||||||
chr12:42166408 | C | T | 6 | a0001c0001t0002g0282 a0001c0002t0002g0084 a0001c0002t0002g0250 others(3): Show |
6 | NA18962.hp2 NA18969.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-4643G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166408 | |||||||
chr12:42166441 | T | C | 5 | a0001c0002t0002g0258 a0001c0002t0002g0259 a0001c0002t0002g0260 others(2): Show |
5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-4676A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166441 | |||||||
chr12:42166447 | A | G | 1 | a0001c0002t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-4682T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166447 | |||||||
chr12:42166548 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.153-4783A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166548 | |||||||
chr12:42166720 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.153-4955A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166720 | |||||||
chr12:42166829 | TA | T | 38 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0003g0003 others(35): Show |
39 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.153-5065delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166829 | |||||||
chr12:42166894 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-5129C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166894 | |||||||
chr12:42167156 | G | T | 1 | a0001c0001t0028g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-5391C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167156 | |||||||
chr12:42167184 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-5419T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167184 | |||||||
chr12:42167331 | G | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-5566C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167331 | |||||||
chr12:42167360 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.153-5595C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167360 | |||||||
chr12:42167596 | A | G | 134 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(131): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-5831T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167596 | |||||||
chr12:42167666 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-5901T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167666 | |||||||
chr12:42167712 | T | C | 1 | a0001c0001t0006g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.153-5947A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167712 | |||||||
chr12:42167750 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.153-5985T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167750 | |||||||
chr12:42167754 | C | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-5989G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167754 | |||||||
chr12:42167913 | T | C | 3 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0004t0016g0122 |
3 | HG02717.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.153-6148A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167913 | |||||||
chr12:42168001 | A | G | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-6236T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168001 | |||||||
chr12:42168175 | A | AT | 16 | a0001c0001t0001g0133 a0001c0001t0001g0179 a0001c0001t0001g0200 others(13): Show |
16 | HG00544.hp1 HG01978.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-6411dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168175 | |||||||
chr12:42168175 | AT | A | 14 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0095 others(11): Show |
14 | HG00642.hp2 HG01192.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-6411delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168175 | |||||||
chr12:42168209 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-6444C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168209 | |||||||
chr12:42168242 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-6477T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168242 | |||||||
chr12:42168286 | C | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-6521G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168286 | |||||||
chr12:42168305 | A | G | 134 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(131): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-6540T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168305 | |||||||
chr12:42168458 | A | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-6693T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168458 | |||||||
chr12:42168461 | T | C | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-6696A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168461 | |||||||
chr12:42168675 | C | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-6910G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168675 | |||||||
chr12:42168698 | C | T | 2 | a0001c0001t0027g0090 a0001c0001t0028g0092 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.153-6933G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168698 | |||||||
chr12:42169027 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-7262G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169027 | |||||||
chr12:42169272 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-7507A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169272 | |||||||
chr12:42169337 | C | A | 2 | a0001c0002t0002g0236 a0001c0002t0002g0351 |
2 | NA18947.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.153-7572G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169337 | |||||||
chr12:42169461 | T | G | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-7696A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169461 | |||||||
chr12:42169527 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-7762A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169527 | |||||||
chr12:42169698 | C | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-7933G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169698 | |||||||
chr12:42169785 | T | C | 11 | a0001c0002t0002g0089 a0001c0002t0002g0163 a0001c0002t0002g0170 others(8): Show |
11 | HG00621.hp1 HG02129.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-8020A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169785 | |||||||
chr12:42169872 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.153-8107A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169872 | |||||||
chr12:42169904 | A | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.153-8139T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169904 | |||||||
chr12:42170018 | G | A | 36 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(33): Show |
37 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.153-8253C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170018 | |||||||
chr12:42170064 | G | A | 1 | a0001c0001t0011g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.153-8299C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170064 | |||||||
chr12:42170111 | A | G | 5 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0150 others(2): Show |
5 | NA18946.hp2 NA18957.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-8346T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170111 | |||||||
chr12:42170187 | G | C | 134 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(131): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-8422C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170187 | |||||||
chr12:42170268 | A | G | 3 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 |
3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-8503T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170268 | |||||||
chr12:42170289 | C | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-8524G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170289 | |||||||
chr12:42170312 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-8547A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170312 | |||||||
chr12:42170605 | T | A | 1 | a0001c0003t0014g0363 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153-8840A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170605 | |||||||
chr12:42170673 | T | TAC | 3 | a0001c0001t0003g0078 a0001c0001t0030g0123 a0001c0004t0016g0122 |
3 | HG02717.hp1 HG02897.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.153-8909_153-8908i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170673 | |||||||
chr12:42170675 | T | C | 36 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(33): Show |
37 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.153-8910A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170675 | |||||||
chr12:42170675 | T | TAC | 5 | a0001c0001t0001g0020 a0001c0001t0001g0355 a0001c0001t0001g0356 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-8912_153-8911d others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170675 | |||||||
chr12:42170675 | T | TACAC | 3 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 |
3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-8914_153-8911d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170675 | |||||||
chr12:42170718 | C | T | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-8953G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170718 | |||||||
chr12:42170845 | C | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-9080G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170845 | |||||||
chr12:42170921 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-9156C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170921 | |||||||
chr12:42170968 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.153-9203C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170968 | |||||||
chr12:42170990 | G | GT | 6 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0001t0017g0125 others(3): Show |
6 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-9226dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170990 | |||||||
chr12:42170991 | T | G | 58 | a0001c0002t0002g0083 a0001c0002t0002g0085 a0001c0002t0002g0089 others(55): Show |
58 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.153-9226A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170991 | |||||||
chr12:42171062 | G | A | 1 | a0001c0002t0024g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.153-9297C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171062 | |||||||
chr12:42171180 | C | T | 1 | a0001c0001t0030g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.153-9415G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171180 | |||||||
chr12:42171207 | G | T | 4 | a0001c0002t0002g0266 a0001c0002t0002g0269 a0001c0002t0002g0270 others(1): Show |
4 | NA18957.hp1 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-9442C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171207 | |||||||
chr12:42171230 | A | T | 1 | a0001c0002t0002g0242 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.153-9465T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171230 | |||||||
chr12:42171233 | C | T | 1 | a0001c0002t0002g0089 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.153-9468G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171233 | |||||||
chr12:42171247 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.153-9482A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171247 | |||||||
chr12:42171269 | G | T | 1 | a0001c0001t0010g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153-9504C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171269 | |||||||
chr12:42171495 | C | A | 9 | a0001c0002t0005g0335 a0001c0002t0005g0336 a0001c0002t0005g0337 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.153-9730G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171495 | |||||||
chr12:42171509 | TA | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
126 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.153-9745delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171509 | |||||||
chr12:42171516 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-9751T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171516 | |||||||
chr12:42171522 | A | C | 1 | a0001c0001t0029g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153-9757T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171522 | |||||||
chr12:42171538 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-9773A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171538 | |||||||
chr12:42171629 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.153-9864T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171629 | |||||||
chr12:42171761 | C | A | 1 | a0001c0002t0002g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.153-9996G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171761 | |||||||
chr12:42171799 | C | CA | 16 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(13): Show |
16 | HG02015.hp1 HG02132.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-10035dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171799 | |||||||
chr12:42171799 | CA | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
263 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.153-10035delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171799 | |||||||
chr12:42171799 | CAA | C | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(3): Show |
6 | HG01069.hp2 HG01169.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-10036_153-1003 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171799 | |||||||
chr12:42171824 | T | C | 1 | a0001c0002t0002g0343 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.153-10059A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171824 | |||||||
chr12:42172006 | C | A | 1 | a0001c0002t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-10241G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172006 | |||||||
chr12:42172304 | T | G | 361 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(358): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.153-10539A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172304 | |||||||
chr12:42172305 | C | T | 1 | a0001c0001t0009g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.153-10540G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172305 | |||||||
chr12:42172480 | T | C | 59 | a0001c0002t0002g0083 a0001c0002t0002g0085 a0001c0002t0002g0089 others(56): Show |
59 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.153-10715A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172480 | |||||||
chr12:42172637 | G | A | 5 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0150 others(2): Show |
5 | NA18946.hp2 NA18957.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-10872C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172637 | |||||||
chr12:42172639 | A | T | 3 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0243 |
3 | NA18990.hp2 NA18993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.153-10874T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172639 | |||||||
chr12:42172727 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-10962C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172727 | |||||||
chr12:42172778 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-11013C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172778 | |||||||
chr12:42172804 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.153-11039A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172804 | |||||||
chr12:42172858 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-11093G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172858 | |||||||
chr12:42172881 | A | G | 2 | a0001c0001t0027g0090 a0001c0001t0028g0092 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.153-11116T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172881 | |||||||
chr12:42173066 | G | C | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.153-11301C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173066 | |||||||
chr12:42173082 | G | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-11317C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173082 | |||||||
chr12:42173161 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-11396A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173161 | |||||||
chr12:42173163 | G | A | 1 | a0001c0002t0002g0322 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.153-11398C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173163 | |||||||
chr12:42173202 | C | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-11437G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173202 | |||||||
chr12:42173253 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-11488C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173253 | |||||||
chr12:42173400 | T | C | 1 | a0001c0002t0002g0289 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.153-11635A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173400 | |||||||
chr12:42173905 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(12): Show |
16 | HG00639.hp2 HG00738.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-12140T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173905 | |||||||
chr12:42173917 | A | G | 5 | a0001c0002t0002g0258 a0001c0002t0002g0259 a0001c0002t0002g0260 others(2): Show |
5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-12152T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173917 | |||||||
chr12:42173998 | C | T | 134 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(131): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-12233G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173998 | |||||||
chr12:42174100 | GA | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
127 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.153-12336delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174100 | |||||||
chr12:42174127 | A | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-12362T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174127 | |||||||
chr12:42174205 | T | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-12440A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174205 | |||||||
chr12:42174209 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.153-12444G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174209 | |||||||
chr12:42174262 | C | T | 1 | a0001c0002t0002g0324 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153-12497G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174262 | |||||||
chr12:42174445 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.153-12680G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174445 | |||||||
chr12:42174642 | G | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-12877C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174642 | |||||||
chr12:42174829 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.153-13064T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174829 | |||||||
chr12:42174891 | A | AT | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-13127dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174891 | |||||||
chr12:42174963 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
89 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.153-13198G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174963 | |||||||
chr12:42175018 | C | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
299 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.153-13253G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175018 | |||||||
chr12:42175112 | T | C | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-13347A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175112 | |||||||
chr12:42175235 | G | A | 8 | a0001c0001t0001g0353 a0001c0001t0001g0355 a0001c0001t0001g0356 others(5): Show |
8 | HG02055.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-13470C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175235 | |||||||
chr12:42175292 | T | C | 4 | a0001c0002t0002g0088 a0001c0002t0002g0232 a0001c0002t0002g0241 others(1): Show |
4 | HG02055.hp1 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-13527A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175292 | |||||||
chr12:42175332 | T | C | 1 | a0001c0002t0002g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.153-13567A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175332 | |||||||
chr12:42175350 | C | A | 2 | a0001c0002t0002g0272 a0001c0002t0002g0288 |
2 | HG01257.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.153-13585G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175350 | |||||||
chr12:42175365 | GGGTAGGT others(6): Show |
G | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-13613_153-1360 others(17): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175365 | |||||||
chr12:42175404 | G | C | 1 | a0001c0002t0002g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.153-13639C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175404 | |||||||
chr12:42175534 | CA | C | 360 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(357): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.153-13770delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175534 | |||||||
chr12:42175740 | C | CA | 39 | a0001c0001t0008g0121 a0001c0002t0002g0083 a0001c0002t0002g0089 others(36): Show |
39 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.153-13976dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAA | 64 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0002t0002g0002 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.153-13977_153-1397 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAA | 29 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0002g0282 others(26): Show |
30 | HG00621.hp2 HG01070.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.153-13978_153-1397 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAA | 11 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0050 others(8): Show |
11 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-13979_153-1397 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAA | 14 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0067 others(11): Show |
14 | HG01433.hp1 HG01975.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-13980_153-1397 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAA | 18 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0066 others(15): Show |
18 | HG00597.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-13981_153-1397 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA | 17 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0046 others(14): Show |
17 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-13982_153-1397 others(11): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(1): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0055 others(8): Show |
11 | HG00408.hp2 HG02071.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-13983_153-1397 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0009g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.153-13985_153-1397 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0077 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.153-13986_153-1397 others(15): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.153-13989_153-1397 others(18): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0062 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.153-13992_153-1397 others(21): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01515.hp2 HG03710.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.153-13994_153-1397 others(23): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(13): Show |
5 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0044 others(2): Show |
5 | HG00639.hp2 HG01358.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-13995_153-1397 others(24): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(14): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-13996_153-1397 others(25): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0049 others(2): Show |
5 | HG00423.hp2 HG01106.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-13997_153-1397 others(26): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(18): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | NA18977.hp1 NA18982.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-14000_153-1397 others(29): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(19): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0047 |
3 | HG01993.hp2 HG02015.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.153-14001_153-1397 others(30): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(20): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0058 others(1): Show |
4 | HG01192.hp2 HG02683.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-14002_153-1397 others(31): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0041 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.153-13976_153-1397 others(35): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0033 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.153-13976_153-1397 others(36): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.153-13976_153-1397 others(40): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | CAAAA | C | 13 | a0001c0001t0001g0012 a0001c0001t0003g0003 a0001c0001t0003g0142 others(10): Show |
14 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-13979_153-1397 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | CAAAAAA | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(3): Show |
7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-13981_153-1397 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-13983_153-1397 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0185 a0001c0001t0001g0196 a0001c0001t0001g0202 others(3): Show |
6 | HG00642.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-13984_153-1397 others(13): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | CAAAAAAA others(3): Show |
C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
72 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.153-13985_153-1397 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175740 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153-13986_153-1397 others(15): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | |||||||
chr12:42175818 | C | G | 6 | a0001c0002t0002g0087 a0001c0002t0002g0319 a0001c0002t0002g0320 others(3): Show |
6 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-14053G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175818 | |||||||
chr12:42175998 | G | C | 1 | a0001c0002t0002g0232 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.153-14233C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175998 | |||||||
chr12:42176068 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.153-14303C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176068 | |||||||
chr12:42176211 | C | CA | 13 | a0001c0001t0001g0196 a0001c0001t0001g0361 a0001c0001t0002g0282 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-14447dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176211 | |||||||
chr12:42176211 | CA | C | 7 | a0001c0001t0003g0167 a0001c0001t0009g0099 a0001c0001t0009g0100 others(4): Show |
7 | HG00597.hp1 HG02258.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-14447delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176211 | |||||||
chr12:42176366 | C | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-14601G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176366 | |||||||
chr12:42176367 | T | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-14602A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176367 | |||||||
chr12:42176538 | T | C | 1 | a0001c0002t0002g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153-14773A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176538 | |||||||
chr12:42176548 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-14783C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176548 | |||||||
chr12:42176563 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.153-14798G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176563 | |||||||
chr12:42176681 | G | T | 1 | a0001c0001t0027g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153-14916C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176681 | |||||||
chr12:42176727 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.153-14962A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176727 | |||||||
chr12:42176779 | T | C | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-15014A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176779 | |||||||
chr12:42176783 | G | A | 1 | a0001c0002t0002g0170 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153-15018C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176783 | |||||||
chr12:42176790 | C | T | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-15025G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176790 | |||||||
chr12:42176840 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.153-15075C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176840 | |||||||
chr12:42176882 | G | A | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
10 | HG00741.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.153-15117C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176882 | |||||||
chr12:42177208 | T | C | 1 | a0001c0001t0003g0161 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.153-15443A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177208 | |||||||
chr12:42177275 | A | G | 1 | a0001c0002t0002g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-15510T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177275 | |||||||
chr12:42177279 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.153-15514G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177279 | |||||||
chr12:42177417 | T | C | 1 | a0001c0001t0004g0118 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.153-15652A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177417 | |||||||
chr12:42177444 | C | A | 5 | a0001c0002t0002g0258 a0001c0002t0002g0259 a0001c0002t0002g0260 others(2): Show |
5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-15679G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177444 | |||||||
chr12:42177484 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.153-15719G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177484 | |||||||
chr12:42177524 | C | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-15759G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177524 | |||||||
chr12:42177576 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.153-15811G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177576 | |||||||
chr12:42177588 | C | G | 1 | a0001c0002t0002g0297 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.153-15823G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177588 | |||||||
chr12:42177593 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-15828T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177593 | |||||||
chr12:42177775 | T | C | 10 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.153-16010A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177775 | |||||||
chr12:42177825 | A | G | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-16060T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177825 | |||||||
chr12:42177929 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-16164G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177929 | |||||||
chr12:42177977 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-16212A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177977 | |||||||
chr12:42178113 | T | C | 38 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(35): Show |
39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-16348A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178113 | |||||||
chr12:42178277 | A | T | 32 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(29): Show |
33 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.153-16512T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178277 | |||||||
chr12:42178302 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-16537C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178302 | |||||||
chr12:42178370 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.153-16605C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178370 | |||||||
chr12:42178382 | G | A | 3 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-16617C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178382 | |||||||
chr12:42178420 | A | G | 2 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.153-16655T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178420 | |||||||
chr12:42178428 | A | G | 1 | a0001c0002t0002g0344 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.153-16663T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178428 | |||||||
chr12:42178505 | C | T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-16740G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178505 | |||||||
chr12:42178611 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-16846A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178611 | |||||||
chr12:42178687 | T | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-16922A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178687 | |||||||
chr12:42178811 | A | T | 1 | a0001c0001t0004g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.153-17046T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178811 | |||||||
chr12:42179103 | T | C | 1 | a0001c0001t0004g0118 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.153-17338A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179103 | |||||||
chr12:42179267 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-17502G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179267 | |||||||
chr12:42179315 | C | G | 1 | a0001c0001t0004g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153-17550G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179315 | |||||||
chr12:42179573 | T | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-17808A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179573 | |||||||
chr12:42179789 | C | CA | 115 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0097 others(112): Show |
119 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.153-18025dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179789 | |||||||
chr12:42179789 | C | CAA | 17 | a0001c0002t0002g0089 a0001c0002t0002g0252 a0001c0002t0002g0253 others(14): Show |
17 | HG00621.hp1 HG01884.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-18026_153-1802 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179789 | |||||||
chr12:42179789 | CA | C | 68 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(65): Show |
69 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.153-18025delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179789 | |||||||
chr12:42179820 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.153-18055C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179820 | |||||||
chr12:42179909 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.153-18144G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179909 | |||||||
chr12:42180020 | T | C | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-18255A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180020 | |||||||
chr12:42180066 | G | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.153-18301C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180066 | |||||||
chr12:42180195 | C | T | 12 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(9): Show |
12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-18430G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180195 | |||||||
chr12:42180221 | G | A | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-18456C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180221 | |||||||
chr12:42180317 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-18552A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180317 | |||||||
chr12:42180390 | A | G | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-18625T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180390 | |||||||
chr12:42180457 | G | A | 1 | a0001c0001t0027g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153-18692C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180457 | |||||||
chr12:42180457 | G | C | 1 | a0001c0001t0009g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.153-18692C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180457 | |||||||
chr12:42180580 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-18815G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180580 | |||||||
chr12:42180581 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-18816C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180581 | |||||||
chr12:42180650 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.153-18885T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180650 | |||||||
chr12:42180736 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0052 a0001c0001t0023g0068 |
3 | HG00408.hp2 NA18961.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.153-18971C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180736 | |||||||
chr12:42181151 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-19386C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181151 | |||||||
chr12:42181379 | A | T | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-19614T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181379 | |||||||
chr12:42181414 | T | C | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-19649A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181414 | |||||||
chr12:42181450 | TCTTGCGT others(10): Show |
T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-19702_153-1968 others(21): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181450 | |||||||
chr12:42181472 | T | C | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-19707A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181472 | |||||||
chr12:42181740 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153-19975G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181740 | |||||||
chr12:42182125 | AAAG | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-20363_153-2036 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182125 | |||||||
chr12:42182244 | G | T | 12 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(9): Show |
12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-20479C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182244 | |||||||
chr12:42182247 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-20482A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182247 | |||||||
chr12:42182264 | A | G | 3 | a0001c0002t0002g0259 a0001c0002t0002g0261 a0001c0002t0002g0262 |
3 | HG01884.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.153-20499T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182264 | |||||||
chr12:42182374 | GA | G | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-20610delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182374 | |||||||
chr12:42182654 | C | G | 1 | a0001c0001t0001g0358 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153-20889G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182654 | |||||||
chr12:42182661 | C | T | 1 | a0001c0002t0002g0264 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.153-20896G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182661 | |||||||
chr12:42182694 | T | C | 1 | a0001c0002t0002g0325 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.153-20929A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182694 | |||||||
chr12:42182735 | A | G | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-20970T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182735 | |||||||
chr12:42182806 | C | A | 2 | a0001c0002t0005g0280 a0001c0002t0005g0281 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.153-21041G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182806 | |||||||
chr12:42182889 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | NA18986.hp2 NA19007.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-21124G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182889 | |||||||
chr12:42182929 | A | C | 2 | a0001c0002t0002g0241 a0001c0002t0002g0242 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.153-21164T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182929 | |||||||
chr12:42182974 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.153-21209C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182974 | |||||||
chr12:42183025 | T | C | 1 | a0001c0001t0028g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-21260A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183025 | |||||||
chr12:42183114 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-21349G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183114 | |||||||
chr12:42183218 | C | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-21453G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183218 | |||||||
chr12:42183427 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.153-21662T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183427 | |||||||
chr12:42183442 | C | G | 2 | a0001c0001t0010g0098 a0001c0001t0010g0101 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153-21677G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183442 | |||||||
chr12:42183733 | T | G | 1 | a0001c0002t0002g0303 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.153-21968A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183733 | |||||||
chr12:42183837 | A | C | 3 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0243 |
3 | NA18990.hp2 NA18993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.153-22072T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183837 | |||||||
chr12:42184275 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.153-22510T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184275 | |||||||
chr12:42184303 | A | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-22538T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184303 | |||||||
chr12:42184413 | G | A | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.153-22648C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184413 | |||||||
chr12:42184726 | C | A | 2 | a0001c0001t0009g0099 a0001c0001t0009g0100 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.153-22961G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184726 | |||||||
chr12:42184997 | C | T | 1 | a0001c0002t0002g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153-23232G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184997 | |||||||
chr12:42185046 | C | T | 2 | a0001c0001t0010g0098 a0001c0001t0010g0101 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153-23281G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185046 | |||||||
chr12:42185050 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-23285A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185050 | |||||||
chr12:42185134 | C | T | 1 | a0001c0001t0004g0106 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.153-23369G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185134 | |||||||
chr12:42185135 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-23370C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185135 | |||||||
chr12:42185171 | T | C | 1 | a0001c0002t0002g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.153-23406A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185171 | |||||||
chr12:42185176 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
76 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.153-23411C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185176 | |||||||
chr12:42185176 | G | GCAAA | 12 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(9): Show |
12 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-23415_153-2341 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185176 | |||||||
chr12:42185176 | GCAAA | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(31): Show |
35 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.153-23415_153-2341 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185176 | |||||||
chr12:42185423 | G | A | 2 | a0001c0001t0027g0090 a0001c0001t0028g0092 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.153-23658C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185423 | |||||||
chr12:42185429 | G | A | 1 | a0001c0002t0002g0250 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.153-23664C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185429 | |||||||
chr12:42185584 | C | T | 14 | a0001c0001t0001g0081 a0001c0001t0001g0173 a0001c0001t0001g0176 others(11): Show |
14 | HG00438.hp1 HG00609.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-23819G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185584 | |||||||
chr12:42185722 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0357 |
4 | HG02559.hp2 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-23957G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185722 | |||||||
chr12:42185921 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(34): Show |
38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.153-24156G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185921 | |||||||
chr12:42185938 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0227 |
2 | NA19007.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.153-24173C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185938 | |||||||
chr12:42186010 | G | A | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-24245C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186010 | |||||||
chr12:42186017 | G | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.153-24252C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186017 | |||||||
chr12:42186065 | C | T | 1 | a0001c0001t0010g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-24300G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186065 | |||||||
chr12:42186117 | G | A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-24352C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186117 | |||||||
chr12:42186121 | G | A | 6 | a0001c0002t0002g0229 a0001c0002t0002g0247 a0001c0002t0002g0264 others(3): Show |
6 | HG02258.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-24356C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186121 | |||||||
chr12:42186170 | C | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-24405G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186170 | |||||||
chr12:42186189 | C | CA | 74 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0018 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.153-24425dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186189 | |||||||
chr12:42186189 | C | CAA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.153-24426_153-2442 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186189 | |||||||
chr12:42186189 | C | CAAA | 46 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0137 others(43): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.153-24427_153-2442 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186189 | |||||||
chr12:42186246 | A | G | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0150 |
3 | NA18946.hp2 NA18957.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.153-24481T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186246 | |||||||
chr12:42186337 | G | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-24572C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186337 | |||||||
chr12:42186340 | CA | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-24576delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186340 | |||||||
chr12:42186410 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-24645C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186410 | |||||||
chr12:42186600 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(34): Show |
38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.153-24835G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186600 | |||||||
chr12:42186731 | G | C | 2 | a0001c0001t0013g0102 a0001c0001t0013g0111 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.153-24966C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186731 | |||||||
chr12:42186943 | A | G | 1 | a0001c0002t0024g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.153-25178T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186943 | |||||||
chr12:42187234 | G | A | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-25469C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187234 | |||||||
chr12:42187308 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-25543A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187308 | |||||||
chr12:42187348 | T | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-25583A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187348 | |||||||
chr12:42187553 | G | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-25788C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187553 | |||||||
chr12:42187615 | C | T | 1 | a0001c0003t0001g0245 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.153-25850G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187615 | |||||||
chr12:42187769 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-26004A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187769 | |||||||
chr12:42187792 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-26027G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187792 | |||||||
chr12:42187801 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-26036C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187801 | |||||||
chr12:42187871 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-26106A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187871 | |||||||
chr12:42187937 | G | C | 3 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-26172C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187937 | |||||||
chr12:42187962 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.153-26197C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187962 | |||||||
chr12:42188155 | T | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26390A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188155 | |||||||
chr12:42188163 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26398G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188163 | |||||||
chr12:42188198 | G | A | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-26433C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188198 | |||||||
chr12:42188336 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-26571G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188336 | |||||||
chr12:42188383 | C | CT | 50 | a0001c0001t0001g0025 a0001c0001t0001g0082 a0001c0001t0001g0137 others(47): Show |
51 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.153-26619dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188383 | |||||||
chr12:42188383 | C | CTT | 6 | a0001c0001t0003g0145 a0001c0001t0003g0169 a0001c0001t0017g0125 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-26620_153-2661 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188383 | |||||||
chr12:42188383 | CT | C | 9 | a0001c0001t0004g0103 a0001c0001t0004g0105 a0001c0001t0004g0106 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.153-26619delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188383 | |||||||
chr12:42188512 | A | G | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-26747T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188512 | |||||||
chr12:42188729 | T | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26964A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188729 | |||||||
chr12:42188730 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26965C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188730 | |||||||
chr12:42188999 | T | C | 32 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(29): Show |
33 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.153-27234A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188999 | |||||||
chr12:42189073 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.153-27308A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189073 | |||||||
chr12:42189082 | G | C | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-27317C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189082 | |||||||
chr12:42189139 | T | G | 1 | a0001c0001t0003g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.153-27374A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189139 | |||||||
chr12:42189271 | G | A | 1 | a0001c0002t0002g0347 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.153-27506C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189271 | |||||||
chr12:42189326 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.153-27561C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189326 | |||||||
chr12:42189387 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.153-27622G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189387 | |||||||
chr12:42189467 | T | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-27702A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189467 | |||||||
chr12:42189503 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0174 others(7): Show |
11 | HG00597.hp2 NA18948.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-27738T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189503 | |||||||
chr12:42189660 | A | G | 1 | a0001c0002t0002g0284 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.153-27895T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189660 | |||||||
chr12:42189697 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153-27932G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189697 | |||||||
chr12:42189847 | A | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-28082T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189847 | |||||||
chr12:42189906 | G | A | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-28141C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189906 | |||||||
chr12:42189944 | A | C | 1 | a0001c0001t0004g0108 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.153-28179T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189944 | |||||||
chr12:42190014 | T | C | 1 | a0001c0002t0002g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153-28249A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190014 | |||||||
chr12:42190261 | T | C | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-28496A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190261 | |||||||
chr12:42190359 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.153-28594T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190359 | |||||||
chr12:42190457 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-28692G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190457 | |||||||
chr12:42190696 | A | G | 1 | a0001c0001t0002g0282 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.153-28931T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190696 | |||||||
chr12:42190726 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.153-28961A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190726 | |||||||
chr12:42191020 | C | T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-29255G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191020 | |||||||
chr12:42191153 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-29388G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191153 | |||||||
chr12:42191294 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.153-29529G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191294 | |||||||
chr12:42191359 | A | G | 1 | a0001c0002t0024g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.153-29594T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191359 | |||||||
chr12:42191539 | C | A | 1 | a0001c0001t0003g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.153-29774G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191539 | |||||||
chr12:42191596 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-29831G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191596 | |||||||
chr12:42191597 | C | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-29832G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191597 | |||||||
chr12:42191740 | C | T | 1 | a0001c0001t0030g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.153-29975G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191740 | |||||||
chr12:42192083 | A | G | 1 | a0001c0002t0022g0249 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.153-30318T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192083 | |||||||
chr12:42192137 | T | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-30372A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192137 | |||||||
chr12:42192237 | G | A | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-30472C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192237 | |||||||
chr12:42192258 | A | G | 1 | a0001c0001t0003g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153-30493T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192258 | |||||||
chr12:42192295 | C | T | 1 | a0001c0001t0010g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153-30530G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192295 | |||||||
chr12:42192314 | C | T | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.153-30549G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192314 | |||||||
chr12:42192668 | G | A | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-30903C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192668 | |||||||
chr12:42192673 | G | T | 1 | a0001c0001t0010g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153-30908C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192673 | |||||||
chr12:42192687 | G | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-30922C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192687 | |||||||
chr12:42192733 | T | C | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-30968A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192733 | |||||||
chr12:42192798 | A | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-31033T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192798 | |||||||
chr12:42192839 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31074G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192839 | |||||||
chr12:42192842 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153-31077G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192842 | |||||||
chr12:42193032 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(11): Show |
15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-31267C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193032 | |||||||
chr12:42193080 | G | A | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-31315C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193080 | |||||||
chr12:42193084 | G | T | 2 | a0001c0001t0029g0091 a0001c0002t0002g0088 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153-31319C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193084 | |||||||
chr12:42193108 | A | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31343T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193108 | |||||||
chr12:42193207 | C | T | 59 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(56): Show |
63 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.153-31442G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193207 | |||||||
chr12:42193213 | G | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31448C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193213 | |||||||
chr12:42193250 | G | A | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-31485C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193250 | |||||||
chr12:42193271 | C | T | 1 | a0001c0002t0002g0330 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.153-31506G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193271 | |||||||
chr12:42193318 | CA | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(14): Show |
18 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.153-31554delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193318 | |||||||
chr12:42193687 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-31922C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193687 | |||||||
chr12:42193732 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31967C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193732 | |||||||
chr12:42193889 | C | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-32124G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193889 | |||||||
chr12:42193962 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.153-32197C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193962 | |||||||
chr12:42194107 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-32342T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194107 | |||||||
chr12:42194376 | G | T | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-32611C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194376 | |||||||
chr12:42194397 | A | G | 38 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(35): Show |
39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-32632T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194397 | |||||||
chr12:42194438 | G | A | 2 | a0001c0002t0007g0265 a0001c0002t0007g0279 |
2 | NA18995.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.153-32673C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194438 | |||||||
chr12:42194462 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0002t0002g0344 |
3 | HG01169.hp2 HG02132.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.153-32697C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194462 | |||||||
chr12:42194482 | A | G | 1 | a0001c0002t0002g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-32717T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194482 | |||||||
chr12:42194539 | G | A | 2 | a0001c0003t0014g0363 a0001c0003t0014g0364 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.153-32774C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194539 | |||||||
chr12:42194874 | T | C | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-33109A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194874 | |||||||
chr12:42194893 | A | T | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-33128T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194893 | |||||||
chr12:42195019 | A | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-33254T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195019 | |||||||
chr12:42195120 | G | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-33355C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195120 | |||||||
chr12:42195137 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-33372C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195137 | |||||||
chr12:42195202 | T | C | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-33437A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195202 | |||||||
chr12:42195309 | G | T | 1 | a0001c0001t0017g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.153-33544C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195309 | |||||||
chr12:42195438 | A | G | 1 | a0001c0001t0028g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-33673T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195438 | |||||||
chr12:42195440 | G | A | 1 | a0001c0002t0002g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-33675C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195440 | |||||||
chr12:42195693 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-33928A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195693 | |||||||
chr12:42195819 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-34054C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195819 | |||||||
chr12:42195894 | G | A | 1 | a0001c0002t0002g0232 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.153-34129C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195894 | |||||||
chr12:42196027 | G | C | 2 | a0001c0001t0010g0098 a0001c0001t0010g0101 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153-34262C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196027 | |||||||
chr12:42196032 | G | C | 1 | a0001c0001t0029g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153-34267C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196032 | |||||||
chr12:42196080 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153-34315C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196080 | |||||||
chr12:42196082 | T | C | 14 | a0001c0001t0001g0081 a0001c0001t0001g0173 a0001c0001t0001g0176 others(11): Show |
14 | HG00438.hp1 HG00609.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-34317A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196082 | |||||||
chr12:42196183 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG00099.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.153-34418G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196183 | |||||||
chr12:42196223 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.153-34458A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196223 | |||||||
chr12:42196227 | G | GA | 60 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(57): Show |
61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.153-34463dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | |||||||
chr12:42196227 | G | GAA | 18 | a0001c0001t0003g0157 a0001c0001t0004g0103 a0001c0001t0004g0104 others(15): Show |
18 | HG00423.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-34464_153-3446 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | |||||||
chr12:42196227 | GA | G | 63 | a0001c0001t0001g0353 a0001c0001t0001g0356 a0001c0001t0001g0358 others(60): Show |
63 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.153-34463delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | |||||||
chr12:42196227 | GAA | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0357 others(2): Show |
6 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-34464_153-3446 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | |||||||
chr12:42196256 | G | A | 1 | a0001c0001t0003g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.153-34491C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196256 | |||||||
chr12:42196270 | AACAGCAT others(8): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.153-34520_153-3450 others(19): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196270 | |||||||
chr12:42196340 | C | A | 1 | a0001c0001t0004g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.153-34575G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196340 | |||||||
chr12:42196365 | TACAGGTT others(4): Show |
T | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.153-34611_153-3460 others(15): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196365 | |||||||
chr12:42196422 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-34657G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196422 | |||||||
chr12:42196426 | T | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-34661A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196426 | |||||||
chr12:42196538 | T | A | 1 | a0001c0001t0004g0108 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.153-34773A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196538 | |||||||
chr12:42196949 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.153-35184A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196949 | |||||||
chr12:42196986 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0355 others(3): Show |
7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-35221G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196986 | |||||||
chr12:42197001 | C | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-35236G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197001 | |||||||
chr12:42197013 | C | A | 2 | a0001c0001t0009g0099 a0001c0001t0009g0100 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.153-35248G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197013 | |||||||
chr12:42197058 | A | G | 1 | a0001c0004t0016g0122 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.153-35293T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197058 | |||||||
chr12:42197093 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-35328A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197093 | |||||||
chr12:42197098 | T | A | 1 | a0001c0001t0028g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-35333A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197098 | |||||||
chr12:42197112 | A | G | 1 | a0001c0001t0004g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153-35347T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197112 | |||||||
chr12:42197127 | G | A | 38 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(35): Show |
39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-35362C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197127 | |||||||
chr12:42197216 | A | G | 5 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-35451T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197216 | |||||||
chr12:42197277 | C | T | 1 | a0001c0002t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-35512G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197277 | |||||||
chr12:42197540 | A | C | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-35775T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197540 | |||||||
chr12:42197591 | G | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-35826C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197591 | |||||||
chr12:42197600 | C | T | 1 | a0001c0001t0030g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.153-35835G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197600 | |||||||
chr12:42197739 | G | C | 38 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(35): Show |
39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-35974C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197739 | |||||||
chr12:42197747 | A | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-35982T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197747 | |||||||
chr12:42197831 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-36066G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197831 | |||||||
chr12:42197854 | A | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-36089T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197854 | |||||||
chr12:42197942 | C | A | 1 | a0001c0002t0002g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153-36177G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197942 | |||||||
chr12:42197993 | A | T | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-36228T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197993 | |||||||
chr12:42198030 | C | A | 1 | a0001c0002t0002g0324 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153-36265G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198030 | |||||||
chr12:42198047 | T | G | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-36282A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198047 | |||||||
chr12:42198105 | C | G | 1 | a0001c0002t0002g0307 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.153-36340G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198105 | |||||||
chr12:42198569 | C | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-36804G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198569 | |||||||
chr12:42198726 | AATTG | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-36965_153-3696 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198726 | |||||||
chr12:42198746 | A | G | 4 | a0001c0001t0009g0099 a0001c0001t0009g0100 a0001c0001t0010g0098 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-36981T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198746 | |||||||
chr12:42198788 | T | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-37023A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198788 | |||||||
chr12:42198796 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-37031C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198796 | |||||||
chr12:42198822 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-37057A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198822 | |||||||
chr12:42198961 | T | A | 1 | a0001c0002t0002g0343 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.153-37196A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198961 | |||||||
chr12:42199008 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-37243A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199008 | |||||||
chr12:42199311 | A | G | 4 | a0001c0001t0029g0091 a0001c0002t0002g0232 a0001c0002t0002g0241 others(1): Show |
4 | HG02717.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-37546T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199311 | |||||||
chr12:42199498 | A | G | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-37733T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199498 | |||||||
chr12:42199634 | A | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-37869T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199634 | |||||||
chr12:42199727 | A | C | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+37872T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199727 | |||||||
chr12:42199772 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.152+37827A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199772 | |||||||
chr12:42199891 | T | C | 7 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(4): Show |
8 | HG00738.hp1 HG01192.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+37708A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199891 | |||||||
chr12:42200087 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+37512G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200087 | |||||||
chr12:42200217 | G | A | 1 | a0001c0002t0002g0300 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.152+37382C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200217 | |||||||
chr12:42200321 | A | G | 1 | a0001c0001t0004g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.152+37278T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200321 | |||||||
chr12:42200377 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+37222C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200377 | |||||||
chr12:42200391 | C | T | 1 | a0001c0002t0002g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.152+37208G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200391 | |||||||
chr12:42200405 | T | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+37194A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200405 | |||||||
chr12:42200422 | C | A | 1 | a0001c0002t0002g0230 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.152+37177G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200422 | |||||||
chr12:42200684 | G | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+36915C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200684 | |||||||
chr12:42200699 | A | G | 1 | a0001c0001t0003g0165 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.152+36900T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200699 | |||||||
chr12:42200707 | G | C | 1 | a0001c0001t0001g0001 | 3 | HG01099.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152+36892C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200707 | |||||||
chr12:42200946 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+36653A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200946 | |||||||
chr12:42201018 | C | G | 1 | a0001c0001t0006g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.152+36581G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201018 | |||||||
chr12:42201128 | T | G | 4 | a0001c0002t0002g0266 a0001c0002t0002g0269 a0001c0002t0002g0270 others(1): Show |
4 | NA18957.hp1 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+36471A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201128 | |||||||
chr12:42201522 | A | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+36077T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201522 | |||||||
chr12:42201523 | T | TTG | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+36074_152+3607 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201523 | |||||||
chr12:42201595 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+36004G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201595 | |||||||
chr12:42201819 | G | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.152+35780C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201819 | |||||||
chr12:42201820 | C | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.152+35779G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201820 | |||||||
chr12:42202105 | C | T | 6 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+35494G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202105 | |||||||
chr12:42202112 | C | A | 1 | a0001c0004t0016g0122 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.152+35487G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202112 | |||||||
chr12:42202130 | G | A | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+35469C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202130 | |||||||
chr12:42202177 | C | T | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+35422G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202177 | |||||||
chr12:42202218 | C | T | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+35381G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202218 | |||||||
chr12:42202249 | T | C | 1 | a0001c0001t0002g0282 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.152+35350A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202249 | |||||||
chr12:42202332 | A | T | 1 | a0001c0002t0002g0326 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152+35267T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202332 | |||||||
chr12:42202412 | C | T | 7 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0222 others(4): Show |
7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+35187G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202412 | |||||||
chr12:42202447 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | NA18747.hp1 NA18954.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+35152T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202447 | |||||||
chr12:42202496 | C | T | 4 | a0001c0001t0001g0353 a0001c0001t0001g0359 a0001c0001t0001g0360 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+35103G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202496 | |||||||
chr12:42202660 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+34939A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202660 | |||||||
chr12:42202875 | G | A | 5 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+34724C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202875 | |||||||
chr12:42203021 | G | C | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+34578C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203021 | |||||||
chr12:42203045 | G | T | 1 | a0001c0002t0002g0241 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152+34554C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203045 | |||||||
chr12:42203066 | C | CA | 11 | a0001c0001t0001g0025 a0001c0001t0001g0081 a0001c0001t0001g0096 others(8): Show |
11 | HG00438.hp1 HG01169.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+34532dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203066 | |||||||
chr12:42203344 | C | A | 4 | a0001c0002t0002g0266 a0001c0002t0002g0269 a0001c0002t0002g0270 others(1): Show |
4 | NA18957.hp1 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+34255G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203344 | |||||||
chr12:42203366 | T | C | 3 | a0001c0002t0002g0284 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG00621.hp2 HG02155.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.152+34233A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203366 | |||||||
chr12:42203453 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+34146A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203453 | |||||||
chr12:42203490 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+34109T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203490 | |||||||
chr12:42203529 | G | A | 1 | a0001c0002t0002g0311 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.152+34070C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203529 | |||||||
chr12:42203643 | AT | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0353 others(9): Show |
13 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.152+33955delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203643 | |||||||
chr12:42203733 | G | A | 7 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
7 | HG00733.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+33866C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203733 | |||||||
chr12:42203740 | A | C | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+33859T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203740 | |||||||
chr12:42203840 | T | C | 1 | a0001c0002t0002g0327 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.152+33759A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203840 | |||||||
chr12:42203886 | C | T | 2 | a0001c0003t0014g0363 a0001c0003t0014g0364 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+33713G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203886 | |||||||
chr12:42203887 | G | A | 1 | a0001c0001t0004g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.152+33712C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203887 | |||||||
chr12:42204020 | C | T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+33579G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204020 | |||||||
chr12:42204146 | G | T | 8 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG00741.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+33453C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204146 | |||||||
chr12:42204161 | T | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+33438A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204161 | |||||||
chr12:42204176 | A | G | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+33423T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204176 | |||||||
chr12:42204279 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+33320G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204279 | |||||||
chr12:42204374 | G | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+33225C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204374 | |||||||
chr12:42204440 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.152+33159A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204440 | |||||||
chr12:42204447 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+33152A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204447 | |||||||
chr12:42204533 | G | A | 1 | a0001c0002t0002g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+33066C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204533 | |||||||
chr12:42204767 | C | G | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+32832G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204767 | |||||||
chr12:42204775 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0227 |
2 | NA19007.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.152+32824G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204775 | |||||||
chr12:42204834 | G | A | 3 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0004t0016g0122 |
3 | HG02717.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152+32765C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204834 | |||||||
chr12:42204836 | A | G | 3 | a0001c0002t0002g0247 a0001c0002t0002g0264 a0001c0002t0002g0331 |
3 | HG02258.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.152+32763T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204836 | |||||||
chr12:42205055 | T | TA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
96 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.152+32543dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205055 | |||||||
chr12:42205055 | TA | T | 23 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(20): Show |
24 | HG00423.hp1 HG00738.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.152+32543delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205055 | |||||||
chr12:42205162 | T | A | 1 | a0001c0001t0001g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.152+32437A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205162 | |||||||
chr12:42205237 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+32362A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205237 | |||||||
chr12:42205320 | C | T | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+32279G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205320 | |||||||
chr12:42205371 | TTCTTC | T | 9 | a0001c0001t0003g0079 a0001c0001t0003g0155 a0001c0001t0003g0156 others(6): Show |
9 | HG01891.hp2 HG01975.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+32223_152+3222 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205371 | |||||||
chr12:42205372 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.152+32227A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205372 | |||||||
chr12:42205378 | C | CT | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(3): Show |
6 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+32220dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205378 | |||||||
chr12:42205585 | G | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+32014C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205585 | |||||||
chr12:42205892 | A | C | 4 | a0001c0001t0009g0099 a0001c0001t0009g0100 a0001c0001t0010g0098 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+31707T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205892 | |||||||
chr12:42205894 | T | A | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+31705A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205894 | |||||||
chr12:42205917 | T | TTTTG | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+31681_152+3168 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205917 | |||||||
chr12:42206105 | A | T | 3 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+31494T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206105 | |||||||
chr12:42206131 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+31468G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206131 | |||||||
chr12:42206297 | T | TA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0036 others(8): Show |
11 | HG00408.hp2 HG01081.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+31301dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206297 | |||||||
chr12:42206297 | TA | T | 180 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0095 others(177): Show |
186 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.152+31301delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206297 | |||||||
chr12:42206297 | TAA | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
86 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.152+31300_152+3130 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206297 | |||||||
chr12:42206323 | G | A | 1 | a0001c0001t0010g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.152+31276C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206323 | |||||||
chr12:42206335 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+31264C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206335 | |||||||
chr12:42206471 | C | T | 2 | a0001c0003t0014g0363 a0001c0003t0014g0364 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+31128G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206471 | |||||||
chr12:42206577 | C | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+31022G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206577 | |||||||
chr12:42206602 | C | T | 1 | a0001c0002t0002g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+30997G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206602 | |||||||
chr12:42206704 | C | CA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0355 others(8): Show |
12 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+30894dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206704 | |||||||
chr12:42206856 | T | C | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+30743A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206856 | |||||||
chr12:42206858 | TCTC | T | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+30738_152+3074 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206858 | |||||||
chr12:42207108 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.152+30491A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207108 | |||||||
chr12:42207112 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(12): Show |
16 | HG00639.hp2 HG00738.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.152+30487T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207112 | |||||||
chr12:42207194 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152+30405T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207194 | |||||||
chr12:42207349 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.152+30250G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207349 | |||||||
chr12:42207469 | TTAA | T | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+30127_152+3012 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207469 | |||||||
chr12:42207531 | T | C | 1 | a0001c0001t0001g0358 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152+30068A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207531 | |||||||
chr12:42207630 | T | C | 1 | a0001c0002t0002g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152+29969A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207630 | |||||||
chr12:42207668 | A | G | 6 | a0001c0001t0001g0056 a0001c0001t0011g0093 a0001c0001t0011g0094 others(3): Show |
6 | HG01891.hp2 HG02165.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+29931T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207668 | |||||||
chr12:42207683 | G | A | 2 | a0001c0001t0009g0099 a0001c0002t0002g0088 |
2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.152+29916C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207683 | |||||||
chr12:42207684 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+29915G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207684 | |||||||
chr12:42207685 | G | C | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0190 others(1): Show |
4 | HG00323.hp2 HG01106.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+29914C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207685 | |||||||
chr12:42207708 | C | T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+29891G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207708 | |||||||
chr12:42207709 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.152+29890C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207709 | |||||||
chr12:42207720 | G | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
288 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.152+29879C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207720 | |||||||
chr12:42207754 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+29845G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207754 | |||||||
chr12:42207754 | C | G | 5 | a0001c0001t0001g0097 a0001c0001t0001g0129 a0001c0002t0002g0239 others(2): Show |
5 | HG03098.hp2 HG03453.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+29845G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207754 | |||||||
chr12:42207794 | G | GGCAGGAG others(12): Show |
86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
91 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.152+29786_152+2980 others(23): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207794 | |||||||
chr12:42207846 | G | A | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+29753C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207846 | |||||||
chr12:42207846 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152+29753C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207846 | |||||||
chr12:42207847 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152+29752A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207847 | |||||||
chr12:42207857 | C | T | 1 | a0001c0002t0002g0345 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.152+29742G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207857 | |||||||
chr12:42207862 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152+29737C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207862 | |||||||
chr12:42207869 | C | T | 1 | a0001c0001t0029g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+29730G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207869 | |||||||
chr12:42207870 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.152+29729C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207870 | |||||||
chr12:42208111 | A | T | 1 | a0001c0001t0003g0162 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.152+29488T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208111 | |||||||
chr12:42208154 | G | A | 3 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 |
3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+29445C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208154 | |||||||
chr12:42208210 | T | C | 7 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0222 others(4): Show |
7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+29389A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208210 | |||||||
chr12:42208267 | T | A | 3 | a0001c0002t0002g0083 a0001c0002t0002g0237 a0001c0002t0002g0345 |
3 | NA18944.hp1 NA19000.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.152+29332A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208267 | |||||||
chr12:42208377 | T | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+29222A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208377 | |||||||
chr12:42208511 | A | T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+29088T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208511 | |||||||
chr12:42208581 | T | A | 1 | a0001c0001t0003g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152+29018A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208581 | |||||||
chr12:42208679 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0174 |
2 | NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.152+28920T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208679 | |||||||
chr12:42208930 | A | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(7): Show |
11 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+28669T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208930 | |||||||
chr12:42208931 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02148.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+28668C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208931 | |||||||
chr12:42209126 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+28473T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209126 | |||||||
chr12:42209133 | A | G | 1 | a0001c0002t0002g0292 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.152+28466T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209133 | |||||||
chr12:42209257 | G | GA | 17 | a0001c0001t0001g0008 a0001c0001t0001g0173 a0001c0001t0001g0353 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+28341dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209257 | |||||||
chr12:42209257 | GA | G | 8 | a0001c0001t0001g0197 a0001c0001t0001g0227 a0001c0001t0002g0282 others(5): Show |
8 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+28341delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209257 | |||||||
chr12:42209304 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+28295G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209304 | |||||||
chr12:42209421 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+28178T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209421 | |||||||
chr12:42209490 | G | A | 6 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0001t0017g0125 others(3): Show |
6 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+28109C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209490 | |||||||
chr12:42209563 | C | CA | 80 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0017 others(77): Show |
82 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.152+28035dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209563 | |||||||
chr12:42209563 | C | CAA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0211 a0001c0001t0004g0106 others(4): Show |
7 | HG01175.hp2 HG01952.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+28034_152+2803 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209563 | |||||||
chr12:42209563 | CA | C | 35 | a0001c0001t0001g0020 a0001c0001t0001g0096 a0001c0001t0001g0126 others(32): Show |
35 | HG00544.hp1 HG00597.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.152+28035delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209563 | |||||||
chr12:42209591 | T | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+28008A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209591 | |||||||
chr12:42209684 | A | G | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+27915T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209684 | |||||||
chr12:42209726 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+27873G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209726 | |||||||
chr12:42209762 | T | C | 1 | a0001c0002t0002g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.152+27837A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209762 | |||||||
chr12:42209828 | C | T | 2 | a0001c0001t0013g0102 a0001c0001t0013g0111 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.152+27771G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209828 | |||||||
chr12:42209960 | G | A | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
10 | HG00741.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+27639C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209960 | |||||||
chr12:42209979 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+27620C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209979 | |||||||
chr12:42210236 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+27363A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210236 | |||||||
chr12:42210330 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+27269C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210330 | |||||||
chr12:42210385 | T | A | 1 | a0001c0002t0005g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152+27214A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210385 | |||||||
chr12:42210537 | C | T | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+27062G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210537 | |||||||
chr12:42210889 | C | T | 2 | a0001c0003t0014g0363 a0001c0003t0014g0364 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+26710G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210889 | |||||||
chr12:42210975 | T | C | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+26624A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210975 | |||||||
chr12:42211225 | G | A | 1 | a0001c0002t0002g0325 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.152+26374C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211225 | |||||||
chr12:42211414 | G | A | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+26185C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211414 | |||||||
chr12:42211427 | C | CA | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.152+26171dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | |||||||
chr12:42211427 | C | CAA | 10 | a0001c0001t0001g0082 a0001c0001t0001g0136 a0001c0001t0001g0185 others(7): Show |
10 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+26170_152+2617 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | |||||||
chr12:42211427 | CA | C | 116 | a0001c0001t0001g0027 a0001c0001t0001g0077 a0001c0001t0001g0095 others(113): Show |
121 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.152+26171delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | |||||||
chr12:42211427 | CAA | C | 10 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0151 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+26170_152+2617 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | |||||||
chr12:42211469 | G | A | 2 | a0001c0002t0002g0272 a0001c0002t0002g0288 |
2 | HG01257.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.152+26130C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211469 | |||||||
chr12:42211495 | T | C | 1 | a0001c0001t0030g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.152+26104A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211495 | |||||||
chr12:42211511 | T | C | 8 | a0001c0002t0002g0170 a0001c0002t0002g0252 a0001c0002t0002g0253 others(5): Show |
8 | HG00621.hp1 HG02135.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+26088A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211511 | |||||||
chr12:42211521 | G | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+26078C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211521 | |||||||
chr12:42211527 | G | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+26072C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211527 | |||||||
chr12:42211597 | T | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+26002A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211597 | |||||||
chr12:42211617 | C | T | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+25982G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211617 | |||||||
chr12:42211742 | C | CA | 17 | a0001c0001t0001g0049 a0001c0001t0001g0172 a0001c0001t0001g0189 others(14): Show |
17 | HG00423.hp2 HG01891.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+25856dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211742 | |||||||
chr12:42211742 | CA | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0076 others(13): Show |
16 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.152+25856delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211742 | |||||||
chr12:42211776 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.152+25823G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211776 | |||||||
chr12:42211781 | G | T | 2 | a0001c0001t0027g0090 a0001c0001t0028g0092 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.152+25818C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211781 | |||||||
chr12:42211806 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.152+25793A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211806 | |||||||
chr12:42211876 | C | A | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+25723G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211876 | |||||||
chr12:42211878 | G | A | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(16): Show |
19 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.152+25721C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211878 | |||||||
chr12:42212034 | CA | C | 12 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(9): Show |
12 | HG01169.hp2 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+25564delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212034 | |||||||
chr12:42212148 | CAAAA | C | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+25447_152+2545 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212148 | |||||||
chr12:42212261 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.152+25338G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212261 | |||||||
chr12:42212280 | T | C | 1 | a0001c0001t0017g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152+25319A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212280 | |||||||
chr12:42212333 | C | T | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+25266G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212333 | |||||||
chr12:42212427 | T | C | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+25172A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212427 | |||||||
chr12:42212564 | A | T | 1 | a0001c0002t0002g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.152+25035T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212564 | |||||||
chr12:42212694 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG01243.hp1 HG01255.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.152+24905C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212694 | |||||||
chr12:42212738 | TCTTA | T | 5 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+24857_152+2486 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212738 | |||||||
chr12:42212894 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
302 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.152+24705G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212894 | |||||||
chr12:42212946 | G | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+24653C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212946 | |||||||
chr12:42213230 | C | T | 1 | a0001c0002t0002g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+24369G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213230 | |||||||
chr12:42213281 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+24318A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213281 | |||||||
chr12:42213784 | T | C | 1 | a0001c0002t0002g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.152+23815A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213784 | |||||||
chr12:42213946 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+23653G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213946 | |||||||
chr12:42213985 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+23614C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213985 | |||||||
chr12:42214199 | T | C | 134 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(131): Show |
138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.152+23400A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214199 | |||||||
chr12:42214236 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.152+23363A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214236 | |||||||
chr12:42214482 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.152+23117C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214482 | |||||||
chr12:42214559 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0202 a0001c0001t0001g0203 |
4 | NA18952.hp1 NA18990.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+23040C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214559 | |||||||
chr12:42214604 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+22995G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214604 | |||||||
chr12:42214685 | G | T | 1 | a0001c0001t0029g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+22914C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214685 | |||||||
chr12:42214687 | A | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+22912T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214687 | |||||||
chr12:42214775 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+22824C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214775 | |||||||
chr12:42214824 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+22775G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214824 | |||||||
chr12:42214883 | G | A | 1 | a0001c0002t0002g0323 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.152+22716C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214883 | |||||||
chr12:42214934 | G | T | 14 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(11): Show |
15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+22665C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214934 | |||||||
chr12:42215156 | C | T | 1 | a0001c0001t0017g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152+22443G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215156 | |||||||
chr12:42215302 | G | T | 2 | a0001c0001t0003g0149 a0001c0001t0003g0150 |
2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.152+22297C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215302 | |||||||
chr12:42215345 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152+22254A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215345 | |||||||
chr12:42215346 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152+22253G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215346 | |||||||
chr12:42215367 | G | T | 1 | a0001c0001t0004g0110 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.152+22232C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215367 | |||||||
chr12:42215405 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+22194G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215405 | |||||||
chr12:42215642 | G | T | 7 | a0001c0001t0003g0158 a0001c0001t0003g0159 a0001c0001t0003g0160 others(4): Show |
7 | HG02129.hp1 HG02523.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+21957C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215642 | |||||||
chr12:42215742 | C | T | 2 | a0001c0002t0002g0304 a0001c0002t0002g0305 |
2 | NA18960.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.152+21857G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215742 | |||||||
chr12:42215775 | C | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+21824G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215775 | |||||||
chr12:42215921 | G | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+21678C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215921 | |||||||
chr12:42215927 | A | AAAAT | 3 | a0001c0001t0001g0026 a0001c0001t0003g0155 a0001c0001t0008g0057 |
3 | HG00639.hp2 HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.152+21668_152+2167 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | |||||||
chr12:42215927 | AAAAT | A | 52 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(49): Show |
53 | HG00423.hp2 HG00738.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.152+21668_152+2167 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | |||||||
chr12:42215927 | AAAATAAA others(1): Show |
A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0354 others(41): Show |
45 | HG00099.hp1 HG00423.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.152+21664_152+2167 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | |||||||
chr12:42215927 | AAAATAAA others(5): Show |
A | 127 | a0001c0001t0001g0051 a0001c0001t0001g0201 a0001c0001t0002g0282 others(124): Show |
131 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.152+21660_152+2167 others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | |||||||
chr12:42215927 | AAAATAAA others(9): Show |
A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
80 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.152+21656_152+2167 others(20): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | |||||||
chr12:42215927 | AAAATAAA others(13): Show |
A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+21652_152+2167 others(24): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | |||||||
chr12:42215982 | A | G | 1 | a0001c0001t0004g0108 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.152+21617T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215982 | |||||||
chr12:42216042 | T | G | 37 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(34): Show |
38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.152+21557A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216042 | |||||||
chr12:42216091 | G | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+21508C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216091 | |||||||
chr12:42216146 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.152+21453G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216146 | |||||||
chr12:42216212 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0174 others(7): Show |
11 | HG00597.hp2 NA18948.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+21387A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216212 | |||||||
chr12:42216266 | C | T | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+21333G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216266 | |||||||
chr12:42216594 | T | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+21005A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216594 | |||||||
chr12:42216680 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.152+20919A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216680 | |||||||
chr12:42216706 | T | C | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+20893A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216706 | |||||||
chr12:42216815 | C | T | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+20784G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216815 | |||||||
chr12:42216975 | C | T | 2 | a0001c0001t0009g0099 a0001c0001t0009g0100 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.152+20624G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216975 | |||||||
chr12:42216991 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152+20608T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216991 | |||||||
chr12:42216992 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+20607A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216992 | |||||||
chr12:42217111 | A | G | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+20488T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217111 | |||||||
chr12:42217114 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.152+20485G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217114 | |||||||
chr12:42217132 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+20467C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217132 | |||||||
chr12:42217676 | T | C | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+19923A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217676 | |||||||
chr12:42217697 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.152+19902A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217697 | |||||||
chr12:42217758 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+19841T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217758 | |||||||
chr12:42218020 | C | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+19579G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218020 | |||||||
chr12:42218029 | T | C | 1 | a0001c0001t0001g0001 | 3 | HG01099.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152+19570A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218029 | |||||||
chr12:42218120 | T | C | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+19479A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218120 | |||||||
chr12:42218170 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+19429T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218170 | |||||||
chr12:42218182 | G | GGA | 8 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0243 others(5): Show |
8 | HG00642.hp1 HG02486.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218182 | |||||||
chr12:42218183 | G | GAGAA | 13 | a0001c0002t0002g0083 a0001c0002t0002g0085 a0001c0002t0002g0170 others(10): Show |
13 | HG01081.hp1 HG01243.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218183 | |||||||
chr12:42218183 | G | GAGAAAC | 28 | a0001c0002t0002g0229 a0001c0002t0002g0230 a0001c0002t0002g0233 others(25): Show |
28 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218183 | |||||||
chr12:42218183 | G | GAGAAACA others(1): Show |
8 | a0001c0002t0002g0089 a0001c0002t0002g0247 a0001c0002t0002g0266 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218183 | |||||||
chr12:42218185 | A | AAC | 64 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(61): Show |
68 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.152+19412_152+1941 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | A | AACAC | 14 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0052 others(11): Show |
14 | HG01515.hp2 HG01943.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.152+19410_152+1941 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | A | AACACAC | 36 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0022 others(33): Show |
36 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.152+19408_152+1941 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | A | AACACACA others(1): Show |
25 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(22): Show |
25 | HG01175.hp2 HG01255.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.152+19406_152+1941 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | A | C | 49 | a0001c0002t0002g0083 a0001c0002t0002g0085 a0001c0002t0002g0089 others(46): Show |
49 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.152+19414T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | A | G | 1 | a0001c0002t0024g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152+19414T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AAC | A | 4 | a0001c0001t0001g0095 a0001c0001t0003g0153 a0001c0001t0009g0100 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+19412_152+1941 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AACAC | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0201 a0001c0001t0001g0202 others(26): Show |
31 | HG00738.hp1 HG02083.hp1 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.152+19410_152+1941 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AACACAC | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0080 others(71): Show |
77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.152+19408_152+1941 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AACACACA others(1): Show |
A | 41 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0077 others(38): Show |
42 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.152+19406_152+1941 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AACACACA others(3): Show |
A | 5 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0003t0001g0244 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+19404_152+1941 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AACACACA others(5): Show |
A | 2 | a0001c0003t0014g0363 a0001c0003t0014g0364 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+19402_152+1941 others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AACACACA others(7): Show |
A | 1 | a0001c0001t0028g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152+19400_152+1941 others(18): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218185 | AACACACA others(9): Show |
A | 2 | a0001c0001t0027g0090 a0001c0001t0029g0091 |
2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+19398_152+1941 others(20): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | |||||||
chr12:42218187 | C | A | 1 | a0001c0002t0024g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152+19412G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218187 | |||||||
chr12:42218375 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+19224C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218375 | |||||||
chr12:42218440 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152+19159A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218440 | |||||||
chr12:42218530 | A | C | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+19069T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218530 | |||||||
chr12:42218660 | A | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+18939T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218660 | |||||||
chr12:42218691 | A | G | 1 | a0001c0002t0002g0253 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.152+18908T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218691 | |||||||
chr12:42218870 | A | G | 6 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+18729T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218870 | |||||||
chr12:42218901 | G | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
7 | HG01099.hp2 HG01515.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+18698C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218901 | |||||||
chr12:42219115 | T | C | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+18484A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219115 | |||||||
chr12:42219122 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0172 a0001c0001t0001g0215 |
5 | HG01099.hp2 HG01515.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+18477A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219122 | |||||||
chr12:42219138 | A | T | 1 | a0001c0002t0002g0348 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152+18461T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219138 | |||||||
chr12:42219142 | G | A | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+18457C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219142 | |||||||
chr12:42219450 | G | A | 1 | a0001c0001t0004g0116 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.152+18149C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219450 | |||||||
chr12:42219468 | T | C | 1 | a0001c0001t0004g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.152+18131A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219468 | |||||||
chr12:42219488 | T | G | 131 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(128): Show |
135 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.152+18111A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219488 | |||||||
chr12:42219509 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+18090A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219509 | |||||||
chr12:42219510 | T | C | 4 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+18089A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219510 | |||||||
chr12:42219564 | T | C | 4 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+18035A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219564 | |||||||
chr12:42219667 | G | A | 2 | a0001c0002t0002g0332 a0001c0002t0002g0333 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.152+17932C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219667 | |||||||
chr12:42219712 | C | A | 1 | a0001c0002t0002g0231 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.152+17887G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219712 | |||||||
chr12:42219754 | C | A | 1 | a0001c0001t0010g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+17845G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219754 | |||||||
chr12:42220074 | G | A | 3 | a0001c0002t0002g0232 a0001c0002t0002g0241 a0001c0002t0002g0242 |
3 | HG02717.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.152+17525C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220074 | |||||||
chr12:42220324 | ATTATC | A | 3 | a0001c0001t0001g0210 a0001c0001t0012g0130 a0001c0001t0012g0131 |
3 | HG01928.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+17270_152+1727 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220324 | |||||||
chr12:42220347 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.152+17252G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220347 | |||||||
chr12:42220421 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+17178T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220421 | |||||||
chr12:42220521 | T | C | 1 | a0001c0001t0004g0106 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.152+17078A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220521 | |||||||
chr12:42220653 | A | C | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+16946T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220653 | |||||||
chr12:42220695 | T | C | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+16904A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220695 | |||||||
chr12:42220722 | T | C | 4 | a0001c0001t0001g0353 a0001c0001t0001g0359 a0001c0001t0001g0360 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+16877A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220722 | |||||||
chr12:42220844 | C | T | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+16755G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220844 | |||||||
chr12:42220904 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.152+16695T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220904 | |||||||
chr12:42221199 | T | C | 1 | a0001c0001t0028g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152+16400A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42221199 | |||||||
chr12:42221473 | A | AG | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.152+16125dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42221473 | |||||||
chr12:42221570 | T | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0080 others(55): Show |
60 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.152+16029A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42221570 | |||||||
chr12:42222055 | C | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+15544G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222055 | |||||||
chr12:42222120 | A | T | 1 | a0001c0001t0033g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+15479T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222120 | |||||||
chr12:42222238 | A | T | 128 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(125): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.152+15361T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222238 | |||||||
chr12:42222520 | G | T | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+15079C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222520 | |||||||
chr12:42222721 | T | C | 1 | a0001c0001t0001g0361 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.152+14878A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222721 | |||||||
chr12:42222754 | A | AT | 17 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0174 others(14): Show |
18 | HG00597.hp2 HG00733.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.152+14844dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222754 | |||||||
chr12:42222893 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+14706A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222893 | |||||||
chr12:42222927 | C | T | 1 | a0001c0002t0002g0253 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.152+14672G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222927 | |||||||
chr12:42222937 | C | CT | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0080 others(77): Show |
82 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.152+14661dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222937 | |||||||
chr12:42223100 | G | A | 1 | a0001c0001t0026g0143 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.152+14499C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223100 | |||||||
chr12:42223186 | T | G | 1 | a0001c0001t0001g0004 | 2 | HG00099.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.152+14413A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223186 | |||||||
chr12:42223249 | T | C | 1 | a0001c0001t0009g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+14350A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223249 | |||||||
chr12:42223300 | A | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+14299T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223300 | |||||||
chr12:42223327 | T | TACACACA others(3): Show |
1 | a0001c0001t0011g0093 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152+14271_152+1427 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223327 | |||||||
chr12:42223327 | T | TACACACA others(5): Show |
2 | a0001c0001t0011g0094 a0001c0001t0027g0090 |
2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.152+14271_152+1427 others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223327 | |||||||
chr12:42223331 | T | C | 4 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+14268A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | |||||||
chr12:42223331 | T | TAC | 141 | a0001c0001t0001g0055 a0001c0001t0001g0096 a0001c0001t0001g0126 others(138): Show |
145 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.152+14266_152+1426 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | |||||||
chr12:42223331 | TAC | T | 6 | a0001c0001t0001g0063 a0001c0001t0004g0118 a0001c0001t0017g0125 others(3): Show |
6 | HG00140.hp2 HG02717.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+14266_152+1426 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | |||||||
chr12:42223331 | TACAC | T | 33 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(30): Show |
34 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.152+14264_152+1426 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | |||||||
chr12:42223401 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.152+14198C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223401 | |||||||
chr12:42223806 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152+13793T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223806 | |||||||
chr12:42223807 | T | G | 128 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(125): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.152+13792A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223807 | |||||||
chr12:42223883 | G | A | 1 | a0001c0001t0033g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+13716C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223883 | |||||||
chr12:42224066 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | NA18747.hp1 NA18954.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+13533C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224066 | |||||||
chr12:42224099 | C | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
280 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.152+13500G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224099 | |||||||
chr12:42224313 | G | A | 1 | a0001c0001t0009g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+13286C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224313 | |||||||
chr12:42224372 | CAATAT | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0357 |
4 | HG02559.hp2 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+13222_152+1322 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224372 | |||||||
chr12:42224512 | T | C | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+13087A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224512 | |||||||
chr12:42224540 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0196 |
2 | NA18954.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.152+13059C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224540 | |||||||
chr12:42224548 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | NA18747.hp1 NA18954.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+13051G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224548 | |||||||
chr12:42224579 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.152+13020G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224579 | |||||||
chr12:42224628 | T | G | 1 | a0001c0002t0002g0318 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152+12971A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224628 | |||||||
chr12:42224643 | C | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(3): Show |
6 | HG01106.hp1 HG01175.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+12956G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224643 | |||||||
chr12:42224728 | A | G | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+12871T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224728 | |||||||
chr12:42224745 | A | G | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+12854T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224745 | |||||||
chr12:42224915 | T | C | 1 | a0001c0001t0004g0106 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.152+12684A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224915 | |||||||
chr12:42225005 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+12594G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225005 | |||||||
chr12:42225214 | TG | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+12384delC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225214 | |||||||
chr12:42225215 | G | T | 1 | a0001c0001t0003g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152+12384C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225215 | |||||||
chr12:42225439 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG00597.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.152+12160C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225439 | |||||||
chr12:42225468 | T | C | 1 | a0001c0002t0002g0242 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152+12131A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225468 | |||||||
chr12:42225629 | T | C | 3 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 |
3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+11970A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225629 | |||||||
chr12:42225632 | G | C | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+11967C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225632 | |||||||
chr12:42225671 | G | A | 1 | a0001c0002t0005g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.152+11928C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225671 | |||||||
chr12:42225693 | C | A | 2 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.152+11906G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225693 | |||||||
chr12:42225722 | G | A | 59 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(56): Show |
63 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.152+11877C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225722 | |||||||
chr12:42225730 | G | A | 1 | a0001c0002t0002g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152+11869C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225730 | |||||||
chr12:42225885 | TTTAAA | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+11709_152+1171 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225885 | |||||||
chr12:42226047 | T | C | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+11552A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226047 | |||||||
chr12:42226126 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0357 |
4 | HG02559.hp2 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+11473A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226126 | |||||||
chr12:42226173 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+11426G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226173 | |||||||
chr12:42226233 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
129 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.152+11366A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226233 | |||||||
chr12:42226287 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.152+11312C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226287 | |||||||
chr12:42226575 | G | A | 138 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(135): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.152+11024C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226575 | |||||||
chr12:42226603 | G | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10996C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226603 | |||||||
chr12:42226686 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
281 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.152+10913C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226686 | |||||||
chr12:42226693 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10906G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226693 | |||||||
chr12:42226694 | G | A | 6 | a0001c0001t0001g0173 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG02040.hp2 NA18941.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+10905C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226694 | |||||||
chr12:42226760 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.152+10839A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226760 | |||||||
chr12:42226776 | C | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+10823G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226776 | |||||||
chr12:42226840 | C | T | 1 | a0001c0002t0002g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.152+10759G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226840 | |||||||
chr12:42226861 | C | T | 3 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+10738G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226861 | |||||||
chr12:42226862 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10737C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226862 | |||||||
chr12:42226884 | G | A | 1 | a0001c0001t0004g0117 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.152+10715C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226884 | |||||||
chr12:42226889 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
97 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.152+10710C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226889 | |||||||
chr12:42226959 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+10640G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226959 | |||||||
chr12:42226997 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152+10602C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226997 | |||||||
chr12:42226997 | G | C | 4 | a0001c0002t0002g0007 a0001c0002t0002g0315 a0001c0002t0002g0316 others(1): Show |
5 | HG02015.hp2 NA18941.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10602C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226997 | |||||||
chr12:42226997 | G | T | 129 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(126): Show |
132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.152+10602C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226997 | |||||||
chr12:42227006 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+10593C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227006 | |||||||
chr12:42227036 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0355 others(3): Show |
7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+10563C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227036 | |||||||
chr12:42227041 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+10558G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227041 | |||||||
chr12:42227047 | C | T | 4 | a0001c0002t0002g0088 a0001c0002t0002g0232 a0001c0002t0002g0241 others(1): Show |
4 | HG02055.hp1 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+10552G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227047 | |||||||
chr12:42227049 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152+10550G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227049 | |||||||
chr12:42227050 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+10549C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227050 | |||||||
chr12:42227053 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+10546G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227053 | |||||||
chr12:42227054 | G | A | 1 | a0001c0002t0002g0318 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152+10545C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227054 | |||||||
chr12:42227064 | G | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+10535C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227064 | |||||||
chr12:42227074 | G | A | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+10525C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227074 | |||||||
chr12:42227078 | G | GCAGCCGC others(13): Show |
5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10520_152+1052 others(24): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227078 | |||||||
chr12:42227099 | G | A | 1 | a0001c0002t0002g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.152+10500C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227099 | |||||||
chr12:42227113 | T | G | 1 | a0001c0001t0009g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152+10486A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227113 | |||||||
chr12:42227129 | C | T | 1 | a0001c0002t0002g0322 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.152+10470G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227129 | |||||||
chr12:42227130 | G | A | 6 | a0001c0002t0002g0087 a0001c0002t0002g0319 a0001c0002t0002g0320 others(3): Show |
6 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+10469C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227130 | |||||||
chr12:42227144 | C | A | 1 | a0001c0002t0002g0322 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.152+10455G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227144 | |||||||
chr12:42227148 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152+10451G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227148 | |||||||
chr12:42227149 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+10450C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227149 | |||||||
chr12:42227175 | G | A | 1 | a0001c0002t0002g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152+10424C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227175 | |||||||
chr12:42227187 | GC | G | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+10411delG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227187 | |||||||
chr12:42227190 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.152+10409G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227190 | |||||||
chr12:42227191 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0174 others(14): Show |
18 | HG00597.hp2 HG00733.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.152+10408C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227191 | |||||||
chr12:42227226 | A | G | 3 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 |
3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+10373T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227226 | |||||||
chr12:42227252 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10347C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227252 | |||||||
chr12:42227296 | G | A | 2 | a0001c0001t0008g0120 a0001c0001t0008g0121 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+10303C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227296 | |||||||
chr12:42227308 | C | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+10291G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227308 | |||||||
chr12:42227311 | C | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+10288G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227311 | |||||||
chr12:42227325 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10274G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227325 | |||||||
chr12:42227353 | G | C | 6 | a0001c0001t0008g0120 a0001c0001t0008g0121 a0001c0001t0017g0125 others(3): Show |
6 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+10246C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227353 | |||||||
chr12:42227359 | T | A | 1 | a0001c0001t0004g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.152+10240A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227359 | |||||||
chr12:42227368 | G | A | 2 | a0001c0002t0002g0241 a0001c0002t0002g0242 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152+10231C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227368 | |||||||
chr12:42227411 | C | T | 1 | a0001c0002t0002g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152+10188G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227411 | |||||||
chr12:42227451 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10148G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227451 | |||||||
chr12:42227490 | C | T | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+10109G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227490 | |||||||
chr12:42227528 | G | A | 6 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+10071C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227528 | |||||||
chr12:42227564 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152+10035C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227564 | |||||||
chr12:42227572 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10027A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227572 | |||||||
chr12:42227615 | C | T | 1 | a0001c0001t0026g0143 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.152+9984G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227615 | |||||||
chr12:42227652 | C | T | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+9947G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227652 | |||||||
chr12:42227677 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.152+9922C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227677 | |||||||
chr12:42227680 | C | T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9919G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227680 | |||||||
chr12:42227681 | G | A | 1 | a0001c0001t0009g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+9918C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227681 | |||||||
chr12:42227686 | C | G | 1 | a0001c0002t0002g0292 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.152+9913G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227686 | |||||||
chr12:42227706 | G | A | 2 | a0001c0001t0010g0098 a0001c0001t0010g0101 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.152+9893C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227706 | |||||||
chr12:42227716 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.152+9883G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227716 | |||||||
chr12:42227732 | CGTCCGGG others(41): Show |
C | 13 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+9819_152+9866d others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227732 | |||||||
chr12:42227733 | G | GTCCGGGA others(44): Show |
2 | a0001c0001t0027g0090 a0001c0001t0028g0092 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.152+9865_152+9866i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227733 | |||||||
chr12:42227733 | G | GTCCGGGA others(43): Show |
3 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0029g0091 |
3 | HG01891.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+9865_152+9866i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227733 | |||||||
chr12:42227736 | C | T | 1 | a0001c0002t0002g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.152+9863G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227736 | |||||||
chr12:42227737 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+9862C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227737 | |||||||
chr12:42227764 | C | T | 3 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+9835G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227764 | |||||||
chr12:42227780 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+9819A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227780 | |||||||
chr12:42227803 | T | C | 9 | a0001c0002t0005g0335 a0001c0002t0005g0336 a0001c0002t0005g0337 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+9796A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227803 | |||||||
chr12:42227808 | C | T | 1 | a0001c0002t0002g0291 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.152+9791G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227808 | |||||||
chr12:42227830 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+9769C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227830 | |||||||
chr12:42227834 | G | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9765C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227834 | |||||||
chr12:42227862 | G | A | 12 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(9): Show |
12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+9737C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227862 | |||||||
chr12:42227866 | C | CGCCAGCC others(447): Show |
1 | a0001c0001t0001g0060 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.152+9279_152+9732d others(456): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227866 | |||||||
chr12:42227867 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+9732C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227867 | |||||||
chr12:42227869 | C | G | 1 | a0001c0001t0012g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+9730G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227869 | |||||||
chr12:42227880 | T | C | 1 | a0001c0002t0002g0288 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.152+9719A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227880 | |||||||
chr12:42227882 | C | T | 1 | a0001c0001t0025g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+9717G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227882 | |||||||
chr12:42227883 | G | A | 5 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(2): Show |
5 | HG02717.hp1 HG02723.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9716C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227883 | |||||||
chr12:42227896 | CGCCTCTG others(629): Show |
C | 1 | a0001c0001t0001g0082 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.152+9067_152+9702d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227896 | |||||||
chr12:42227897 | G | A | 38 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(35): Show |
39 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.152+9702C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227897 | |||||||
chr12:42227911 | G | A | 17 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0155 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+9688C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227911 | |||||||
chr12:42227944 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+9655T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227944 | |||||||
chr12:42227964 | A | C | 4 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0150 others(1): Show |
4 | NA18946.hp2 NA18957.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9635T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227964 | |||||||
chr12:42227977 | G | A | 1 | a0001c0001t0004g0113 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.152+9622C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227977 | |||||||
chr12:42227988 | C | T | 14 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(11): Show |
15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+9611G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227988 | |||||||
chr12:42228007 | T | C | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9592A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228007 | |||||||
chr12:42228010 | A | G | 7 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0011g0093 others(4): Show |
7 | HG01169.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+9589T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228010 | |||||||
chr12:42228020 | T | TG | 10 | a0001c0001t0001g0008 a0001c0001t0001g0064 a0001c0001t0001g0354 others(7): Show |
11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+9578dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228020 | |||||||
chr12:42228020 | TGGGGGGT others(449): Show |
T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0126 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152+9123_152+9578d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228020 | |||||||
chr12:42228020 | TGGGGGGT others(453): Show |
T | 57 | a0001c0002t0002g0083 a0001c0002t0002g0089 a0001c0002t0002g0170 others(54): Show |
57 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.152+9119_152+9578d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228020 | |||||||
chr12:42228126 | C | T | 1 | a0001c0001t0004g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.152+9473G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228126 | |||||||
chr12:42228132 | G | A | 4 | a0001c0001t0010g0101 a0001c0001t0027g0090 a0001c0001t0028g0092 others(1): Show |
4 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9467C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228132 | |||||||
chr12:42228135 | C | T | 79 | a0001c0001t0001g0095 a0001c0001t0001g0127 a0001c0001t0001g0128 others(76): Show |
83 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.152+9464G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228135 | |||||||
chr12:42228144 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152+9455C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228144 | |||||||
chr12:42228146 | TG | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
220 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.152+9452delC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228146 | |||||||
chr12:42228153 | G | T | 21 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(18): Show |
21 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.152+9446C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228153 | |||||||
chr12:42228154 | G | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0175 others(15): Show |
19 | HG00597.hp2 HG00733.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+9445C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228154 | |||||||
chr12:42228158 | G | GC | 9 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0181 others(6): Show |
9 | HG00597.hp2 HG01192.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+9440dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228158 | |||||||
chr12:42228169 | G | GC | 4 | a0001c0002t0002g0303 a0001c0002t0002g0308 a0001c0002t0002g0309 others(1): Show |
4 | HG01993.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9429_152+9430i others(3): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228169 | |||||||
chr12:42228182 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
10 | HG00597.hp2 NA18948.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+9417C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228182 | |||||||
chr12:42228186 | G | A | 12 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(9): Show |
12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+9413C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228186 | |||||||
chr12:42228186 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.152+9413C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228186 | |||||||
chr12:42228196 | T | TG | 24 | a0001c0001t0001g0010 a0001c0001t0001g0070 a0001c0001t0001g0133 others(21): Show |
24 | HG00544.hp1 HG00597.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.152+9402dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228196 | |||||||
chr12:42228202 | G | T | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9397C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228202 | |||||||
chr12:42228207 | G | GC | 12 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0095 others(9): Show |
12 | HG00597.hp1 HG02109.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+9391dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228207 | |||||||
chr12:42228214 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG01175.hp2 HG01346.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9385C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228214 | |||||||
chr12:42228218 | G | A | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+9381C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228218 | |||||||
chr12:42228231 | G | A | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9368C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228231 | |||||||
chr12:42228235 | T | G | 6 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0002t0002g0303 others(3): Show |
6 | HG01891.hp2 HG01993.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+9364A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228235 | |||||||
chr12:42228246 | GGGGGTGT others(42): Show |
G | 4 | a0001c0002t0002g0303 a0001c0002t0002g0308 a0001c0002t0002g0309 others(1): Show |
4 | HG01993.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9304_152+9352d others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228246 | |||||||
chr12:42228251 | T | G | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9348A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228251 | |||||||
chr12:42228256 | G | GC | 11 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0189 others(8): Show |
11 | HG00597.hp1 HG00597.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+9342dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228256 | |||||||
chr12:42228264 | C | A | 4 | a0001c0001t0001g0353 a0001c0001t0001g0359 a0001c0001t0001g0360 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9335G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228264 | |||||||
chr12:42228267 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0354 a0001c0001t0001g0355 others(3): Show |
7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+9332C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228267 | |||||||
chr12:42228268 | C | CGCCAGCC others(42): Show |
1 | a0001c0001t0027g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.152+9330_152+9331i others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228268 | |||||||
chr12:42228268 | C | CGCCAGCC others(42): Show |
3 | a0001c0001t0001g0005 a0001c0001t0008g0120 a0001c0001t0008g0121 |
3 | HG03486.hp2 NA18952.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.152+9330_152+9331i others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228268 | |||||||
chr12:42228268 | CGCCAGCC others(123): Show |
C | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9201_152+9330d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228268 | |||||||
chr12:42228281 | G | A | 2 | a0001c0001t0028g0092 a0001c0001t0029g0091 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+9318C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228281 | |||||||
chr12:42228295 | T | TGGGGGGG others(45): Show |
1 | a0001c0002t0002g0327 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(46): Show |
2 | a0001c0002t0002g0326 a0001c0002t0002g0328 |
2 | HG03209.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.152+9303_152+9304i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(44): Show |
57 | a0001c0001t0001g0205 a0001c0001t0002g0282 a0001c0002t0002g0002 others(54): Show |
59 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(45): Show |
14 | a0001c0001t0003g0153 a0001c0002t0002g0006 a0001c0002t0002g0087 others(11): Show |
15 | HG01192.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(46): Show |
3 | a0001c0001t0003g0166 a0001c0001t0003g0169 a0001c0002t0002g0002 |
3 | HG00408.hp1 HG03831.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.152+9303_152+9304i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(47): Show |
1 | a0001c0001t0004g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.152+9303_152+9304i others(56): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(45): Show |
1 | a0001c0001t0003g0161 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(43): Show |
84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(44): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0080 others(32): Show |
37 | HG00738.hp1 HG01099.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(45): Show |
16 | a0001c0001t0001g0213 a0001c0001t0001g0355 a0001c0001t0001g0356 others(13): Show |
16 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228295 | T | TGGGGGGG others(46): Show |
3 | a0001c0001t0004g0104 a0001c0001t0004g0119 a0001c0001t0033g0154 |
3 | HG02922.hp1 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.152+9303_152+9304i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | |||||||
chr12:42228296 | G | GGGGGGGT others(43): Show |
2 | a0001c0001t0028g0092 a0001c0001t0029g0091 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+9302_152+9303i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228296 | |||||||
chr12:42228309 | C | T | 1 | a0001c0001t0001g0001 | 3 | HG01099.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152+9290G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228309 | |||||||
chr12:42228320 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.152+9279C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228320 | |||||||
chr12:42228328 | A | G | 4 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 others(1): Show |
4 | HG02280.hp2 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9271T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228328 | |||||||
chr12:42228333 | A | G | 6 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+9266T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228333 | |||||||
chr12:42228360 | C | T | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(15): Show |
18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+9239G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228360 | |||||||
chr12:42228385 | A | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
89 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.152+9214T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228385 | |||||||
chr12:42228389 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+9210A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228389 | |||||||
chr12:42228393 | T | TGCCCGGC others(43): Show |
1 | a0001c0001t0006g0226 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.152+9205_152+9206i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228393 | |||||||
chr12:42228393 | T | TGCCCGGC others(42): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0140 others(15): Show |
19 | HG00597.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.152+9157_152+9205d others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228393 | |||||||
chr12:42228426 | G | GGGGGGGT others(41): Show |
4 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9172_152+9173i others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228426 | |||||||
chr12:42228435 | A | G | 6 | a0001c0001t0029g0091 a0001c0003t0001g0244 a0001c0003t0001g0245 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+9164T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228435 | |||||||
chr12:42228441 | C | T | 1 | a0001c0004t0016g0122 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.152+9158G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228441 | |||||||
chr12:42228446 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
220 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.152+9153A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228446 | |||||||
chr12:42228474 | T | TG | 21 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0015 others(18): Show |
21 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.152+9124dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | |||||||
chr12:42228474 | T | TGGGGGGG others(44): Show |
2 | a0001c0001t0004g0107 a0001c0001t0004g0115 |
2 | HG01081.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.152+9124_152+9125i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | |||||||
chr12:42228474 | T | TGGGGGGG others(43): Show |
7 | a0001c0001t0001g0185 a0001c0001t0004g0105 a0001c0001t0004g0110 others(4): Show |
7 | HG00423.hp1 HG00642.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+9124_152+9125i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | |||||||
chr12:42228474 | T | TGGGGGGG others(44): Show |
7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG02071.hp2 HG03704.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+9124_152+9125i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | |||||||
chr12:42228474 | T | TGGGGGGG others(46): Show |
1 | a0001c0001t0004g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.152+9124_152+9125i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | |||||||
chr12:42228475 | G | GGGGGGGT others(41): Show |
72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
74 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.152+9123_152+9124i others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228475 | |||||||
chr12:42228475 | G | GGGGGGGT others(40): Show |
1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152+9123_152+9124i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228475 | |||||||
chr12:42228476 | G | GGGGGGGT others(41): Show |
1 | a0001c0001t0003g0159 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.152+9122_152+9123i others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | |||||||
chr12:42228476 | G | GGGGGGTC others(40): Show |
1 | a0001c0001t0001g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+9122_152+9123i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | |||||||
chr12:42228476 | G | GGGGGGTC others(40): Show |
28 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0095 others(25): Show |
29 | HG01192.hp1 HG01975.hp2 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+9122_152+9123i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | |||||||
chr12:42228476 | G | GGGGGTCA others(39): Show |
1 | a0001c0001t0029g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+9122_152+9123i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | |||||||
chr12:42228477 | G | GGGGGGTC others(40): Show |
2 | a0001c0001t0026g0143 a0001c0002t0002g0330 |
2 | HG02738.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.152+9121_152+9122i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228477 | |||||||
chr12:42228477 | G | GGGGGTCA others(39): Show |
1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152+9121_152+9122i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228477 | |||||||
chr12:42228477 | G | GGGGGTCA others(39): Show |
78 | a0001c0001t0002g0282 a0001c0001t0003g0003 a0001c0001t0003g0142 others(75): Show |
83 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.152+9121_152+9122i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228477 | |||||||
chr12:42228479 | G | GGGTCAGC others(40): Show |
2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+9119_152+9120i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228479 | |||||||
chr12:42228479 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.152+9120C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228479 | |||||||
chr12:42228480 | G | GGTCAGCC others(39): Show |
2 | a0001c0002t0002g0314 a0001c0002t0002g0325 |
2 | HG00609.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.152+9118_152+9119i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228480 | |||||||
chr12:42228497 | C | T | 6 | a0001c0001t0033g0154 a0001c0003t0001g0244 a0001c0003t0001g0245 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+9102G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228497 | |||||||
chr12:42228501 | T | C | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9098A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228501 | |||||||
chr12:42228510 | G | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9089C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228510 | |||||||
chr12:42228515 | G | A | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9084C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228515 | |||||||
chr12:42228519 | G | A | 1 | a0001c0003t0014g0364 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152+9080C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228519 | |||||||
chr12:42228531 | G | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+9068C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228531 | |||||||
chr12:42228532 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
286 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.152+9067A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228532 | |||||||
chr12:42228543 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.152+9056C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228543 | |||||||
chr12:42228571 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9028G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228571 | |||||||
chr12:42228580 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.152+9019C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228580 | |||||||
chr12:42228596 | A | C | 10 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+9003T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228596 | |||||||
chr12:42228612 | G | T | 1 | a0001c0002t0002g0086 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.152+8987C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228612 | |||||||
chr12:42228613 | T | G | 8 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 others(5): Show |
8 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+8986A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228613 | |||||||
chr12:42228623 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.152+8976G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228623 | |||||||
chr12:42228628 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8971G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228628 | |||||||
chr12:42228636 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8963G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228636 | |||||||
chr12:42228645 | C | T | 10 | a0001c0002t0002g0089 a0001c0002t0002g0170 a0001c0002t0002g0252 others(7): Show |
10 | HG00621.hp1 HG02135.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+8954G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228645 | |||||||
chr12:42228656 | T | TG | 81 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(78): Show |
84 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.152+8942dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228656 | |||||||
chr12:42228656 | T | TGG | 19 | a0001c0001t0001g0008 a0001c0001t0001g0356 a0001c0001t0001g0357 others(16): Show |
20 | HG00609.hp2 HG02132.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.152+8941_152+8942d others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228656 | |||||||
chr12:42228671 | C | A | 4 | a0001c0001t0009g0099 a0001c0001t0009g0100 a0001c0001t0010g0098 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+8928G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228671 | |||||||
chr12:42228689 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.152+8910G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228689 | |||||||
chr12:42228695 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA18962.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.152+8904C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228695 | |||||||
chr12:42228705 | T | G | 1 | a0001c0001t0003g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.152+8894A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228705 | |||||||
chr12:42228710 | G | A | 7 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0222 others(4): Show |
7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+8889C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228710 | |||||||
chr12:42228727 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152+8872C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228727 | |||||||
chr12:42228772 | C | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8827G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228772 | |||||||
chr12:42228805 | G | T | 4 | a0001c0001t0003g0079 a0001c0001t0003g0155 a0001c0001t0003g0156 others(1): Show |
4 | HG01975.hp2 HG01978.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+8794C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228805 | |||||||
chr12:42228809 | G | A | 1 | a0001c0001t0010g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+8790C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228809 | |||||||
chr12:42228816 | C | T | 1 | a0001c0001t0006g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.152+8783G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228816 | |||||||
chr12:42228834 | A | G | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+8765T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228834 | |||||||
chr12:42228840 | G | A | 9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(6): Show |
9 | HG00544.hp1 HG00597.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+8759C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228840 | |||||||
chr12:42228849 | C | T | 1 | a0001c0002t0002g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152+8750G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228849 | |||||||
chr12:42228850 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8749C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228850 | |||||||
chr12:42228854 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+8745T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228854 | |||||||
chr12:42228891 | A | AGCCGCCC others(117): Show |
1 | a0001c0001t0009g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152+8707_152+8708i others(126): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228891 | |||||||
chr12:42228901 | C | T | 1 | a0001c0002t0002g0231 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.152+8698G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228901 | |||||||
chr12:42229013 | G | A | 3 | a0001c0001t0027g0090 a0001c0001t0028g0092 a0001c0001t0029g0091 |
3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+8586C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229013 | |||||||
chr12:42229015 | G | A | 1 | a0001c0001t0001g0358 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152+8584C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229015 | |||||||
chr12:42229032 | T | C | 1 | a0001c0001t0029g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+8567A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229032 | |||||||
chr12:42229034 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
89 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.152+8565C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229034 | |||||||
chr12:42229038 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+8561A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229038 | |||||||
chr12:42229204 | T | C | 133 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(130): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+8395A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229204 | |||||||
chr12:42229221 | G | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+8378C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229221 | |||||||
chr12:42229227 | A | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+8372T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229227 | |||||||
chr12:42229243 | T | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(34): Show |
38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.152+8356A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229243 | |||||||
chr12:42229275 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+8324C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229275 | |||||||
chr12:42229415 | AT | A | 8 | a0001c0002t0002g0230 a0001c0002t0002g0247 a0001c0002t0002g0250 others(5): Show |
8 | HG00544.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+8183delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229415 | |||||||
chr12:42229416 | T | A | 126 | a0001c0001t0001g0035 a0001c0001t0002g0282 a0001c0002t0002g0002 others(123): Show |
130 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.152+8183A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229416 | |||||||
chr12:42229419 | A | T | 125 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(122): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.152+8180T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229419 | |||||||
chr12:42229421 | T | A | 125 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(122): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.152+8178A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | |||||||
chr12:42229421 | T | TA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.152+8177dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | |||||||
chr12:42229421 | T | TAA | 11 | a0001c0001t0001g0219 a0001c0001t0004g0119 a0001c0001t0011g0093 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+8176_152+8177d others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | |||||||
chr12:42229421 | TA | T | 33 | a0001c0001t0003g0003 a0001c0001t0003g0079 a0001c0001t0003g0142 others(30): Show |
34 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.152+8177delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | |||||||
chr12:42229549 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+8050T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229549 | |||||||
chr12:42229975 | A | G | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+7624T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229975 | |||||||
chr12:42230054 | G | A | 1 | a0001c0002t0002g0334 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.152+7545C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230054 | |||||||
chr12:42230057 | G | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(34): Show |
38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.152+7542C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230057 | |||||||
chr12:42230084 | C | T | 1 | a0001c0001t0010g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+7515G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230084 | |||||||
chr12:42230188 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.152+7411G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230188 | |||||||
chr12:42230212 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+7387C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230212 | |||||||
chr12:42230235 | G | A | 7 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0222 others(4): Show |
7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+7364C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230235 | |||||||
chr12:42230261 | AAAAG | A | 4 | a0001c0001t0001g0353 a0001c0001t0001g0359 a0001c0001t0001g0360 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+7334_152+7337d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230261 | |||||||
chr12:42230262 | AAAGAAAG others(2): Show |
A | 10 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0006g0220 others(7): Show |
10 | HG02155.hp2 HG03017.hp2 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+7328_152+7336d others(11): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230262 | |||||||
chr12:42230266 | A | AAAGAGAA others(7): Show |
5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+7319_152+7332d others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230266 | |||||||
chr12:42230289 | G | GAAGA | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+7306_152+7309d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230289 | |||||||
chr12:42230315 | A | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+7284T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230315 | |||||||
chr12:42230391 | G | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+7208C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230391 | |||||||
chr12:42230428 | A | G | 1 | a0001c0002t0002g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.152+7171T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230428 | |||||||
chr12:42230541 | C | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
299 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.152+7058G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230541 | |||||||
chr12:42230544 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152+7055C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230544 | |||||||
chr12:42230737 | G | A | 1 | a0001c0001t0032g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+6862C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230737 | |||||||
chr12:42230779 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+6820T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230779 | |||||||
chr12:42230883 | G | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+6716C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230883 | |||||||
chr12:42230986 | T | TA | 9 | a0001c0002t0005g0335 a0001c0002t0005g0336 a0001c0002t0005g0337 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+6612dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230986 | |||||||
chr12:42231255 | A | C | 1 | a0001c0002t0002g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152+6344T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231255 | |||||||
chr12:42231278 | G | A | 4 | a0001c0001t0017g0125 a0001c0001t0018g0124 a0001c0001t0030g0123 others(1): Show |
4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+6321C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231278 | |||||||
chr12:42231477 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.152+6122C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231477 | |||||||
chr12:42231499 | T | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0126 others(2): Show |
5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+6100A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231499 | |||||||
chr12:42231674 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+5925G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231674 | |||||||
chr12:42231726 | C | A | 1 | a0001c0001t0003g0079 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.152+5873G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231726 | |||||||
chr12:42231889 | T | C | 2 | a0001c0001t0011g0093 a0001c0001t0011g0094 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+5710A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231889 | |||||||
chr12:42232328 | T | C | 3 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 |
3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+5271A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232328 | |||||||
chr12:42232412 | C | T | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+5187G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232412 | |||||||
chr12:42232672 | C | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+4927G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232672 | |||||||
chr12:42232771 | TAAGC | T | 5 | a0001c0003t0001g0244 a0001c0003t0001g0245 a0001c0003t0001g0246 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+4824_152+4827d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232771 | |||||||
chr12:42232990 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152+4609C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232990 | |||||||
chr12:42233027 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.152+4572A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233027 | |||||||
chr12:42233050 | G | A | 1 | a0001c0001t0033g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+4549C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233050 | |||||||
chr12:42233176 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.152+4423G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233176 | |||||||
chr12:42233202 | T | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+4397A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233202 | |||||||
chr12:42233317 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152+4282T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233317 | |||||||
chr12:42233356 | C | G | 1 | a0001c0001t0003g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.152+4243G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233356 | |||||||
chr12:42233484 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.152+4115A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233484 | |||||||
chr12:42233613 | G | C | 1 | a0001c0001t0012g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+3986C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233613 | |||||||
chr12:42233712 | T | C | 2 | a0001c0002t0002g0343 a0001c0002t0002g0344 |
2 | HG02132.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.152+3887A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233712 | |||||||
chr12:42233988 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+3611A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233988 | |||||||
chr12:42234188 | AAAAGAGA others(4): Show |
A | 3 | a0001c0001t0001g0096 a0001c0001t0011g0093 a0001c0001t0011g0094 |
3 | HG01169.hp2 HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+3400_152+3410d others(13): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234188 | |||||||
chr12:42234189 | AAAGAGAA others(3): Show |
A | 2 | a0001c0001t0028g0092 a0001c0001t0029g0091 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+3400_152+3409d others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234189 | |||||||
chr12:42234190 | AAGAGAAA others(7): Show |
A | 25 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(22): Show |
25 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.152+3395_152+3408d others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234190 | |||||||
chr12:42234192 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0070 |
2 | HG01192.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.152+3407C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | |||||||
chr12:42234192 | G | GAGAAA | 17 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0097 others(14): Show |
18 | HG00738.hp1 HG02109.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.152+3402_152+3406d others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | |||||||
chr12:42234192 | G | GAGAAAAG others(3): Show |
2 | a0001c0001t0003g0145 a0001c0001t0010g0101 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.152+3397_152+3406d others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | |||||||
chr12:42234192 | GAGAAA | G | 46 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(43): Show |
46 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.152+3402_152+3406d others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | |||||||
chr12:42234192 | GAGAAAAG others(3): Show |
G | 11 | a0001c0001t0001g0062 a0001c0001t0001g0177 a0001c0001t0001g0179 others(8): Show |
11 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+3397_152+3406d others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | |||||||
chr12:42234192 | GAGAAAAG others(8): Show |
G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.152+3392_152+3406d others(17): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | |||||||
chr12:42234202 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.152+3397T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234202 | |||||||
chr12:42234204 | G | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+3395C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234204 | |||||||
chr12:42234207 | A | G | 25 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(22): Show |
25 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.152+3392T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234207 | |||||||
chr12:42234434 | A | C | 1 | a0001c0001t0003g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.152+3165T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234434 | |||||||
chr12:42234478 | C | A | 1 | a0001c0001t0033g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+3121G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234478 | |||||||
chr12:42234711 | C | T | 1 | a0001c0001t0029g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+2888G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234711 | |||||||
chr12:42234805 | T | A | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+2794A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234805 | |||||||
chr12:42234921 | G | A | 2 | a0001c0003t0014g0363 a0001c0003t0014g0364 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+2678C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234921 | |||||||
chr12:42234935 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.152+2664G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234935 | |||||||
chr12:42235387 | T | TATTAATA others(7): Show |
1 | a0001c0002t0002g0345 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.152+2198_152+2211d others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235387 | |||||||
chr12:42235489 | T | C | 1 | a0001c0002t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152+2110A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235489 | |||||||
chr12:42235536 | T | C | 6 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+2063A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235536 | |||||||
chr12:42235560 | G | GAC | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+2038_152+2039i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235560 | |||||||
chr12:42235566 | A | C | 1 | a0001c0002t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.152+2033T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235566 | |||||||
chr12:42235748 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+1851A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235748 | |||||||
chr12:42235757 | T | C | 2 | a0001c0002t0002g0089 a0001c0002t0002g0347 |
2 | HG04184.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.152+1842A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235757 | |||||||
chr12:42235783 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152+1816G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235783 | |||||||
chr12:42235799 | A | T | 14 | a0001c0001t0003g0003 a0001c0001t0003g0142 a0001c0001t0003g0144 others(11): Show |
15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+1800T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235799 | |||||||
chr12:42235871 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.152+1728T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235871 | |||||||
chr12:42236238 | C | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1361G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236238 | |||||||
chr12:42236281 | A | C | 1 | a0001c0002t0024g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152+1318T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236281 | |||||||
chr12:42236330 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(71): Show |
78 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.152+1269A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236330 | |||||||
chr12:42236425 | A | C | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1174T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236425 | |||||||
chr12:42236474 | T | C | 3 | a0001c0002t0002g0348 a0001c0002t0002g0349 a0001c0002t0002g0350 |
3 | HG03669.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.152+1125A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236474 | |||||||
chr12:42236567 | A | AAC | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+1031_152+1032i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236567 | |||||||
chr12:42236568 | A | ACG | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1030_152+1031i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236568 | |||||||
chr12:42236569 | G | C | 1 | a0001c0002t0002g0351 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152+1030C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236569 | |||||||
chr12:42236570 | T | A | 1 | a0001c0002t0002g0351 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152+1029A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236570 | |||||||
chr12:42236612 | G | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0078 a0001c0001t0003g0079 others(28): Show |
32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+987C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236612 | |||||||
chr12:42236615 | T | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
68 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.152+984A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236615 | |||||||
chr12:42236664 | C | A | 137 | a0001c0001t0002g0282 a0001c0002t0002g0002 a0001c0002t0002g0006 others(134): Show |
141 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.152+935G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236664 | |||||||
chr12:42236817 | A | G | 2 | a0001c0003t0014g0363 a0001c0003t0014g0364 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+782T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236817 | |||||||
chr12:42236950 | T | A | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+649A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236950 | |||||||
chr12:42237101 | C | G | 1 | a0001c0001t0027g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.152+498G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237101 | |||||||
chr12:42237302 | A | G | 5 | a0001c0001t0011g0093 a0001c0001t0011g0094 a0001c0001t0027g0090 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+297T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237302 | |||||||
chr12:42237532 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.152+67C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237532 | |||||||
chr12:42237557 | A | AC | 17 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(14): Show |
17 | HG00438.hp1 HG01978.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.152+41dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237557 | |||||||
chr12:42237587 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+12G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237587 | |||||||
chr12:42237851 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.27-127A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 1/3 | chr12 | 42237851 | |||||||
chr12:42237905 | G | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0353 a0001c0001t0001g0354 others(8): Show |
12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-181C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 1/3 | chr12 | 42237905 |