Item | Value |
---|---|
geneid | 387338 |
ensemblid | ENSG00000117481.11 |
hgncid | 31802 |
symbol | NSUN4 |
name | NOP2/Sun RNA methyltransferase 4 |
refseq_nuc | NM_199044.4 |
refseq_prot | NP_950245.2 |
ensembl_nuc | ENST00000474844.6 |
ensembl_prot | ENSP00000419740.1 |
mane_status | MANE Select |
chr | chr1 |
start | 46340807 |
end | 46365018 |
strand | + |
ver | v1.2 |
region | chr1:46340807-46365018 |
region5000 | chr1:46335807-46370018 |
regionname0 | NSUN4_chr1_46340807_46365018 |
regionname5000 | NSUN4_chr1_46335807_46370018 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 384 | 145 | 60 | 28 | 44 | 3 | 8 | 37 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0002 | 0/0 | 384 | 108 | 9 | 24 | 61 | 8 | 6 | 41 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0003 | 0/0 | 384 | 87 | 5 | 7 | 50 | 4 | 21 | 39 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0004 | 0/0 | 384 | 28 | 8 | 12 | 2 | 3 | 3 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0005 | 0/0 | 384 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0006 | 0/0 | 384 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0007 | 0/0 | 384 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0008 | 0/0 | 280 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(275): Show |
chr1 | 46335807 | 46370018 |
a0009 | 0/0 | 384 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0010 | 0/0 | 384 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
a0011 | 0/0 | 384 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | MAALT others(379): Show |
chr1 | 46335807 | 46370018 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1152 | 145 | 60 | 28 | 44 | 3 | 8 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0002c0002 | 0/0 | 1152 | 108 | 9 | 24 | 61 | 8 | 6 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0003c0003 | 0/0 | 1152 | 87 | 5 | 7 | 50 | 4 | 21 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0004c0004 | 0/0 | 1152 | 28 | 8 | 12 | 2 | 3 | 3 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0005c0005 | 0/0 | 1152 | 11 | 11 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0006c0006 | 0/0 | 1152 | 3 | 0 | 3 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0007c0007 | 0/0 | 1152 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0008c0009 | 0/0 | 1152 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0009c0011 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0010c0010 | 0/0 | 1152 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 | ||
a0011c0008 | 0/0 | 1152 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATGGC others(1147): Show |
chr1 | 46335807 | 46370018 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4349 | 8 | 0 | 2 | 6 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0002 | 1/1 | 4347 | 88 | 25 | 19 | 31 | 3 | 8 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4342): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0005 | 0/0 | 4348 | 10 | 3 | 1 | 6 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0007 | 0/0 | 4350 | 10 | 8 | 2 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0011 | 0/0 | 4348 | 2 | 0 | 1 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0016 | 0/0 | 4351 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4346): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0017 | 0/0 | 4347 | 3 | 2 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4342): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0021 | 0/0 | 4349 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0022 | 0/0 | 4348 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0023 | 0/0 | 4348 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0026 | 0/0 | 4348 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0028 | 0/0 | 4347 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4342): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0029 | 0/0 | 4348 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0030 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0035 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4342): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0039 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0040 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0041 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4342): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0042 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0043 | 0/0 | 4348 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0044 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4342): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0045 | 0/0 | 4351 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4346): Show |
chr1 | 46335807 | 46370018 |
a0001c0001t0050 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0001 | 0/0 | 4349 | 84 | 7 | 20 | 46 | 7 | 4 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0005 | 0/0 | 4348 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0009 | 0/0 | 4350 | 8 | 1 | 1 | 5 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0011 | 0/0 | 4348 | 4 | 0 | 0 | 4 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0012 | 0/0 | 4349 | 5 | 1 | 3 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0020 | 0/0 | 4350 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0037 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0002c0002t0038 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0003 | 0/0 | 4348 | 52 | 4 | 3 | 36 | 0 | 9 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0006 | 0/0 | 4348 | 12 | 0 | 2 | 0 | 3 | 7 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0008 | 0/0 | 4349 | 9 | 1 | 0 | 7 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0014 | 0/0 | 4349 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0024 | 0/0 | 4350 | 2 | 0 | 0 | 1 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0025 | 0/0 | 4349 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0031 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0032 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0033 | 0/0 | 4348 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0034 | 0/0 | 4348 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0046 | 0/0 | 4348 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0047 | 0/0 | 4348 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0048 | 0/0 | 4348 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0003c0003t0049 | 0/0 | 4348 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0004c0004t0004 | 0/0 | 4350 | 15 | 1 | 8 | 1 | 3 | 2 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0004c0004t0013 | 0/0 | 4350 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0004c0004t0018 | 0/0 | 4351 | 3 | 0 | 2 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4346): Show |
chr1 | 46335807 | 46370018 |
a0004c0004t0019 | 0/0 | 4351 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4346): Show |
chr1 | 46335807 | 46370018 |
a0004c0004t0052 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0004c0004t0054 | 0/0 | 4352 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4347): Show |
chr1 | 46335807 | 46370018 |
a0004c0004t0055 | 0/0 | 4351 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4346): Show |
chr1 | 46335807 | 46370018 |
a0005c0005t0010 | 0/0 | 4350 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4345): Show |
chr1 | 46335807 | 46370018 |
a0005c0005t0015 | 0/0 | 4351 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4346): Show |
chr1 | 46335807 | 46370018 |
a0005c0005t0036 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0006c0006t0002 | 0/0 | 4347 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4342): Show |
chr1 | 46335807 | 46370018 |
a0006c0006t0005 | 0/0 | 4348 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0007c0007t0027 | 0/0 | 4349 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0008c0009t0014 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0009c0011t0051 | 0/0 | 4348 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
a0010c0010t0053 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | ATCCC others(4344): Show |
chr1 | 46335807 | 46370018 |
a0011c0008t0003 | 0/0 | 4348 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | ACCCC others(4343): Show |
chr1 | 46335807 | 46370018 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0003 | 0/0 | 8 | 0 | 4 | 1 | 2 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0011g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0016g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0016g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0017g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0017g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0021g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0021g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0022g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0022g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0023g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0023g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0026g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0026g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0028g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0028g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0029g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0030g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0035g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0039g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0040g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0041g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0042g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0043g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0044g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0045g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0001c0001t0050g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0002 | 0/0 | 11 | 2 | 1 | 7 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0006 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0009g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0009g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0011g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0012g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0012g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0012g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0012g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0020g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0037g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0002c0002t0038g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0001 | 0/0 | 11 | 1 | 0 | 6 | 0 | 4 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0006g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0008g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0008g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0008g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0014g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0014g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0024g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0024g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0025g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0025g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0031g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0032g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0033g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0034g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0046g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0047g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0048g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0003c0003t0049g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0013g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0013g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0018g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0018g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0018g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0019g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0019g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0052g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0054g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0004c0004t0055g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0010g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0010g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0015g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0005c0005t0036g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0006c0006t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0006c0006t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0006c0006t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0007c0007t0027g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0007c0007t0027g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0008c0009t0014g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0009c0011t0051g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0010c0010t0053g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
a0011c0008t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0212 | EUR | GBR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00140 | hp1 | a0004 | c0004 | t0004 | g0271 | EUR | GBR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00140 | hp2 | a0003 | c0003 | t0006 | g0153 | EUR | GBR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0251 | EUR | FIN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00323 | hp1 | a0002 | c0002 | t0012 | g0258 | EUR | FIN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | FIN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00408 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00423 | hp2 | a0003 | c0003 | t0008 | g0005 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00544 | hp1 | a0004 | c0004 | t0004 | g0290 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00544 | hp2 | a0004 | c0004 | t0052 | g0265 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00609 | hp1 | a0002 | c0002 | t0005 | g0238 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00621 | hp1 | a0002 | c0002 | t0009 | g0011 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00621 | hp2 | a0002 | c0002 | t0009 | g0198 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0132 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00642 | hp2 | a0002 | c0002 | t0012 | g0232 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00673 | hp1 | a0003 | c0003 | t0003 | g0171 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00733 | hp1 | a0003 | c0003 | t0006 | g0016 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00733 | hp2 | a0003 | c0003 | t0033 | g0263 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00735 | hp1 | a0004 | c0004 | t0018 | g0270 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00735 | hp2 | a0003 | c0003 | t0003 | g0010 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG00741 | hp2 | a0004 | c0004 | t0004 | g0282 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01069 | hp2 | a0001 | c0001 | t0029 | g0127 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01081 | hp2 | a0004 | c0004 | t0004 | g0278 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01109 | hp2 | a0002 | c0002 | t0012 | g0218 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01167 | hp2 | a0004 | c0004 | t0004 | g0277 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01168 | hp2 | a0002 | c0002 | t0012 | g0245 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01169 | hp1 | a0004 | c0004 | t0004 | g0285 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01192 | hp1 | a0003 | c0003 | t0032 | g0084 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01243 | hp2 | a0004 | c0004 | t0055 | g0288 | AMR | PUR | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01255 | hp1 | a0004 | c0004 | t0018 | g0273 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01256 | hp1 | a0004 | c0004 | t0004 | g0281 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01256 | hp2 | a0003 | c0003 | t0006 | g0151 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01258 | hp1 | a0004 | c0004 | t0004 | g0272 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01258 | hp2 | a0004 | c0004 | t0004 | g0275 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01261 | hp1 | a0001 | c0001 | t0011 | g0050 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01261 | hp2 | a0004 | c0004 | t0004 | g0279 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01346 | hp1 | a0006 | c0006 | t0005 | g0047 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01346 | hp2 | a0002 | c0002 | t0009 | g0007 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01433 | hp1 | a0006 | c0006 | t0002 | g0012 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01515 | hp1 | a0003 | c0003 | t0034 | g0083 | EUR | IBS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0032 | EUR | IBS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01516 | hp1 | a0004 | c0004 | t0004 | g0289 | EUR | IBS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0219 | EUR | IBS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0031 | EUR | IBS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0032 | EUR | IBS | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01884 | hp2 | a0001 | c0001 | t0041 | g0141 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0134 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01891 | hp2 | a0005 | c0005 | t0015 | g0190 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01943 | hp1 | a0001 | c0001 | t0017 | g0112 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01975 | hp1 | a0006 | c0006 | t0002 | g0053 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01981 | hp1 | a0004 | c0004 | t0054 | g0269 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01981 | hp2 | a0001 | c0001 | t0040 | g0008 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02015 | hp1 | a0003 | c0003 | t0003 | g0186 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02015 | hp2 | a0002 | c0002 | t0011 | g0229 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02027 | hp2 | a0002 | c0002 | t0009 | g0240 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0130 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0138 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02056 | hp1 | a0003 | c0003 | t0003 | g0180 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02056 | hp2 | a0003 | c0003 | t0024 | g0157 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02074 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02080 | hp1 | a0003 | c0003 | t0003 | g0173 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02080 | hp2 | a0003 | c0003 | t0003 | g0029 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02132 | hp1 | a0002 | c0002 | t0005 | g0034 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02132 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02145 | hp1 | a0004 | c0004 | t0013 | g0286 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02145 | hp2 | a0002 | c0002 | t0009 | g0207 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02155 | hp1 | a0003 | c0003 | t0047 | g0162 | EAS | CDX | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | CDX | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | CDX | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CDX | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02257 | hp1 | a0005 | c0005 | t0010 | g0191 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02280 | hp1 | a0003 | c0003 | t0003 | g0176 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02293 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02300 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | KHV | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02572 | hp1 | a0001 | c0001 | t0022 | g0082 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02602 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02602 | hp2 | a0003 | c0003 | t0014 | g0014 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02615 | hp2 | a0001 | c0001 | t0026 | g0023 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02622 | hp1 | a0001 | c0001 | t0017 | g0025 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02622 | hp2 | a0001 | c0001 | t0039 | g0195 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02630 | hp1 | a0001 | c0001 | t0043 | g0089 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02630 | hp2 | a0001 | c0001 | t0017 | g0025 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0139 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02683 | hp2 | a0004 | c0004 | t0004 | g0283 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02698 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02698 | hp2 | a0003 | c0003 | t0031 | g0152 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02717 | hp1 | a0007 | c0007 | t0027 | g0268 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02735 | hp1 | a0003 | c0003 | t0006 | g0086 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02735 | hp2 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02738 | hp1 | a0003 | c0003 | t0014 | g0146 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02738 | hp2 | a0003 | c0003 | t0024 | g0163 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02818 | hp2 | a0002 | c0002 | t0012 | g0002 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02895 | hp1 | a0001 | c0001 | t0028 | g0142 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02895 | hp2 | a0003 | c0003 | t0003 | g0149 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02896 | hp1 | a0005 | c0005 | t0010 | g0030 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02897 | hp1 | a0001 | c0001 | t0028 | g0143 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02897 | hp2 | a0005 | c0005 | t0010 | g0030 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02922 | hp1 | a0004 | c0004 | t0019 | g0276 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02922 | hp2 | a0004 | c0004 | t0013 | g0036 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02965 | hp1 | a0005 | c0005 | t0010 | g0193 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02965 | hp2 | a0004 | c0004 | t0013 | g0036 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02970 | hp1 | a0001 | c0001 | t0050 | g0009 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02970 | hp2 | a0001 | c0001 | t0042 | g0264 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03017 | hp1 | a0003 | c0003 | t0003 | g0170 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03041 | hp2 | a0005 | c0005 | t0036 | g0194 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03098 | hp1 | a0005 | c0005 | t0015 | g0192 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0133 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03139 | hp1 | a0001 | c0001 | t0023 | g0088 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03139 | hp2 | a0003 | c0003 | t0003 | g0001 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03195 | hp2 | a0005 | c0005 | t0010 | g0196 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0140 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03225 | hp2 | a0004 | c0004 | t0019 | g0284 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03239 | hp1 | a0003 | c0003 | t0006 | g0144 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03486 | hp1 | a0003 | c0003 | t0008 | g0145 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03486 | hp2 | a0001 | c0001 | t0045 | g0131 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03490 | hp2 | a0003 | c0003 | t0006 | g0014 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03491 | hp2 | a0003 | c0003 | t0003 | g0183 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03516 | hp1 | a0001 | c0001 | t0021 | g0135 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0090 | AFR | ESN | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03579 | hp1 | a0005 | c0005 | t0010 | g0017 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03579 | hp2 | a0003 | c0003 | t0003 | g0147 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03654 | hp1 | a0003 | c0003 | t0006 | g0087 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03669 | hp1 | a0004 | c0004 | t0018 | g0280 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03688 | hp1 | a0003 | c0003 | t0008 | g0189 | SAS | STU | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0260 | SAS | STU | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03710 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03710 | hp2 | a0003 | c0003 | t0006 | g0014 | SAS | PJL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03831 | hp1 | a0002 | c0002 | t0009 | g0019 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03831 | hp2 | a0003 | c0003 | t0003 | g0174 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03834 | hp2 | a0004 | c0004 | t0004 | g0291 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03927 | hp1 | a0003 | c0003 | t0006 | g0148 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03942 | hp1 | a0003 | c0003 | t0003 | g0168 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03942 | hp2 | a0008 | c0009 | t0014 | g0085 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0200 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG04199 | hp1 | a0003 | c0003 | t0003 | g0164 | SAS | STU | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG04199 | hp2 | a0002 | c0002 | t0037 | g0246 | SAS | STU | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | YRI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18612 | hp1 | a0002 | c0002 | t0038 | g0002 | EAS | CHB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | CHB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | CHB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18906 | hp1 | a0009 | c0011 | t0051 | g0266 | AFR | YRI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | YRI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18941 | hp2 | a0003 | c0003 | t0003 | g0158 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18944 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18948 | hp1 | a0002 | c0002 | t0011 | g0007 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18949 | hp1 | a0003 | c0003 | t0008 | g0028 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18949 | hp2 | a0002 | c0002 | t0009 | g0011 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18950 | hp1 | a0003 | c0003 | t0003 | g0161 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18956 | hp1 | a0003 | c0003 | t0025 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18957 | hp2 | a0002 | c0002 | t0011 | g0241 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18959 | hp2 | a0010 | c0010 | t0053 | g0038 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18962 | hp2 | a0003 | c0003 | t0003 | g0187 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18968 | hp1 | a0003 | c0003 | t0003 | g0175 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18970 | hp2 | a0003 | c0003 | t0008 | g0005 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18973 | hp1 | a0003 | c0003 | t0048 | g0177 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18974 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18975 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18977 | hp1 | a0002 | c0002 | t0020 | g0002 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0182 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18979 | hp2 | a0003 | c0003 | t0008 | g0028 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18981 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18984 | hp1 | a0003 | c0003 | t0003 | g0184 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18985 | hp1 | a0003 | c0003 | t0003 | g0178 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18986 | hp2 | a0003 | c0003 | t0049 | g0181 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18988 | hp1 | a0003 | c0003 | t0003 | g0169 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18988 | hp2 | a0003 | c0003 | t0003 | g0160 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18989 | hp2 | a0003 | c0003 | t0003 | g0159 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18994 | hp2 | a0002 | c0002 | t0009 | g0235 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18998 | hp2 | a0003 | c0003 | t0008 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19004 | hp2 | a0003 | c0003 | t0003 | g0166 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19005 | hp2 | a0003 | c0003 | t0003 | g0156 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19006 | hp1 | a0003 | c0003 | t0003 | g0167 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19030 | hp1 | a0001 | c0001 | t0022 | g0081 | AFR | LWK | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | LWK | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0136 | AFR | LWK | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19043 | hp2 | a0001 | c0001 | t0021 | g0137 | AFR | LWK | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19055 | hp2 | a0003 | c0003 | t0008 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19056 | hp1 | a0003 | c0003 | t0025 | g0185 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19060 | hp2 | a0003 | c0003 | t0003 | g0165 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19062 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19062 | hp2 | a0002 | c0002 | t0005 | g0224 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19063 | hp2 | a0003 | c0003 | t0003 | g0155 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19064 | hp2 | a0003 | c0003 | t0003 | g0154 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19065 | hp1 | a0003 | c0003 | t0008 | g0005 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19068 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19074 | hp1 | a0002 | c0002 | t0011 | g0259 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19075 | hp1 | a0003 | c0003 | t0003 | g0188 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19081 | hp2 | a0003 | c0003 | t0003 | g0172 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19087 | hp2 | a0001 | c0001 | t0011 | g0066 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19088 | hp1 | a0003 | c0003 | t0003 | g0029 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19090 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19090 | hp2 | a0002 | c0002 | t0020 | g0217 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19091 | hp1 | a0003 | c0003 | t0003 | g0179 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | YRI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA19240 | hp2 | a0007 | c0007 | t0027 | g0267 | AFR | YRI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20129 | hp1 | a0001 | c0001 | t0016 | g0129 | AFR | ASW | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ASW | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | TSI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20752 | hp2 | a0003 | c0003 | t0006 | g0016 | EUR | TSI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20805 | hp1 | a0003 | c0003 | t0006 | g0150 | EUR | TSI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20805 | hp2 | a0004 | c0004 | t0004 | g0274 | EUR | TSI | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20905 | hp1 | a0003 | c0003 | t0006 | g0016 | SAS | GIH | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20905 | hp2 | a0011 | c0008 | t0003 | g0001 | SAS | GIH | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02109 | hp1 | a0001 | c0001 | t0030 | g0126 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02109 | hp2 | a0004 | c0004 | t0004 | g0035 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02486 | hp1 | a0001 | c0001 | t0044 | g0091 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02486 | hp2 | a0004 | c0004 | t0013 | g0287 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02559 | hp1 | a0004 | c0004 | t0019 | g0035 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | ACB | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03471 | hp1 | a0001 | c0001 | t0035 | g0024 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG06807 | hp1 | a0001 | c0001 | t0026 | g0113 | AFR | USA | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
HG06807 | hp2 | a0005 | c0005 | t0015 | g0017 | AFR | USA | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18955 | hp1 | a0003 | c0003 | t0046 | g0001 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA18955 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA20300 | hp2 | a0005 | c0005 | t0010 | g0017 | AFR | USA | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | LWK | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | LWK | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0079 | REF | REF | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0116 | REF | REF | NSUN4_chr1_46335807_46370018 | NSUN4 | chr1 | 46335807 | 46370018 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46340878 | C | T | 3 | a0004 a0009 a0010 |
30 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(27): Show |
missense_variant | MODERATE | c.52C>T | p.Leu18Phe | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/6 | 72/4347 | 52/1155 | 18/384 | chr1 | 46340878 | |||
chr1:46344858 | A | G | 1 | a0002 | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
missense_variant | MODERATE | c.151A>G | p.Thr51Ala | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/6 | 171/4347 | 151/1155 | 51/384 | chr1 | 46344858 | |||
chr1:46345091 | C | A | 1 | a0005 | 11 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(8): Show |
missense_variant | MODERATE | c.384C>A | p.Asn128Lys | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/6 | 404/4347 | 384/1155 | 128/384 | chr1 | 46345091 | |||
chr1:46345125 | A | G | 1 | a0006 | 3 | HG01346.hp1 HG01433.hp1 HG01975.hp1 |
missense_variant | MODERATE | c.418A>G | p.Ser140Gly | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/6 | 438/4347 | 418/1155 | 140/384 | chr1 | 46345125 | |||
chr1:46360774 | G | A | 1 | a0011 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.824G>A | p.Arg275Gln | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/6 | 844/4347 | 824/1155 | 275/384 | chr1 | 46360774 | |||
chr1:46360791 | C | T | 1 | a0008 | 1 | HG03942.hp2 | stop_gained | HIGH | c.841C>T | p.Arg281* | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/6 | 861/4347 | 841/1155 | 281/384 | chr1 | 46360791 | |||
chr1:46361665 | T | C | 2 | a0007 a0010 |
3 | HG02717.hp1 NA18959.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.974T>C | p.Ile325Thr | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 994/4347 | 974/1155 | 325/384 | chr1 | 46361665 | |||
chr1:46361784 | A | G | 4 | a0003 a0008 a0009 others(1): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
missense_variant | MODERATE | c.1093A>G | p.Ile365Val | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1113/4347 | 1093/1155 | 365/384 | chr1 | 46361784 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46344998 | T | C | 3 | a0004c0004 a0007c0007 a0010c0010 |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
synonymous_variant | LOW | c.291T>C | p.Asp97Asp | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/6 | 311/4347 | 291/1155 | 97/384 | chr1 | 46344998 | |||
chr1:46361813 | C | T | 3 | a0004c0004 a0007c0007 a0010c0010 |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
synonymous_variant | LOW | c.1122C>T | p.Pro374Pro | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1142/4347 | 1122/1155 | 374/384 | chr1 | 46361813 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46340808 | C | T | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
30 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-19C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/6 | 19 | chr1 | 46340808 | ||||||
chr1:46361940 | C | T | 1 | a0001c0001t0028 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*94C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 94 | chr1 | 46361940 | ||||||
chr1:46362056 | A | C | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*210A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 210 | chr1 | 46362056 | ||||||
chr1:46362097 | C | T | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*251C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 251 | chr1 | 46362097 | ||||||
chr1:46362106 | G | A | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG01069.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*260G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 260 | chr1 | 46362106 | ||||||
chr1:46362199 | G | A | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*353G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 353 | chr1 | 46362199 | ||||||
chr1:46362358 | A | G | 1 | a0001c0001t0026 | 2 | HG02615.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*512A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 512 | chr1 | 46362358 | ||||||
chr1:46362437 | A | G | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*591A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 591 | chr1 | 46362437 | ||||||
chr1:46362438 | C | A | 7 | a0003c0003t0006 a0003c0003t0014 a0003c0003t0031 others(4): Show |
19 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*592C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 592 | chr1 | 46362438 | ||||||
chr1:46362489 | C | T | 1 | a0001c0001t0050 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*643C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 643 | chr1 | 46362489 | ||||||
chr1:46362688 | C | T | 17 | a0003c0003t0003 a0003c0003t0006 a0003c0003t0008 others(14): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*842C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 842 | chr1 | 46362688 | ||||||
chr1:46362788 | C | T | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*942C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 942 | chr1 | 46362788 | ||||||
chr1:46362985 | C | CT | 8 | a0001c0001t0030 a0004c0004t0004 a0004c0004t0013 others(5): Show |
30 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1152dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1153 | INFO_REALIGN_3_PRIME | chr1 | 46362985 | |||||
chr1:46363028 | A | G | 8 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(5): Show |
30 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1182A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1182 | chr1 | 46363028 | ||||||
chr1:46363059 | G | A | 1 | a0001c0001t0035 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1213 | chr1 | 46363059 | ||||||
chr1:46363062 | T | C | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1216T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1216 | chr1 | 46363062 | ||||||
chr1:46363079 | C | A | 1 | a0003c0003t0046 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1233 | chr1 | 46363079 | ||||||
chr1:46363303 | C | T | 1 | a0001c0001t0028 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1457C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1457 | chr1 | 46363303 | ||||||
chr1:46363341 | A | G | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1495A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1495 | chr1 | 46363341 | ||||||
chr1:46363423 | C | G | 1 | a0001c0001t0045 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1577 | chr1 | 46363423 | ||||||
chr1:46363632 | A | T | 1 | a0003c0003t0049 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1786 | chr1 | 46363632 | ||||||
chr1:46363720 | A | G | 2 | a0004c0004t0013 a0004c0004t0055 |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1874A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 1874 | chr1 | 46363720 | ||||||
chr1:46364036 | G | T | 1 | a0001c0001t0044 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2190G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2190 | chr1 | 46364036 | ||||||
chr1:46364141 | C | CA | 21 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(18): Show |
142 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*2314dupA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2315 | INFO_REALIGN_3_PRIME | chr1 | 46364141 | |||||
chr1:46364141 | C | CAA | 4 | a0002c0002t0020 a0005c0005t0010 a0005c0005t0015 others(1): Show |
13 | HG01891.hp2 HG02257.hp1 HG02896.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2313_*2314dupAA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2315 | INFO_REALIGN_3_PRIME | chr1 | 46364141 | |||||
chr1:46364262 | T | TG | 3 | a0001c0001t0023 a0001c0001t0042 a0001c0001t0043 |
4 | HG02630.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2419dupG | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2420 | INFO_REALIGN_3_PRIME | chr1 | 46364262 | |||||
chr1:46364332 | C | CA | 29 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0022 others(26): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2507dupA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2508 | INFO_REALIGN_3_PRIME | chr1 | 46364332 | |||||
chr1:46364332 | C | CAA | 16 | a0001c0001t0007 a0001c0001t0021 a0001c0001t0040 others(13): Show |
64 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2506_*2507dupAA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2508 | INFO_REALIGN_3_PRIME | chr1 | 46364332 | |||||
chr1:46364332 | C | CAAA | 4 | a0001c0001t0016 a0001c0001t0045 a0004c0004t0019 others(1): Show |
8 | HG01981.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2505_*2507dupAAA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2508 | INFO_REALIGN_3_PRIME | chr1 | 46364332 | |||||
chr1:46364415 | G | A | 1 | a0002c0002t0012 | 5 | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2569G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2569 | chr1 | 46364415 | ||||||
chr1:46364439 | G | A | 1 | a0003c0003t0047 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2593G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2593 | chr1 | 46364439 | ||||||
chr1:46364466 | C | T | 1 | a0003c0003t0034 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2620C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2620 | chr1 | 46364466 | ||||||
chr1:46364499 | G | A | 1 | a0002c0002t0037 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2653G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2653 | chr1 | 46364499 | ||||||
chr1:46364524 | C | T | 1 | a0001c0001t0017 | 3 | HG01943.hp1 HG02622.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2678C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2678 | chr1 | 46364524 | ||||||
chr1:46364577 | C | T | 4 | a0001c0001t0039 a0005c0005t0010 a0005c0005t0015 others(1): Show |
12 | HG01891.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2731C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2731 | chr1 | 46364577 | ||||||
chr1:46364585 | C | T | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2739C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2739 | chr1 | 46364585 | ||||||
chr1:46364632 | A | C | 1 | a0003c0003t0048 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2786A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2786 | chr1 | 46364632 | ||||||
chr1:46364758 | G | A | 40 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0021 others(37): Show |
158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*2912G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2912 | chr1 | 46364758 | ||||||
chr1:46364775 | A | C | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0018 others(6): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2929A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 2929 | chr1 | 46364775 | ||||||
chr1:46364921 | G | T | 1 | a0002c0002t0038 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3075G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 3075 | chr1 | 46364921 | ||||||
chr1:46364962 | C | T | 1 | a0001c0001t0043 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3116C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 6/6 | 3116 | chr1 | 46364962 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46340988 | G | A | 1 | a0001c0001t0007g0037 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.93+69G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46340988 | |||||||
chr1:46341031 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.93+112A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341031 | |||||||
chr1:46341046 | T | A | 1 | a0004c0004t0052g0265 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.93+127T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341046 | |||||||
chr1:46341069 | C | G | 1 | a0004c0004t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.93+150C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341069 | |||||||
chr1:46341080 | C | G | 1 | a0003c0003t0033g0263 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.93+161C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341080 | |||||||
chr1:46341080 | C | T | 1 | a0001c0001t0042g0264 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.93+161C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341080 | |||||||
chr1:46341287 | C | T | 84 | a0001c0001t0002g0197 a0002c0002t0001g0002 a0002c0002t0001g0006 others(81): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.93+368C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341287 | |||||||
chr1:46341301 | C | G | 10 | a0001c0001t0039g0195 a0005c0005t0010g0017 a0005c0005t0010g0030 others(7): Show |
12 | HG01891.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.93+382C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341301 | |||||||
chr1:46341445 | C | A | 31 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.93+526C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341445 | |||||||
chr1:46341481 | C | A | 1 | a0001c0001t0002g0039 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.93+562C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341481 | |||||||
chr1:46341744 | T | G | 31 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.93+825T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341744 | |||||||
chr1:46341773 | A | G | 31 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.93+854A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341773 | |||||||
chr1:46341925 | G | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0061 others(49): Show |
65 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.93+1006G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46341925 | |||||||
chr1:46342025 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.93+1106C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342025 | |||||||
chr1:46342033 | T | G | 1 | a0002c0002t0009g0198 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.93+1114T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342033 | |||||||
chr1:46342039 | C | T | 59 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(56): Show |
81 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.93+1120C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342039 | |||||||
chr1:46342081 | C | T | 2 | a0002c0002t0001g0261 a0002c0002t0001g0262 |
2 | NA18997.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.93+1162C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342081 | |||||||
chr1:46342370 | C | T | 48 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(45): Show |
68 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.93+1451C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342370 | |||||||
chr1:46342388 | G | T | 1 | a0004c0004t0004g0290 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.93+1469G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342388 | |||||||
chr1:46342508 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.93+1589C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342508 | |||||||
chr1:46342522 | T | A | 1 | a0004c0004t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.93+1603T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342522 | |||||||
chr1:46342549 | G | T | 3 | a0001c0001t0028g0142 a0001c0001t0028g0143 a0001c0001t0041g0141 |
3 | HG01884.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.93+1630G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342549 | |||||||
chr1:46342552 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.93+1633A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342552 | |||||||
chr1:46342691 | C | T | 3 | a0001c0001t0007g0139 a0001c0001t0007g0140 a0001c0001t0016g0138 |
3 | HG02055.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.93+1772C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342691 | |||||||
chr1:46342754 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.93+1835C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342754 | |||||||
chr1:46342790 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.93+1871A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342790 | |||||||
chr1:46342892 | G | A | 2 | a0001c0001t0022g0081 a0001c0001t0022g0082 |
2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.94-1909G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342892 | |||||||
chr1:46342996 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-1805G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46342996 | |||||||
chr1:46343023 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-1778T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343023 | |||||||
chr1:46343055 | G | A | 1 | a0004c0004t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.94-1746G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343055 | |||||||
chr1:46343100 | G | C | 1 | a0003c0003t0006g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.94-1701G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343100 | |||||||
chr1:46343180 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-1621C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343180 | |||||||
chr1:46343186 | G | GC | 67 | a0002c0002t0001g0199 a0003c0003t0003g0001 a0003c0003t0003g0005 others(64): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.94-1609dupC | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 46343186 | ||||||
chr1:46343188 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-1613C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343188 | |||||||
chr1:46343344 | C | T | 15 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(12): Show |
17 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.94-1457C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343344 | |||||||
chr1:46343350 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.94-1451C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343350 | |||||||
chr1:46343353 | G | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-1448G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343353 | |||||||
chr1:46343599 | C | T | 3 | a0001c0001t0007g0139 a0001c0001t0007g0140 a0001c0001t0016g0138 |
3 | HG02055.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.94-1202C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343599 | |||||||
chr1:46343649 | C | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-1152C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343649 | |||||||
chr1:46343747 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-1054A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343747 | |||||||
chr1:46343819 | C | T | 19 | a0003c0003t0003g0147 a0003c0003t0003g0149 a0003c0003t0006g0014 others(16): Show |
22 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.94-982C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343819 | |||||||
chr1:46343838 | A | G | 2 | a0004c0004t0052g0265 a0010c0010t0053g0038 |
2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.94-963A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46343838 | |||||||
chr1:46344110 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-691T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46344110 | |||||||
chr1:46344290 | G | A | 2 | a0007c0007t0027g0267 a0007c0007t0027g0268 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94-511G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46344290 | |||||||
chr1:46344440 | G | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-361G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46344440 | |||||||
chr1:46344632 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-169T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46344632 | |||||||
chr1:46344731 | G | A | 13 | a0001c0001t0023g0088 a0001c0001t0023g0090 a0001c0001t0039g0195 others(10): Show |
15 | HG01891.hp2 HG02257.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.94-70G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | chr1 | 46344731 | |||||||
chr1:46344733 | TG | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.94-63delG | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 46344733 | ||||||
chr1:46345165 | T | C | 1 | a0002c0002t0001g0200 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.437+21T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345165 | |||||||
chr1:46345170 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.437+26C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345170 | |||||||
chr1:46345278 | AT | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.437+141delT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46345278 | ||||||
chr1:46345298 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.437+154A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345298 | |||||||
chr1:46345355 | G | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.437+211G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345355 | |||||||
chr1:46345543 | A | ATG | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.437+403_437+404dup others(2): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46345543 | ||||||
chr1:46345574 | C | T | 2 | a0001c0001t0029g0127 a0001c0001t0030g0126 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.437+430C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345574 | |||||||
chr1:46345638 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.437+494A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345638 | |||||||
chr1:46345661 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.437+517T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345661 | |||||||
chr1:46345699 | AAGG | A | 7 | a0002c0002t0001g0018 a0002c0002t0001g0201 a0002c0002t0001g0202 others(4): Show |
9 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.437+558_437+560del others(3): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46345699 | ||||||
chr1:46345740 | A | C | 10 | a0001c0001t0039g0195 a0005c0005t0010g0017 a0005c0005t0010g0030 others(7): Show |
12 | HG01891.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.437+596A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345740 | |||||||
chr1:46345770 | A | G | 1 | a0002c0002t0001g0260 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.437+626A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345770 | |||||||
chr1:46345806 | A | G | 2 | a0001c0001t0029g0127 a0001c0001t0030g0126 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.437+662A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345806 | |||||||
chr1:46345871 | C | T | 48 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(45): Show |
68 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.437+727C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345871 | |||||||
chr1:46345872 | G | A | 3 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 |
3 | HG02040.hp2 NA18967.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.437+728G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345872 | |||||||
chr1:46345887 | C | T | 1 | a0001c0001t0042g0264 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.437+743C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46345887 | |||||||
chr1:46346024 | G | A | 2 | a0001c0001t0016g0129 a0001c0001t0016g0130 |
2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.437+880G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346024 | |||||||
chr1:46346150 | C | CA | 33 | a0001c0001t0001g0043 a0001c0001t0002g0039 a0001c0001t0002g0128 others(30): Show |
40 | HG00099.hp2 HG01081.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.438-751dupA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46346150 | ||||||
chr1:46346150 | C | CAA | 37 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(34): Show |
40 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.438-752_438-751dup others(2): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46346150 | ||||||
chr1:46346150 | C | CAAA | 8 | a0001c0001t0022g0081 a0001c0001t0045g0131 a0004c0004t0018g0270 others(5): Show |
8 | HG00544.hp2 HG00735.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.438-753_438-751dup others(3): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46346150 | ||||||
chr1:46346150 | CA | C | 13 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0121 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.438-751delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46346150 | ||||||
chr1:46346157 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.438-764A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346157 | |||||||
chr1:46346320 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.438-601C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346320 | |||||||
chr1:46346370 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.438-551T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346370 | |||||||
chr1:46346520 | C | G | 1 | a0001c0001t0039g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.438-401C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346520 | |||||||
chr1:46346539 | G | A | 2 | a0001c0001t0028g0142 a0001c0001t0028g0143 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.438-382G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346539 | |||||||
chr1:46346547 | G | C | 3 | a0001c0001t0007g0139 a0001c0001t0007g0140 a0001c0001t0016g0138 |
3 | HG02055.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.438-374G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346547 | |||||||
chr1:46346549 | CT | C | 3 | a0001c0001t0007g0139 a0001c0001t0007g0140 a0001c0001t0016g0138 |
3 | HG02055.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.438-371delT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346549 | |||||||
chr1:46346551 | C | A | 3 | a0001c0001t0007g0139 a0001c0001t0007g0140 a0001c0001t0016g0138 |
3 | HG02055.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.438-370C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346551 | |||||||
chr1:46346551 | C | CA | 140 | a0001c0001t0001g0096 a0001c0001t0002g0004 a0001c0001t0002g0022 others(137): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.438-347dupA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46346551 | ||||||
chr1:46346551 | C | CAA | 19 | a0001c0001t0002g0128 a0001c0001t0007g0009 a0001c0001t0007g0132 others(16): Show |
21 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.438-348_438-347dup others(2): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46346551 | ||||||
chr1:46346551 | CA | C | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0002c0002t0011g0259 others(5): Show |
8 | HG00323.hp2 HG01074.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.438-347delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 46346551 | ||||||
chr1:46346629 | C | T | 15 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(12): Show |
17 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.438-292C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346629 | |||||||
chr1:46346667 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.438-254C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346667 | |||||||
chr1:46346680 | T | C | 3 | a0001c0001t0029g0127 a0001c0001t0030g0126 a0001c0001t0041g0141 |
3 | HG01069.hp2 HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.438-241T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346680 | |||||||
chr1:46346688 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.438-233C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346688 | |||||||
chr1:46346702 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.438-219T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346702 | |||||||
chr1:46346772 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.438-149A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346772 | |||||||
chr1:46346833 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.438-88G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346833 | |||||||
chr1:46346847 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.438-74A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346847 | |||||||
chr1:46346887 | G | T | 2 | a0001c0001t0028g0142 a0001c0001t0028g0143 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.438-34G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 2/5 | chr1 | 46346887 | |||||||
chr1:46347180 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+105G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347180 | |||||||
chr1:46347200 | A | G | 2 | a0001c0001t0028g0142 a0001c0001t0028g0143 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.592+125A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347200 | |||||||
chr1:46347216 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+141C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347216 | |||||||
chr1:46347367 | A | G | 2 | a0004c0004t0052g0265 a0010c0010t0053g0038 |
2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.592+292A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347367 | |||||||
chr1:46347449 | A | C | 84 | a0001c0001t0001g0120 a0002c0002t0001g0002 a0002c0002t0001g0006 others(81): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.592+374A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347449 | |||||||
chr1:46347449 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+374A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347449 | |||||||
chr1:46347471 | C | G | 1 | a0005c0005t0036g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.592+396C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347471 | |||||||
chr1:46347595 | T | C | 48 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(45): Show |
68 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.592+520T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347595 | |||||||
chr1:46347771 | T | G | 3 | a0001c0001t0029g0127 a0001c0001t0030g0126 a0001c0001t0041g0141 |
3 | HG01069.hp2 HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.592+696T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347771 | |||||||
chr1:46347803 | T | G | 1 | a0005c0005t0010g0030 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.592+728T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347803 | |||||||
chr1:46347859 | C | CT | 89 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(86): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.592+795dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46347859 | ||||||
chr1:46347871 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+796C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347871 | |||||||
chr1:46347896 | G | A | 21 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(18): Show |
21 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.592+821G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347896 | |||||||
chr1:46347916 | C | T | 2 | a0007c0007t0027g0267 a0007c0007t0027g0268 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.592+841C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347916 | |||||||
chr1:46347917 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+842A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347917 | |||||||
chr1:46347947 | G | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+872G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347947 | |||||||
chr1:46347963 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+888C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347963 | |||||||
chr1:46347991 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+916C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46347991 | |||||||
chr1:46348023 | G | A | 1 | a0003c0003t0003g0160 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.592+948G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348023 | |||||||
chr1:46348176 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0061 others(51): Show |
67 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.592+1101G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348176 | |||||||
chr1:46348188 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1113C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348188 | |||||||
chr1:46348209 | C | T | 1 | a0004c0004t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.592+1134C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348209 | |||||||
chr1:46348216 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1141T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348216 | |||||||
chr1:46348295 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1220C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348295 | |||||||
chr1:46348299 | C | T | 1 | a0001c0001t0042g0264 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.592+1224C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348299 | |||||||
chr1:46348310 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1235G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348310 | |||||||
chr1:46348336 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1261C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348336 | |||||||
chr1:46348357 | G | A | 17 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(14): Show |
19 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.592+1282G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348357 | |||||||
chr1:46348420 | T | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1345T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348420 | |||||||
chr1:46348559 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1484A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348559 | |||||||
chr1:46348593 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1518C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348593 | |||||||
chr1:46348601 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1526T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348601 | |||||||
chr1:46348657 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1582T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348657 | |||||||
chr1:46348680 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+1605G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348680 | |||||||
chr1:46348709 | C | CA | 116 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0001g0120 others(113): Show |
145 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.592+1661dupA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348709 | ||||||
chr1:46348709 | C | CAA | 21 | a0001c0001t0022g0081 a0001c0001t0029g0127 a0002c0002t0001g0031 others(18): Show |
25 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.592+1660_592+1661d others(4): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348709 | ||||||
chr1:46348709 | CA | C | 10 | a0001c0001t0002g0074 a0001c0001t0002g0119 a0001c0001t0002g0124 others(7): Show |
10 | HG02300.hp2 HG02717.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.592+1661delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348709 | ||||||
chr1:46348709 | CAAAA | C | 11 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(8): Show |
13 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.592+1658_592+1661d others(6): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348709 | ||||||
chr1:46348709 | CAAAAAA | C | 19 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(16): Show |
19 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.592+1656_592+1661d others(8): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348709 | ||||||
chr1:46348709 | CAAAAAAA | C | 9 | a0002c0002t0001g0251 a0004c0004t0004g0285 a0004c0004t0004g0291 others(6): Show |
10 | HG00280.hp2 HG00544.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.592+1655_592+1661d others(9): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348709 | ||||||
chr1:46348808 | G | GT | 6 | a0001c0001t0002g0105 a0001c0001t0044g0091 a0003c0003t0006g0087 others(3): Show |
6 | HG02486.hp1 HG02683.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+1757dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | G | GTTT | 18 | a0001c0001t0007g0140 a0001c0001t0016g0138 a0001c0001t0022g0082 others(15): Show |
22 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.592+1755_592+1757d others(5): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | G | GTTTT | 51 | a0001c0001t0001g0120 a0001c0001t0002g0073 a0001c0001t0007g0139 others(48): Show |
69 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.592+1754_592+1757d others(6): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | G | GTTTTT | 40 | a0001c0001t0021g0135 a0001c0001t0028g0142 a0001c0001t0028g0143 others(37): Show |
46 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.592+1753_592+1757d others(7): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | G | GTTTTTT | 8 | a0001c0001t0021g0137 a0001c0001t0023g0088 a0002c0002t0001g0202 others(5): Show |
8 | HG02145.hp2 HG02148.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.592+1752_592+1757d others(8): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | GT | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0061 others(57): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.592+1757delT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | GTTTTT | G | 16 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(13): Show |
18 | HG00639.hp1 HG00642.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.592+1753_592+1757d others(7): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | GTTTTTT | G | 42 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(39): Show |
62 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.592+1752_592+1757d others(8): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348808 | GTTTTTTT others(5): Show |
G | 1 | a0003c0003t0003g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592+1746_592+1757d others(14): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46348808 | ||||||
chr1:46348819 | T | G | 2 | a0001c0001t0002g0107 a0001c0001t0005g0106 |
2 | HG00738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.592+1744T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348819 | |||||||
chr1:46348836 | A | G | 3 | a0004c0004t0013g0036 a0004c0004t0013g0286 a0004c0004t0055g0288 |
4 | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+1761A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348836 | |||||||
chr1:46348837 | A | G | 3 | a0001c0001t0007g0139 a0001c0001t0007g0140 a0001c0001t0016g0138 |
3 | HG02055.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.592+1762A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348837 | |||||||
chr1:46348846 | G | A | 31 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.592+1771G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348846 | |||||||
chr1:46348900 | C | T | 2 | a0001c0001t0023g0088 a0001c0001t0023g0090 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.592+1825C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348900 | |||||||
chr1:46348918 | A | G | 125 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(122): Show |
152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.592+1843A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46348918 | |||||||
chr1:46349048 | C | T | 5 | a0002c0002t0001g0006 a0002c0002t0001g0032 a0002c0002t0001g0212 others(2): Show |
10 | HG00099.hp2 HG01099.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.592+1973C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349048 | |||||||
chr1:46349089 | A | T | 28 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.592+2014A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349089 | |||||||
chr1:46349104 | C | T | 1 | a0001c0001t0043g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.592+2029C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349104 | |||||||
chr1:46349130 | TG | T | 6 | a0003c0003t0003g0029 a0003c0003t0003g0167 a0003c0003t0003g0169 others(3): Show |
8 | HG02015.hp1 HG02080.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.592+2057delG | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46349130 | ||||||
chr1:46349135 | TG | T | 47 | a0002c0002t0009g0240 a0003c0003t0003g0001 a0003c0003t0003g0005 others(44): Show |
67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.592+2061delG | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349135 | |||||||
chr1:46349136 | G | T | 13 | a0003c0003t0003g0029 a0003c0003t0003g0159 a0003c0003t0003g0167 others(10): Show |
15 | HG00673.hp1 HG02015.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.592+2061G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349136 | |||||||
chr1:46349143 | T | G | 5 | a0003c0003t0003g0159 a0003c0003t0003g0170 a0003c0003t0003g0171 others(2): Show |
5 | HG00673.hp1 HG02056.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+2068T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349143 | |||||||
chr1:46349144 | G | GT | 7 | a0001c0001t0011g0066 a0001c0001t0028g0142 a0001c0001t0028g0143 others(4): Show |
7 | HG00639.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.592+2082dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46349144 | ||||||
chr1:46349144 | G | T | 5 | a0003c0003t0003g0159 a0003c0003t0003g0170 a0003c0003t0003g0171 others(2): Show |
5 | HG00673.hp1 HG02056.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+2069G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349144 | |||||||
chr1:46349148 | T | TTTG | 28 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.592+2075_592+2076i others(5): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46349148 | ||||||
chr1:46349158 | G | C | 2 | a0001c0001t0016g0129 a0001c0001t0016g0130 |
2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.592+2083G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349158 | |||||||
chr1:46349209 | G | A | 1 | a0004c0004t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.592+2134G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349209 | |||||||
chr1:46349221 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+2146A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349221 | |||||||
chr1:46349232 | C | T | 1 | a0002c0002t0005g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.592+2157C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349232 | |||||||
chr1:46349233 | G | A | 3 | a0001c0001t0029g0127 a0001c0001t0030g0126 a0001c0001t0041g0141 |
3 | HG01069.hp2 HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.592+2158G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349233 | |||||||
chr1:46349253 | C | A | 2 | a0007c0007t0027g0267 a0007c0007t0027g0268 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.592+2178C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349253 | |||||||
chr1:46349266 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+2191G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349266 | |||||||
chr1:46349281 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+2206G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349281 | |||||||
chr1:46349285 | A | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+2210A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349285 | |||||||
chr1:46349303 | C | A | 1 | a0003c0003t0003g0173 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.592+2228C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349303 | |||||||
chr1:46349331 | A | G | 31 | a0003c0003t0003g0180 a0004c0004t0004g0035 a0004c0004t0004g0271 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.592+2256A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349331 | |||||||
chr1:46349341 | C | T | 78 | a0001c0001t0002g0094 a0002c0002t0001g0233 a0003c0003t0003g0001 others(75): Show |
99 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.592+2266C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349341 | |||||||
chr1:46349419 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+2344C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349419 | |||||||
chr1:46349432 | G | A | 2 | a0001c0001t0029g0127 a0001c0001t0030g0126 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.592+2357G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349432 | |||||||
chr1:46349482 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+2407G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349482 | |||||||
chr1:46349535 | C | T | 1 | a0002c0002t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.592+2460C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349535 | |||||||
chr1:46349703 | A | T | 3 | a0002c0002t0001g0031 a0002c0002t0001g0216 a0002c0002t0001g0219 |
4 | HG01081.hp1 HG01175.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+2628A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349703 | |||||||
chr1:46349706 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+2631C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349706 | |||||||
chr1:46349839 | GA | G | 3 | a0004c0004t0004g0291 a0004c0004t0052g0265 a0010c0010t0053g0038 |
3 | HG00544.hp2 HG03834.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.592+2766delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46349839 | ||||||
chr1:46349880 | A | G | 2 | a0001c0001t0007g0037 a0001c0001t0007g0136 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.592+2805A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349880 | |||||||
chr1:46349955 | C | G | 4 | a0004c0004t0013g0036 a0004c0004t0013g0286 a0004c0004t0013g0287 others(1): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+2880C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349955 | |||||||
chr1:46349975 | A | G | 1 | a0002c0002t0001g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.593-2893A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46349975 | |||||||
chr1:46350077 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2791T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350077 | |||||||
chr1:46350126 | T | G | 5 | a0001c0001t0001g0099 a0001c0001t0002g0108 a0001c0001t0002g0109 others(2): Show |
5 | HG00738.hp2 HG01071.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-2742T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350126 | |||||||
chr1:46350164 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2704C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350164 | |||||||
chr1:46350208 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2660A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350208 | |||||||
chr1:46350226 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2642T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350226 | |||||||
chr1:46350245 | A | G | 2 | a0007c0007t0027g0267 a0007c0007t0027g0268 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.593-2623A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350245 | |||||||
chr1:46350258 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2610C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350258 | |||||||
chr1:46350298 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2570T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350298 | |||||||
chr1:46350331 | G | A | 59 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(56): Show |
81 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.593-2537G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350331 | |||||||
chr1:46350411 | G | A | 1 | a0004c0004t0004g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.593-2457G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350411 | |||||||
chr1:46350591 | C | T | 1 | a0004c0004t0004g0282 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.593-2277C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350591 | |||||||
chr1:46350660 | G | A | 4 | a0002c0002t0001g0234 a0002c0002t0001g0242 a0002c0002t0005g0238 others(1): Show |
4 | HG00423.hp1 HG00609.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-2208G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350660 | |||||||
chr1:46350668 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2200A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350668 | |||||||
chr1:46350736 | CAGGTATG others(1): Show |
C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2128_593-2121d others(10): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46350736 | ||||||
chr1:46350757 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2111T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350757 | |||||||
chr1:46350793 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-2075G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350793 | |||||||
chr1:46350972 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1896A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350972 | |||||||
chr1:46350987 | T | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1881T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46350987 | |||||||
chr1:46351134 | C | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0061 others(278): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.593-1734C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351134 | |||||||
chr1:46351214 | A | G | 1 | a0002c0002t0001g0262 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.593-1654A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351214 | |||||||
chr1:46351256 | C | T | 34 | a0001c0001t0007g0037 a0001c0001t0007g0136 a0001c0001t0023g0088 others(31): Show |
35 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.593-1612C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351256 | |||||||
chr1:46351257 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.593-1611G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351257 | |||||||
chr1:46351296 | G | A | 1 | a0003c0003t0003g0149 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.593-1572G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351296 | |||||||
chr1:46351421 | A | G | 2 | a0001c0001t0029g0127 a0001c0001t0030g0126 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.593-1447A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351421 | |||||||
chr1:46351438 | G | A | 1 | a0002c0002t0001g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.593-1430G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351438 | |||||||
chr1:46351453 | C | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1415C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351453 | |||||||
chr1:46351503 | G | A | 1 | a0001c0001t0011g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.593-1365G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351503 | |||||||
chr1:46351659 | C | CT | 157 | a0001c0001t0001g0043 a0001c0001t0001g0096 a0001c0001t0001g0099 others(154): Show |
206 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.593-1186dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46351659 | ||||||
chr1:46351659 | C | CTT | 15 | a0001c0001t0016g0130 a0001c0001t0016g0138 a0002c0002t0001g0211 others(12): Show |
16 | HG00642.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.593-1187_593-1186d others(4): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46351659 | ||||||
chr1:46351659 | CTTT | C | 25 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(22): Show |
26 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-1188_593-1186d others(5): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46351659 | ||||||
chr1:46351681 | T | TG | 4 | a0003c0003t0006g0144 a0003c0003t0006g0150 a0003c0003t0006g0153 others(1): Show |
4 | HG00140.hp2 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-1187_593-1186i others(3): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351681 | |||||||
chr1:46351734 | G | A | 4 | a0004c0004t0013g0036 a0004c0004t0013g0286 a0004c0004t0013g0287 others(1): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1134G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351734 | |||||||
chr1:46351809 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1059T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351809 | |||||||
chr1:46351953 | C | T | 2 | a0001c0001t0002g0197 a0001c0001t0005g0044 |
2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.593-915C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46351953 | |||||||
chr1:46352083 | G | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-785G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352083 | |||||||
chr1:46352098 | T | C | 28 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.593-770T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352098 | |||||||
chr1:46352147 | T | TAA | 28 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.593-707_593-706dup others(2): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46352147 | ||||||
chr1:46352147 | TA | T | 9 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0002c0002t0001g0098 others(6): Show |
9 | HG02965.hp1 HG03491.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.593-706delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46352147 | ||||||
chr1:46352211 | G | A | 2 | a0001c0001t0029g0127 a0001c0001t0030g0126 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.593-657G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352211 | |||||||
chr1:46352224 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.593-644G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352224 | |||||||
chr1:46352277 | T | C | 125 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(122): Show |
152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.593-591T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352277 | |||||||
chr1:46352278 | G | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-590G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352278 | |||||||
chr1:46352451 | TA | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-407delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 46352451 | ||||||
chr1:46352494 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-374G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352494 | |||||||
chr1:46352541 | C | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-327C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352541 | |||||||
chr1:46352547 | T | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-321T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352547 | |||||||
chr1:46352616 | A | G | 28 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.593-252A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352616 | |||||||
chr1:46352659 | T | A | 2 | a0001c0001t0021g0135 a0001c0001t0021g0137 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.593-209T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352659 | |||||||
chr1:46352702 | C | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-166C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352702 | |||||||
chr1:46352703 | C | T | 4 | a0004c0004t0013g0036 a0004c0004t0013g0286 a0004c0004t0013g0287 others(1): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-165C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352703 | |||||||
chr1:46352719 | T | C | 1 | a0002c0002t0001g0247 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.593-149T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352719 | |||||||
chr1:46352744 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-124A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352744 | |||||||
chr1:46352745 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-123T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352745 | |||||||
chr1:46352770 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-98G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352770 | |||||||
chr1:46352780 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-88A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352780 | |||||||
chr1:46352807 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-61C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352807 | |||||||
chr1:46352830 | A | G | 14 | a0001c0001t0001g0096 a0001c0001t0002g0015 a0001c0001t0002g0026 others(11): Show |
18 | HG00733.hp2 HG01192.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.593-38A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352830 | |||||||
chr1:46352836 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-32T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 3/5 | chr1 | 46352836 | |||||||
chr1:46353053 | T | C | 5 | a0001c0001t0023g0088 a0001c0001t0023g0090 a0001c0001t0028g0142 others(2): Show |
5 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+25T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353053 | |||||||
chr1:46353164 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+136T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353164 | |||||||
chr1:46353226 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+198T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353226 | |||||||
chr1:46353249 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+221A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353249 | |||||||
chr1:46353302 | T | C | 2 | a0001c0001t0021g0135 a0001c0001t0021g0137 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.753+274T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353302 | |||||||
chr1:46353349 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+321A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353349 | |||||||
chr1:46353516 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.753+488G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353516 | |||||||
chr1:46353632 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+604C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353632 | |||||||
chr1:46353636 | C | T | 2 | a0001c0001t0029g0127 a0001c0001t0030g0126 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.753+608C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353636 | |||||||
chr1:46353769 | G | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+741G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353769 | |||||||
chr1:46353781 | GTATAT | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+763_753+767del others(5): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46353781 | ||||||
chr1:46353854 | TTTTTAAT others(4): Show |
T | 1 | a0010c0010t0053g0038 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.753+829_753+839del others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46353854 | ||||||
chr1:46353927 | G | A | 1 | a0003c0003t0003g0161 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.753+899G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46353927 | |||||||
chr1:46354107 | A | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+1079A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354107 | |||||||
chr1:46354110 | GTT | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+1093_753+1094d others(4): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46354110 | ||||||
chr1:46354166 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.753+1138G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354166 | |||||||
chr1:46354176 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+1148G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354176 | |||||||
chr1:46354194 | C | A | 1 | a0001c0001t0021g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.753+1166C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354194 | |||||||
chr1:46354194 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+1166C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354194 | |||||||
chr1:46354211 | G | T | 1 | a0003c0003t0003g0166 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.753+1183G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354211 | |||||||
chr1:46354212 | T | G | 1 | a0003c0003t0003g0166 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.753+1184T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354212 | |||||||
chr1:46354319 | G | A | 3 | a0002c0002t0001g0208 a0002c0002t0001g0221 a0002c0002t0001g0223 |
3 | HG02257.hp2 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.753+1291G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354319 | |||||||
chr1:46354510 | G | A | 4 | a0004c0004t0013g0036 a0004c0004t0013g0286 a0004c0004t0013g0287 others(1): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+1482G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354510 | |||||||
chr1:46354661 | CT | C | 32 | a0002c0002t0001g0219 a0003c0003t0031g0152 a0004c0004t0004g0035 others(29): Show |
33 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.753+1645delT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46354661 | ||||||
chr1:46354730 | C | G | 10 | a0001c0001t0039g0195 a0005c0005t0010g0017 a0005c0005t0010g0030 others(7): Show |
12 | HG01891.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.753+1702C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354730 | |||||||
chr1:46354747 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+1719T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354747 | |||||||
chr1:46354779 | C | T | 1 | a0004c0004t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.753+1751C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354779 | |||||||
chr1:46354843 | AT | A | 85 | a0001c0001t0001g0043 a0001c0001t0005g0071 a0002c0002t0001g0002 others(82): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.753+1822delT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46354843 | ||||||
chr1:46354857 | G | A | 1 | a0001c0001t0022g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.753+1829G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354857 | |||||||
chr1:46354889 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.753+1861T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354889 | |||||||
chr1:46354917 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+1889A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46354917 | |||||||
chr1:46355109 | C | A | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.753+2081C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355109 | |||||||
chr1:46355224 | G | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+2196G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355224 | |||||||
chr1:46355303 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+2275C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355303 | |||||||
chr1:46355346 | A | G | 1 | a0003c0003t0003g0027 | 2 | HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.753+2318A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355346 | |||||||
chr1:46355402 | T | A | 18 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(15): Show |
20 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.753+2374T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355402 | |||||||
chr1:46355686 | A | G | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0005g0103 |
3 | HG02723.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.753+2658A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355686 | |||||||
chr1:46355724 | A | C | 4 | a0003c0003t0006g0144 a0003c0003t0006g0150 a0003c0003t0006g0153 others(1): Show |
4 | HG00140.hp2 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+2696A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355724 | |||||||
chr1:46355777 | G | A | 1 | a0004c0004t0004g0272 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.753+2749G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355777 | |||||||
chr1:46355830 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+2802C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46355830 | |||||||
chr1:46356014 | CA | C | 43 | a0001c0001t0001g0061 a0001c0001t0002g0039 a0001c0001t0002g0046 others(40): Show |
44 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.753+3001delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46356014 | ||||||
chr1:46356022 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+2994A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356022 | |||||||
chr1:46356028 | A | C | 66 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(63): Show |
89 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.753+3000A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356028 | |||||||
chr1:46356132 | C | T | 1 | a0004c0004t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.753+3104C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356132 | |||||||
chr1:46356167 | G | T | 2 | a0004c0004t0052g0265 a0010c0010t0053g0038 |
2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.753+3139G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356167 | |||||||
chr1:46356277 | T | C | 1 | a0002c0002t0001g0249 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.753+3249T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356277 | |||||||
chr1:46356290 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+3262C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356290 | |||||||
chr1:46356329 | C | A | 1 | a0003c0003t0003g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.753+3301C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356329 | |||||||
chr1:46356329 | C | G | 4 | a0004c0004t0013g0036 a0004c0004t0013g0286 a0004c0004t0013g0287 others(1): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+3301C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356329 | |||||||
chr1:46356380 | A | C | 2 | a0001c0001t0017g0025 a0001c0001t0017g0112 |
3 | HG01943.hp1 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.753+3352A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356380 | |||||||
chr1:46356401 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+3373G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356401 | |||||||
chr1:46356467 | C | T | 26 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(23): Show |
26 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.753+3439C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356467 | |||||||
chr1:46356475 | G | A | 26 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(23): Show |
26 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.753+3447G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356475 | |||||||
chr1:46356488 | G | C | 46 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(43): Show |
48 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.753+3460G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356488 | |||||||
chr1:46356508 | C | T | 24 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(21): Show |
24 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.753+3480C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356508 | |||||||
chr1:46356509 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.753+3481G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356509 | |||||||
chr1:46356552 | T | C | 28 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+3524T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356552 | |||||||
chr1:46356614 | C | A | 2 | a0007c0007t0027g0267 a0007c0007t0027g0268 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.753+3586C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356614 | |||||||
chr1:46356619 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+3591T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356619 | |||||||
chr1:46356625 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+3597A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356625 | |||||||
chr1:46356650 | G | A | 8 | a0003c0003t0003g0156 a0003c0003t0003g0160 a0003c0003t0003g0178 others(5): Show |
8 | HG02056.hp1 HG02155.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.753+3622G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356650 | |||||||
chr1:46356686 | G | A | 9 | a0001c0001t0001g0096 a0001c0001t0002g0015 a0001c0001t0002g0026 others(6): Show |
12 | HG00733.hp2 HG01192.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.753+3658G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356686 | |||||||
chr1:46356700 | A | AG | 28 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(25): Show |
29 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.753+3672_753+3673i others(3): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356700 | |||||||
chr1:46356733 | G | C | 3 | a0001c0001t0023g0088 a0001c0001t0023g0090 a0001c0001t0043g0089 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.753+3705G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356733 | |||||||
chr1:46356768 | G | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.753+3740G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356768 | |||||||
chr1:46356928 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-3776T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46356928 | |||||||
chr1:46357289 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-3415C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357289 | |||||||
chr1:46357326 | T | C | 97 | a0003c0003t0003g0001 a0003c0003t0003g0005 a0003c0003t0003g0010 others(94): Show |
121 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.754-3378T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357326 | |||||||
chr1:46357382 | C | T | 2 | a0004c0004t0052g0265 a0010c0010t0053g0038 |
2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.754-3322C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357382 | |||||||
chr1:46357421 | C | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-3283C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357421 | |||||||
chr1:46357534 | G | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-3170G>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357534 | |||||||
chr1:46357589 | C | T | 2 | a0001c0001t0028g0142 a0001c0001t0028g0143 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.754-3115C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357589 | |||||||
chr1:46357626 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-3078A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357626 | |||||||
chr1:46357716 | C | CT | 8 | a0003c0003t0003g0156 a0003c0003t0003g0160 a0003c0003t0003g0178 others(5): Show |
8 | HG02056.hp1 HG02155.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-2978dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46357716 | ||||||
chr1:46357763 | A | G | 10 | a0001c0001t0039g0195 a0005c0005t0010g0017 a0005c0005t0010g0030 others(7): Show |
12 | HG01891.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.754-2941A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46357763 | |||||||
chr1:46358029 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2675C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358029 | |||||||
chr1:46358087 | G | GTATT | 14 | a0002c0002t0001g0018 a0002c0002t0001g0201 a0002c0002t0001g0202 others(11): Show |
16 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.754-2595_754-2592d others(6): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46358087 | ||||||
chr1:46358118 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.754-2586C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358118 | |||||||
chr1:46358181 | C | T | 2 | a0001c0001t0028g0142 a0001c0001t0028g0143 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.754-2523C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358181 | |||||||
chr1:46358245 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2459A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358245 | |||||||
chr1:46358257 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2447G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358257 | |||||||
chr1:46358338 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2366T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358338 | |||||||
chr1:46358376 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2328A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358376 | |||||||
chr1:46358398 | A | AT | 32 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0057 others(29): Show |
34 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.754-2284dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46358398 | ||||||
chr1:46358398 | AT | A | 33 | a0001c0001t0001g0120 a0001c0001t0002g0067 a0001c0001t0002g0078 others(30): Show |
35 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.754-2284delT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46358398 | ||||||
chr1:46358398 | ATT | A | 148 | a0001c0001t0023g0088 a0001c0001t0023g0090 a0001c0001t0030g0126 others(145): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.754-2285_754-2284d others(4): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46358398 | ||||||
chr1:46358398 | ATTT | A | 6 | a0001c0001t0029g0127 a0002c0002t0001g0205 a0002c0002t0011g0241 others(3): Show |
6 | HG01069.hp2 HG01256.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-2286_754-2284d others(5): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46358398 | ||||||
chr1:46358424 | A | T | 1 | a0002c0002t0001g0231 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.754-2280A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358424 | |||||||
chr1:46358431 | C | A | 1 | a0002c0002t0001g0255 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.754-2273C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358431 | |||||||
chr1:46358464 | C | T | 1 | a0002c0002t0001g0244 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.754-2240C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358464 | |||||||
chr1:46358470 | C | T | 7 | a0001c0001t0028g0142 a0001c0001t0028g0143 a0001c0001t0041g0141 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.754-2234C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358470 | |||||||
chr1:46358471 | G | A | 1 | a0003c0003t0003g0154 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.754-2233G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358471 | |||||||
chr1:46358511 | T | C | 120 | a0001c0001t0007g0009 a0001c0001t0007g0037 a0001c0001t0007g0132 others(117): Show |
146 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.754-2193T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358511 | |||||||
chr1:46358526 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2178C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358526 | |||||||
chr1:46358536 | G | A | 1 | a0001c0001t0041g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.754-2168G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358536 | |||||||
chr1:46358652 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2052G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358652 | |||||||
chr1:46358687 | G | A | 84 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(81): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.754-2017G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358687 | |||||||
chr1:46358691 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2013T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358691 | |||||||
chr1:46358699 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-2005A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358699 | |||||||
chr1:46358811 | A | C | 3 | a0001c0001t0023g0088 a0001c0001t0023g0090 a0001c0001t0043g0089 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.754-1893A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358811 | |||||||
chr1:46358976 | G | A | 13 | a0001c0001t0023g0088 a0001c0001t0023g0090 a0001c0001t0039g0195 others(10): Show |
15 | HG01891.hp2 HG02257.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.754-1728G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46358976 | |||||||
chr1:46359184 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1520C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359184 | |||||||
chr1:46359247 | C | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1457C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359247 | |||||||
chr1:46359260 | A | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1444A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359260 | |||||||
chr1:46359281 | C | T | 1 | a0003c0003t0049g0181 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.754-1423C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359281 | |||||||
chr1:46359504 | T | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1200T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359504 | |||||||
chr1:46359544 | C | T | 1 | a0004c0004t0004g0279 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.754-1160C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359544 | |||||||
chr1:46359550 | AAT | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1153_754-1152d others(4): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359550 | |||||||
chr1:46359551 | A | AT | 6 | a0001c0001t0002g0128 a0001c0001t0022g0081 a0002c0002t0009g0207 others(3): Show |
6 | HG02145.hp2 HG02572.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-1136dupT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46359551 | ||||||
chr1:46359554 | T | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1150T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359554 | |||||||
chr1:46359589 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1115C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359589 | |||||||
chr1:46359590 | G | C | 1 | a0001c0001t0001g0068 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.754-1114G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359590 | |||||||
chr1:46359591 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.754-1113C>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359591 | |||||||
chr1:46359731 | T | G | 1 | a0002c0002t0001g0248 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.754-973T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359731 | |||||||
chr1:46359761 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-943C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359761 | |||||||
chr1:46359772 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0051 |
2 | NA18948.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.754-932T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359772 | |||||||
chr1:46359779 | A | T | 4 | a0004c0004t0013g0036 a0004c0004t0013g0286 a0004c0004t0013g0287 others(1): Show |
5 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-925A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359779 | |||||||
chr1:46359798 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.754-906G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359798 | |||||||
chr1:46359812 | T | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-892T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359812 | |||||||
chr1:46359836 | T | C | 2 | a0001c0001t0022g0081 a0001c0001t0022g0082 |
2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.754-868T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359836 | |||||||
chr1:46359979 | T | C | 1 | a0002c0002t0011g0241 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.754-725T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46359979 | |||||||
chr1:46360004 | C | T | 21 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(18): Show |
21 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.754-700C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360004 | |||||||
chr1:46360005 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-699A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360005 | |||||||
chr1:46360024 | T | G | 1 | a0003c0003t0006g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.754-680T>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360024 | |||||||
chr1:46360045 | C | T | 84 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(81): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.754-659C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360045 | |||||||
chr1:46360090 | A | G | 1 | a0010c0010t0053g0038 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.754-614A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360090 | |||||||
chr1:46360092 | G | C | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-612G>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360092 | |||||||
chr1:46360093 | G | A | 2 | a0004c0004t0052g0265 a0010c0010t0053g0038 |
2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.754-611G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360093 | |||||||
chr1:46360102 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-602G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360102 | |||||||
chr1:46360111 | C | T | 1 | a0002c0002t0001g0215 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.754-593C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360111 | |||||||
chr1:46360148 | A | G | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-556A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360148 | |||||||
chr1:46360207 | C | T | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-497C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360207 | |||||||
chr1:46360228 | C | CA | 9 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0002g0052 others(6): Show |
10 | HG01934.hp2 HG01943.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.754-454dupA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360228 | ||||||
chr1:46360228 | C | CAA | 7 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0108 others(4): Show |
7 | HG00673.hp2 HG00738.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.754-455_754-454dup others(2): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360228 | ||||||
chr1:46360228 | C | CAAAA | 7 | a0004c0004t0004g0035 a0004c0004t0004g0275 a0004c0004t0004g0282 others(4): Show |
7 | HG00741.hp2 HG01258.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-457_754-454dup others(4): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360228 | ||||||
chr1:46360228 | C | CAAAAA | 7 | a0004c0004t0004g0272 a0004c0004t0004g0274 a0004c0004t0004g0279 others(4): Show |
7 | HG00544.hp1 HG00735.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-458_754-454dup others(5): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360228 | ||||||
chr1:46360228 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0007g0132 a0001c0001t0007g0139 a0003c0003t0003g0182 |
3 | HG00642.hp1 HG02647.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.754-463_754-454dup others(10): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360228 | ||||||
chr1:46360242 | AAAAAAAA others(2): Show |
A | 7 | a0005c0005t0010g0017 a0005c0005t0010g0030 a0005c0005t0010g0193 others(4): Show |
9 | HG02896.hp1 HG02897.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.754-460_754-452del others(9): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360242 | ||||||
chr1:46360242 | AAAAAAAA others(4): Show |
A | 1 | a0002c0002t0009g0235 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.754-460_754-450del others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360242 | ||||||
chr1:46360243 | AAAAAAAA others(5): Show |
A | 5 | a0002c0002t0001g0011 a0002c0002t0001g0216 a0002c0002t0001g0244 others(2): Show |
5 | HG01081.hp1 HG01978.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-459_754-448del others(12): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360243 | ||||||
chr1:46360244 | AAAAAAAT others(4): Show |
A | 7 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0019 others(4): Show |
7 | HG00280.hp2 HG02074.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-458_754-448del others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360244 | ||||||
chr1:46360245 | AAAAAATA others(3): Show |
A | 1 | a0002c0002t0001g0031 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.754-457_754-448del others(10): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360245 | ||||||
chr1:46360245 | AAAAAATA others(5): Show |
A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(56): Show |
72 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.754-457_754-446del others(12): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360245 | ||||||
chr1:46360246 | AAAAATAT others(4): Show |
A | 4 | a0002c0002t0001g0018 a0002c0002t0001g0033 a0002c0002t0001g0223 others(1): Show |
4 | HG01928.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-456_754-446del others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360246 | ||||||
chr1:46360247 | AAAATATA others(3): Show |
A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0215 |
2 | NA18947.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.754-455_754-446del others(10): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360247 | ||||||
chr1:46360247 | AAAATATA others(5): Show |
A | 7 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0208 others(4): Show |
9 | HG01074.hp2 HG01346.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.754-455_754-444del others(12): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360247 | ||||||
chr1:46360248 | AAATATAT others(4): Show |
A | 3 | a0001c0001t0039g0195 a0002c0002t0001g0002 a0002c0002t0009g0198 |
3 | HG00621.hp2 HG02622.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.754-454_754-444del others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360248 | ||||||
chr1:46360248 | AAATATAT others(6): Show |
A | 1 | a0002c0002t0001g0255 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.754-454_754-442del others(13): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360248 | ||||||
chr1:46360249 | A | AAAAAAAA others(32): Show |
1 | a0003c0003t0008g0145 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(39): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(20): Show |
1 | a0003c0003t0003g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(27): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(30): Show |
1 | a0003c0003t0003g0175 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(37): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(18): Show |
1 | a0003c0003t0003g0001 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(25): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(24): Show |
1 | a0003c0003t0003g0169 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(31): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(26): Show |
3 | a0001c0001t0042g0264 a0001c0001t0043g0089 a0004c0004t0055g0288 |
3 | HG01243.hp2 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(33): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(21): Show |
2 | a0003c0003t0003g0159 a0003c0003t0025g0001 |
2 | NA18956.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(28): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(23): Show |
2 | a0003c0003t0003g0001 a0003c0003t0003g0149 |
2 | HG02895.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(30): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(25): Show |
1 | a0003c0003t0003g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(32): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(27): Show |
2 | a0003c0003t0003g0010 a0007c0007t0027g0268 |
2 | HG02717.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(34): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(29): Show |
1 | a0003c0003t0003g0001 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(36): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(10): Show |
1 | a0003c0003t0003g0174 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(17): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(14): Show |
1 | a0003c0003t0006g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(21): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(20): Show |
2 | a0001c0001t0007g0037 a0003c0003t0003g0155 |
2 | HG03130.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(27): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(24): Show |
2 | a0003c0003t0003g0173 a0009c0011t0051g0266 |
2 | HG02080.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(31): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(28): Show |
2 | a0003c0003t0003g0180 a0004c0004t0004g0291 |
2 | HG02056.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(35): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(30): Show |
1 | a0003c0003t0003g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(37): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(9): Show |
1 | a0003c0003t0003g0168 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(16): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(15): Show |
3 | a0003c0003t0006g0014 a0003c0003t0006g0153 a0008c0009t0014g0085 |
3 | HG00140.hp2 HG03490.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(22): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(17): Show |
1 | a0003c0003t0006g0014 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(24): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(19): Show |
3 | a0003c0003t0003g0001 a0003c0003t0003g0029 a0004c0004t0013g0286 |
3 | HG02145.hp1 HG02698.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(26): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(21): Show |
3 | a0003c0003t0003g0001 a0003c0003t0003g0161 a0003c0003t0024g0157 |
3 | HG02056.hp2 HG02735.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(28): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(23): Show |
3 | a0003c0003t0003g0029 a0003c0003t0003g0154 a0003c0003t0008g0028 |
3 | HG02080.hp2 NA18949.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(30): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(25): Show |
3 | a0003c0003t0003g0187 a0003c0003t0008g0028 a0003c0003t0047g0162 |
3 | HG02155.hp1 NA18962.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(32): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(27): Show |
1 | a0007c0007t0027g0267 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(34): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(29): Show |
2 | a0003c0003t0003g0160 a0011c0008t0003g0001 |
2 | NA18988.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(36): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(35): Show |
1 | a0003c0003t0025g0185 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(42): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(14): Show |
2 | a0003c0003t0006g0086 a0003c0003t0031g0152 |
2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(21): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(18): Show |
2 | a0003c0003t0003g0001 a0003c0003t0003g0167 |
3 | NA18975.hp2 NA19006.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(25): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(20): Show |
4 | a0003c0003t0003g0158 a0003c0003t0008g0005 a0004c0004t0013g0036 others(1): Show |
4 | HG02486.hp2 HG02922.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-454_754-453ins others(27): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(22): Show |
1 | a0004c0004t0013g0036 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(29): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(24): Show |
2 | a0001c0001t0007g0136 a0003c0003t0008g0001 |
3 | NA18998.hp2 NA19043.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(31): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0021g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(16): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0023g0088 a0003c0003t0003g0186 |
2 | HG02015.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(18): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(13): Show |
4 | a0003c0003t0006g0016 a0003c0003t0006g0148 a0003c0003t0006g0150 others(1): Show |
4 | HG02602.hp2 HG03927.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-454_754-453ins others(20): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(15): Show |
2 | a0003c0003t0003g0010 a0003c0003t0014g0146 |
2 | HG00735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(22): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(17): Show |
1 | a0003c0003t0003g0001 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(24): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(19): Show |
5 | a0001c0001t0045g0131 a0003c0003t0003g0001 a0003c0003t0003g0010 others(2): Show |
5 | HG00408.hp1 HG02132.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-454_754-453ins others(26): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(21): Show |
2 | a0003c0003t0008g0005 a0003c0003t0046g0001 |
2 | HG00423.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(28): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(27): Show |
1 | a0003c0003t0003g0166 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(34): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0007g0140 a0003c0003t0003g0027 |
3 | HG02293.hp1 HG02300.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0016g0130 a0001c0001t0016g0138 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(13): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(12): Show |
1 | a0003c0003t0006g0016 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(19): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(14): Show |
3 | a0003c0003t0006g0016 a0003c0003t0006g0087 a0003c0003t0006g0151 |
3 | HG01256.hp2 HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(21): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(18): Show |
1 | a0003c0003t0003g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(25): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(20): Show |
2 | a0003c0003t0003g0005 a0003c0003t0008g0189 |
2 | HG03688.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.754-454_754-453ins others(27): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(22): Show |
4 | a0003c0003t0003g0005 a0003c0003t0003g0156 a0003c0003t0003g0176 others(1): Show |
4 | HG02280.hp1 NA18955.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-454_754-453ins others(29): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(24): Show |
2 | a0003c0003t0003g0165 a0003c0003t0024g0163 |
2 | HG02738.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(31): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0022g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(14): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(15): Show |
3 | a0001c0001t0021g0137 a0001c0001t0029g0127 a0001c0001t0030g0126 |
3 | HG01069.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(22): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(21): Show |
1 | a0003c0003t0003g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(28): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(27): Show |
1 | a0003c0003t0003g0171 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(34): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0007g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(10): Show |
2 | a0001c0001t0022g0082 a0001c0001t0023g0090 |
2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(17): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(20): Show |
1 | a0003c0003t0003g0172 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.754-454_754-453ins others(27): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0007g0009 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(12): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAA others(13): Show |
1 | a0003c0003t0003g0001 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(20): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAAAAAAT others(4): Show |
3 | a0001c0001t0007g0009 a0001c0001t0007g0133 a0001c0001t0050g0009 |
3 | HG02809.hp2 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.754-454_754-453ins others(11): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | A | AAATATAT others(12): Show |
1 | a0003c0003t0003g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.754-454_754-453ins others(19): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | AAT | A | 25 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(22): Show |
34 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.754-428_754-427del others(2): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360249 | AATATATA others(5): Show |
A | 3 | a0002c0002t0001g0222 a0002c0002t0001g0239 a0002c0002t0011g0007 |
3 | NA18948.hp1 NA18991.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.754-438_754-427del others(12): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360249 | ||||||
chr1:46360250 | AT | A | 29 | a0001c0001t0001g0003 a0001c0001t0002g0004 a0001c0001t0002g0012 others(26): Show |
35 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.754-453delT | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360250 | |||||||
chr1:46360250 | ATAT | A | 11 | a0001c0001t0001g0120 a0001c0001t0002g0013 a0001c0001t0002g0055 others(8): Show |
13 | HG01074.hp1 HG03017.hp1 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-453_754-451del others(3): Show |
NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360250 | |||||||
chr1:46360251 | T | A | 63 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0068 others(60): Show |
64 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.754-453T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360251 | |||||||
chr1:46360253 | T | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0061 others(94): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.754-451T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360253 | |||||||
chr1:46360255 | T | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0002g0003 others(76): Show |
97 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.754-449T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360255 | |||||||
chr1:46360257 | T | A | 34 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0021 others(31): Show |
41 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.754-447T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360257 | |||||||
chr1:46360259 | T | A | 12 | a0001c0001t0002g0022 a0001c0001t0002g0057 a0001c0001t0005g0092 others(9): Show |
13 | HG00544.hp2 HG01256.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-445T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360259 | |||||||
chr1:46360261 | T | A | 5 | a0001c0001t0002g0022 a0001c0001t0028g0142 a0001c0001t0028g0143 others(2): Show |
6 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-443T>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360261 | |||||||
chr1:46360278 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-426G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360278 | |||||||
chr1:46360282 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.754-422A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360282 | |||||||
chr1:46360439 | TA | T | 34 | a0001c0001t0002g0039 a0001c0001t0002g0056 a0001c0001t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.754-251delA | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 46360439 | ||||||
chr1:46360473 | A | T | 1 | a0001c0001t0041g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.754-231A>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360473 | |||||||
chr1:46360507 | A | C | 2 | a0001c0001t0021g0135 a0001c0001t0021g0137 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.754-197A>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360507 | |||||||
chr1:46360516 | A | G | 1 | a0002c0002t0001g0234 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.754-188A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 4/5 | chr1 | 46360516 | |||||||
chr1:46360915 | C | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.878+87C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46360915 | |||||||
chr1:46361000 | A | G | 3 | a0001c0001t0023g0088 a0001c0001t0023g0090 a0001c0001t0043g0089 |
3 | HG02630.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.878+172A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46361000 | |||||||
chr1:46361014 | A | G | 7 | a0003c0003t0003g0005 a0003c0003t0003g0165 a0003c0003t0003g0172 others(4): Show |
10 | HG00423.hp2 HG02056.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.878+186A>G | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46361014 | |||||||
chr1:46361101 | C | T | 2 | a0004c0004t0052g0265 a0010c0010t0053g0038 |
2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.878+273C>T | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46361101 | |||||||
chr1:46361133 | C | A | 1 | a0001c0001t0043g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.878+305C>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46361133 | |||||||
chr1:46361253 | T | C | 2 | a0001c0001t0029g0127 a0001c0001t0030g0126 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.879-317T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46361253 | |||||||
chr1:46361322 | T | C | 1 | a0003c0003t0024g0163 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.879-248T>C | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46361322 | |||||||
chr1:46361378 | G | A | 30 | a0004c0004t0004g0035 a0004c0004t0004g0271 a0004c0004t0004g0272 others(27): Show |
31 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.879-192G>A | NSUN4 | ENSG00000117481.11 | transcript | ENST00000474844.6 | protein_coding | 5/5 | chr1 | 46361378 |