Item | Value |
---|---|
geneid | 2248 |
ensemblid | ENSG00000186895.4 |
hgncid | 3681 |
symbol | FGF3 |
name | fibroblast growth factor 3 |
refseq_nuc | NM_005247.4 |
refseq_prot | NP_005238.1 |
ensembl_nuc | ENST00000334134.4 |
ensembl_prot | ENSP00000334122.2 |
mane_status | MANE Select |
chr | chr11 |
start | 69809968 |
end | 69819416 |
strand | - |
ver | v1.2 |
region | chr11:69809968-69819416 |
region5000 | chr11:69804968-69824416 |
regionname0 | FGF3_chr11_69809968_69819416 |
regionname5000 | FGF3_chr11_69804968_69824416 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 239 | 417 | 92 | 80 | 184 | 16 | 43 | 142 | FGF3_chr11_69804968_69824416 | FGF3 | MGLIW others(234): Show |
chr11 | 69804968 | 69824416 |
a0002 | 0/0 | 130 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | MGLIW others(125): Show |
chr11 | 69804968 | 69824416 |
a0003 | 0/0 | 239 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | MGLIW others(234): Show |
chr11 | 69804968 | 69824416 |
a0004 | 0/0 | 239 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | MGLIW others(234): Show |
chr11 | 69804968 | 69824416 |
a0005 | 0/0 | 239 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | MGLIW others(234): Show |
chr11 | 69804968 | 69824416 |
a0006 | 0/0 | 239 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | MGLIW others(234): Show |
chr11 | 69804968 | 69824416 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 717 | 389 | 83 | 75 | 176 | 14 | 39 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0001c0002 | 0/0 | 717 | 20 | 4 | 4 | 7 | 2 | 3 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0001c0003 | 0/0 | 717 | 6 | 5 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0001c0006 | 0/0 | 717 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0001c0010 | 0/0 | 717 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0002c0005 | 0/0 | 730 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(725): Show |
chr11 | 69804968 | 69824416 | ||
a0003c0004 | 0/0 | 717 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0004c0008 | 0/0 | 717 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0005c0007 | 0/0 | 717 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 | ||
a0006c0009 | 0/0 | 717 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | ATGGG others(712): Show |
chr11 | 69804968 | 69824416 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1540 | 374 | 75 | 72 | 176 | 14 | 35 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0001t0002 | 0/0 | 1540 | 9 | 5 | 3 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0001t0003 | 0/0 | 1540 | 2 | 0 | 0 | 0 | 0 | 2 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0001t0004 | 0/0 | 1540 | 2 | 2 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0001t0005 | 0/0 | 1540 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0001t0006 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0002t0001 | 0/0 | 1540 | 20 | 4 | 4 | 7 | 2 | 3 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0003t0001 | 0/0 | 1540 | 6 | 5 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0006t0001 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0001c0010t0001 | 0/0 | 1540 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0002c0005t0001 | 0/0 | 1553 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1548): Show |
chr11 | 69804968 | 69824416 |
a0003c0004t0007 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0004c0008t0001 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0005c0007t0001 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
a0006c0009t0001 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | AGAGC others(1535): Show |
chr11 | 69804968 | 69824416 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 74 | 3 | 13 | 46 | 6 | 6 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0002 | 0/0 | 47 | 3 | 8 | 27 | 2 | 7 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0003 | 0/0 | 31 | 1 | 8 | 16 | 1 | 5 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0004 | 0/0 | 19 | 6 | 3 | 8 | 1 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0006 | 0/0 | 14 | 5 | 4 | 1 | 0 | 4 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0007 | 0/0 | 13 | 0 | 3 | 9 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0008 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0009 | 0/0 | 12 | 0 | 9 | 0 | 2 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0010 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0011 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0012 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0013 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0015 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0016 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0018 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0002t0001g0005 | 0/0 | 16 | 0 | 4 | 7 | 2 | 3 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0002t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0003t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0001c0010t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0002c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0003c0004t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0004c0008t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0005c0007t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
a0006c0009t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0038 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | IBS | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02683 | hp1 | a0002 | c0005 | t0001 | g0099 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0106 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02965 | hp2 | a0003 | c0004 | t0007 | g0111 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04115 | hp2 | a0001 | c0010 | t0001 | g0090 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | YRI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18966 | hp1 | a0001 | c0006 | t0001 | g0064 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19010 | hp1 | a0005 | c0007 | t0001 | g0097 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | LWK | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19088 | hp1 | a0006 | c0009 | t0001 | g0086 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ASW | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | TSI | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | GIH | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG03471 | hp2 | a0004 | c0008 | t0001 | g0070 | AFR | MSL | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | USA | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0087 | REF | REF | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0056 | REF | REF | FGF3_chr11_69804968_69824416 | FGF3 | chr11 | 69804968 | 69824416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69810390 | C | T | 1 | a0004 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.635G>A | p.Arg212Gln | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 3/3 | 1118/1540 | 635/720 | 212/239 | chr11 | 69810390 | |||
chr11:69810396 | C | T | 1 | a0005 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.629G>A | p.Arg210Gln | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 3/3 | 1112/1540 | 629/720 | 210/239 | chr11 | 69810396 | |||
chr11:69810440 | C | A | 1 | a0006 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.585G>T | p.Gln195His | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 3/3 | 1068/1540 | 585/720 | 195/239 | chr11 | 69810440 | |||
chr11:69810674 | A | AAACTCGC others(6): Show |
1 | a0002 | 1 | HG02683.hp1 | frameshift_variant | HIGH | c.338_350dupCCGAGTGC others(5): Show |
p.Val118fs | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 3/3 | 833/1540 | 350/720 | 117/239 | chr11 | 69810674 | |||
chr11:69816341 | C | G | 1 | a0003 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.303G>C | p.Lys101Asn | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/3 | 786/1540 | 303/720 | 101/239 | chr11 | 69816341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69810602 | A | G | 1 | a0001c0006 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.423T>C | p.Pro141Pro | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 3/3 | 906/1540 | 423/720 | 141/239 | chr11 | 69810602 | |||
chr11:69810617 | C | T | 1 | a0001c0002 | 20 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
synonymous_variant | LOW | c.408G>A | p.Thr136Thr | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 3/3 | 891/1540 | 408/720 | 136/239 | chr11 | 69810617 | |||
chr11:69816365 | G | A | 1 | a0001c0010 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.279C>T | p.Ser93Ser | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/3 | 762/1540 | 279/720 | 93/239 | chr11 | 69816365 | |||
chr11:69818865 | C | A | 2 | a0001c0002 a0001c0003 |
26 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(23): Show |
synonymous_variant | LOW | c.69G>T | p.Ala23Ala | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/3 | 552/1540 | 69/720 | 23/239 | chr11 | 69818865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69818996 | G | A | 1 | a0003c0004t0007 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-63C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/3 | 63 | chr11 | 69818996 | ||||||
chr11:69819057 | C | A | 1 | a0001c0001t0002 | 9 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-124G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/3 | 124 | chr11 | 69819057 | ||||||
chr11:69819082 | A | T | 1 | a0001c0001t0006 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/3 | 149 | chr11 | 69819082 | ||||||
chr11:69819226 | C | A | 1 | a0001c0001t0003 | 2 | HG03490.hp2 HG03492.hp2 |
5_prime_UTR_variant | MODIFIER | c.-293G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/3 | 293 | chr11 | 69819226 | ||||||
chr11:69819259 | A | C | 1 | a0001c0001t0005 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-326T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/3 | 326 | chr11 | 69819259 | ||||||
chr11:69819264 | C | A | 1 | a0001c0001t0004 | 2 | HG02630.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-331G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/3 | 331 | chr11 | 69819264 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69810705 | G | A | 1 | a0001c0001t0002g0039 | 2 | HG01361.hp2 HG01496.hp1 |
splice_region_variant&intron_variant | LOW | c.325-5C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810705 | |||||||
chr11:69810719 | A | G | 1 | a0001c0001t0001g0023 | 3 | HG03453.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.325-19T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810719 | |||||||
chr11:69810743 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(51): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.325-43A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810743 | |||||||
chr11:69810800 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0069 |
2 | NA18960.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.325-100G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810800 | |||||||
chr11:69810903 | T | A | 1 | a0001c0001t0002g0040 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.325-203A>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810903 | |||||||
chr11:69810907 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.325-207G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810907 | |||||||
chr11:69810962 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(51): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.325-262C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810962 | |||||||
chr11:69810967 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.325-267G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69810967 | |||||||
chr11:69811158 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0076 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.325-458T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811158 | |||||||
chr11:69811306 | C | T | 1 | a0001c0001t0001g0020 | 3 | HG02895.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.325-606G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811306 | |||||||
chr11:69811387 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
4 | HG00642.hp1 HG02559.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-687A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811387 | |||||||
chr11:69811450 | C | CA | 12 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0050 others(9): Show |
24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.325-751dupT | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811450 | |||||||
chr11:69811450 | CA | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
26 | HG01496.hp2 HG02615.hp1 HG03098.hp1 others(23): Show |
intron_variant | MODIFIER | c.325-751delT | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811450 | |||||||
chr11:69811450 | CAA | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(39): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.325-752_325-751del others(2): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811450 | |||||||
chr11:69811451 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-751T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811451 | |||||||
chr11:69811463 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0104 |
6 | HG02615.hp1 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-763T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811463 | |||||||
chr11:69811467 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.325-767T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811467 | |||||||
chr11:69811473 | G | GA | 4 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0089 others(1): Show |
7 | HG02615.hp1 HG03098.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-774dupT | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811473 | |||||||
chr11:69811473 | GA | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0021 others(5): Show |
48 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.325-774delT | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811473 | |||||||
chr11:69811498 | A | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(51): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.325-798T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811498 | |||||||
chr11:69811529 | G | C | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.325-829C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811529 | |||||||
chr11:69811533 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-833T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811533 | |||||||
chr11:69811703 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.325-1003G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811703 | |||||||
chr11:69811704 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.325-1004T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811704 | |||||||
chr11:69811923 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.325-1223T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811923 | |||||||
chr11:69811925 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.325-1225A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69811925 | |||||||
chr11:69812046 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.325-1346C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812046 | |||||||
chr11:69812150 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(15): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.325-1450G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812150 | |||||||
chr11:69812193 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.325-1493G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812193 | |||||||
chr11:69812240 | C | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(56): Show |
231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.325-1540G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812240 | |||||||
chr11:69812247 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(63): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.325-1547T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812247 | |||||||
chr11:69812262 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0089 |
8 | NA18973.hp1 NA18974.hp2 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-1562G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812262 | |||||||
chr11:69812283 | G | C | 1 | a0003c0004t0007g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.325-1583C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812283 | |||||||
chr11:69812449 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.325-1749G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812449 | |||||||
chr11:69812503 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.325-1803G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812503 | |||||||
chr11:69812549 | C | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(24): Show |
75 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.325-1849G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812549 | |||||||
chr11:69812605 | T | G | 1 | a0001c0002t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.325-1905A>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812605 | |||||||
chr11:69812613 | G | T | 1 | a0001c0001t0001g0030 | 2 | HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.325-1913C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812613 | |||||||
chr11:69812620 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.325-1920G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812620 | |||||||
chr11:69812683 | C | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(14): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.325-1983G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812683 | |||||||
chr11:69812772 | G | A | 8 | a0001c0002t0001g0005 a0001c0002t0001g0024 a0001c0002t0001g0110 others(5): Show |
26 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.325-2072C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812772 | |||||||
chr11:69812894 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.325-2194T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812894 | |||||||
chr11:69812898 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-2198A>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812898 | |||||||
chr11:69812899 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-2199C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812899 | |||||||
chr11:69812934 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.325-2234G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812934 | |||||||
chr11:69812954 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.325-2254C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812954 | |||||||
chr11:69812959 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-2259T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812959 | |||||||
chr11:69812960 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-2260C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812960 | |||||||
chr11:69812994 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.325-2294T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69812994 | |||||||
chr11:69813305 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.325-2605G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813305 | |||||||
chr11:69813331 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.325-2631T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813331 | |||||||
chr11:69813395 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.325-2695C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813395 | |||||||
chr11:69813410 | T | C | 4 | a0001c0001t0002g0039 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
5 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-2710A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813410 | |||||||
chr11:69813465 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-2765A>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813465 | |||||||
chr11:69813467 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.325-2767T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813467 | |||||||
chr11:69813523 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.324+2797C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813523 | |||||||
chr11:69813576 | ATGGATGG others(65): Show |
A | 1 | a0001c0001t0001g0048 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324+2672_324+2743d others(74): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813576 | |||||||
chr11:69813584 | ATAGATGG others(25): Show |
A | 8 | a0001c0001t0001g0004 a0001c0001t0002g0039 a0001c0001t0002g0040 others(5): Show |
10 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+2704_324+2735d others(34): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813584 | |||||||
chr11:69813585 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+2735A>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813585 | |||||||
chr11:69813586 | A | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(24): Show |
74 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.324+2734T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813586 | |||||||
chr11:69813586 | A | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.324+2734T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813586 | |||||||
chr11:69813592 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.324+2728C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813592 | |||||||
chr11:69813596 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.324+2724C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813596 | |||||||
chr11:69813608 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.324+2712T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813608 | |||||||
chr11:69813612 | ATGGG | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(22): Show |
72 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.324+2704_324+2707d others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813612 | |||||||
chr11:69813616 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324+2704C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813616 | |||||||
chr11:69813618 | G | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(29): Show |
82 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.324+2702C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813618 | |||||||
chr11:69813624 | A | ATGGATGG others(57): Show |
11 | a0001c0001t0001g0011 a0001c0001t0004g0042 a0001c0001t0006g0044 others(8): Show |
38 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.324+2695_324+2696i others(66): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813624 | |||||||
chr11:69813624 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+2696T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813624 | |||||||
chr11:69813632 | A | C | 1 | a0002c0005t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324+2688T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813632 | |||||||
chr11:69813632 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(18): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.324+2688T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813632 | |||||||
chr11:69813636 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+2684T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813636 | |||||||
chr11:69813640 | G | A | 1 | a0002c0005t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324+2680C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813640 | |||||||
chr11:69813640 | G | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(16): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.324+2680C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813640 | |||||||
chr11:69813641 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+2679A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813641 | |||||||
chr11:69813642 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.324+2678C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813642 | |||||||
chr11:69813642 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+2678C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813642 | |||||||
chr11:69813646 | G | GGATGGAT others(33): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(14): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.324+2673_324+2674i others(42): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813646 | |||||||
chr11:69813648 | G | A | 2 | a0001c0001t0001g0037 a0001c0003t0001g0109 |
3 | HG01884.hp1 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+2672C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813648 | |||||||
chr11:69813648 | G | C | 11 | a0001c0001t0001g0011 a0001c0001t0004g0042 a0001c0001t0006g0044 others(8): Show |
38 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.324+2672C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813648 | |||||||
chr11:69813648 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+2672C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813648 | |||||||
chr11:69813656 | A | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(26): Show |
78 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.324+2664T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813656 | |||||||
chr11:69813662 | G | A | 1 | a0002c0005t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324+2658C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813662 | |||||||
chr11:69813664 | G | A | 2 | a0001c0001t0001g0037 a0001c0003t0001g0109 |
3 | HG01884.hp1 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+2656C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813664 | |||||||
chr11:69813665 | T | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0104 |
6 | HG02615.hp1 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2655A>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813665 | |||||||
chr11:69813670 | G | A | 2 | a0001c0001t0001g0037 a0001c0003t0001g0109 |
3 | HG01884.hp1 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+2650C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813670 | |||||||
chr11:69813672 | C | A | 1 | a0003c0004t0007g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.324+2648G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813672 | |||||||
chr11:69813672 | C | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0004g0042 others(10): Show |
41 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.324+2648G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813672 | |||||||
chr11:69813680 | A | ATGGG | 3 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0104 |
6 | HG02615.hp1 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2639_324+2640i others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813680 | |||||||
chr11:69813686 | G | A | 2 | a0001c0001t0001g0037 a0001c0003t0001g0109 |
3 | HG01884.hp1 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+2634C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813686 | |||||||
chr11:69813688 | G | A | 11 | a0001c0001t0001g0011 a0001c0001t0004g0042 a0001c0001t0006g0044 others(8): Show |
38 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.324+2632C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813688 | |||||||
chr11:69813688 | G | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0104 |
6 | HG02615.hp1 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2632C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813688 | |||||||
chr11:69813692 | A | ATGGG | 22 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(19): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.324+2627_324+2628i others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813692 | |||||||
chr11:69813696 | A | C | 1 | a0002c0005t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324+2624T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813696 | |||||||
chr11:69813696 | A | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(15): Show |
50 | HG00280.hp2 HG00438.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.324+2624T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813696 | |||||||
chr11:69813702 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.324+2618T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813702 | |||||||
chr11:69813704 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(48): Show |
219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.324+2616C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813704 | |||||||
chr11:69813708 | A | ATGGG | 1 | a0001c0001t0001g0023 | 3 | HG03453.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.324+2611_324+2612i others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813708 | |||||||
chr11:69813712 | A | ATGGG | 3 | a0001c0001t0001g0011 a0001c0001t0004g0042 a0001c0003t0001g0038 |
13 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+2607_324+2608i others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813712 | |||||||
chr11:69813712 | A | C | 2 | a0001c0001t0001g0037 a0001c0003t0001g0109 |
3 | HG01884.hp1 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+2608T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813712 | |||||||
chr11:69813712 | A | G | 11 | a0001c0001t0001g0036 a0001c0001t0001g0104 a0001c0001t0006g0044 others(8): Show |
29 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+2608T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813712 | |||||||
chr11:69813716 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.324+2604T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813716 | |||||||
chr11:69813718 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.324+2602T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813718 | |||||||
chr11:69813720 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(43): Show |
191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.324+2600C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813720 | |||||||
chr11:69813724 | A | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0060 others(1): Show |
7 | HG00597.hp1 HG02015.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+2596T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813724 | |||||||
chr11:69813728 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0059 others(11): Show |
42 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.324+2592T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813728 | |||||||
chr11:69813736 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
47 | HG00280.hp2 HG00438.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.324+2584C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813736 | |||||||
chr11:69813736 | G | C | 2 | a0001c0001t0001g0059 a0001c0003t0001g0108 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.324+2584C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813736 | |||||||
chr11:69813740 | A | T | 1 | a0001c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324+2580T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813740 | |||||||
chr11:69813744 | C | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0037 others(4): Show |
11 | HG01255.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.324+2576G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813744 | |||||||
chr11:69813744 | C | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(38): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.324+2576G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813744 | |||||||
chr11:69813744 | CTGGATGG others(41): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.324+2528_324+2575d others(50): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813744 | |||||||
chr11:69813748 | A | T | 9 | a0001c0001t0001g0011 a0001c0001t0004g0042 a0001c0001t0006g0044 others(6): Show |
36 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.324+2572T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813748 | |||||||
chr11:69813752 | A | ATGGATGG others(77): Show |
2 | a0001c0001t0001g0037 a0001c0003t0001g0109 |
3 | HG01884.hp1 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+2567_324+2568i others(86): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813752 | |||||||
chr11:69813752 | A | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0004g0042 others(7): Show |
37 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.324+2568T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813752 | |||||||
chr11:69813752 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(41): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.324+2568T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813752 | |||||||
chr11:69813756 | A | ATGGCTGG others(1): Show |
5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(2): Show |
11 | HG01243.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.324+2563_324+2564i others(10): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813756 | |||||||
chr11:69813756 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.324+2564T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813756 | |||||||
chr11:69813758 | G | GGGTGGAT | 2 | a0001c0001t0001g0016 a0001c0001t0001g0051 |
5 | HG01346.hp1 HG01928.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+2555_324+2561d others(9): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813758 | |||||||
chr11:69813760 | G | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(26): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.324+2560C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813760 | |||||||
chr11:69813764 | A | ATGGCTGG others(5): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0031 others(5): Show |
28 | HG00280.hp2 HG01257.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.324+2555_324+2556i others(14): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813764 | |||||||
chr11:69813764 | A | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(20): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.324+2556T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813764 | |||||||
chr11:69813768 | G | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(10): Show |
37 | HG00280.hp2 HG01255.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.324+2552C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813768 | |||||||
chr11:69813768 | G | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(24): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.324+2552C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813768 | |||||||
chr11:69813768 | G | GTGGA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(12): Show |
43 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.324+2548_324+2551d others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813768 | |||||||
chr11:69813768 | G | GTGGATGG others(1): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(18): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.324+2544_324+2551d others(10): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813768 | |||||||
chr11:69813768 | G | GTGGATGG others(5): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0067 others(5): Show |
11 | HG02015.hp1 HG03471.hp2 HG03486.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+2540_324+2551d others(14): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813768 | |||||||
chr11:69813768 | G | GTGGATGG others(5): Show |
9 | a0001c0001t0001g0011 a0001c0001t0004g0042 a0001c0001t0006g0044 others(6): Show |
36 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.324+2551_324+2552i others(14): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813768 | |||||||
chr11:69813772 | A | ATGGCTGG others(13): Show |
1 | a0001c0001t0001g0023 | 3 | HG03453.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.324+2547_324+2548i others(22): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813772 | |||||||
chr11:69813772 | A | ATGGG | 10 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0046 others(7): Show |
32 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.324+2547_324+2548i others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813772 | |||||||
chr11:69813772 | A | ATGGGTGG others(21): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0104 |
3 | HG02615.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.324+2547_324+2548i others(30): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813772 | |||||||
chr11:69813772 | A | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0031 others(5): Show |
28 | HG00280.hp2 HG01257.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.324+2548T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813772 | |||||||
chr11:69813772 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0089 a0001c0001t0001g0095 others(1): Show |
12 | HG00438.hp2 HG01243.hp2 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+2548T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813772 | |||||||
chr11:69813776 | A | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0089 a0001c0001t0001g0095 others(1): Show |
12 | HG00438.hp2 HG01243.hp2 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+2544T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813776 | |||||||
chr11:69813776 | A | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0045 others(2): Show |
8 | HG01243.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+2544T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813776 | |||||||
chr11:69813780 | A | ATGGG | 11 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0034 others(8): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.324+2539_324+2540i others(6): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813780 | |||||||
chr11:69813780 | A | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(18): Show |
66 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.324+2540T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813780 | |||||||
chr11:69813784 | A | C | 1 | a0002c0005t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324+2536T>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813784 | |||||||
chr11:69813784 | A | G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0033 others(6): Show |
13 | HG00423.hp1 HG01243.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+2536T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813784 | |||||||
chr11:69813788 | A | ATGGGTGG others(5): Show |
1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+2531_324+2532i others(14): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813788 | |||||||
chr11:69813788 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(28): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.324+2532T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813788 | |||||||
chr11:69813792 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(14): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.324+2528T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813792 | |||||||
chr11:69813796 | A | ATGGGTGG others(5): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0095 |
10 | HG00438.hp2 HG01243.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+2523_324+2524i others(14): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813796 | |||||||
chr11:69813796 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0033 others(9): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.324+2524T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813796 | |||||||
chr11:69813800 | A | ATGGATGG others(9): Show |
1 | a0001c0001t0002g0039 | 2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.324+2519_324+2520i others(18): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813800 | |||||||
chr11:69813800 | A | ATGGATGG others(5): Show |
4 | a0001c0001t0002g0040 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+2519_324+2520i others(14): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813800 | |||||||
chr11:69813800 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0095 a0001c0001t0001g0101 others(2): Show |
6 | HG00423.hp1 HG02155.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2520T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813800 | |||||||
chr11:69813808 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(42): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.324+2512C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813808 | |||||||
chr11:69813816 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(42): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.324+2504C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813816 | |||||||
chr11:69813824 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(15): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.324+2496C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813824 | |||||||
chr11:69813832 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0002c0005t0001g0099 |
3 | HG02622.hp2 HG02683.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.324+2488C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813832 | |||||||
chr11:69813840 | C | A | 1 | a0002c0005t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324+2480G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813840 | |||||||
chr11:69813844 | T | G | 1 | a0002c0005t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324+2476A>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813844 | |||||||
chr11:69813877 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.324+2443A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813877 | |||||||
chr11:69813918 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.324+2402C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813918 | |||||||
chr11:69813926 | TGGTGGAT others(9): Show |
T | 1 | a0001c0001t0006g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.324+2378_324+2393d others(18): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813926 | |||||||
chr11:69813930 | GGATGGGT others(1): Show |
G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.324+2382_324+2389d others(10): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813930 | |||||||
chr11:69813951 | G | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(13): Show |
54 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.324+2369C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813951 | |||||||
chr11:69813997 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
14 | HG02080.hp1 NA18940.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.324+2323C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69813997 | |||||||
chr11:69814069 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.324+2251C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814069 | |||||||
chr11:69814077 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.324+2243T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814077 | |||||||
chr11:69814247 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(22): Show |
72 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.324+2073G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814247 | |||||||
chr11:69814248 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.324+2072T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814248 | |||||||
chr11:69814258 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.324+2062G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814258 | |||||||
chr11:69814272 | G | C | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2048C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814272 | |||||||
chr11:69814274 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2046C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814274 | |||||||
chr11:69814276 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2044C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814276 | |||||||
chr11:69814277 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2043A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814277 | |||||||
chr11:69814278 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2042C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814278 | |||||||
chr11:69814279 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2041C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814279 | |||||||
chr11:69814280 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2040C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814280 | |||||||
chr11:69814281 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2039G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814281 | |||||||
chr11:69814285 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2035T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814285 | |||||||
chr11:69814287 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.324+2033T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814287 | |||||||
chr11:69814329 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.324+1991C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814329 | |||||||
chr11:69814330 | C | G | 1 | a0001c0001t0001g0088 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.324+1990G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814330 | |||||||
chr11:69814338 | G | C | 1 | a0001c0001t0005g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324+1982C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814338 | |||||||
chr11:69814356 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.324+1964G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814356 | |||||||
chr11:69814390 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(13): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.324+1930C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814390 | |||||||
chr11:69814431 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.324+1889G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814431 | |||||||
chr11:69814607 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01099.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.324+1713G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814607 | |||||||
chr11:69814622 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.324+1698C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814622 | |||||||
chr11:69814752 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.324+1568A>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814752 | |||||||
chr11:69814841 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0089 |
8 | NA18973.hp1 NA18974.hp2 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+1479C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814841 | |||||||
chr11:69814929 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0004g0042 |
13 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+1391T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69814929 | |||||||
chr11:69815040 | T | G | 1 | a0001c0001t0005g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324+1280A>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815040 | |||||||
chr11:69815107 | GTGGATGG others(1): Show |
G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.324+1205_324+1212d others(10): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815107 | |||||||
chr11:69815137 | A | AGGTGGAT others(1): Show |
7 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0112 others(4): Show |
9 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+1175_324+1182d others(10): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815137 | |||||||
chr11:69815142 | GATGGGTG others(17): Show |
G | 1 | a0001c0001t0001g0026 | 2 | HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.324+1154_324+1177d others(26): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815142 | |||||||
chr11:69815212 | TGGTGGAT others(17): Show |
T | 1 | a0001c0001t0001g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.324+1084_324+1107d others(26): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815212 | |||||||
chr11:69815248 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.324+1072C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815248 | |||||||
chr11:69815253 | G | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(13): Show |
54 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.324+1067C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815253 | |||||||
chr11:69815265 | G | GGTGGATG others(25): Show |
1 | a0001c0001t0002g0040 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.324+1023_324+1054d others(34): Show |
FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815265 | |||||||
chr11:69815297 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0049 others(4): Show |
44 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.324+1023T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815297 | |||||||
chr11:69815398 | A | G | 1 | a0001c0003t0001g0106 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+922T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815398 | |||||||
chr11:69815565 | G | A | 1 | a0001c0002t0001g0005 | 16 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.324+755C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815565 | |||||||
chr11:69815567 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.324+753C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815567 | |||||||
chr11:69815695 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.324+625G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815695 | |||||||
chr11:69815736 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(13): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.324+584C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815736 | |||||||
chr11:69815801 | C | T | 7 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0112 others(4): Show |
9 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+519G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815801 | |||||||
chr11:69815909 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(55): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.324+411A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815909 | |||||||
chr11:69815990 | G | A | 1 | a0003c0004t0007g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.324+330C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69815990 | |||||||
chr11:69816039 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.324+281C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69816039 | |||||||
chr11:69816205 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.324+115C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69816205 | |||||||
chr11:69816210 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.324+110C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69816210 | |||||||
chr11:69816278 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324+42C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69816278 | |||||||
chr11:69816291 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.324+29G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69816291 | |||||||
chr11:69816305 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.324+15T>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69816305 | |||||||
chr11:69816309 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.324+11G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 2/2 | chr11 | 69816309 | |||||||
chr11:69816529 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 |
3 | HG02258.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.221-106C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816529 | |||||||
chr11:69816553 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA19054.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.221-130C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816553 | |||||||
chr11:69816556 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.221-133C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816556 | |||||||
chr11:69816630 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.221-207G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816630 | |||||||
chr11:69816672 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0025 |
5 | HG01243.hp1 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-249G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816672 | |||||||
chr11:69816707 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.221-284C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816707 | |||||||
chr11:69816723 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.221-300G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816723 | |||||||
chr11:69816819 | C | G | 1 | a0001c0001t0002g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.221-396G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816819 | |||||||
chr11:69816963 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.221-540C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816963 | |||||||
chr11:69816985 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.221-562C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816985 | |||||||
chr11:69816996 | T | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0104 |
3 | HG02615.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.221-573A>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69816996 | |||||||
chr11:69817035 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.221-612A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817035 | |||||||
chr11:69817165 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0104 |
6 | HG02615.hp1 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-742C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817165 | |||||||
chr11:69817383 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.221-960C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817383 | |||||||
chr11:69817481 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.221-1058A>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817481 | |||||||
chr11:69817506 | C | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.221-1083G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817506 | |||||||
chr11:69817507 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-1084C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817507 | |||||||
chr11:69817617 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220+1097C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817617 | |||||||
chr11:69817621 | A | T | 1 | a0001c0001t0003g0041 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.220+1093T>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817621 | |||||||
chr11:69817800 | C | A | 1 | a0003c0004t0007g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.220+914G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817800 | |||||||
chr11:69817807 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.220+907G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817807 | |||||||
chr11:69817924 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.220+790C>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817924 | |||||||
chr11:69817969 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.220+745G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817969 | |||||||
chr11:69817975 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0079 |
6 | HG02809.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+739C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69817975 | |||||||
chr11:69818039 | C | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(13): Show |
54 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.220+675G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818039 | |||||||
chr11:69818095 | AT | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(15): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.220+618delA | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818095 | |||||||
chr11:69818130 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.220+584C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818130 | |||||||
chr11:69818229 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.220+485C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818229 | |||||||
chr11:69818247 | G | C | 1 | a0001c0001t0001g0023 | 3 | HG03453.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.220+467C>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818247 | |||||||
chr11:69818269 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(29): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.220+445C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818269 | |||||||
chr11:69818351 | G | A | 3 | a0001c0002t0001g0005 a0001c0002t0001g0024 a0001c0002t0001g0110 |
20 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.220+363C>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818351 | |||||||
chr11:69818539 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0104 |
6 | HG02615.hp1 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+175A>G | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818539 | |||||||
chr11:69818542 | C | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0004g0042 others(11): Show |
42 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.220+172G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818542 | |||||||
chr11:69818606 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.220+108G>A | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818606 | |||||||
chr11:69818617 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
14 | HG02080.hp1 NA18940.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+97G>T | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818617 | |||||||
chr11:69818656 | C | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.220+58G>C | FGF3 | ENSG00000186895.4 | transcript | ENST00000334134.4 | protein_coding | 1/2 | chr11 | 69818656 |