Item | Value |
---|---|
geneid | 56341 |
ensemblid | ENSG00000111218.12 |
hgncid | 5188 |
symbol | PRMT8 |
name | protein arginine methyltransferase 8 |
refseq_nuc | NM_019854.5 |
refseq_prot | NP_062828.3 |
ensembl_nuc | ENST00000382622.4 |
ensembl_prot | ENSP00000372067.3 |
mane_status | MANE Select |
chr | chr12 |
start | 3491203 |
end | 3593973 |
strand | + |
ver | v1.2 |
region | chr12:3491203-3593973 |
region5000 | chr12:3486203-3598973 |
regionname0 | PRMT8_chr12_3491203_3593973 |
regionname5000 | PRMT8_chr12_3486203_3598973 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 394 | 363 | 89 | 68 | 154 | 16 | 34 | 112 | PRMT8_chr12_3486203_3598973 | PRMT8 | MGMKH others(389): Show |
chr12 | 3486203 | 3598973 |
a0002 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | MGMKH others(389): Show |
chr12 | 3486203 | 3598973 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1182 | 311 | 70 | 60 | 131 | 16 | 32 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0002 | 0/0 | 1182 | 36 | 14 | 5 | 15 | 0 | 2 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0003 | 0/0 | 1182 | 4 | 0 | 0 | 4 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0004 | 0/0 | 1182 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0005 | 0/0 | 1182 | 4 | 3 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0006 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0007 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0009 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0001c0010 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 | ||
a0002c0008 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | ATGGG others(1177): Show |
chr12 | 3486203 | 3598973 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2399 | 288 | 60 | 52 | 127 | 16 | 31 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0002 | 0/0 | 2399 | 4 | 3 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0003 | 0/0 | 2399 | 8 | 0 | 8 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0004 | 0/0 | 2405 | 3 | 0 | 0 | 3 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2400): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0006 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0007 | 0/0 | 2399 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0008 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0010 | 0/0 | 2399 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0012 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0013 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0001t0014 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0002t0002 | 0/0 | 2399 | 32 | 13 | 4 | 13 | 0 | 2 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0002t0005 | 0/0 | 2405 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2400): Show |
chr12 | 3486203 | 3598973 |
a0001c0002t0009 | 0/0 | 2399 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0002t0011 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0003t0001 | 0/0 | 2399 | 4 | 0 | 0 | 4 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0004t0001 | 0/0 | 2399 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0005t0001 | 0/0 | 2399 | 3 | 2 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0005t0006 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0006t0001 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0007t0001 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0009t0001 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0001c0010t0002 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
a0002c0008t0001 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | GCTTC others(2394): Show |
chr12 | 3486203 | 3598973 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0359 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0001t0014g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0002t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0004t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0004t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0004t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0004t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0005t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0005t0006g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0007t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0009t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0001c0010t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
a0002c0008t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0330 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0310 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01069 | hp1 | a0001 | c0002 | t0009 | g0034 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0174 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0333 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01346 | hp2 | a0001 | c0005 | t0001 | g0324 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0345 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0343 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02145 | hp2 | a0001 | c0005 | t0001 | g0199 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0334 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0297 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0335 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0122 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0329 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02647 | hp1 | a0001 | c0005 | t0006 | g0355 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0331 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0328 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02895 | hp1 | a0001 | c0002 | t0011 | g0101 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02976 | hp1 | a0001 | c0001 | t0014 | g0003 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03098 | hp1 | a0002 | c0008 | t0001 | g0356 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0053 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0323 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0184 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0028 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04115 | hp1 | a0001 | c0001 | t0010 | g0196 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0325 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18951 | hp1 | a0001 | c0007 | t0001 | g0208 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0277 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18981 | hp1 | a0001 | c0006 | t0001 | g0026 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18990 | hp2 | a0001 | c0010 | t0002 | g0147 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18992 | hp1 | a0001 | c0002 | t0005 | g0041 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18995 | hp1 | a0001 | c0009 | t0001 | g0107 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0087 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0353 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20129 | hp1 | a0001 | c0001 | t0013 | g0056 | AFR | ASW | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0320 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | GIH | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0193 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA18955 | hp2 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0259 | REF | REF | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0359 | REF | REF | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:3592301 | G | C | 1 | a0002 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1050G>C | p.Arg350Ser | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/10 | 1473/2399 | 1050/1185 | 350/394 | chr12 | 3592301 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:3540614 | C | T | 1 | a0001c0010 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.84C>T | p.Ser28Ser | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 507/2399 | 84/1185 | 28/394 | chr12 | 3540614 | |||
chr12:3540632 | C | G | 1 | a0001c0005 | 4 | HG01346.hp2 HG02145.hp2 HG02559.hp1 others(1): Show |
synonymous_variant | LOW | c.102C>G | p.Pro34Pro | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 525/2399 | 102/1185 | 34/394 | chr12 | 3540632 | |||
chr12:3540641 | C | T | 1 | a0001c0009 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.111C>T | p.Val37Val | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 534/2399 | 111/1185 | 37/394 | chr12 | 3540641 | |||
chr12:3540764 | C | T | 1 | a0001c0004 | 4 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(1): Show |
synonymous_variant | LOW | c.234C>T | p.Asp78Asp | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 657/2399 | 234/1185 | 78/394 | chr12 | 3540764 | |||
chr12:3540788 | C | T | 1 | a0001c0010 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.258C>T | p.His86His | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 681/2399 | 258/1185 | 86/394 | chr12 | 3540788 | |||
chr12:3568821 | G | A | 2 | a0001c0006 a0001c0007 |
2 | NA18951.hp1 NA18981.hp1 |
synonymous_variant | LOW | c.597G>A | p.Thr199Thr | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/10 | 1020/2399 | 597/1185 | 199/394 | chr12 | 3568821 | |||
chr12:3592298 | G | A | 2 | a0001c0002 a0001c0010 |
37 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(34): Show |
synonymous_variant | LOW | c.1047G>A | p.Arg349Arg | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/10 | 1470/2399 | 1047/1185 | 349/394 | chr12 | 3592298 | |||
chr12:3592301 | G | A | 2 | a0001c0003 a0001c0006 |
5 | NA18967.hp1 NA18981.hp1 NA18984.hp1 others(2): Show |
synonymous_variant | LOW | c.1050G>A | p.Arg350Arg | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/10 | 1473/2399 | 1050/1185 | 350/394 | chr12 | 3592301 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:3491220 | G | T | 1 | a0001c0001t0014 | 1 | HG02976.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-406G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/10 | chr12 | 3491220 | |||||||
chr12:3491269 | C | A | 1 | a0001c0001t0003 | 8 | HG01167.hp1 HG01169.hp2 HG01256.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-357C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/10 | 357 | chr12 | 3491269 | ||||||
chr12:3491293 | A | ACCGCCG | 2 | a0001c0001t0004 a0001c0002t0005 |
5 | NA18955.hp2 NA18968.hp1 NA18987.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-319_-314dupCGCCGC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/10 | 313 | INFO_REALIGN_3_PRIME | chr12 | 3491293 | |||||
chr12:3593210 | G | A | 1 | a0001c0001t0008 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 28 | chr12 | 3593210 | ||||||
chr12:3593259 | G | C | 1 | a0001c0002t0009 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*77G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 77 | chr12 | 3593259 | ||||||
chr12:3593389 | C | G | 1 | a0001c0001t0013 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*207C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 207 | chr12 | 3593389 | ||||||
chr12:3593423 | G | A | 1 | a0001c0001t0010 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 241 | chr12 | 3593423 | ||||||
chr12:3593453 | G | T | 1 | a0001c0001t0007 | 2 | HG02615.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*271G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 271 | chr12 | 3593453 | ||||||
chr12:3593623 | C | A | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0002t0002 others(4): Show |
43 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*441C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 441 | chr12 | 3593623 | ||||||
chr12:3593626 | G | A | 1 | a0001c0002t0011 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 444 | chr12 | 3593626 | ||||||
chr12:3593662 | C | T | 1 | a0001c0001t0012 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 480 | chr12 | 3593662 | ||||||
chr12:3593736 | G | A | 2 | a0001c0001t0006 a0001c0005t0006 |
2 | HG02647.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*554G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 554 | chr12 | 3593736 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:3491729 | G | C | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+29G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491729 | |||||||
chr12:3491749 | G | C | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+49G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491749 | |||||||
chr12:3491801 | T | C | 352 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(349): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.75+101T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491801 | |||||||
chr12:3491831 | CCTGT | C | 5 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0001c0001t0001g0351 others(2): Show |
5 | NA18951.hp2 NA18970.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+132_75+135delCT others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491831 | |||||||
chr12:3491832 | C | CTG | 25 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0049 others(22): Show |
25 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.75+188_75+189dupGT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | C | CTGTG | 7 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0231 others(4): Show |
8 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+186_75+189dupGT others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0229 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+180_75+189dupGT others(8): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.75+178_75+189dupGT others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | C | G | 1 | a0001c0001t0001g0025 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.75+132C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491832 | |||||||
chr12:3491832 | CTG | C | 55 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.75+188_75+189delGT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTG | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(46): Show |
49 | HG00280.hp2 HG00597.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+186_75+189delGT others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTGTG | C | 56 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0029 others(53): Show |
56 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.75+184_75+189delGT others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTGTGT others(1): Show |
C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0060 others(33): Show |
36 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.75+182_75+189delGT others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTGTGT others(3): Show |
C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0116 others(35): Show |
38 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+180_75+189delGT others(8): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTGTGT others(5): Show |
C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0195 others(5): Show |
8 | HG00642.hp1 HG00673.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+178_75+189delGT others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTGTGT others(7): Show |
C | 11 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(8): Show |
11 | HG01175.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+176_75+189delGT others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTGTGT others(9): Show |
C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0311 a0001c0001t0001g0327 |
3 | HG02148.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.75+174_75+189delGT others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491832 | CTGTGTGT others(11): Show |
C | 11 | a0001c0001t0001g0095 a0001c0001t0001g0118 a0001c0001t0001g0119 others(8): Show |
11 | HG01346.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+172_75+189delGT others(16): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | ||||||
chr12:3491833 | TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+134_75+144delGT others(9): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491833 | |||||||
chr12:3491845 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+145T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491845 | |||||||
chr12:3491864 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.75+164G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491864 | |||||||
chr12:3492006 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+306C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492006 | |||||||
chr12:3492175 | C | G | 5 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 others(2): Show |
5 | HG00639.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+475C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492175 | |||||||
chr12:3492210 | C | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(51): Show |
54 | HG00280.hp2 HG00558.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.75+510C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492210 | |||||||
chr12:3492250 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.75+550A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492250 | |||||||
chr12:3492374 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+674C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492374 | |||||||
chr12:3492507 | C | G | 1 | a0001c0001t0001g0338 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+807C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492507 | |||||||
chr12:3492655 | A | G | 10 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+955A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492655 | |||||||
chr12:3492903 | C | G | 1 | a0001c0001t0001g0337 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.75+1203C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492903 | |||||||
chr12:3492910 | C | G | 1 | a0001c0001t0001g0336 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.75+1210C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492910 | |||||||
chr12:3493203 | C | G | 2 | a0001c0001t0002g0334 a0001c0002t0002g0335 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.75+1503C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493203 | |||||||
chr12:3493347 | G | C | 1 | a0001c0001t0001g0349 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.75+1647G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493347 | |||||||
chr12:3493370 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): Show |
58 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.75+1670T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493370 | |||||||
chr12:3493535 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(51): Show |
55 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+1835C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493535 | |||||||
chr12:3493561 | G | GGTGCAGA others(20): Show |
1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+1868_75+1894dup others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3493561 | ||||||
chr12:3493581 | T | A | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+1881T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493581 | |||||||
chr12:3493636 | G | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1936G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493636 | |||||||
chr12:3493818 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+2118G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493818 | |||||||
chr12:3493997 | C | T | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+2297C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493997 | |||||||
chr12:3494300 | C | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0327 a0001c0001t0006g0328 |
3 | HG02723.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+2600C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494300 | |||||||
chr12:3494382 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75+2682T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494382 | |||||||
chr12:3494461 | A | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0040 others(2): Show |
5 | NA18955.hp2 NA18968.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2761A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494461 | |||||||
chr12:3494645 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.75+2945C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494645 | |||||||
chr12:3494718 | C | T | 3 | a0001c0001t0001g0094 a0001c0002t0002g0325 a0001c0005t0001g0324 |
3 | HG01346.hp2 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.75+3018C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494718 | |||||||
chr12:3494727 | C | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0276 a0001c0001t0001g0279 others(52): Show |
55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+3027C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494727 | |||||||
chr12:3494822 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.75+3122G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494822 | |||||||
chr12:3494951 | G | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0276 a0001c0001t0001g0279 others(52): Show |
55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+3251G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494951 | |||||||
chr12:3495098 | G | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.75+3398G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495098 | |||||||
chr12:3495110 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+3410T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495110 | |||||||
chr12:3495309 | G | A | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+3609G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495309 | |||||||
chr12:3495438 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+3738C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495438 | |||||||
chr12:3495468 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+3768C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495468 | |||||||
chr12:3495524 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+3824C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495524 | |||||||
chr12:3495583 | C | G | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+3883C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495583 | |||||||
chr12:3495643 | A | G | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG02165.hp2 NA18949.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.75+3943A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495643 | |||||||
chr12:3495738 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+4038T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495738 | |||||||
chr12:3495743 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG00280.hp1 HG01099.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.75+4043G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495743 | |||||||
chr12:3495840 | G | T | 11 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(8): Show |
11 | HG00597.hp2 NA18939.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+4140G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495840 | |||||||
chr12:3496085 | C | G | 2 | a0001c0001t0001g0352 a0001c0003t0001g0353 |
2 | NA18951.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.75+4385C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496085 | |||||||
chr12:3496199 | G | GATATAT | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0151 others(1): Show |
4 | HG01169.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4510_75+4515dup others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(3): Show |
15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0120 others(12): Show |
15 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+4506_75+4515dup others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(5): Show |
8 | a0001c0001t0001g0091 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG01346.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+4504_75+4515dup others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(7): Show |
1 | a0001c0001t0001g0287 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.75+4502_75+4515dup others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(9): Show |
3 | a0001c0001t0001g0312 a0001c0001t0001g0315 a0001c0001t0001g0347 |
3 | HG01192.hp2 HG01433.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75+4500_75+4515dup others(16): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(11): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0304 a0001c0001t0003g0288 others(1): Show |
4 | HG01256.hp1 HG01361.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(13): Show |
5 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
5 | HG02083.hp1 HG02451.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(20): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(15): Show |
4 | a0001c0001t0001g0090 a0001c0001t0001g0299 a0001c0001t0001g0300 others(1): Show |
4 | HG00639.hp2 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(17): Show |
1 | a0001c0001t0001g0284 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(24): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(19): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0285 |
2 | HG03139.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496199 | G | GATATATA others(23): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0283 |
2 | HG00423.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | ||||||
chr12:3496212 | A | ATTT | 7 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
8 | HG01256.hp2 HG01258.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+4513_75+4514ins others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496212 | ||||||
chr12:3496212 | A | ATTTT | 18 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0244 others(15): Show |
18 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+4513_75+4514ins others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496212 | ||||||
chr12:3496212 | A | ATTTTT | 13 | a0001c0001t0001g0100 a0001c0001t0001g0261 a0001c0001t0001g0262 others(10): Show |
13 | HG00280.hp1 HG01081.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+4513_75+4514ins others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496212 | ||||||
chr12:3496214 | A | ATATATAT others(4): Show |
11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG00140.hp2 HG01109.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01074.hp2 HG01891.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(13): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0021 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(22): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0286 |
2 | HG02818.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(26): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0272 |
2 | HG00558.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(33): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(38): Show |
1 | a0001c0001t0001g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(45): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(40): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(43): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0012 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(44): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0014 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(36): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(32): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(27): Show |
1 | a0001c0002t0011g0101 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(34): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(38): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(46): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0019 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(31): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(39): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(24): Show |
2 | a0001c0002t0002g0020 a0001c0002t0002g0053 |
2 | HG03139.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(31): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(34): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(39): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(22): Show |
1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(33): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(40): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0339 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0075 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0354 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(25): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(14): Show |
1 | a0001c0009t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA18971.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(18): Show |
3 | a0001c0001t0001g0108 a0001c0001t0001g0340 a0001c0002t0002g0109 |
3 | HG01071.hp1 HG02055.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(25): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0078 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01261.hp1 NA18959.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(15): Show |
3 | a0001c0001t0001g0079 a0001c0001t0001g0114 a0001c0002t0002g0080 |
3 | HG01069.hp2 NA18942.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0002t0002g0115 |
3 | HG01070.hp1 HG03579.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0061 |
2 | HG01071.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(24): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(21): Show |
1 | a0001c0002t0002g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0125 |
2 | HG02080.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(20): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0126 a0001c0005t0006g0355 |
2 | HG02135.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(16): Show |
4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0130 others(1): Show |
4 | HG02055.hp2 HG02896.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0322 |
2 | NA18939.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(20): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0085 a0001c0001t0001g0148 a0001c0010t0002g0147 |
3 | NA18963.hp1 NA18990.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0066 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0149 a0001c0002t0002g0150 |
2 | HG01358.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(24): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0002t0002g0086 |
3 | HG02886.hp1 HG02970.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(12): Show |
1 | a0001c0001t0007g0323 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(3): Show |
6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0183 others(3): Show |
6 | HG01934.hp1 HG02451.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0097 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0190 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0195 |
3 | HG00438.hp1 HG00558.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(4): Show |
1 | a0001c0001t0010g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | A | T | 48 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(45): Show |
49 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+4514A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496214 | |||||||
chr12:3496214 | AT | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0351 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+4540delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | ATTT | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0350 a0001c0002t0002g0043 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4538_75+4540del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496214 | ATTTTT | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+4536_75+4540del others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | ||||||
chr12:3496215 | T | TATATATA others(2): Show |
9 | a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0001g0119 others(6): Show |
9 | HG00099.hp2 HG02056.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(9): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(4): Show |
8 | a0001c0001t0001g0121 a0001c0001t0001g0132 a0001c0001t0001g0134 others(5): Show |
8 | HG01070.hp2 HG01981.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(13): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(8): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0302 a0001c0001t0001g0320 others(1): Show |
4 | HG02523.hp1 HG03195.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(15): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(10): Show |
8 | a0001c0001t0001g0303 a0001c0001t0001g0316 a0001c0001t0001g0317 others(5): Show |
8 | HG01074.hp1 HG01175.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(17): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(12): Show |
6 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(3): Show |
6 | HG00099.hp1 HG01123.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(14): Show |
7 | a0001c0001t0001g0280 a0001c0001t0001g0292 a0001c0001t0001g0298 others(4): Show |
7 | HG00639.hp1 HG00673.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(16): Show |
2 | a0001c0001t0001g0293 a0001c0001t0001g0301 |
2 | NA18944.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(18): Show |
2 | a0001c0001t0001g0281 a0001c0001t0001g0294 |
2 | NA18959.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(25): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(20): Show |
3 | a0001c0002t0002g0278 a0001c0002t0002g0282 a0001c0003t0001g0277 |
3 | NA18967.hp1 NA18994.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(22): Show |
2 | a0001c0001t0001g0276 a0001c0001t0001g0279 |
2 | NA18747.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496215 | T | TATATATA others(24): Show |
1 | a0001c0001t0001g0338 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(31): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | |||||||
chr12:3496216 | T | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0116 others(26): Show |
29 | HG00438.hp2 HG00639.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+4516T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496216 | |||||||
chr12:3496217 | T | A | 32 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0118 others(29): Show |
32 | HG00639.hp1 HG01123.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.75+4517T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496217 | |||||||
chr12:3496218 | T | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0116 others(12): Show |
15 | HG00438.hp2 HG01169.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+4518T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496218 | |||||||
chr12:3496219 | T | A | 24 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0119 others(21): Show |
24 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+4519T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496219 | |||||||
chr12:3496220 | T | A | 9 | a0001c0001t0001g0095 a0001c0001t0001g0116 a0001c0001t0001g0117 others(6): Show |
9 | HG01169.hp1 HG01256.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+4520T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496220 | |||||||
chr12:3496221 | T | A | 23 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(20): Show |
23 | HG00642.hp1 HG01123.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+4521T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496221 | |||||||
chr12:3496222 | T | A | 11 | a0001c0001t0001g0052 a0001c0001t0001g0095 a0001c0001t0001g0116 others(8): Show |
11 | HG01169.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+4522T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496222 | |||||||
chr12:3496223 | T | A | 21 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(18): Show |
21 | HG00642.hp1 HG01517.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.75+4523T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496223 | |||||||
chr12:3496224 | T | A | 7 | a0001c0001t0001g0052 a0001c0001t0001g0095 a0001c0001t0001g0287 others(4): Show |
7 | HG01175.hp1 HG01891.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+4524T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496224 | |||||||
chr12:3496225 | T | A | 18 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(15): Show |
18 | HG00642.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+4525T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496225 | |||||||
chr12:3496226 | T | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0095 a0001c0001t0001g0287 others(3): Show |
6 | HG01891.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+4526T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496226 | |||||||
chr12:3496227 | T | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0327 a0001c0001t0002g0334 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4527T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496227 | |||||||
chr12:3496228 | T | A | 3 | a0001c0001t0001g0095 a0001c0001t0006g0328 a0001c0002t0002g0051 |
3 | HG01891.hp2 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.75+4528T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496228 | |||||||
chr12:3496229 | T | A | 3 | a0001c0001t0001g0203 a0001c0001t0002g0334 a0001c0002t0002g0335 |
3 | HG02258.hp2 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.75+4529T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496229 | |||||||
chr12:3496241 | G | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0083 |
3 | NA18969.hp2 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.75+4541G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496241 | |||||||
chr12:3496301 | T | C | 1 | a0001c0001t0013g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.75+4601T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496301 | |||||||
chr12:3496386 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+4686G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496386 | |||||||
chr12:3496392 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.75+4692T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496392 | |||||||
chr12:3496659 | T | A | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+4959T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496659 | |||||||
chr12:3496742 | T | C | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+5042T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496742 | |||||||
chr12:3496747 | G | A | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+5047G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496747 | |||||||
chr12:3496848 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(10): Show |
13 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+5148T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496848 | |||||||
chr12:3496914 | A | AT | 18 | a0001c0001t0001g0039 a0001c0001t0001g0113 a0001c0001t0001g0130 others(15): Show |
18 | HG01175.hp1 HG01433.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+5233dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | ||||||
chr12:3496914 | AT | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(64): Show |
67 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.75+5233delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | ||||||
chr12:3496914 | ATT | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(40): Show |
44 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.75+5232_75+5233del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | ||||||
chr12:3496914 | ATTT | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0085 others(5): Show |
8 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+5231_75+5233del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | ||||||
chr12:3496939 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+5239G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496939 | |||||||
chr12:3497310 | C | T | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+5610C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497310 | |||||||
chr12:3497452 | T | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(15): Show |
19 | HG00597.hp2 HG00733.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+5752T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497452 | |||||||
chr12:3497476 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75+5776T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497476 | |||||||
chr12:3497720 | TC | T | 37 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(34): Show |
37 | HG00280.hp2 HG01069.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+6023delC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3497720 | ||||||
chr12:3497741 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0126 a0001c0001t0001g0145 others(1): Show |
4 | HG01261.hp1 HG02135.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+6041T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497741 | |||||||
chr12:3498175 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+6475C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498175 | |||||||
chr12:3498176 | A | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+6476A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498176 | |||||||
chr12:3498402 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.75+6702G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498402 | |||||||
chr12:3498523 | A | G | 6 | a0001c0001t0001g0146 a0001c0001t0001g0226 a0001c0001t0001g0255 others(3): Show |
6 | HG00733.hp2 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+6823A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498523 | |||||||
chr12:3498573 | C | T | 1 | a0001c0002t0002g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+6873C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498573 | |||||||
chr12:3498606 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+6906G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498606 | |||||||
chr12:3498845 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+7145C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498845 | |||||||
chr12:3498974 | C | G | 3 | a0001c0001t0003g0002 a0001c0001t0003g0224 a0001c0001t0003g0225 |
4 | HG01256.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+7274C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498974 | |||||||
chr12:3499041 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.75+7341T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499041 | |||||||
chr12:3499159 | A | AT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(56): Show |
60 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.75+7464dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499159 | ||||||
chr12:3499165 | A | T | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+7465A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499165 | |||||||
chr12:3499177 | A | AT | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(47): Show |
50 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.75+7487dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499177 | ||||||
chr12:3499177 | ATT | A | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+7486_75+7487del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499177 | ||||||
chr12:3499181 | T | A | 9 | a0001c0001t0001g0039 a0001c0001t0001g0095 a0001c0001t0001g0192 others(6): Show |
9 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+7481T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499181 | |||||||
chr12:3499193 | CT | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): Show |
75 | HG00099.hp1 HG00558.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.75+7508delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499193 | ||||||
chr12:3499193 | CTT | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0075 others(16): Show |
20 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.75+7507_75+7508del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499193 | ||||||
chr12:3499215 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
53 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.75+7515C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499215 | |||||||
chr12:3499346 | C | A | 2 | a0001c0001t0001g0343 a0001c0001t0001g0345 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.75+7646C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499346 | |||||||
chr12:3499354 | G | A | 72 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.75+7654G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499354 | |||||||
chr12:3499377 | G | A | 13 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(10): Show |
13 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+7677G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499377 | |||||||
chr12:3499399 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0002t0002g0325 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+7699C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499399 | |||||||
chr12:3499450 | A | T | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+7750A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499450 | |||||||
chr12:3499683 | C | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0298 a0001c0001t0001g0304 |
3 | NA18612.hp2 NA18979.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.75+7983C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499683 | |||||||
chr12:3500016 | A | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(9): Show |
12 | HG00597.hp2 NA18939.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+8316A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500016 | |||||||
chr12:3500024 | C | T | 81 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(78): Show |
82 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.75+8324C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500024 | |||||||
chr12:3500025 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00733.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.75+8325G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500025 | |||||||
chr12:3500122 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
53 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.75+8422C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500122 | |||||||
chr12:3500136 | C | T | 82 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(79): Show |
83 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.75+8436C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500136 | |||||||
chr12:3500141 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+8441T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500141 | |||||||
chr12:3500238 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18980.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.75+8538A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500238 | |||||||
chr12:3500258 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.75+8558C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500258 | |||||||
chr12:3500345 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.75+8645A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500345 | |||||||
chr12:3500408 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(12): Show |
16 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+8708T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500408 | |||||||
chr12:3500414 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.75+8714T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500414 | |||||||
chr12:3500516 | C | T | 1 | a0001c0001t0006g0328 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.75+8816C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500516 | |||||||
chr12:3500517 | G | A | 71 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.75+8817G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500517 | |||||||
chr12:3500518 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0002t0002g0325 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+8818G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500518 | |||||||
chr12:3500723 | C | G | 6 | a0001c0001t0001g0332 a0001c0001t0012g0087 a0001c0004t0001g0329 others(3): Show |
6 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+9023C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500723 | |||||||
chr12:3500945 | T | G | 6 | a0001c0001t0001g0332 a0001c0001t0012g0087 a0001c0004t0001g0329 others(3): Show |
6 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+9245T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500945 | |||||||
chr12:3500980 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+9280C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500980 | |||||||
chr12:3501059 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.75+9359G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501059 | |||||||
chr12:3501107 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.75+9407G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501107 | |||||||
chr12:3501137 | G | C | 8 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(5): Show |
8 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+9437G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501137 | |||||||
chr12:3501206 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(25): Show |
29 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+9506G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501206 | |||||||
chr12:3501248 | C | T | 6 | a0001c0001t0001g0038 a0001c0001t0001g0111 a0001c0001t0001g0125 others(3): Show |
6 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+9548C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501248 | |||||||
chr12:3501249 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.75+9549G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501249 | |||||||
chr12:3501368 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0002t0002g0325 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+9668C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501368 | |||||||
chr12:3501538 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+9838C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501538 | |||||||
chr12:3501596 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
53 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.75+9896G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501596 | |||||||
chr12:3501671 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75+9971T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501671 | |||||||
chr12:3501683 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01952.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.75+9983C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501683 | |||||||
chr12:3501693 | G | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+9993G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501693 | |||||||
chr12:3501744 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
131 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.75+10044C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501744 | |||||||
chr12:3501951 | G | T | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10251G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501951 | |||||||
chr12:3501958 | T | C | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10258T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501958 | |||||||
chr12:3502026 | T | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0057 others(26): Show |
30 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.75+10326T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502026 | |||||||
chr12:3502036 | C | T | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10336C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502036 | |||||||
chr12:3502069 | T | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0276 a0001c0001t0001g0279 others(53): Show |
56 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.75+10369T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502069 | |||||||
chr12:3502150 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.75+10450A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502150 | |||||||
chr12:3502282 | A | C | 1 | a0001c0001t0001g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75+10582A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502282 | |||||||
chr12:3502336 | T | G | 3 | a0001c0001t0001g0322 a0001c0001t0007g0323 a0001c0002t0011g0101 |
3 | HG02895.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+10636T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502336 | |||||||
chr12:3502397 | G | T | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10697G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502397 | |||||||
chr12:3502411 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+10711C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502411 | |||||||
chr12:3502412 | G | A | 6 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+10712G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502412 | |||||||
chr12:3502428 | A | G | 1 | a0001c0001t0001g0362 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.75+10728A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502428 | |||||||
chr12:3502543 | T | C | 2 | a0001c0001t0001g0076 a0001c0002t0002g0080 |
2 | NA18942.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.75+10843T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502543 | |||||||
chr12:3502570 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0002t0002g0325 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+10870T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502570 | |||||||
chr12:3502584 | G | C | 1 | a0001c0001t0007g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.75+10884G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502584 | |||||||
chr12:3502609 | C | T | 2 | a0001c0001t0002g0129 a0001c0002t0002g0150 |
2 | HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.75+10909C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502609 | |||||||
chr12:3502718 | T | C | 2 | a0001c0001t0001g0132 a0001c0002t0002g0133 |
2 | HG01070.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.75+11018T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502718 | |||||||
chr12:3502823 | T | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+11123T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502823 | |||||||
chr12:3502856 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.75+11156G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502856 | |||||||
chr12:3502954 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75+11254A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502954 | |||||||
chr12:3503037 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.75+11337T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503037 | |||||||
chr12:3503102 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+11402C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503102 | |||||||
chr12:3503103 | G | A | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+11403G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503103 | |||||||
chr12:3503156 | A | C | 5 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(2): Show |
5 | HG00597.hp2 NA18942.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+11456A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503156 | |||||||
chr12:3503183 | A | G | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+11483A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503183 | |||||||
chr12:3503297 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
51 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.75+11597C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503297 | |||||||
chr12:3503397 | G | A | 2 | a0001c0001t0004g0007 a0001c0001t0004g0008 |
2 | NA18968.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.75+11697G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503397 | |||||||
chr12:3503562 | A | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+11862A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503562 | |||||||
chr12:3503591 | T | C | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+11891T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503591 | |||||||
chr12:3503598 | A | T | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+11898A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503598 | |||||||
chr12:3503608 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.75+11908G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503608 | |||||||
chr12:3503670 | A | G | 62 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.75+11970A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503670 | |||||||
chr12:3503848 | G | A | 5 | a0001c0001t0001g0332 a0001c0004t0001g0329 a0001c0004t0001g0330 others(2): Show |
5 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+12148G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503848 | |||||||
chr12:3503900 | T | G | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+12200T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503900 | |||||||
chr12:3503935 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0255 a0001c0002t0011g0101 |
3 | HG00733.hp2 HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.75+12235G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503935 | |||||||
chr12:3503961 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+12261A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503961 | |||||||
chr12:3503989 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.75+12289C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503989 | |||||||
chr12:3503990 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0276 a0001c0001t0001g0279 others(52): Show |
55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+12290G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503990 | |||||||
chr12:3503993 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0276 a0001c0001t0001g0279 others(52): Show |
55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+12293T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503993 | |||||||
chr12:3503994 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.75+12294C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503994 | |||||||
chr12:3503995 | G | A | 3 | a0001c0001t0001g0239 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG02040.hp1 HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.75+12295G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503995 | |||||||
chr12:3504097 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+12397A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504097 | |||||||
chr12:3504157 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+12457G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504157 | |||||||
chr12:3504178 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+12478G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504178 | |||||||
chr12:3504233 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+12533T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504233 | |||||||
chr12:3504248 | A | G | 84 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(81): Show |
85 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.75+12548A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504248 | |||||||
chr12:3504273 | A | G | 82 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(79): Show |
83 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.75+12573A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504273 | |||||||
chr12:3504361 | G | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+12661G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504361 | |||||||
chr12:3504379 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0221 a0001c0001t0001g0242 others(4): Show |
7 | HG02055.hp1 HG02056.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+12679C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504379 | |||||||
chr12:3504385 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0195 a0001c0001t0001g0221 others(5): Show |
8 | HG02055.hp1 HG02056.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+12685A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504385 | |||||||
chr12:3504399 | G | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0195 a0001c0001t0001g0221 others(3): Show |
6 | HG02055.hp1 HG02056.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+12699G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504399 | |||||||
chr12:3504401 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.75+12701T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504401 | |||||||
chr12:3504412 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.75+12712C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504412 | |||||||
chr12:3504434 | G | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0267 |
2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.75+12734G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504434 | |||||||
chr12:3504441 | G | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0047 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+12741G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504441 | |||||||
chr12:3504443 | C | G | 12 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0047 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+12743C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504443 | |||||||
chr12:3504446 | C | T | 99 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0044 others(96): Show |
100 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.75+12746C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504446 | |||||||
chr12:3504451 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0248 a0001c0001t0001g0357 others(1): Show |
4 | HG01884.hp1 HG02056.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+12751A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504451 | |||||||
chr12:3504455 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0248 |
2 | HG02056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12755C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504455 | |||||||
chr12:3504456 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0248 |
2 | HG02056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12756C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504456 | |||||||
chr12:3504457 | T | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0248 |
2 | HG02056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12757T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504457 | |||||||
chr12:3504460 | C | T | 2 | a0001c0001t0001g0357 a0001c0001t0001g0361 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.75+12760C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504460 | |||||||
chr12:3504461 | G | C | 1 | a0001c0001t0001g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.75+12761G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504461 | |||||||
chr12:3504476 | G | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0231 a0001c0001t0001g0321 |
3 | HG01169.hp1 NA18997.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12776G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504476 | |||||||
chr12:3504478 | G | A | 1 | a0001c0005t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+12778G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504478 | |||||||
chr12:3504485 | G | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.75+12785G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504485 | |||||||
chr12:3504487 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.75+12787G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504487 | |||||||
chr12:3504493 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.75+12793T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504493 | |||||||
chr12:3504514 | G | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+12814G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504514 | |||||||
chr12:3504540 | G | A | 2 | a0001c0001t0001g0357 a0001c0001t0001g0361 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.75+12840G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504540 | |||||||
chr12:3504556 | C | G | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+12856C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504556 | |||||||
chr12:3504574 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0108 a0001c0001t0001g0114 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+12874T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504574 | |||||||
chr12:3504576 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0059 others(10): Show |
13 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+12876T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504576 | |||||||
chr12:3504577 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.75+12877G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504577 | |||||||
chr12:3504592 | C | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0036 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+12892C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504592 | |||||||
chr12:3504616 | A | T | 71 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.75+12916A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504616 | |||||||
chr12:3504623 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0114 |
3 | HG01069.hp2 HG01071.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.75+12923C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504623 | |||||||
chr12:3504653 | T | C | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+12953T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504653 | |||||||
chr12:3504671 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.75+12971C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504671 | |||||||
chr12:3504721 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0002g0246 |
2 | HG02083.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.75+13021G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504721 | |||||||
chr12:3504728 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.75+13028A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504728 | |||||||
chr12:3504745 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.75+13045C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504745 | |||||||
chr12:3504746 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.75+13046G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504746 | |||||||
chr12:3504765 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0134 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13065G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504765 | |||||||
chr12:3504772 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0005t0001g0193 |
3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13072T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504772 | |||||||
chr12:3504777 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.75+13077A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504777 | |||||||
chr12:3504783 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.75+13083G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504783 | |||||||
chr12:3504783 | G | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0005t0001g0193 |
3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13083G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504783 | |||||||
chr12:3504786 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.75+13086C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504786 | |||||||
chr12:3504805 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0131 a0001c0001t0001g0134 others(2): Show |
5 | HG01099.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+13105T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504805 | |||||||
chr12:3504809 | C | G | 2 | a0001c0001t0001g0067 a0001c0002t0002g0065 |
2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.75+13109C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504809 | |||||||
chr12:3504855 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0005t0001g0193 |
3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13155T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504855 | |||||||
chr12:3504876 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0005t0001g0193 |
3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13176T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504876 | |||||||
chr12:3504891 | A | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0276 a0001c0001t0001g0279 others(50): Show |
53 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.75+13191A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504891 | |||||||
chr12:3504901 | G | A | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+13201G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504901 | |||||||
chr12:3504915 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0005t0001g0193 |
3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13215C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504915 | |||||||
chr12:3504922 | C | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+13222C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504922 | |||||||
chr12:3504961 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0005t0001g0193 |
3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13261T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504961 | |||||||
chr12:3504977 | G | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
14 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+13277G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504977 | |||||||
chr12:3505056 | C | T | 2 | a0001c0001t0001g0126 a0001c0002t0002g0115 |
2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.75+13356C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505056 | |||||||
chr12:3505067 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+13367C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505067 | |||||||
chr12:3505334 | C | T | 1 | a0001c0004t0001g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.75+13634C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505334 | |||||||
chr12:3505389 | C | T | 82 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(79): Show |
83 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.75+13689C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505389 | |||||||
chr12:3505390 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+13690G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505390 | |||||||
chr12:3505403 | C | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0130 others(5): Show |
8 | HG02523.hp2 NA18959.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+13703C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505403 | |||||||
chr12:3505601 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(64): Show |
68 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.75+13901G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505601 | |||||||
chr12:3505653 | A | G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
9 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+13953A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505653 | |||||||
chr12:3505911 | C | T | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+14211C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505911 | |||||||
chr12:3505998 | G | A | 14 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(11): Show |
14 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+14298G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505998 | |||||||
chr12:3506013 | A | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+14313A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506013 | |||||||
chr12:3506039 | G | T | 3 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0002t0002g0265 |
3 | NA18967.hp2 NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.75+14339G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506039 | |||||||
chr12:3506398 | C | T | 7 | a0001c0001t0001g0332 a0001c0001t0012g0087 a0001c0002t0002g0086 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+14698C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506398 | |||||||
chr12:3506489 | T | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+14789T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506489 | |||||||
chr12:3506725 | G | T | 1 | a0001c0001t0010g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+15025G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506725 | |||||||
chr12:3506902 | T | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+15202T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506902 | |||||||
chr12:3506931 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.75+15231A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506931 | |||||||
chr12:3506981 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | NA18939.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.75+15281G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506981 | |||||||
chr12:3507118 | C | CT | 32 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0038 others(29): Show |
32 | HG02129.hp1 HG02257.hp2 HG02273.hp2 others(29): Show |
intron_variant | MODIFIER | c.75+15439dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507118 | ||||||
chr12:3507118 | CT | C | 18 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(15): Show |
18 | HG00642.hp1 HG01169.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+15439delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507118 | ||||||
chr12:3507182 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+15482C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507182 | |||||||
chr12:3507314 | C | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
70 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.75+15614C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507314 | |||||||
chr12:3507367 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75+15667C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507367 | |||||||
chr12:3507446 | C | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0002t0002g0325 others(1): Show |
4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+15746C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507446 | |||||||
chr12:3507613 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+15913G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507613 | |||||||
chr12:3507644 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.75+15944C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507644 | |||||||
chr12:3507646 | C | T | 9 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0146 others(6): Show |
9 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+15946C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507646 | |||||||
chr12:3507758 | C | CT | 16 | a0001c0001t0001g0095 a0001c0001t0001g0112 a0001c0001t0001g0113 others(13): Show |
16 | HG02258.hp1 HG02258.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+16076dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507758 | ||||||
chr12:3507758 | CT | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
40 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.75+16076delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507758 | ||||||
chr12:3507804 | G | A | 3 | a0001c0001t0001g0307 a0001c0001t0001g0309 a0001c0002t0002g0310 |
3 | HG00673.hp1 HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.75+16104G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507804 | |||||||
chr12:3507819 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(73): Show |
77 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.75+16119T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507819 | |||||||
chr12:3507962 | C | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0002t0002g0063 |
3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+16262C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507962 | |||||||
chr12:3508145 | A | AT | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+16452dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3508145 | ||||||
chr12:3508149 | T | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(12): Show |
16 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+16449T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508149 | |||||||
chr12:3508300 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.75+16600C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508300 | |||||||
chr12:3508311 | C | A | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+16611C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508311 | |||||||
chr12:3508321 | G | A | 1 | a0001c0001t0003g0224 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.75+16621G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508321 | |||||||
chr12:3508380 | T | C | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+16680T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508380 | |||||||
chr12:3508458 | G | A | 12 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(9): Show |
12 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+16758G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508458 | |||||||
chr12:3508473 | T | G | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+16773T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508473 | |||||||
chr12:3508566 | T | A | 12 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(9): Show |
12 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+16866T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508566 | |||||||
chr12:3508683 | C | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.75+16983C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508683 | |||||||
chr12:3509058 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75+17358C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509058 | |||||||
chr12:3509103 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(60): Show |
64 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.75+17403A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509103 | |||||||
chr12:3509129 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.75+17429G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509129 | |||||||
chr12:3509199 | G | A | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+17499G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509199 | |||||||
chr12:3509302 | T | C | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+17602T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509302 | |||||||
chr12:3509519 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+17819A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509519 | |||||||
chr12:3509681 | G | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0003t0001g0277 |
3 | NA18967.hp1 NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.75+17981G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509681 | |||||||
chr12:3509784 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.75+18084G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509784 | |||||||
chr12:3509876 | A | G | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(4): Show |
7 | HG02071.hp1 HG02735.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+18176A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509876 | |||||||
chr12:3509941 | G | A | 1 | a0001c0002t0002g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.75+18241G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509941 | |||||||
chr12:3510023 | C | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0276 a0001c0001t0001g0279 others(49): Show |
52 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.75+18323C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510023 | |||||||
chr12:3510098 | T | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+18398T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510098 | |||||||
chr12:3510103 | G | T | 70 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.75+18403G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510103 | |||||||
chr12:3510372 | A | G | 23 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(20): Show |
23 | HG00280.hp2 HG01069.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+18672A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510372 | |||||||
chr12:3510433 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0019 others(1): Show |
4 | HG00558.hp2 HG02027.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+18733A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510433 | |||||||
chr12:3510580 | C | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.75+18880C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510580 | |||||||
chr12:3510758 | C | T | 2 | a0001c0002t0002g0325 a0001c0005t0001g0324 |
2 | HG01346.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.75+19058C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510758 | |||||||
chr12:3511048 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+19348C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511048 | |||||||
chr12:3511322 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.75+19622G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511322 | |||||||
chr12:3511759 | C | A | 37 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(34): Show |
37 | HG00280.hp2 HG01069.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+20059C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511759 | |||||||
chr12:3511849 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 |
3 | HG01192.hp1 HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.75+20149A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511849 | |||||||
chr12:3511867 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0007g0323 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+20167C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511867 | |||||||
chr12:3512006 | C | G | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+20306C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512006 | |||||||
chr12:3512009 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0151 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.75+20309G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512009 | |||||||
chr12:3512054 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+20354A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512054 | |||||||
chr12:3512185 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.75+20485G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512185 | |||||||
chr12:3512326 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01952.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.75+20626T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512326 | |||||||
chr12:3512536 | T | C | 1 | a0001c0004t0001g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.75+20836T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512536 | |||||||
chr12:3512576 | C | G | 10 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+20876C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512576 | |||||||
chr12:3512722 | C | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21022C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512722 | |||||||
chr12:3512803 | G | A | 12 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(9): Show |
12 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+21103G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512803 | |||||||
chr12:3512819 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+21119T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512819 | |||||||
chr12:3512892 | A | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21192A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512892 | |||||||
chr12:3513058 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.75+21358C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513058 | |||||||
chr12:3513098 | G | A | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+21398G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513098 | |||||||
chr12:3513104 | C | A | 5 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0159 others(2): Show |
5 | NA18940.hp2 NA18949.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+21404C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513104 | |||||||
chr12:3513168 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0256 |
2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.75+21468G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513168 | |||||||
chr12:3513231 | C | G | 78 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(75): Show |
79 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.75+21531C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513231 | |||||||
chr12:3513348 | G | T | 7 | a0001c0001t0001g0332 a0001c0001t0012g0087 a0001c0002t0002g0086 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21648G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513348 | |||||||
chr12:3513350 | T | A | 7 | a0001c0001t0001g0332 a0001c0001t0012g0087 a0001c0002t0002g0086 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21650T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513350 | |||||||
chr12:3513444 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.75+21744G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513444 | |||||||
chr12:3513558 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG00597.hp2 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.75+21858T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513558 | |||||||
chr12:3513610 | G | A | 12 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0062 others(9): Show |
12 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+21910G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513610 | |||||||
chr12:3513634 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+21934A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513634 | |||||||
chr12:3513651 | G | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21951G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513651 | |||||||
chr12:3513993 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
51 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.75+22293T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513993 | |||||||
chr12:3514124 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22424G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514124 | |||||||
chr12:3514211 | C | CT | 8 | a0001c0001t0001g0070 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG00735.hp1 HG00735.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+22525dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3514211 | ||||||
chr12:3514211 | C | CTTT | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(41): Show |
45 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.75+22523_75+22525d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3514211 | ||||||
chr12:3514211 | CT | C | 6 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+22525delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3514211 | ||||||
chr12:3514222 | T | C | 1 | a0001c0001t0008g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.75+22522T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514222 | |||||||
chr12:3514298 | C | T | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+22598C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514298 | |||||||
chr12:3514389 | G | A | 8 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0130 others(5): Show |
8 | HG02523.hp2 NA18959.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+22689G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514389 | |||||||
chr12:3514406 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.75+22706G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514406 | |||||||
chr12:3514429 | G | A | 7 | a0001c0001t0001g0332 a0001c0001t0012g0087 a0001c0002t0002g0086 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+22729G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514429 | |||||||
chr12:3514508 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22808G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514508 | |||||||
chr12:3514510 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.75+22810T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514510 | |||||||
chr12:3514518 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22818C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514518 | |||||||
chr12:3514547 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22847G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514547 | |||||||
chr12:3514673 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0327 a0001c0001t0006g0328 |
3 | HG02723.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+22973T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514673 | |||||||
chr12:3514678 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22978G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514678 | |||||||
chr12:3514776 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18980.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.75+23076C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514776 | |||||||
chr12:3514792 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75+23092C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514792 | |||||||
chr12:3514807 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23107G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514807 | |||||||
chr12:3514968 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23268G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514968 | |||||||
chr12:3515006 | C | T | 12 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0062 others(9): Show |
12 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+23306C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515006 | |||||||
chr12:3515018 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75+23318C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515018 | |||||||
chr12:3515041 | T | TA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23348dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3515041 | ||||||
chr12:3515102 | A | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+23402A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515102 | |||||||
chr12:3515140 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.75+23440A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515140 | |||||||
chr12:3515158 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23458C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515158 | |||||||
chr12:3515191 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+23491G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515191 | |||||||
chr12:3515244 | T | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+23544T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515244 | |||||||
chr12:3515342 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23642A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515342 | |||||||
chr12:3515506 | A | G | 3 | a0001c0001t0001g0244 a0001c0001t0003g0243 a0001c0001t0003g0245 |
3 | HG01167.hp1 HG01169.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.75+23806A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515506 | |||||||
chr12:3515589 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.75+23889C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515589 | |||||||
chr12:3515590 | G | A | 7 | a0001c0001t0001g0332 a0001c0001t0012g0087 a0001c0002t0002g0086 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+23890G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515590 | |||||||
chr12:3515591 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0003g0243 a0001c0001t0003g0245 |
3 | HG01167.hp1 HG01169.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.75+23891G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515591 | |||||||
chr12:3515640 | C | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+23940C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515640 | |||||||
chr12:3515652 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23952A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515652 | |||||||
chr12:3515698 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23998T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515698 | |||||||
chr12:3515755 | G | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+24055G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515755 | |||||||
chr12:3515787 | G | A | 8 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(5): Show |
8 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+24087G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515787 | |||||||
chr12:3515879 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+24179C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515879 | |||||||
chr12:3515931 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.75+24231T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515931 | |||||||
chr12:3516007 | T | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.75+24307T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516007 | |||||||
chr12:3516198 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0023 |
2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.76-24408G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516198 | |||||||
chr12:3516295 | T | C | 1 | a0001c0002t0002g0206 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-24311T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516295 | |||||||
chr12:3516315 | GTTCA | G | 9 | a0001c0001t0001g0095 a0001c0001t0001g0111 a0001c0001t0001g0158 others(6): Show |
9 | HG00423.hp1 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-24267_76-24264d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3516315 | ||||||
chr12:3516315 | GTTCATTC others(1): Show |
G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0130 others(5): Show |
8 | HG02523.hp2 NA18959.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-24271_76-24264d others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3516315 | ||||||
chr12:3516315 | GTTCATTC others(5): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.76-24275_76-24264d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3516315 | ||||||
chr12:3516612 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-23994G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516612 | |||||||
chr12:3516762 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.76-23844G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516762 | |||||||
chr12:3517159 | G | T | 4 | a0001c0001t0001g0332 a0001c0004t0001g0329 a0001c0004t0001g0330 others(1): Show |
4 | HG00642.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-23447G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517159 | |||||||
chr12:3517222 | A | G | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-23384A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517222 | |||||||
chr12:3517240 | G | A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0225 |
3 | HG01256.hp2 HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.76-23366G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517240 | |||||||
chr12:3517330 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.76-23276G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517330 | |||||||
chr12:3517356 | G | A | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-23250G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517356 | |||||||
chr12:3517560 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0146 others(6): Show |
9 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-23046G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517560 | |||||||
chr12:3517595 | C | T | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-23011C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517595 | |||||||
chr12:3517933 | C | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0075 others(15): Show |
19 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-22673C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517933 | |||||||
chr12:3518077 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(68): Show |
72 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.76-22529G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518077 | |||||||
chr12:3518113 | C | T | 12 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0062 others(9): Show |
12 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-22493C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518113 | |||||||
chr12:3518130 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-22476C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518130 | |||||||
chr12:3518170 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-22436G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518170 | |||||||
chr12:3518189 | G | T | 1 | a0001c0001t0013g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.76-22417G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518189 | |||||||
chr12:3518237 | T | C | 6 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-22369T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518237 | |||||||
chr12:3518285 | C | A | 283 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0024 others(280): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.76-22321C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518285 | |||||||
chr12:3518397 | C | CT | 19 | a0001c0001t0001g0033 a0001c0001t0001g0098 a0001c0001t0001g0111 others(16): Show |
19 | HG01099.hp2 HG01169.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-22197dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518397 | ||||||
chr12:3518397 | C | CTT | 188 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(185): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.76-22198_76-22197d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518397 | ||||||
chr12:3518397 | C | CTTT | 9 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0106 others(6): Show |
9 | HG02818.hp1 HG02922.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-22199_76-22197d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518397 | ||||||
chr12:3518400 | T | G | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.76-22206T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518400 | |||||||
chr12:3518409 | T | TTA | 68 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.76-22197_76-22196i others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518409 | |||||||
chr12:3518410 | A | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0049 others(4): Show |
7 | HG01069.hp1 HG01515.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-22196A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518410 | |||||||
chr12:3518427 | T | C | 285 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0024 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.76-22179T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518427 | |||||||
chr12:3518476 | C | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.76-22130C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518476 | |||||||
chr12:3518483 | T | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.76-22123T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518483 | |||||||
chr12:3518509 | C | G | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-22097C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518509 | |||||||
chr12:3518667 | G | A | 2 | a0001c0001t0001g0033 a0001c0002t0009g0034 |
2 | HG01069.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.76-21939G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518667 | |||||||
chr12:3518835 | G | A | 291 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0024 others(288): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.76-21771G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518835 | |||||||
chr12:3518992 | GA | G | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0127 others(5): Show |
8 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-21607delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518992 | ||||||
chr12:3519012 | A | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0272 others(2): Show |
5 | HG01346.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-21594A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519012 | |||||||
chr12:3519138 | A | T | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.76-21468A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519138 | |||||||
chr12:3519307 | T | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0194 others(55): Show |
58 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.76-21299T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519307 | |||||||
chr12:3519399 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0019 others(1): Show |
4 | HG00558.hp2 HG02027.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-21207T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519399 | |||||||
chr12:3519403 | G | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-21203G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519403 | |||||||
chr12:3519480 | T | C | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-21126T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519480 | |||||||
chr12:3519540 | T | C | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-21066T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519540 | |||||||
chr12:3519639 | T | C | 7 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0146 others(4): Show |
7 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-20967T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519639 | |||||||
chr12:3519765 | G | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0254 |
2 | NA19066.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.76-20841G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519765 | |||||||
chr12:3519795 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76-20811G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519795 | |||||||
chr12:3520020 | T | A | 7 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-20586T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520020 | |||||||
chr12:3520083 | C | G | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-20523C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520083 | |||||||
chr12:3520110 | C | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0120 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-20496C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520110 | |||||||
chr12:3520163 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.76-20443G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520163 | |||||||
chr12:3520200 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-20406G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520200 | |||||||
chr12:3520200 | G | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0197 others(53): Show |
56 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.76-20406G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520200 | |||||||
chr12:3520203 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-20403G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520203 | |||||||
chr12:3520246 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.76-20360A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520246 | |||||||
chr12:3520247 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.76-20359C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520247 | |||||||
chr12:3520248 | G | A | 84 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.76-20358G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520248 | |||||||
chr12:3520509 | A | G | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-20097A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520509 | |||||||
chr12:3520680 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.76-19926A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520680 | |||||||
chr12:3520712 | A | G | 1 | a0001c0002t0002g0296 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.76-19894A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520712 | |||||||
chr12:3520757 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0120 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-19849G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520757 | |||||||
chr12:3520899 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.76-19707T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520899 | |||||||
chr12:3520913 | G | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.76-19693G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520913 | |||||||
chr12:3521180 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-19426G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521180 | |||||||
chr12:3521267 | A | T | 1 | a0001c0001t0001g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.76-19339A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521267 | |||||||
chr12:3521340 | G | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0039 others(4): Show |
7 | HG00280.hp1 HG02698.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-19266G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521340 | |||||||
chr12:3521348 | C | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0104 others(59): Show |
63 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.76-19258C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521348 | |||||||
chr12:3521349 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.76-19257G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521349 | |||||||
chr12:3521371 | C | T | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02165.hp2 NA18949.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-19235C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521371 | |||||||
chr12:3521389 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19217C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521389 | |||||||
chr12:3521390 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19216A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521390 | |||||||
chr12:3521400 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19206C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521400 | |||||||
chr12:3521401 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19205C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521401 | |||||||
chr12:3521402 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19204C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521402 | |||||||
chr12:3521448 | C | T | 1 | a0001c0002t0002g0282 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.76-19158C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521448 | |||||||
chr12:3521492 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0148 |
2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.76-19114T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521492 | |||||||
chr12:3521575 | A | C | 2 | a0001c0002t0002g0086 a0001c0002t0002g0325 |
2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.76-19031A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521575 | |||||||
chr12:3521607 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0120 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-18999G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521607 | |||||||
chr12:3521676 | G | T | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0233 others(2): Show |
5 | NA18951.hp1 NA18965.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-18930G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521676 | |||||||
chr12:3521833 | A | G | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-18773A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521833 | |||||||
chr12:3521931 | TA | T | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.76-18673delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3521931 | ||||||
chr12:3521947 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0120 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-18659A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521947 | |||||||
chr12:3522128 | GC | G | 75 | a0001c0001t0001g0036 a0001c0001t0001g0096 a0001c0001t0001g0098 others(72): Show |
75 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.76-18473delC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522128 | ||||||
chr12:3522202 | C | A | 82 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.76-18404C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522202 | |||||||
chr12:3522233 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.76-18373A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522233 | |||||||
chr12:3522265 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.76-18341C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522265 | |||||||
chr12:3522405 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
17 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-18201C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522405 | |||||||
chr12:3522449 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.76-18157A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522449 | |||||||
chr12:3522479 | G | T | 3 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0002t0002g0265 |
3 | NA18967.hp2 NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.76-18127G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522479 | |||||||
chr12:3522596 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.76-18010G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522596 | |||||||
chr12:3522648 | TA | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(315): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.76-17938delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522648 | ||||||
chr12:3522648 | TAA | T | 26 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0090 others(23): Show |
26 | HG00733.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.76-17939_76-17938d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522648 | ||||||
chr12:3522662 | A | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0118 others(3): Show |
6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-17944A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522662 | |||||||
chr12:3522665 | A | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.76-17941A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522665 | |||||||
chr12:3522726 | G | A | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG02523.hp2 HG02976.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-17880G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522726 | |||||||
chr12:3522778 | AAAAC | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0207 a0001c0005t0001g0193 |
3 | HG00280.hp1 HG02559.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.76-17816_76-17813d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522778 | ||||||
chr12:3522790 | C | CA | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-17810dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522790 | ||||||
chr12:3522793 | AAAAC | A | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-17801_76-17798d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522793 | ||||||
chr12:3522801 | C | CA | 5 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0118 others(2): Show |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-17802dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522801 | ||||||
chr12:3522805 | C | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0118 others(3): Show |
6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-17801C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522805 | |||||||
chr12:3522805 | CA | C | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG02523.hp2 HG02976.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-17792delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522805 | ||||||
chr12:3522926 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-17680C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522926 | |||||||
chr12:3522944 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.76-17662C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522944 | |||||||
chr12:3523007 | GA | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.76-17589delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3523007 | ||||||
chr12:3523369 | T | C | 81 | a0001c0001t0001g0036 a0001c0001t0001g0096 a0001c0001t0001g0098 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.76-17237T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523369 | |||||||
chr12:3523436 | G | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-17170G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523436 | |||||||
chr12:3523556 | A | T | 1 | a0001c0001t0001g0341 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.76-17050A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523556 | |||||||
chr12:3523797 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0112 others(9): Show |
12 | HG02523.hp2 HG02630.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-16809T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523797 | |||||||
chr12:3523880 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.76-16726G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523880 | |||||||
chr12:3524332 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-16274C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524332 | |||||||
chr12:3524642 | T | TA | 17 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(14): Show |
17 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-15944dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3524642 | ||||||
chr12:3524642 | TA | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(135): Show |
139 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.76-15944delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3524642 | ||||||
chr12:3524678 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-15928A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524678 | |||||||
chr12:3524712 | G | A | 1 | a0001c0001t0001g0352 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.76-15894G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524712 | |||||||
chr12:3524960 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0104 others(4): Show |
7 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-15646T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524960 | |||||||
chr12:3525076 | G | C | 17 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
17 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-15530G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525076 | |||||||
chr12:3525117 | G | A | 1 | a0001c0002t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.76-15489G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525117 | |||||||
chr12:3525165 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-15441T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525165 | |||||||
chr12:3525522 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.76-15084A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525522 | |||||||
chr12:3525805 | A | C | 12 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(9): Show |
12 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-14801A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525805 | |||||||
chr12:3525908 | A | T | 1 | a0001c0001t0001g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76-14698A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525908 | |||||||
chr12:3525926 | A | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0067 others(96): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.76-14680A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525926 | |||||||
chr12:3526491 | G | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-14115G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526491 | |||||||
chr12:3526513 | T | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0130 a0001c0001t0001g0207 others(1): Show |
4 | NA18747.hp1 NA18959.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-14093T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526513 | |||||||
chr12:3526515 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-14091C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526515 | |||||||
chr12:3526565 | T | C | 24 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0102 others(21): Show |
24 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-14041T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526565 | |||||||
chr12:3526616 | T | C | 2 | a0001c0001t0002g0334 a0001c0002t0002g0335 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.76-13990T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526616 | |||||||
chr12:3526743 | C | A | 2 | a0001c0001t0001g0088 a0001c0001t0007g0089 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-13863C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526743 | |||||||
chr12:3526919 | A | G | 7 | a0001c0001t0001g0069 a0001c0001t0001g0097 a0001c0001t0001g0136 others(4): Show |
7 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-13687A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526919 | |||||||
chr12:3526921 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.76-13685T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526921 | |||||||
chr12:3526958 | A | C | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-13648A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526958 | |||||||
chr12:3526994 | G | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0149 others(2): Show |
5 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-13612G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526994 | |||||||
chr12:3527335 | G | GGCGGGCA others(13): Show |
1 | a0001c0002t0002g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-13269_76-13250d others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3527335 | ||||||
chr12:3527350 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-13256C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3527350 | |||||||
chr12:3527475 | G | A | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-13131G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3527475 | |||||||
chr12:3527565 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.76-13041T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3527565 | |||||||
chr12:3528062 | C | T | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-12544C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528062 | |||||||
chr12:3528195 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.76-12411T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528195 | |||||||
chr12:3528231 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0006 |
3 | HG01257.hp2 HG01258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.76-12375C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528231 | |||||||
chr12:3528232 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-12374G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528232 | |||||||
chr12:3528284 | G | A | 80 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(77): Show |
80 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.76-12322G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528284 | |||||||
chr12:3528499 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-12107C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528499 | |||||||
chr12:3528501 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.76-12105G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528501 | |||||||
chr12:3528503 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.76-12103C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528503 | |||||||
chr12:3528633 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(13): Show |
17 | HG00597.hp2 HG00733.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-11973G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528633 | |||||||
chr12:3528653 | AT | A | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-11945delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3528653 | ||||||
chr12:3528679 | T | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0002t0002g0063 |
3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-11927T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528679 | |||||||
chr12:3528706 | AT | A | 11 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG02523.hp2 HG02976.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-11895delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3528706 | ||||||
chr12:3528852 | T | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0102 others(21): Show |
24 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-11754T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528852 | |||||||
chr12:3529114 | C | G | 12 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(9): Show |
12 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-11492C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529114 | |||||||
chr12:3529153 | C | G | 5 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(2): Show |
5 | HG00597.hp2 NA18942.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-11453C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529153 | |||||||
chr12:3529251 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.76-11355C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529251 | |||||||
chr12:3529267 | TGG | T | 6 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-11336_76-11335d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3529267 | ||||||
chr12:3529352 | C | G | 75 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(72): Show |
75 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.76-11254C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529352 | |||||||
chr12:3529362 | C | A | 2 | a0001c0001t0004g0007 a0001c0001t0004g0008 |
2 | NA18968.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.76-11244C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529362 | |||||||
chr12:3529396 | G | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-11210G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529396 | |||||||
chr12:3529835 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.76-10771A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529835 | |||||||
chr12:3529836 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.76-10770C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529836 | |||||||
chr12:3529849 | A | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0149 others(2): Show |
5 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-10757A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529849 | |||||||
chr12:3529849 | A | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-10757A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529849 | |||||||
chr12:3529919 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.76-10687C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529919 | |||||||
chr12:3529922 | G | A | 11 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG02523.hp2 HG02976.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-10684G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529922 | |||||||
chr12:3529988 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-10618T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529988 | |||||||
chr12:3530393 | G | T | 1 | a0001c0002t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-10213G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530393 | |||||||
chr12:3530591 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0112 others(9): Show |
12 | HG02523.hp2 HG02630.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-10015A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530591 | |||||||
chr12:3530643 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-9963C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530643 | |||||||
chr12:3530683 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.76-9923G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530683 | |||||||
chr12:3530743 | C | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0067 others(101): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.76-9863C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530743 | |||||||
chr12:3530774 | C | T | 6 | a0001c0001t0001g0300 a0001c0001t0001g0317 a0001c0001t0001g0318 others(3): Show |
7 | HG00639.hp2 HG01074.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-9832C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530774 | |||||||
chr12:3530798 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0272 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-9808G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530798 | |||||||
chr12:3530898 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-9708C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530898 | |||||||
chr12:3531128 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(14): Show |
18 | HG00597.hp2 HG00733.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-9478C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531128 | |||||||
chr12:3531175 | G | GT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0102 others(22): Show |
25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-9430dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3531175 | ||||||
chr12:3531187 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0006g0328 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.76-9419A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531187 | |||||||
chr12:3531324 | A | T | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-9282A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531324 | |||||||
chr12:3531572 | G | T | 1 | a0001c0002t0002g0206 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-9034G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531572 | |||||||
chr12:3531582 | A | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0102 others(23): Show |
26 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.76-9024A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531582 | |||||||
chr12:3531648 | T | C | 25 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0102 others(22): Show |
25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-8958T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531648 | |||||||
chr12:3531674 | C | T | 1 | a0001c0003t0001g0155 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.76-8932C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531674 | |||||||
chr12:3531716 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0007g0323 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.76-8890C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531716 | |||||||
chr12:3531717 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0197 others(52): Show |
56 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.76-8889G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531717 | |||||||
chr12:3531789 | T | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0102 others(22): Show |
25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-8817T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531789 | |||||||
chr12:3531879 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0195 |
2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.76-8727G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531879 | |||||||
chr12:3532050 | A | G | 2 | a0001c0002t0002g0086 a0001c0002t0002g0325 |
2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.76-8556A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532050 | |||||||
chr12:3532060 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0068 a0001c0001t0001g0071 others(6): Show |
9 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-8546G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532060 | |||||||
chr12:3532071 | G | C | 1 | a0001c0002t0002g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-8535G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532071 | |||||||
chr12:3532091 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-8515C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532091 | |||||||
chr12:3532109 | A | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG00438.hp1 HG00558.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-8497A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532109 | |||||||
chr12:3532111 | C | T | 4 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-8495C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532111 | |||||||
chr12:3532151 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.76-8455G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532151 | |||||||
chr12:3532396 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.76-8210G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532396 | |||||||
chr12:3532478 | G | T | 32 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(29): Show |
32 | HG00735.hp1 HG01069.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.76-8128G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532478 | |||||||
chr12:3532506 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.76-8100G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532506 | |||||||
chr12:3532552 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-8054C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532552 | |||||||
chr12:3532569 | G | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.76-8037G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532569 | |||||||
chr12:3532611 | C | CA | 47 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0023 others(44): Show |
47 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.76-7965dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | ||||||
chr12:3532611 | C | CAA | 19 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0083 others(16): Show |
19 | HG01358.hp2 HG02109.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.76-7966_76-7965dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | ||||||
chr12:3532611 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0126 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.76-7974_76-7965dup others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | ||||||
chr12:3532611 | CA | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0062 others(61): Show |
65 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.76-7965delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | ||||||
chr12:3532611 | CAA | C | 14 | a0001c0001t0001g0138 a0001c0001t0001g0153 a0001c0001t0001g0159 others(11): Show |
14 | HG00597.hp1 HG01123.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-7966_76-7965del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | ||||||
chr12:3532611 | CAAA | C | 68 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(65): Show |
68 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.76-7967_76-7965del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | ||||||
chr12:3532611 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-7974_76-7965del others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | ||||||
chr12:3532763 | A | C | 78 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0068 others(75): Show |
78 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.76-7843A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532763 | |||||||
chr12:3532970 | G | A | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-7636G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532970 | |||||||
chr12:3533053 | T | G | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-7553T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533053 | |||||||
chr12:3533103 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.76-7503T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533103 | |||||||
chr12:3533181 | A | G | 6 | a0001c0001t0001g0332 a0001c0004t0001g0329 a0001c0004t0001g0330 others(3): Show |
6 | HG00642.hp1 HG01175.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-7425A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533181 | |||||||
chr12:3533260 | G | A | 1 | a0001c0001t0007g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.76-7346G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533260 | |||||||
chr12:3533512 | T | A | 1 | a0001c0001t0001g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.76-7094T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533512 | |||||||
chr12:3533571 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.76-7035C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533571 | |||||||
chr12:3533842 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.76-6764A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533842 | |||||||
chr12:3534008 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6598C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534008 | |||||||
chr12:3534118 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6488C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534118 | |||||||
chr12:3534123 | T | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6483T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534123 | |||||||
chr12:3534221 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0195 |
2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.76-6385T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534221 | |||||||
chr12:3534403 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6203C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534403 | |||||||
chr12:3534406 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.76-6200C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534406 | |||||||
chr12:3534467 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.76-6139C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534467 | |||||||
chr12:3534516 | C | G | 11 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG02523.hp2 HG02976.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-6090C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534516 | |||||||
chr12:3534524 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.76-6082C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534524 | |||||||
chr12:3534752 | G | A | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-5854G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534752 | |||||||
chr12:3534823 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-5783G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534823 | |||||||
chr12:3534876 | G | A | 8 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-5730G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534876 | |||||||
chr12:3534975 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.76-5631G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534975 | |||||||
chr12:3535002 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.76-5604A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535002 | |||||||
chr12:3535004 | C | T | 6 | a0001c0001t0001g0095 a0001c0001t0001g0192 a0001c0001t0001g0203 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-5602C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535004 | |||||||
chr12:3535026 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-5580T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535026 | |||||||
chr12:3535174 | C | T | 1 | a0001c0005t0001g0324 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.76-5432C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535174 | |||||||
chr12:3535225 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-5381C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535225 | |||||||
chr12:3535261 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.76-5345G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535261 | |||||||
chr12:3535367 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-5239G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535367 | |||||||
chr12:3535433 | T | G | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(17): Show |
20 | HG00735.hp1 HG01069.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-5173T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535433 | |||||||
chr12:3535481 | G | A | 115 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0067 others(112): Show |
115 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-5125G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535481 | |||||||
chr12:3535527 | C | T | 19 | a0001c0001t0001g0083 a0001c0001t0001g0092 a0001c0001t0001g0093 others(16): Show |
19 | HG00642.hp1 HG01175.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.76-5079C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535527 | |||||||
chr12:3535608 | G | C | 3 | a0001c0001t0001g0322 a0001c0001t0007g0323 a0001c0002t0011g0101 |
3 | HG02895.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.76-4998G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535608 | |||||||
chr12:3535787 | C | T | 5 | a0001c0001t0001g0332 a0001c0004t0001g0329 a0001c0004t0001g0330 others(2): Show |
5 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-4819C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535787 | |||||||
chr12:3535862 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0005t0001g0199 others(1): Show |
4 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-4744C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535862 | |||||||
chr12:3535908 | C | G | 2 | a0001c0001t0001g0126 a0001c0002t0002g0115 |
2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.76-4698C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535908 | |||||||
chr12:3535948 | A | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.76-4658A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535948 | |||||||
chr12:3535963 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.76-4643C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535963 | |||||||
chr12:3535980 | C | A | 1 | a0001c0001t0010g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.76-4626C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535980 | |||||||
chr12:3536008 | T | C | 3 | a0001c0001t0001g0119 a0001c0002t0002g0053 a0001c0002t0002g0335 |
3 | HG02572.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.76-4598T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536008 | |||||||
chr12:3536186 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0104 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-4420C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536186 | |||||||
chr12:3536265 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0088 others(28): Show |
31 | HG00642.hp1 HG01175.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-4341T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536265 | |||||||
chr12:3536267 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0088 others(28): Show |
31 | HG00642.hp1 HG01175.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-4339T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536267 | |||||||
chr12:3536480 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-4126G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536480 | |||||||
chr12:3536504 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0118 others(2): Show |
5 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-4102G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536504 | |||||||
chr12:3536522 | C | T | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.76-4084C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536522 | |||||||
chr12:3537046 | T | C | 7 | a0001c0001t0001g0284 a0001c0001t0001g0287 a0001c0001t0001g0294 others(4): Show |
7 | HG00438.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-3560T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537046 | |||||||
chr12:3537076 | T | A | 25 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0001g0104 others(22): Show |
25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-3530T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537076 | |||||||
chr12:3537102 | A | T | 25 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0001g0104 others(22): Show |
25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-3504A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537102 | |||||||
chr12:3537282 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-3324G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537282 | |||||||
chr12:3537284 | T | G | 9 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-3322T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537284 | |||||||
chr12:3537402 | G | C | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3204G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537402 | |||||||
chr12:3537452 | C | A | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-3154C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537452 | |||||||
chr12:3537540 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.76-3066T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537540 | |||||||
chr12:3537758 | A | G | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-2848A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537758 | |||||||
chr12:3537996 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0005t0001g0199 others(1): Show |
4 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-2610T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537996 | |||||||
chr12:3538102 | T | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(139): Show |
142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.76-2504T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538102 | |||||||
chr12:3538117 | C | G | 1 | a0001c0002t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-2489C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538117 | |||||||
chr12:3538239 | A | T | 10 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(7): Show |
10 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-2367A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538239 | |||||||
chr12:3538365 | C | T | 9 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
9 | HG01109.hp2 HG01261.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-2241C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538365 | |||||||
chr12:3538471 | C | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0149 others(2): Show |
5 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-2135C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538471 | |||||||
chr12:3538600 | C | T | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
152 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.76-2006C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538600 | |||||||
chr12:3538625 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.76-1981C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538625 | |||||||
chr12:3538669 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.76-1937G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538669 | |||||||
chr12:3538704 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.76-1902A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538704 | |||||||
chr12:3538876 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0005t0001g0199 others(1): Show |
4 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1730G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538876 | |||||||
chr12:3538926 | G | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(314): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.76-1680G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538926 | |||||||
chr12:3538985 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.76-1621C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538985 | |||||||
chr12:3539080 | T | C | 3 | a0001c0001t0001g0360 a0001c0002t0002g0086 a0002c0008t0001g0356 |
3 | HG01109.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.76-1526T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539080 | |||||||
chr12:3539233 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-1373A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539233 | |||||||
chr12:3539368 | C | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(304): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.76-1238C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539368 | |||||||
chr12:3539929 | C | T | 1 | a0001c0001t0001g0349 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.76-677C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539929 | |||||||
chr12:3540160 | A | G | 77 | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0001g0061 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.76-446A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540160 | |||||||
chr12:3540215 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.76-391G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540215 | |||||||
chr12:3540245 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0210 a0001c0001t0001g0218 |
3 | HG00140.hp1 HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.76-361C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540245 | |||||||
chr12:3540392 | T | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
123 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.76-214T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540392 | |||||||
chr12:3540392 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.76-214T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540392 | |||||||
chr12:3540447 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.76-159G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540447 | |||||||
chr12:3540522 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-84G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540522 | |||||||
chr12:3540798 | T | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01261.hp2 HG01358.hp1 |
splice_region_variant&intron_variant | LOW | c.261+7T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540798 | |||||||
chr12:3540804 | G | A | 1 | a0001c0002t0002g0123 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.261+13G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540804 | |||||||
chr12:3540967 | C | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0165 |
2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.261+176C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540967 | |||||||
chr12:3540990 | T | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(353): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.261+199T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540990 | |||||||
chr12:3541120 | G | A | 1 | a0001c0001t0001g0352 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.261+329G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541120 | |||||||
chr12:3541197 | G | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0165 |
2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.261+406G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541197 | |||||||
chr12:3541215 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.261+424T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541215 | |||||||
chr12:3541226 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.261+435G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541226 | |||||||
chr12:3541277 | C | T | 107 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0054 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.261+486C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541277 | |||||||
chr12:3541337 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.261+546A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541337 | |||||||
chr12:3541529 | T | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(86): Show |
89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.261+738T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541529 | |||||||
chr12:3541566 | G | A | 3 | a0001c0004t0001g0329 a0001c0004t0001g0330 a0001c0004t0001g0331 |
3 | HG00642.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.261+775G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541566 | |||||||
chr12:3541665 | C | T | 4 | a0001c0004t0001g0329 a0001c0004t0001g0330 a0001c0004t0001g0331 others(1): Show |
4 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+874C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541665 | |||||||
chr12:3541783 | G | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+992G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541783 | |||||||
chr12:3541909 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.261+1118C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541909 | |||||||
chr12:3541953 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(1): Show |
4 | HG01192.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1162G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541953 | |||||||
chr12:3541994 | A | C | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.261+1203A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541994 | |||||||
chr12:3542021 | A | AT | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+1231dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3542021 | ||||||
chr12:3542061 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.261+1270C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542061 | |||||||
chr12:3542222 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.261+1431G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542222 | |||||||
chr12:3542225 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.261+1434C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542225 | |||||||
chr12:3542232 | T | C | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+1441T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542232 | |||||||
chr12:3542283 | G | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+1492G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542283 | |||||||
chr12:3542438 | G | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0327 |
3 | HG01261.hp2 HG01358.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.261+1647G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542438 | |||||||
chr12:3542470 | C | T | 2 | a0001c0001t0001g0264 a0001c0002t0002g0265 |
2 | NA18967.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.261+1679C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542470 | |||||||
chr12:3542528 | A | G | 3 | a0001c0001t0001g0322 a0001c0001t0007g0323 a0001c0002t0002g0325 |
3 | HG03209.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.261+1737A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542528 | |||||||
chr12:3542542 | T | C | 2 | a0001c0001t0001g0058 a0001c0002t0002g0043 |
2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.261+1751T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542542 | |||||||
chr12:3542586 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.261+1795G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542586 | |||||||
chr12:3542615 | C | T | 1 | a0001c0001t0001g0349 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.261+1824C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542615 | |||||||
chr12:3542727 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.261+1936G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542727 | |||||||
chr12:3543045 | A | G | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.261+2254A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543045 | |||||||
chr12:3543135 | C | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0227 |
3 | HG03490.hp1 HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.261+2344C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543135 | |||||||
chr12:3543201 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.261+2410C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543201 | |||||||
chr12:3543248 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.261+2457G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543248 | |||||||
chr12:3543460 | T | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(104): Show |
107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.261+2669T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543460 | |||||||
chr12:3543470 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(104): Show |
107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.261+2679C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543470 | |||||||
chr12:3543590 | G | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(104): Show |
107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.261+2799G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543590 | |||||||
chr12:3543592 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.261+2801C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543592 | |||||||
chr12:3543600 | G | A | 3 | a0001c0001t0001g0119 a0001c0002t0002g0053 a0001c0002t0002g0335 |
3 | HG02572.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.261+2809G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543600 | |||||||
chr12:3543723 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.261+2932A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543723 | |||||||
chr12:3543767 | A | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(353): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.261+2976A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543767 | |||||||
chr12:3543834 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.261+3043G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543834 | |||||||
chr12:3543854 | A | G | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+3063A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543854 | |||||||
chr12:3543892 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.261+3101A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543892 | |||||||
chr12:3544141 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(319): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.261+3350G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544141 | |||||||
chr12:3544612 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0327 |
3 | HG01261.hp2 HG01358.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.261+3821C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544612 | |||||||
chr12:3544613 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.261+3822G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544613 | |||||||
chr12:3544670 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0258 a0001c0001t0001g0290 others(5): Show |
8 | HG00099.hp1 HG00741.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+3879A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544670 | |||||||
chr12:3544752 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261+3961A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544752 | |||||||
chr12:3544784 | C | T | 2 | a0001c0001t0001g0126 a0001c0002t0002g0115 |
2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.261+3993C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544784 | |||||||
chr12:3544812 | C | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.261+4021C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544812 | |||||||
chr12:3545190 | C | G | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.261+4399C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545190 | |||||||
chr12:3545285 | C | T | 349 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(346): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.261+4494C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545285 | |||||||
chr12:3545321 | A | G | 1 | a0001c0005t0001g0324 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.261+4530A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545321 | |||||||
chr12:3545608 | G | A | 31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(28): Show |
31 | HG00280.hp1 HG00642.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.262-4328G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545608 | |||||||
chr12:3545648 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-4288C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545648 | |||||||
chr12:3545682 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.262-4254C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545682 | |||||||
chr12:3545685 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.262-4251G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545685 | |||||||
chr12:3545929 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(94): Show |
99 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.262-4007G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545929 | |||||||
chr12:3546016 | T | C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0119 a0001c0001t0001g0128 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-3920T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546016 | |||||||
chr12:3546096 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.262-3840C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546096 | |||||||
chr12:3546486 | G | A | 3 | a0001c0001t0001g0360 a0001c0002t0002g0086 a0002c0008t0001g0356 |
3 | HG01109.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.262-3450G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546486 | |||||||
chr12:3546519 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.262-3417C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546519 | |||||||
chr12:3546595 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0167 |
2 | NA18940.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.262-3341C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546595 | |||||||
chr12:3546739 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.262-3197C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546739 | |||||||
chr12:3546812 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0360 others(2): Show |
5 | HG01109.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-3124G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546812 | |||||||
chr12:3546834 | G | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-3102G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546834 | |||||||
chr12:3546953 | A | G | 23 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0075 others(20): Show |
23 | HG00597.hp2 HG00733.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.262-2983A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546953 | |||||||
chr12:3547050 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-2886A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547050 | |||||||
chr12:3547184 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.262-2752G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547184 | |||||||
chr12:3547261 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
87 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.262-2675G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547261 | |||||||
chr12:3547407 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0271 others(1): Show |
4 | HG02071.hp2 HG02165.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-2529A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547407 | |||||||
chr12:3547481 | A | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0149 a0001c0001t0002g0129 others(1): Show |
4 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-2455A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547481 | |||||||
chr12:3547496 | G | A | 1 | a0001c0002t0002g0206 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.262-2440G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547496 | |||||||
chr12:3547504 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00733.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.262-2432A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547504 | |||||||
chr12:3547568 | C | T | 33 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(30): Show |
33 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.262-2368C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547568 | |||||||
chr12:3547615 | C | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-2321C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547615 | |||||||
chr12:3547659 | A | G | 33 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(30): Show |
33 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.262-2277A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547659 | |||||||
chr12:3547764 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.262-2172A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547764 | |||||||
chr12:3547934 | AG | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG02559.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1999delG | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3547934 | ||||||
chr12:3548238 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.262-1698T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548238 | |||||||
chr12:3548470 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.262-1466G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548470 | |||||||
chr12:3548520 | A | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(110): Show |
113 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.262-1416A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548520 | |||||||
chr12:3548574 | G | GA | 26 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(23): Show |
26 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.262-1354dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3548574 | ||||||
chr12:3548574 | GA | G | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(7): Show |
10 | NA18939.hp2 NA18942.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-1354delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3548574 | ||||||
chr12:3548692 | T | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(353): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.262-1244T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548692 | |||||||
chr12:3548721 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.262-1215A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548721 | |||||||
chr12:3548741 | A | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0001g0118 others(8): Show |
11 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.262-1195A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548741 | |||||||
chr12:3549186 | T | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(143): Show |
146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.262-750T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549186 | |||||||
chr12:3549497 | CT | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.262-426delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3549497 | ||||||
chr12:3549497 | CTT | C | 10 | a0001c0001t0001g0060 a0001c0001t0001g0096 a0001c0001t0001g0112 others(7): Show |
10 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-427_262-426del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3549497 | ||||||
chr12:3549510 | T | A | 9 | a0001c0001t0001g0033 a0001c0001t0001g0078 a0001c0001t0001g0081 others(6): Show |
9 | HG00597.hp2 HG01069.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.262-426T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549510 | |||||||
chr12:3549510 | TA | T | 39 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(36): Show |
39 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.262-418delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3549510 | ||||||
chr12:3549511 | A | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0327 others(1): Show |
4 | HG01261.hp2 HG01358.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-425A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549511 | |||||||
chr12:3549565 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-371G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549565 | |||||||
chr12:3549608 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.262-328C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549608 | |||||||
chr12:3549609 | G | A | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262-327G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549609 | |||||||
chr12:3549719 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.262-217G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549719 | |||||||
chr12:3549723 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.262-213T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549723 | |||||||
chr12:3550159 | C | T | 18 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0075 others(15): Show |
18 | HG00733.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.417+68C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550159 | |||||||
chr12:3550310 | C | T | 16 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0126 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.417+219C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550310 | |||||||
chr12:3550399 | G | T | 1 | a0001c0001t0014g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.417+308G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550399 | |||||||
chr12:3550410 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.417+319G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550410 | |||||||
chr12:3550496 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0210 |
2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.417+405C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550496 | |||||||
chr12:3550597 | A | G | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+506A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550597 | |||||||
chr12:3550611 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0094 a0001c0001t0001g0322 others(8): Show |
11 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.417+520C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550611 | |||||||
chr12:3550727 | G | T | 3 | a0001c0001t0001g0322 a0001c0001t0007g0323 a0001c0002t0002g0325 |
3 | HG03209.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.417+636G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550727 | |||||||
chr12:3550818 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0003g0225 |
2 | HG01346.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.417+727G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550818 | |||||||
chr12:3551004 | C | T | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.417+913C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551004 | |||||||
chr12:3551048 | T | C | 3 | a0001c0004t0001g0329 a0001c0004t0001g0330 a0001c0004t0001g0331 |
3 | HG00642.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.417+957T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551048 | |||||||
chr12:3551076 | A | AC | 98 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0067 others(95): Show |
98 | HG00140.hp2 HG00558.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.417+994dupC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 3551076 | ||||||
chr12:3551076 | A | ACC | 42 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(39): Show |
42 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.417+993_417+994dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 3551076 | ||||||
chr12:3551076 | A | ACCC | 20 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(17): Show |
20 | HG00642.hp1 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.417+992_417+994dup others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 3551076 | ||||||
chr12:3551080 | C | G | 1 | a0001c0001t0001g0081 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.417+989C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551080 | |||||||
chr12:3551085 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0360 others(2): Show |
5 | HG01109.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+994C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551085 | |||||||
chr12:3551226 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0094 a0001c0001t0001g0322 others(8): Show |
11 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.417+1135C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551226 | |||||||
chr12:3551227 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+1136G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551227 | |||||||
chr12:3551369 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0008g0122 a0001c0002t0002g0123 |
3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.417+1278C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551369 | |||||||
chr12:3551459 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.417+1368G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551459 | |||||||
chr12:3551489 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.417+1398C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551489 | |||||||
chr12:3551632 | C | T | 2 | a0001c0001t0001g0352 a0001c0003t0001g0353 |
2 | NA18951.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.417+1541C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551632 | |||||||
chr12:3551788 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.417+1697C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551788 | |||||||
chr12:3551813 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(94): Show |
99 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.417+1722G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551813 | |||||||
chr12:3552183 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.418-1468C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552183 | |||||||
chr12:3552372 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.418-1279C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552372 | |||||||
chr12:3552393 | T | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(171): Show |
174 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.418-1258T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552393 | |||||||
chr12:3552419 | AC | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(23): Show |
27 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418-1231delC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552419 | |||||||
chr12:3552450 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0128 a0001c0001t0001g0134 |
3 | HG02280.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.418-1201C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552450 | |||||||
chr12:3552463 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.418-1188A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552463 | |||||||
chr12:3552530 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.418-1121C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552530 | |||||||
chr12:3552795 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0343 a0001c0001t0001g0344 others(1): Show |
4 | HG00639.hp1 HG01261.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-856C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552795 | |||||||
chr12:3552846 | C | CTTAGCA | 4 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.418-805_418-804ins others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552846 | |||||||
chr12:3552875 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.418-776A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552875 | |||||||
chr12:3552902 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.418-749G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552902 | |||||||
chr12:3552956 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-695G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552956 | |||||||
chr12:3553060 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.418-591C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553060 | |||||||
chr12:3553078 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
87 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.418-573C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553078 | |||||||
chr12:3553088 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.418-563A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553088 | |||||||
chr12:3553118 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.418-533G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553118 | |||||||
chr12:3553217 | C | T | 2 | a0001c0001t0001g0132 a0001c0002t0002g0133 |
2 | HG01070.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.418-434C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553217 | |||||||
chr12:3553265 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02300.hp1 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.418-386C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553265 | |||||||
chr12:3553305 | C | T | 1 | a0001c0001t0013g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.418-346C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553305 | |||||||
chr12:3553315 | G | C | 18 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(15): Show |
18 | HG00280.hp1 HG01123.hp2 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.418-336G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553315 | |||||||
chr12:3553444 | C | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0295 a0001c0001t0013g0056 |
4 | HG01257.hp2 HG01258.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-207C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553444 | |||||||
chr12:3553488 | G | T | 2 | a0001c0001t0001g0348 a0001c0001t0002g0334 |
2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.418-163G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553488 | |||||||
chr12:3553489 | G | C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.418-162G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553489 | |||||||
chr12:3553590 | G | A | 9 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.418-61G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553590 | |||||||
chr12:3553756 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.481+42C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553756 | |||||||
chr12:3553799 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0295 a0001c0001t0013g0056 |
4 | HG01257.hp2 HG01258.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+85G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553799 | |||||||
chr12:3553800 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.481+86C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553800 | |||||||
chr12:3553808 | A | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+94A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553808 | |||||||
chr12:3553835 | A | G | 10 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(7): Show |
10 | HG01891.hp1 HG02056.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+121A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553835 | |||||||
chr12:3553984 | C | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0258 a0001c0001t0001g0290 others(6): Show |
9 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+270C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553984 | |||||||
chr12:3554676 | AG | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+967delG | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3554676 | ||||||
chr12:3554681 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0008g0122 a0001c0002t0002g0123 |
3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.481+967G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554681 | |||||||
chr12:3554699 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+985G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554699 | |||||||
chr12:3554774 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+1060C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554774 | |||||||
chr12:3554832 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.481+1118A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554832 | |||||||
chr12:3554918 | T | G | 4 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0040 others(1): Show |
4 | NA18955.hp2 NA18968.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+1204T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554918 | |||||||
chr12:3554949 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+1235G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554949 | |||||||
chr12:3554952 | C | A | 2 | a0001c0001t0001g0058 a0001c0002t0002g0043 |
2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.481+1238C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554952 | |||||||
chr12:3555271 | C | T | 58 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(55): Show |
58 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.481+1557C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555271 | |||||||
chr12:3555468 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.481+1754G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555468 | |||||||
chr12:3555538 | C | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(115): Show |
118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+1824C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555538 | |||||||
chr12:3555617 | A | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0127 a0001c0001t0001g0149 others(3): Show |
6 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+1903A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555617 | |||||||
chr12:3555780 | AGGACCTG others(157): Show |
A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(123): Show |
126 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.481+2077_481+2240d others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3555780 | ||||||
chr12:3555791 | GTGCATTG others(157): Show |
G | 52 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(49): Show |
52 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.481+2150_481+2313d others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3555791 | ||||||
chr12:3555931 | A | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(96): Show |
101 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.481+2217A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555931 | |||||||
chr12:3555967 | T | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(123): Show |
126 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.481+2253T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555967 | |||||||
chr12:3556013 | C | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0360 others(4): Show |
7 | HG01109.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+2299C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556013 | |||||||
chr12:3556040 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+2326G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556040 | |||||||
chr12:3556150 | A | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.481+2436A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556150 | |||||||
chr12:3556520 | G | A | 19 | a0001c0001t0001g0136 a0001c0001t0001g0177 a0001c0001t0001g0181 others(16): Show |
19 | HG01361.hp2 HG01934.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.481+2806G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556520 | |||||||
chr12:3556635 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+2921G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556635 | |||||||
chr12:3556673 | T | A | 1 | a0001c0001t0001g0354 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.481+2959T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556673 | |||||||
chr12:3556673 | TA | T | 9 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0003g0243 others(6): Show |
9 | HG00642.hp1 HG01169.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+2969delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3556673 | ||||||
chr12:3556674 | A | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
96 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.481+2960A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556674 | |||||||
chr12:3556675 | A | T | 5 | a0001c0001t0001g0211 a0001c0001t0001g0231 a0001c0001t0001g0322 others(2): Show |
5 | HG03209.hp2 NA18906.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+2961A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556675 | |||||||
chr12:3556739 | G | A | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.481+3025G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556739 | |||||||
chr12:3556747 | G | A | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.481+3033G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556747 | |||||||
chr12:3556826 | AGTGGAGG others(21): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.481+3145_481+3172d others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3556826 | ||||||
chr12:3556861 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.481+3147G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556861 | |||||||
chr12:3556920 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.481+3206C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556920 | |||||||
chr12:3556923 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481+3209C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556923 | |||||||
chr12:3557376 | G | A | 2 | a0001c0001t0001g0126 a0001c0002t0002g0115 |
2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.481+3662G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557376 | |||||||
chr12:3557384 | A | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(353): Show |
358 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.481+3670A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557384 | |||||||
chr12:3557412 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.481+3698C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557412 | |||||||
chr12:3557460 | G | A | 3 | a0001c0001t0001g0322 a0001c0001t0007g0323 a0001c0002t0002g0325 |
3 | HG03209.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.481+3746G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557460 | |||||||
chr12:3557539 | G | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG02559.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+3825G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557539 | |||||||
chr12:3557584 | C | A | 1 | a0001c0010t0002g0147 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.481+3870C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557584 | |||||||
chr12:3557643 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+3929G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557643 | |||||||
chr12:3557652 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.481+3938C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557652 | |||||||
chr12:3557819 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0311 |
2 | HG00738.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.481+4105G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557819 | |||||||
chr12:3557994 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.481+4280C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557994 | |||||||
chr12:3558225 | T | TCTCCCCT others(2): Show |
10 | a0001c0001t0001g0070 a0001c0001t0001g0094 a0001c0001t0001g0322 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+4532_481+4540d others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558225 | ||||||
chr12:3558225 | T | TCTCCCCT others(20): Show |
1 | a0001c0002t0002g0325 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.481+4514_481+4540d others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558225 | ||||||
chr12:3558301 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+4587A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558301 | |||||||
chr12:3558302 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+4588T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558302 | |||||||
chr12:3558371 | C | T | 2 | a0001c0001t0001g0039 a0001c0002t0002g0028 |
2 | HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.481+4657C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558371 | |||||||
chr12:3558463 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.481+4749G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558463 | |||||||
chr12:3558464 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.481+4750T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558464 | |||||||
chr12:3558658 | T | C | 17 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0001g0062 others(14): Show |
17 | HG01099.hp1 HG01109.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.481+4944T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558658 | |||||||
chr12:3558683 | T | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(115): Show |
118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+4969T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558683 | |||||||
chr12:3558930 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+5216C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558930 | |||||||
chr12:3558949 | T | G | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(116): Show |
119 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.481+5235T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558949 | |||||||
chr12:3558949 | TCTATCTA others(5): Show |
T | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.481+5247_481+5258d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558949 | ||||||
chr12:3558961 | C | CCTAT | 92 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0033 others(89): Show |
92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.481+5274_481+5277d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | C | CCTATCTA others(21): Show |
1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481+5254_481+5255i others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | C | CCTATCTA others(1): Show |
61 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(58): Show |
61 | HG00597.hp1 HG00597.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.481+5270_481+5277d others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | C | CCTATCTA others(5): Show |
61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
62 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.481+5266_481+5277d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | C | CCTATCTA others(9): Show |
14 | a0001c0001t0001g0111 a0001c0001t0001g0140 a0001c0001t0001g0141 others(11): Show |
14 | HG00099.hp1 HG01074.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.481+5262_481+5277d others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | C | CCTATCTA others(13): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0207 others(5): Show |
9 | HG01257.hp2 HG01258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+5258_481+5277d others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | C | CCTATCTA others(17): Show |
2 | a0001c0001t0001g0343 a0001c0001t0001g0345 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.481+5254_481+5277d others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.481+5247C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558961 | |||||||
chr12:3558961 | CCTAT | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG01175.hp1 HG01261.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+5274_481+5277d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558961 | CCTATCTA others(5): Show |
C | 3 | a0001c0001t0001g0144 a0001c0001t0008g0122 a0001c0002t0002g0123 |
3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.481+5266_481+5277d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | ||||||
chr12:3558984 | ATCTATCT others(1): Show |
A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+5278_481+5285d others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558984 | ||||||
chr12:3558992 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.481+5278G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558992 | |||||||
chr12:3559048 | T | G | 1 | a0001c0001t0001g0354 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.481+5334T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559048 | |||||||
chr12:3559235 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.481+5521G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559235 | |||||||
chr12:3559489 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.481+5775G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559489 | |||||||
chr12:3559503 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0008g0122 a0001c0002t0002g0123 |
3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.481+5789G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559503 | |||||||
chr12:3559584 | T | A | 4 | a0001c0004t0001g0329 a0001c0004t0001g0330 a0001c0004t0001g0331 others(1): Show |
4 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+5870T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559584 | |||||||
chr12:3559823 | G | A | 122 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(119): Show |
122 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.481+6109G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559823 | |||||||
chr12:3559835 | G | A | 3 | a0001c0001t0001g0119 a0001c0002t0002g0053 a0001c0002t0002g0335 |
3 | HG02572.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.481+6121G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559835 | |||||||
chr12:3559938 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.481+6224C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559938 | |||||||
chr12:3560036 | C | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(115): Show |
118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+6322C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560036 | |||||||
chr12:3560088 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0327 |
3 | HG01261.hp2 HG01358.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.481+6374C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560088 | |||||||
chr12:3560172 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.481+6458G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560172 | |||||||
chr12:3560458 | G | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(115): Show |
118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+6744G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560458 | |||||||
chr12:3560665 | A | G | 8 | a0001c0001t0001g0212 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | NA18966.hp2 NA18977.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+6951A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560665 | |||||||
chr12:3560873 | C | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(108): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.481+7159C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560873 | |||||||
chr12:3560979 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.481+7265G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560979 | |||||||
chr12:3560985 | T | G | 117 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(114): Show |
117 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.481+7271T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560985 | |||||||
chr12:3561167 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0173 |
2 | HG01074.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.481+7453C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561167 | |||||||
chr12:3561186 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+7472G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561186 | |||||||
chr12:3561252 | G | A | 4 | a0001c0001t0001g0357 a0001c0001t0001g0358 a0001c0001t0001g0361 others(1): Show |
4 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-7454G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561252 | |||||||
chr12:3561500 | C | T | 1 | a0001c0005t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.482-7206C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561500 | |||||||
chr12:3561559 | C | G | 1 | a0001c0002t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.482-7147C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561559 | |||||||
chr12:3561688 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0257 |
2 | HG00733.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.482-7018G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561688 | |||||||
chr12:3562125 | A | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0301 |
2 | NA18944.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.482-6581A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562125 | |||||||
chr12:3562149 | G | A | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482-6557G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562149 | |||||||
chr12:3562340 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482-6366G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562340 | |||||||
chr12:3562357 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.482-6349G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562357 | |||||||
chr12:3562390 | G | A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0055 others(17): Show |
20 | HG00597.hp2 HG00733.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.482-6316G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562390 | |||||||
chr12:3562506 | G | A | 58 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(55): Show |
58 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.482-6200G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562506 | |||||||
chr12:3562547 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.482-6159G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562547 | |||||||
chr12:3562747 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0006g0328 |
3 | HG02723.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.482-5959T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562747 | |||||||
chr12:3562752 | T | C | 1 | a0001c0002t0002g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.482-5954T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562752 | |||||||
chr12:3563024 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.482-5682G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563024 | |||||||
chr12:3563258 | C | T | 3 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 |
3 | HG00639.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.482-5448C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563258 | |||||||
chr12:3563259 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0118 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.482-5447G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563259 | |||||||
chr12:3563287 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02300.hp1 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.482-5419G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563287 | |||||||
chr12:3563290 | C | T | 2 | a0001c0003t0001g0155 a0001c0003t0001g0277 |
2 | NA18967.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.482-5416C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563290 | |||||||
chr12:3563374 | T | A | 3 | a0001c0001t0001g0144 a0001c0001t0008g0122 a0001c0002t0002g0123 |
3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482-5332T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563374 | |||||||
chr12:3563433 | G | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.482-5273G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563433 | |||||||
chr12:3563553 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0095 others(10): Show |
13 | HG00099.hp1 HG00741.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.482-5153G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563553 | |||||||
chr12:3563554 | CAGG | C | 16 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0126 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.482-5149_482-5147d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3563554 | ||||||
chr12:3563563 | G | T | 30 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(27): Show |
30 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.482-5143G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563563 | |||||||
chr12:3563609 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0008g0122 a0001c0002t0002g0123 |
3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482-5097C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563609 | |||||||
chr12:3563617 | T | G | 1 | a0001c0002t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.482-5089T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563617 | |||||||
chr12:3563695 | G | A | 2 | a0001c0001t0001g0058 a0001c0002t0002g0043 |
2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.482-5011G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563695 | |||||||
chr12:3563811 | G | C | 3 | a0001c0004t0001g0329 a0001c0004t0001g0330 a0001c0004t0001g0331 |
3 | HG00642.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.482-4895G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563811 | |||||||
chr12:3563928 | G | GC | 112 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(109): Show |
112 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.482-4772dupC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3563928 | ||||||
chr12:3563935 | A | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(115): Show |
118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-4771A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563935 | |||||||
chr12:3563935 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
180 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.482-4771A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563935 | |||||||
chr12:3564172 | C | T | 21 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0055 others(18): Show |
21 | HG00597.hp2 HG00733.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.482-4534C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564172 | |||||||
chr12:3564204 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0350 others(1): Show |
4 | NA18980.hp1 NA19064.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-4502G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564204 | |||||||
chr12:3564271 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-4435G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564271 | |||||||
chr12:3564333 | C | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(112): Show |
115 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.482-4373C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564333 | |||||||
chr12:3564334 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-4372G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564334 | |||||||
chr12:3564377 | G | C | 1 | a0001c0007t0001g0208 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.482-4329G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564377 | |||||||
chr12:3564429 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.482-4277A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564429 | |||||||
chr12:3564526 | CAGG | C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0162 others(1): Show |
4 | HG02056.hp2 HG02080.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-4177_482-4175d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3564526 | ||||||
chr12:3564590 | T | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-4116T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564590 | |||||||
chr12:3564602 | C | A | 1 | a0001c0001t0001g0337 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.482-4104C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564602 | |||||||
chr12:3564626 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.482-4080G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564626 | |||||||
chr12:3564676 | G | A | 116 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(113): Show |
116 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.482-4030G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564676 | |||||||
chr12:3564759 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.482-3947G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564759 | |||||||
chr12:3564907 | T | C | 6 | a0001c0001t0001g0212 a0001c0001t0001g0231 a0001c0001t0001g0234 others(3): Show |
6 | NA18966.hp2 NA18977.hp1 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-3799T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564907 | |||||||
chr12:3565292 | G | A | 1 | a0001c0004t0001g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.482-3414G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565292 | |||||||
chr12:3565336 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.482-3370G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565336 | |||||||
chr12:3565397 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.482-3309C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565397 | |||||||
chr12:3565507 | G | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(115): Show |
118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-3199G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565507 | |||||||
chr12:3565665 | A | G | 117 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0027 others(114): Show |
117 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.482-3041A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565665 | |||||||
chr12:3565697 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0008g0122 a0001c0002t0002g0123 |
3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482-3009C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565697 | |||||||
chr12:3565710 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.482-2996A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565710 | |||||||
chr12:3565714 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0012g0087 |
2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.482-2992A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565714 | |||||||
chr12:3565931 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0309 |
2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.482-2775A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565931 | |||||||
chr12:3566054 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.482-2652C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566054 | |||||||
chr12:3566102 | A | G | 24 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(21): Show |
24 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-2604A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566102 | |||||||
chr12:3566178 | GT | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0350 others(1): Show |
4 | NA18980.hp1 NA19064.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-2527delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566178 | |||||||
chr12:3566586 | T | A | 1 | a0001c0001t0001g0279 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.482-2120T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566586 | |||||||
chr12:3566637 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-2069A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566637 | |||||||
chr12:3566660 | G | A | 1 | a0001c0001t0008g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.482-2046G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566660 | |||||||
chr12:3566675 | C | A | 1 | a0001c0001t0001g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.482-2031C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566675 | |||||||
chr12:3566824 | A | T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0130 others(3): Show |
6 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-1882A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566824 | |||||||
chr12:3566941 | A | G | 1 | a0001c0001t0008g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.482-1765A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566941 | |||||||
chr12:3566955 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.482-1751A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566955 | |||||||
chr12:3567080 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.482-1626C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567080 | |||||||
chr12:3567160 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.482-1546A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567160 | |||||||
chr12:3567664 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.482-1042G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567664 | |||||||
chr12:3567679 | C | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0006g0328 |
3 | HG02723.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.482-1027C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567679 | |||||||
chr12:3567756 | C | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0357 a0001c0001t0001g0358 others(3): Show |
6 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-950C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567756 | |||||||
chr12:3567811 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.482-895T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567811 | |||||||
chr12:3567851 | A | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0075 others(14): Show |
17 | HG00741.hp2 HG01123.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.482-855A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567851 | |||||||
chr12:3567871 | T | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02300.hp1 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.482-835T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567871 | |||||||
chr12:3567929 | C | T | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482-777C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567929 | |||||||
chr12:3568003 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.482-703C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568003 | |||||||
chr12:3568028 | C | T | 8 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-678C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568028 | |||||||
chr12:3568033 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.482-673C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568033 | |||||||
chr12:3568072 | C | CA | 86 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.482-618dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | ||||||
chr12:3568072 | C | CAA | 7 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-619_482-618dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | ||||||
chr12:3568072 | CAA | C | 13 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.482-619_482-618del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | ||||||
chr12:3568072 | CAAA | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0027 others(26): Show |
29 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-620_482-618del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | ||||||
chr12:3568162 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.482-544A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568162 | |||||||
chr12:3568186 | T | C | 3 | a0001c0001t0001g0358 a0001c0001t0001g0362 a0001c0001t0007g0089 |
3 | HG01167.hp2 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.482-520T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568186 | |||||||
chr12:3568306 | C | CAGAGGTG others(7): Show |
1 | a0001c0001t0001g0354 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.482-400_482-399ins others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568306 | |||||||
chr12:3568320 | A | G | 2 | a0001c0001t0001g0340 a0001c0001t0001g0354 |
2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.482-386A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568320 | |||||||
chr12:3568332 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.482-374C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568332 | |||||||
chr12:3568339 | G | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0090 others(4): Show |
7 | HG02896.hp2 HG02897.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-367G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568339 | |||||||
chr12:3568347 | T | TA | 6 | a0001c0001t0001g0058 a0001c0001t0001g0134 a0001c0001t0001g0360 others(3): Show |
6 | HG01109.hp2 HG01952.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-347dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568347 | ||||||
chr12:3568347 | TA | T | 170 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(167): Show |
170 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.482-347delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568347 | ||||||
chr12:3568352 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0192 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.482-354A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568352 | |||||||
chr12:3568395 | G | GGTT | 207 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(204): Show |
207 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.482-307_482-305dup others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568395 | ||||||
chr12:3568461 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0064 a0001c0001t0001g0084 others(5): Show |
8 | HG03209.hp2 HG06807.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-245G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568461 | |||||||
chr12:3568478 | C | T | 18 | a0001c0001t0001g0097 a0001c0001t0001g0112 a0001c0001t0001g0131 others(15): Show |
18 | HG00673.hp2 HG02258.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.482-228C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568478 | |||||||
chr12:3568610 | AG | A | 9 | a0001c0001t0001g0185 a0001c0001t0001g0202 a0001c0001t0001g0227 others(6): Show |
9 | HG00735.hp2 HG00738.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-93delG | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568610 | ||||||
chr12:3568628 | T | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-78T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568628 | |||||||
chr12:3568872 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.624+24C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3568872 | |||||||
chr12:3568914 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.624+66G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3568914 | |||||||
chr12:3568954 | G | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0102 others(3): Show |
6 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+106G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3568954 | |||||||
chr12:3569023 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0047 others(6): Show |
9 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+175C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569023 | |||||||
chr12:3569085 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0074 others(14): Show |
19 | HG00140.hp1 HG00558.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.624+237A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569085 | |||||||
chr12:3569207 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625-270G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569207 | |||||||
chr12:3569214 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.625-263C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569214 | |||||||
chr12:3569355 | C | G | 3 | a0001c0001t0001g0350 a0001c0003t0001g0353 a0001c0007t0001g0208 |
3 | NA18951.hp1 NA19065.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.625-122C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569355 | |||||||
chr12:3569386 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.625-91C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569386 | |||||||
chr12:3569402 | A | G | 26 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0067 others(23): Show |
26 | HG00558.hp2 HG00597.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.625-75A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569402 | |||||||
chr12:3569579 | G | A | 79 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0024 others(76): Show |
80 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.712+15G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569579 | |||||||
chr12:3569586 | C | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0134 others(2): Show |
5 | HG01261.hp2 HG01358.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.712+22C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569586 | |||||||
chr12:3569752 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.712+188A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569752 | |||||||
chr12:3569776 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0003g0313 |
2 | HG01192.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.712+212C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569776 | |||||||
chr12:3570020 | T | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0135 a0001c0001t0001g0176 others(4): Show |
7 | HG01361.hp2 HG02273.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+456T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570020 | |||||||
chr12:3570108 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.712+544G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570108 | |||||||
chr12:3570233 | G | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0022 others(47): Show |
50 | HG00558.hp2 HG00597.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.712+669G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570233 | |||||||
chr12:3570388 | A | G | 11 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0111 others(8): Show |
12 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.712+824A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570388 | |||||||
chr12:3570412 | A | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0099 others(9): Show |
12 | HG00438.hp1 HG00741.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+848A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570412 | |||||||
chr12:3570452 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.712+888G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570452 | |||||||
chr12:3570489 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0272 |
3 | HG02109.hp1 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.712+925G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570489 | |||||||
chr12:3570557 | G | A | 70 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0022 others(67): Show |
70 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.712+993G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570557 | |||||||
chr12:3570613 | T | A | 70 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0022 others(67): Show |
70 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.712+1049T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570613 | |||||||
chr12:3570672 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.712+1108C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570672 | |||||||
chr12:3570693 | G | A | 68 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0022 others(65): Show |
68 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.712+1129G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570693 | |||||||
chr12:3570861 | A | T | 22 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0187 others(19): Show |
22 | HG00621.hp2 HG00673.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.712+1297A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570861 | |||||||
chr12:3571014 | C | T | 80 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0022 others(77): Show |
81 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.712+1450C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571014 | |||||||
chr12:3571169 | G | C | 1 | a0001c0006t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.712+1605G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571169 | |||||||
chr12:3571189 | A | C | 11 | a0001c0001t0001g0011 a0001c0001t0002g0103 a0001c0001t0002g0129 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.712+1625A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571189 | |||||||
chr12:3571396 | G | A | 2 | a0001c0001t0002g0129 a0001c0002t0011g0101 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.712+1832G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571396 | |||||||
chr12:3571404 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.712+1840C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571404 | |||||||
chr12:3571493 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0187 |
2 | HG00621.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.712+1929G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571493 | |||||||
chr12:3571700 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.712+2136C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571700 | |||||||
chr12:3571902 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.712+2338A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571902 | |||||||
chr12:3571913 | T | G | 2 | a0001c0001t0001g0132 a0001c0002t0009g0034 |
2 | HG01069.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.712+2349T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571913 | |||||||
chr12:3572186 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.712+2622A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572186 | |||||||
chr12:3572241 | C | T | 2 | a0001c0002t0002g0050 a0001c0002t0002g0335 |
2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.712+2677C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572241 | |||||||
chr12:3572345 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712+2781T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572345 | |||||||
chr12:3572503 | A | C | 1 | a0001c0001t0001g0232 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.712+2939A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572503 | |||||||
chr12:3572633 | C | T | 7 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(4): Show |
8 | HG00558.hp1 HG00733.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.712+3069C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572633 | |||||||
chr12:3572658 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
94 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.712+3094C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572658 | |||||||
chr12:3572667 | A | C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(4): Show |
8 | HG00558.hp1 HG00733.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.712+3103A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572667 | |||||||
chr12:3573150 | A | T | 9 | a0001c0001t0002g0103 a0001c0002t0002g0045 a0001c0002t0002g0046 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.712+3586A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573150 | |||||||
chr12:3573317 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0049 others(73): Show |
78 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.713-3554A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573317 | |||||||
chr12:3573467 | T | C | 2 | a0001c0001t0001g0110 a0001c0005t0001g0324 |
2 | HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.713-3404T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573467 | |||||||
chr12:3573591 | G | A | 1 | a0001c0002t0002g0206 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.713-3280G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573591 | |||||||
chr12:3573781 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.713-3090C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573781 | |||||||
chr12:3573923 | C | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | NA19074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.713-2948C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573923 | |||||||
chr12:3574078 | A | G | 1 | a0001c0001t0007g0323 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.713-2793A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574078 | |||||||
chr12:3574221 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0049 others(61): Show |
65 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.713-2650A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574221 | |||||||
chr12:3574398 | A | G | 10 | a0001c0001t0001g0022 a0001c0001t0002g0103 a0001c0001t0007g0089 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.713-2473A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574398 | |||||||
chr12:3574528 | C | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18980.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.713-2343C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574528 | |||||||
chr12:3574630 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0049 others(59): Show |
63 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.713-2241G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574630 | |||||||
chr12:3574760 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.713-2111C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574760 | |||||||
chr12:3574876 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0049 others(56): Show |
60 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.713-1995A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574876 | |||||||
chr12:3574944 | A | G | 1 | a0001c0004t0001g0330 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.713-1927A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574944 | |||||||
chr12:3575006 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.713-1865A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575006 | |||||||
chr12:3575632 | A | G | 5 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0203 others(2): Show |
5 | HG01346.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-1239A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575632 | |||||||
chr12:3575876 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.713-995C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575876 | |||||||
chr12:3575890 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0002g0129 a0001c0001t0002g0334 |
3 | HG01891.hp1 HG02258.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.713-981G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575890 | |||||||
chr12:3575908 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.713-963A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575908 | |||||||
chr12:3575912 | G | A | 26 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0035 others(23): Show |
26 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.713-959G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575912 | |||||||
chr12:3575934 | A | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(137): Show |
140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.713-937A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575934 | |||||||
chr12:3576323 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.713-548T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576323 | |||||||
chr12:3576338 | T | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.713-533T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576338 | |||||||
chr12:3576424 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.713-447G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576424 | |||||||
chr12:3576543 | G | C | 2 | a0001c0001t0001g0203 a0001c0001t0014g0003 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.713-328G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576543 | |||||||
chr12:3576544 | AAGGAAGA others(26): Show |
A | 2 | a0001c0001t0001g0203 a0001c0001t0014g0003 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.713-326_713-294del others(33): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576544 | |||||||
chr12:3576597 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0049 others(59): Show |
63 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.713-274A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576597 | |||||||
chr12:3576700 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.713-171A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576700 | |||||||
chr12:3576714 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.713-157A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576714 | |||||||
chr12:3576829 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.713-42G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576829 | |||||||
chr12:3576850 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0007g0089 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.713-21C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576850 | |||||||
chr12:3577031 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0212 a0001c0001t0001g0247 |
3 | HG02074.hp1 NA18977.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.828+45C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577031 | |||||||
chr12:3577151 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.828+165C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577151 | |||||||
chr12:3577228 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.828+242G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577228 | |||||||
chr12:3577229 | C | T | 21 | a0001c0002t0002g0020 a0001c0002t0002g0043 a0001c0002t0002g0063 others(18): Show |
21 | HG00673.hp1 HG00738.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.828+243C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577229 | |||||||
chr12:3577281 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0014g0003 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.828+295C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577281 | |||||||
chr12:3577302 | C | T | 9 | a0001c0001t0002g0103 a0001c0002t0002g0045 a0001c0002t0002g0046 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+316C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577302 | |||||||
chr12:3577316 | T | G | 21 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0079 others(18): Show |
21 | HG00558.hp2 HG00735.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.828+330T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577316 | |||||||
chr12:3577405 | A | T | 1 | a0001c0001t0002g0129 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.828+419A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577405 | |||||||
chr12:3577406 | CACACCTT others(76): Show |
C | 2 | a0001c0001t0001g0203 a0001c0001t0014g0003 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.828+485_828+567del others(83): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3577406 | ||||||
chr12:3577462 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.828+476G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577462 | |||||||
chr12:3577479 | C | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.828+493C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577479 | |||||||
chr12:3577488 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.828+502A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577488 | |||||||
chr12:3577678 | AT | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.828+702delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3577678 | ||||||
chr12:3577684 | T | C | 49 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0079 others(46): Show |
49 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.828+698T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577684 | |||||||
chr12:3577754 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.828+768G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577754 | |||||||
chr12:3577776 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.828+790T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577776 | |||||||
chr12:3577891 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0002g0129 a0001c0001t0002g0334 others(1): Show |
4 | HG01891.hp1 HG02258.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.828+905C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577891 | |||||||
chr12:3577953 | C | G | 9 | a0001c0001t0002g0103 a0001c0002t0002g0045 a0001c0002t0002g0046 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+967C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577953 | |||||||
chr12:3578055 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+1069A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578055 | |||||||
chr12:3578086 | T | TAAAG | 92 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(89): Show |
94 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.828+1101_828+1102i others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3578086 | ||||||
chr12:3578221 | C | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0144 a0001c0001t0002g0129 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.828+1235C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578221 | |||||||
chr12:3578331 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(89): Show |
94 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.828+1345T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578331 | |||||||
chr12:3578340 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(72): Show |
76 | HG00099.hp1 HG00558.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.828+1354T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578340 | |||||||
chr12:3578347 | C | A | 2 | a0001c0001t0001g0327 a0001c0001t0012g0087 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.828+1361C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578347 | |||||||
chr12:3578391 | A | AT | 18 | a0001c0001t0001g0022 a0001c0001t0001g0074 a0001c0001t0001g0081 others(15): Show |
19 | HG00558.hp1 HG00597.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.828+1418dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3578391 | ||||||
chr12:3578623 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.828+1637A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578623 | |||||||
chr12:3578668 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0332 |
2 | HG01358.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.828+1682G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578668 | |||||||
chr12:3578700 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.828+1714G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578700 | |||||||
chr12:3579018 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0200 |
2 | NA18992.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.828+2032T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579018 | |||||||
chr12:3579151 | T | C | 1 | a0001c0001t0007g0323 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.828+2165T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579151 | |||||||
chr12:3579245 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.828+2259G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579245 | |||||||
chr12:3579262 | A | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0083 a0001c0001t0001g0148 others(11): Show |
14 | HG00423.hp1 HG00438.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.828+2276A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579262 | |||||||
chr12:3579282 | G | T | 1 | a0001c0002t0002g0325 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.828+2296G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579282 | |||||||
chr12:3579532 | G | A | 10 | a0001c0001t0002g0103 a0001c0002t0002g0045 a0001c0002t0002g0046 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.828+2546G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579532 | |||||||
chr12:3579551 | C | A | 1 | a0001c0001t0001g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.828+2565C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579551 | |||||||
chr12:3579577 | C | T | 2 | a0001c0001t0001g0327 a0001c0001t0012g0087 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.828+2591C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579577 | |||||||
chr12:3579677 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.828+2691T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579677 | |||||||
chr12:3579678 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0012g0087 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.828+2692G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579678 | |||||||
chr12:3579727 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.828+2741G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579727 | |||||||
chr12:3579821 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(88): Show |
93 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.828+2835A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579821 | |||||||
chr12:3580036 | T | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.829-3022T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580036 | |||||||
chr12:3580094 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.829-2964G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580094 | |||||||
chr12:3580113 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0142 others(2): Show |
5 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.829-2945C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580113 | |||||||
chr12:3580217 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.829-2841G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580217 | |||||||
chr12:3580335 | T | TGC | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0182 |
3 | HG01261.hp2 HG01358.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.829-2721_829-2720d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580335 | ||||||
chr12:3580337 | C | CGT | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.829-2692_829-2691d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | ||||||
chr12:3580337 | C | CGTGT | 50 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0054 others(47): Show |
51 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.829-2694_829-2691d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | ||||||
chr12:3580337 | C | CGTGTGT | 4 | a0001c0001t0001g0127 a0001c0001t0007g0323 a0001c0001t0008g0122 others(1): Show |
4 | HG02055.hp2 HG02135.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-2696_829-2691d others(8): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | ||||||
chr12:3580337 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.829-2700_829-2691d others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | ||||||
chr12:3580337 | CGT | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0110 others(5): Show |
8 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-2692_829-2691d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | ||||||
chr12:3580354 | G | GTA | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0100 others(6): Show |
9 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.829-2703_829-2702i others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580354 | ||||||
chr12:3580371 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0314 a0001c0001t0001g0326 others(2): Show |
6 | HG00099.hp1 HG01081.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.829-2687C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580371 | |||||||
chr12:3580379 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0049 others(76): Show |
81 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.829-2679T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580379 | |||||||
chr12:3580396 | A | C | 1 | a0001c0001t0007g0323 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.829-2662A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580396 | |||||||
chr12:3580450 | A | G | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-2608A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580450 | |||||||
chr12:3580484 | G | A | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-2574G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580484 | |||||||
chr12:3580518 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(21): Show |
25 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.829-2540A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580518 | |||||||
chr12:3580679 | C | T | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.829-2379C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580679 | |||||||
chr12:3580737 | A | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0088 others(8): Show |
11 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.829-2321A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580737 | |||||||
chr12:3580869 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-2189C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580869 | |||||||
chr12:3580998 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.829-2060G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580998 | |||||||
chr12:3581083 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.829-1975A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581083 | |||||||
chr12:3581225 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0144 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.829-1833G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581225 | |||||||
chr12:3581322 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.829-1736C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581322 | |||||||
chr12:3581388 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(63): Show |
67 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.829-1670A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581388 | |||||||
chr12:3581418 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.829-1640C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581418 | |||||||
chr12:3581533 | G | T | 2 | a0001c0001t0001g0327 a0001c0001t0012g0087 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.829-1525G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581533 | |||||||
chr12:3581647 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-1411C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581647 | |||||||
chr12:3581711 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.829-1347A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581711 | |||||||
chr12:3581791 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.829-1267G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581791 | |||||||
chr12:3581866 | A | G | 1 | a0001c0002t0002g0214 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.829-1192A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581866 | |||||||
chr12:3581917 | A | G | 6 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0327 others(3): Show |
6 | HG00642.hp1 HG01346.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.829-1141A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581917 | |||||||
chr12:3581966 | T | C | 9 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0051 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-1092T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581966 | |||||||
chr12:3582053 | C | G | 2 | a0001c0001t0001g0327 a0001c0001t0012g0087 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.829-1005C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582053 | |||||||
chr12:3582070 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0007g0089 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.829-988A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582070 | |||||||
chr12:3582198 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0172 |
2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.829-860G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582198 | |||||||
chr12:3582271 | G | A | 38 | a0001c0001t0001g0185 a0001c0002t0002g0020 a0001c0002t0002g0028 others(35): Show |
38 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.829-787G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582271 | |||||||
chr12:3582272 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.829-786C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582272 | |||||||
chr12:3582328 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.829-730A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582328 | |||||||
chr12:3582393 | T | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0060 others(10): Show |
13 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.829-665T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582393 | |||||||
chr12:3582443 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0083 a0001c0001t0001g0299 others(1): Show |
4 | NA18968.hp2 NA18969.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-615C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582443 | |||||||
chr12:3582590 | G | A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(5): Show |
9 | HG00558.hp1 HG00733.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-468G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582590 | |||||||
chr12:3582630 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.829-428C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582630 | |||||||
chr12:3582662 | A | C | 1 | a0001c0001t0001g0221 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.829-396A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582662 | |||||||
chr12:3582766 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.829-292T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582766 | |||||||
chr12:3582799 | A | C | 2 | a0001c0001t0002g0103 a0001c0001t0002g0129 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.829-259A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582799 | |||||||
chr12:3582813 | G | A | 1 | a0001c0002t0002g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.829-245G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582813 | |||||||
chr12:3582876 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.829-182C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582876 | |||||||
chr12:3582940 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0007g0089 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.829-118A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582940 | |||||||
chr12:3582947 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0187 |
3 | HG00621.hp2 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.829-111T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582947 | |||||||
chr12:3583237 | C | T | 5 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0327 others(2): Show |
5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+29C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583237 | |||||||
chr12:3583370 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0327 others(4): Show |
7 | HG01346.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+162T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583370 | |||||||
chr12:3583540 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0007g0089 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.979+332T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583540 | |||||||
chr12:3583544 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.979+336G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583544 | |||||||
chr12:3583741 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.979+533G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583741 | |||||||
chr12:3583746 | C | T | 7 | a0001c0002t0002g0028 a0001c0002t0002g0050 a0001c0002t0002g0184 others(4): Show |
7 | HG00735.hp1 HG01069.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+538C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583746 | |||||||
chr12:3583848 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.979+640C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583848 | |||||||
chr12:3583861 | G | A | 1 | a0001c0002t0002g0184 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.979+653G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583861 | |||||||
chr12:3583936 | T | C | 1 | a0001c0002t0002g0080 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.979+728T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583936 | |||||||
chr12:3584380 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.979+1172G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584380 | |||||||
chr12:3584477 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0094 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.979+1269G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584477 | |||||||
chr12:3584487 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0129 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979+1279C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584487 | |||||||
chr12:3584511 | A | G | 1 | a0001c0001t0001g0352 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.979+1303A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584511 | |||||||
chr12:3584645 | A | C | 2 | a0001c0001t0001g0249 a0001c0001t0004g0040 |
2 | HG02040.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.979+1437A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584645 | |||||||
chr12:3584718 | A | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(154): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.979+1510A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584718 | |||||||
chr12:3584730 | G | A | 1 | a0001c0003t0001g0260 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.979+1522G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584730 | |||||||
chr12:3584816 | C | T | 2 | a0001c0001t0001g0327 a0001c0001t0012g0087 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.979+1608C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584816 | |||||||
chr12:3585301 | G | A | 154 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(151): Show |
154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.979+2093G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585301 | |||||||
chr12:3585322 | C | T | 7 | a0001c0002t0002g0028 a0001c0002t0002g0050 a0001c0002t0002g0184 others(4): Show |
7 | HG00735.hp1 HG01069.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+2114C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585322 | |||||||
chr12:3585345 | C | CT | 202 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(199): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.979+2164dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | ||||||
chr12:3585345 | C | CTT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(94): Show |
99 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.979+2163_979+2164d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | ||||||
chr12:3585345 | C | CTTT | 9 | a0001c0001t0001g0030 a0001c0001t0001g0102 a0001c0001t0001g0116 others(6): Show |
9 | HG01934.hp1 HG01993.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.979+2162_979+2164d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | ||||||
chr12:3585345 | CTTTTTTT others(3): Show |
C | 1 | a0001c0009t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.979+2155_979+2164d others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | ||||||
chr12:3585345 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0236 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.979+2154_979+2164d others(13): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | ||||||
chr12:3585345 | CTTTTTTT others(6): Show |
C | 1 | a0001c0004t0001g0330 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.979+2152_979+2164d others(15): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | ||||||
chr12:3585436 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.979+2228G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585436 | |||||||
chr12:3585532 | A | AT | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.979+2339dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585532 | ||||||
chr12:3585650 | G | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0044 others(11): Show |
14 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.979+2442G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585650 | |||||||
chr12:3585704 | G | A | 2 | a0001c0001t0002g0334 a0001c0004t0001g0330 |
2 | HG00642.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.979+2496G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585704 | |||||||
chr12:3585714 | C | T | 5 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0327 others(2): Show |
5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2506C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585714 | |||||||
chr12:3585722 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0299 a0001c0009t0001g0107 |
3 | NA18968.hp2 NA18995.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.979+2514G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585722 | |||||||
chr12:3585728 | T | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0008 |
2 | NA18968.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.979+2520T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585728 | |||||||
chr12:3585964 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.979+2756C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585964 | |||||||
chr12:3586078 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.979+2870T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586078 | |||||||
chr12:3586179 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.979+2971A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586179 | |||||||
chr12:3586279 | G | A | 1 | a0001c0004t0001g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.979+3071G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586279 | |||||||
chr12:3586315 | T | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0327 others(2): Show |
5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+3107T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586315 | |||||||
chr12:3586354 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.979+3146G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586354 | |||||||
chr12:3586452 | C | T | 2 | a0001c0001t0007g0089 a0001c0001t0007g0323 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.979+3244C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586452 | |||||||
chr12:3586468 | A | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0202 a0001c0001t0001g0209 others(1): Show |
4 | NA18969.hp1 NA19009.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+3260A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586468 | |||||||
chr12:3586635 | A | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0102 a0001c0001t0001g0104 others(2): Show |
5 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+3427A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586635 | |||||||
chr12:3586840 | T | A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0327 others(2): Show |
5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+3632T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586840 | |||||||
chr12:3586858 | C | T | 1 | a0001c0002t0011g0101 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.979+3650C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586858 | |||||||
chr12:3586946 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.979+3738C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586946 | |||||||
chr12:3586947 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0129 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979+3739G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586947 | |||||||
chr12:3587052 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.979+3844C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587052 | |||||||
chr12:3587202 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.979+3994T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587202 | |||||||
chr12:3587463 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0187 a0001c0001t0001g0308 |
3 | HG00621.hp2 NA18998.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.979+4255G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587463 | |||||||
chr12:3587512 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0137 |
3 | HG02300.hp1 HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.979+4304C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587512 | |||||||
chr12:3587515 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.979+4307G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587515 | |||||||
chr12:3587541 | T | C | 7 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0327 others(4): Show |
7 | HG01346.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+4333T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587541 | |||||||
chr12:3587781 | T | C | 1 | a0001c0004t0001g0330 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.980-4450T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587781 | |||||||
chr12:3587787 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.980-4444C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587787 | |||||||
chr12:3587804 | G | A | 1 | a0001c0002t0009g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.980-4427G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587804 | |||||||
chr12:3587875 | C | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0129 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-4356C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587875 | |||||||
chr12:3588203 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0144 |
3 | HG01891.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.980-4028T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588203 | |||||||
chr12:3588244 | A | C | 9 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0160 others(6): Show |
10 | HG00558.hp1 HG00733.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.980-3987A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588244 | |||||||
chr12:3588593 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0129 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-3638C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588593 | |||||||
chr12:3588673 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(80): Show |
85 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.980-3558A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588673 | |||||||
chr12:3589086 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0129 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-3145G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589086 | |||||||
chr12:3589140 | A | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0144 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.980-3091A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589140 | |||||||
chr12:3589186 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.980-3045A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589186 | |||||||
chr12:3589307 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0203 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.980-2924C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589307 | |||||||
chr12:3589312 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.980-2919C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589312 | |||||||
chr12:3589671 | G | T | 1 | a0001c0001t0001g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.980-2560G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589671 | |||||||
chr12:3589677 | C | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0088 others(8): Show |
11 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.980-2554C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589677 | |||||||
chr12:3589681 | G | A | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-2550G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589681 | |||||||
chr12:3589755 | A | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0088 others(8): Show |
11 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.980-2476A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589755 | |||||||
chr12:3589761 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.980-2470G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589761 | |||||||
chr12:3589815 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.980-2416C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589815 | |||||||
chr12:3589860 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(1): Show |
4 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-2371G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589860 | |||||||
chr12:3589877 | A | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0144 others(3): Show |
6 | HG01891.hp1 HG02896.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-2354A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589877 | |||||||
chr12:3590027 | G | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(71): Show |
75 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.980-2204G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590027 | |||||||
chr12:3590048 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.980-2183G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590048 | |||||||
chr12:3590097 | G | A | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-2134G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590097 | |||||||
chr12:3590142 | A | G | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-2089A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590142 | |||||||
chr12:3590396 | G | A | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.980-1835G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590396 | |||||||
chr12:3590495 | C | G | 1 | a0001c0001t0012g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-1736C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590495 | |||||||
chr12:3590497 | T | C | 2 | a0001c0001t0002g0103 a0001c0001t0002g0129 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-1734T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590497 | |||||||
chr12:3590520 | T | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0144 others(2): Show |
5 | HG01891.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-1711T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590520 | |||||||
chr12:3590522 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0144 |
3 | HG01891.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.980-1709C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590522 | |||||||
chr12:3590632 | T | TA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(14): Show |
17 | HG00642.hp2 HG01071.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.980-1583dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3590632 | ||||||
chr12:3590632 | TA | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(55): Show |
59 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.980-1583delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3590632 | ||||||
chr12:3590781 | T | C | 6 | a0001c0001t0001g0215 a0001c0001t0001g0219 a0001c0001t0001g0222 others(3): Show |
6 | NA18612.hp1 NA18943.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.980-1450T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590781 | |||||||
chr12:3590871 | G | A | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.980-1360G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590871 | |||||||
chr12:3590912 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.980-1319G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590912 | |||||||
chr12:3590921 | G | A | 37 | a0001c0002t0002g0020 a0001c0002t0002g0028 a0001c0002t0002g0043 others(34): Show |
37 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.980-1310G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590921 | |||||||
chr12:3591217 | G | A | 2 | a0001c0001t0007g0089 a0001c0001t0007g0323 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.980-1014G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591217 | |||||||
chr12:3591407 | C | CT | 138 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(135): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.980-803dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3591407 | ||||||
chr12:3591407 | C | CTT | 21 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(18): Show |
21 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.980-804_980-803dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3591407 | ||||||
chr12:3591407 | CT | C | 41 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0263 others(38): Show |
41 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.980-803delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3591407 | ||||||
chr12:3591608 | G | T | 1 | a0001c0004t0001g0330 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.980-623G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591608 | |||||||
chr12:3591621 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.980-610T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591621 | |||||||
chr12:3591896 | A | C | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.980-335A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591896 | |||||||
chr12:3591975 | G | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(1): Show |
4 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-256G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591975 | |||||||
chr12:3592224 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0055 others(23): Show |
27 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(24): Show |
splice_region_variant&intron_variant | LOW | c.980-7C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3592224 | |||||||
chr12:3592503 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1101+151G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592503 | |||||||
chr12:3592531 | C | G | 1 | a0001c0001t0002g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1101+179C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592531 | |||||||
chr12:3592725 | C | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(3): Show |
6 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+373C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592725 | |||||||
chr12:3592743 | A | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(3): Show |
6 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1102-356A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592743 | |||||||
chr12:3592748 | C | G | 3 | a0001c0002t0002g0046 a0001c0002t0002g0051 a0001c0002t0002g0086 |
3 | HG01884.hp2 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1102-351C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592748 | |||||||
chr12:3592783 | A | G | 51 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0074 others(48): Show |
51 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1102-316A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592783 | |||||||
chr12:3592823 | T | C | 6 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(3): Show |
6 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1102-276T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592823 | |||||||
chr12:3592852 | C | T | 44 | a0001c0001t0001g0074 a0001c0001t0001g0160 a0001c0001t0001g0171 others(41): Show |
44 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1102-247C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592852 | |||||||
chr12:3593053 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1102-46A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3593053 |