Item | Value |
---|---|
geneid | 152273 |
ensemblid | ENSG00000154783.12 |
hgncid | 19117 |
symbol | FGD5 |
name | FYVE, RhoGEF and PH domain containing 5 |
refseq_nuc | NM_152536.4 |
refseq_prot | NP_689749.3 |
ensembl_nuc | ENST00000285046.10 |
ensembl_prot | ENSP00000285046.5 |
mane_status | MANE Select |
chr | chr3 |
start | 14818962 |
end | 14934571 |
strand | + |
ver | v1.2 |
region | chr3:14818962-14934571 |
region5000 | chr3:14813962-14939571 |
regionname0 | FGD5_chr3_14818962_14934571 |
regionname5000 | FGD5_chr3_14813962_14939571 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1462 | 242 | 38 | 57 | 102 | 16 | 27 | 71 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0002 | 0/0 | 1462 | 47 | 0 | 3 | 41 | 0 | 3 | 34 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0003 | 0/0 | 1462 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0004 | 0/0 | 1462 | 9 | 1 | 3 | 2 | 0 | 3 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0005 | 0/0 | 1462 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0006 | 0/0 | 1462 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0007 | 0/0 | 1462 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0008 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0009 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0010 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0011 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0012 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0013 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0014 | 0/0 | 1468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1463): Show |
chr3 | 14813962 | 14939571 |
a0015 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0016 | 0/0 | 1462 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0017 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0018 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0019 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0020 | 0/0 | 1462 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0021 | 0/0 | 1462 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0022 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0023 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0024 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0025 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
a0026 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | MFRGP others(1457): Show |
chr3 | 14813962 | 14939571 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4386 | 178 | 26 | 45 | 78 | 13 | 16 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0001c0002 | 1/1 | 4386 | 54 | 6 | 12 | 24 | 3 | 7 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0001c0008 | 0/0 | 4386 | 3 | 3 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0001c0013 | 0/0 | 4386 | 2 | 0 | 0 | 0 | 0 | 2 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0001c0014 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0001c0022 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0001c0030 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0001c0031 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0002c0003 | 0/0 | 4386 | 43 | 0 | 3 | 37 | 0 | 3 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0002c0007 | 0/0 | 4386 | 4 | 0 | 0 | 4 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0003c0005 | 0/0 | 4386 | 7 | 6 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0003c0009 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0003c0017 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0003c0018 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0003c0019 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0004c0006 | 0/0 | 4386 | 7 | 1 | 2 | 1 | 0 | 3 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0004c0010 | 0/0 | 4386 | 2 | 0 | 1 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0005c0004 | 0/0 | 4386 | 8 | 8 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0006c0011 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0006c0033 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0007c0012 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0008c0035 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0009c0029 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0010c0025 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0011c0020 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0012c0039 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0013c0032 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0014c0015 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4399): Show |
chr3 | 14813962 | 14939571 | ||
a0015c0038 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0016c0016 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0017c0037 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0018c0040 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0019c0036 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0020c0023 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0021c0024 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0022c0026 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0023c0028 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0024c0034 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0025c0021 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 | ||
a0026c0027 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | ATGTT others(4381): Show |
chr3 | 14813962 | 14939571 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5903 | 158 | 20 | 39 | 70 | 13 | 16 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0002 | 0/0 | 5901 | 7 | 1 | 4 | 2 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5896): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0003 | 0/0 | 5903 | 4 | 0 | 0 | 4 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0004 | 0/0 | 5903 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0005 | 0/0 | 5903 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0008 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0011 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0012 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0015 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0016 | 0/0 | 5903 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0001t0017 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0001 | 1/1 | 5903 | 42 | 6 | 8 | 20 | 3 | 3 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0002 | 0/0 | 5901 | 5 | 0 | 3 | 2 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5896): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0005 | 0/0 | 5903 | 2 | 0 | 0 | 0 | 0 | 2 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0007 | 0/0 | 5903 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0009 | 0/0 | 5903 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0010 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0014 | 0/0 | 5903 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0002t0018 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0008t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0008t0004 | 0/0 | 5903 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0013t0001 | 0/0 | 5903 | 2 | 0 | 0 | 0 | 0 | 2 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0014t0001 | 0/0 | 5903 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0022t0001 | 0/0 | 5903 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0030t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0001c0031t0001 | 0/0 | 5903 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0002c0003t0001 | 0/0 | 5903 | 39 | 0 | 3 | 33 | 0 | 3 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0002c0003t0002 | 0/0 | 5901 | 2 | 0 | 0 | 2 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5896): Show |
chr3 | 14813962 | 14939571 |
a0002c0003t0003 | 0/0 | 5903 | 2 | 0 | 0 | 2 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0002c0007t0001 | 0/0 | 5903 | 4 | 0 | 0 | 4 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0003c0005t0001 | 0/0 | 5903 | 5 | 4 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0003c0005t0006 | 0/0 | 5903 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0003c0009t0001 | 0/0 | 5903 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0003c0017t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0003c0018t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0003c0019t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0004c0006t0001 | 0/0 | 5903 | 7 | 1 | 2 | 1 | 0 | 3 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0004c0010t0001 | 0/0 | 5903 | 2 | 0 | 1 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0005c0004t0001 | 0/0 | 5903 | 8 | 8 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0006c0011t0001 | 0/0 | 5903 | 2 | 2 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0006c0033t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0007c0012t0001 | 0/0 | 5903 | 2 | 0 | 0 | 2 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0008c0035t0001 | 0/0 | 5903 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0009c0029t0001 | 0/0 | 5903 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0010c0025t0001 | 0/0 | 5903 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0011c0020t0002 | 0/0 | 5901 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5896): Show |
chr3 | 14813962 | 14939571 |
a0012c0039t0001 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0013c0032t0001 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0014c0015t0001 | 0/0 | 5921 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5916): Show |
chr3 | 14813962 | 14939571 |
a0015c0038t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0016c0016t0001 | 0/0 | 5903 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0017c0037t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0018c0040t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0019c0036t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0020c0023t0001 | 0/0 | 5903 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0021c0024t0001 | 0/0 | 5903 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0022c0026t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0023c0028t0001 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0024c0034t0013 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0025c0021t0001 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
a0026c0027t0001 | 0/0 | 5903 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | CAAAA others(5898): Show |
chr3 | 14813962 | 14939571 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0011g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0016g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0007g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0009g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0010g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0014g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0002t0018g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0008t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0008t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0013t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0013t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0014t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0014t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0022t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0030t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0001c0031t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0007t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0007t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0002c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0005t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0005t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0005t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0005t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0009t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0009t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0017t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0018t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0003c0019t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0006t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0006t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0010t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0004c0010t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0005c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0006c0011t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0006c0011t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0006c0033t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0007c0012t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0007c0012t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0008c0035t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0009c0029t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0010c0025t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0011c0020t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0012c0039t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0013c0032t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0014c0015t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0015c0038t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0016c0016t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0017c0037t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0018c0040t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0019c0036t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0020c0023t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0021c0024t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0022c0026t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0023c0028t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0024c0034t0013g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0025c0021t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
a0026c0027t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | FIN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00544 | hp1 | a0001 | c0002 | t0010 | g0263 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00558 | hp2 | a0002 | c0003 | t0001 | g0178 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0330 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0195 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00673 | hp1 | a0001 | c0001 | t0011 | g0340 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00741 | hp1 | a0008 | c0035 | t0001 | g0165 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0233 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01081 | hp1 | a0003 | c0005 | t0001 | g0003 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01081 | hp2 | a0004 | c0010 | t0001 | g0161 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01106 | hp1 | a0004 | c0006 | t0001 | g0080 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01169 | hp2 | a0009 | c0029 | t0001 | g0103 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0176 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01255 | hp1 | a0010 | c0025 | t0001 | g0017 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01257 | hp1 | a0001 | c0002 | t0014 | g0160 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01261 | hp2 | a0001 | c0001 | t0016 | g0050 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0209 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0186 | EUR | IBS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | IBS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | IBS | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01934 | hp2 | a0002 | c0003 | t0001 | g0179 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01943 | hp1 | a0011 | c0020 | t0002 | g0269 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0267 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01975 | hp2 | a0004 | c0006 | t0001 | g0101 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02071 | hp2 | a0002 | c0003 | t0001 | g0221 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02074 | hp2 | a0004 | c0010 | t0001 | g0091 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02129 | hp2 | a0004 | c0006 | t0001 | g0044 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02132 | hp2 | a0001 | c0002 | t0018 | g0264 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0268 | AMR | PEL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02165 | hp1 | a0012 | c0039 | t0001 | g0092 | EAS | CDX | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02165 | hp2 | a0013 | c0032 | t0001 | g0222 | EAS | CDX | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02257 | hp1 | a0004 | c0006 | t0001 | g0078 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02257 | hp2 | a0003 | c0009 | t0001 | g0251 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02258 | hp1 | a0006 | c0033 | t0001 | g0008 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02258 | hp2 | a0003 | c0019 | t0001 | g0255 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02523 | hp1 | a0002 | c0003 | t0001 | g0194 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02572 | hp1 | a0015 | c0038 | t0001 | g0258 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02615 | hp1 | a0001 | c0014 | t0001 | g0018 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02615 | hp2 | a0001 | c0001 | t0017 | g0046 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02622 | hp1 | a0006 | c0011 | t0001 | g0007 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02630 | hp1 | a0003 | c0018 | t0001 | g0249 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0227 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0197 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02723 | hp2 | a0005 | c0004 | t0001 | g0038 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02735 | hp2 | a0001 | c0002 | t0007 | g0157 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02738 | hp2 | a0016 | c0016 | t0001 | g0068 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0032 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02895 | hp1 | a0003 | c0005 | t0006 | g0257 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02895 | hp2 | a0005 | c0004 | t0001 | g0021 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02896 | hp1 | a0001 | c0014 | t0001 | g0019 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02896 | hp2 | a0005 | c0004 | t0001 | g0040 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02897 | hp1 | a0003 | c0005 | t0006 | g0254 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02897 | hp2 | a0005 | c0004 | t0001 | g0037 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02965 | hp1 | a0001 | c0001 | t0015 | g0022 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02970 | hp1 | a0003 | c0005 | t0001 | g0005 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02976 | hp1 | a0003 | c0005 | t0001 | g0252 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02976 | hp2 | a0005 | c0004 | t0001 | g0041 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03130 | hp1 | a0005 | c0004 | t0001 | g0042 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03139 | hp1 | a0017 | c0037 | t0001 | g0253 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03139 | hp2 | a0003 | c0005 | t0001 | g0256 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03195 | hp1 | a0003 | c0009 | t0001 | g0250 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03195 | hp2 | a0006 | c0011 | t0001 | g0006 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03209 | hp1 | a0001 | c0008 | t0004 | g0047 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03225 | hp2 | a0018 | c0040 | t0001 | g0057 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03486 | hp2 | a0003 | c0005 | t0001 | g0061 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03490 | hp2 | a0020 | c0023 | t0001 | g0075 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03491 | hp1 | a0021 | c0024 | t0001 | g0281 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03516 | hp2 | a0001 | c0008 | t0004 | g0048 | AFR | ESN | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03540 | hp2 | a0022 | c0026 | t0001 | g0009 | AFR | GWD | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03579 | hp2 | a0023 | c0028 | t0001 | g0011 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0119 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03669 | hp1 | a0001 | c0031 | t0001 | g0066 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03688 | hp1 | a0001 | c0002 | t0005 | g0118 | SAS | STU | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | STU | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03710 | hp2 | a0001 | c0002 | t0009 | g0270 | SAS | PJL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03831 | hp2 | a0004 | c0006 | t0001 | g0077 | SAS | BEB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03834 | hp1 | a0001 | c0013 | t0001 | g0304 | SAS | BEB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG04115 | hp2 | a0004 | c0006 | t0001 | g0082 | SAS | STU | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG04184 | hp1 | a0001 | c0022 | t0001 | g0146 | SAS | BEB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG04184 | hp2 | a0001 | c0013 | t0001 | g0305 | SAS | BEB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0228 | SAS | STU | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG04199 | hp2 | a0004 | c0006 | t0001 | g0081 | SAS | STU | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18522 | hp2 | a0005 | c0004 | t0001 | g0036 | AFR | YRI | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0177 | EAS | CHB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | CHB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18939 | hp1 | a0002 | c0007 | t0001 | g0241 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18942 | hp2 | a0002 | c0003 | t0001 | g0336 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18948 | hp1 | a0024 | c0034 | t0013 | g0196 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18953 | hp2 | a0002 | c0007 | t0001 | g0243 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0184 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18959 | hp1 | a0002 | c0003 | t0001 | g0199 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0210 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0315 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0188 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18980 | hp1 | a0002 | c0007 | t0001 | g0242 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18991 | hp1 | a0007 | c0012 | t0001 | g0060 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18991 | hp2 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18992 | hp2 | a0002 | c0003 | t0001 | g0202 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18993 | hp2 | a0002 | c0003 | t0001 | g0180 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18995 | hp1 | a0002 | c0003 | t0003 | g0225 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18998 | hp1 | a0002 | c0003 | t0003 | g0224 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19002 | hp1 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19005 | hp1 | a0002 | c0003 | t0002 | g0189 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19010 | hp1 | a0002 | c0003 | t0001 | g0215 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19010 | hp2 | a0002 | c0003 | t0001 | g0216 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | LWK | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19043 | hp1 | a0001 | c0030 | t0001 | g0230 | AFR | LWK | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19043 | hp2 | a0005 | c0004 | t0001 | g0039 | AFR | LWK | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19054 | hp1 | a0025 | c0021 | t0001 | g0191 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19056 | hp2 | a0002 | c0007 | t0001 | g0240 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19058 | hp2 | a0002 | c0003 | t0001 | g0212 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19062 | hp1 | a0002 | c0003 | t0001 | g0234 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19064 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19068 | hp1 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19070 | hp1 | a0002 | c0003 | t0001 | g0213 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19074 | hp1 | a0007 | c0012 | t0001 | g0059 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0214 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19081 | hp2 | a0026 | c0027 | t0001 | g0201 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19082 | hp1 | a0002 | c0003 | t0001 | g0200 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA19091 | hp2 | a0002 | c0003 | t0002 | g0182 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0327 | EUR | TSI | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0163 | EUR | TSI | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0122 | SAS | GIH | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02559 | hp1 | a0003 | c0017 | t0001 | g0004 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG02559 | hp2 | a0014 | c0015 | t0001 | g0229 | AFR | ACB | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG03471 | hp2 | a0019 | c0036 | t0001 | g0245 | AFR | MSL | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | USA | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
HG06807 | hp2 | a0001 | c0008 | t0001 | g0049 | AFR | USA | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0127 | REF | REF | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0164 | REF | REF | FGD5_chr3_14813962_14939571 | FGD5 | chr3 | 14813962 | 14939571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:14819333 | G | T | 1 | a0018 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.262G>T | p.Ala88Ser | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 372/5903 | 262/4389 | 88/1462 | chr3 | 14819333 | |||
chr3:14819359 | G | GGAAGAGG others(11): Show |
1 | a0014 | 1 | HG02559.hp2 | disruptive_inframe_insertion | MODERATE | c.296_313dupAAGAGGAG others(10): Show |
p.Glu99_Glu104dup | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 424/5903 | 314/4389 | 105/1462 | INFO_REALIGN_3_PRIME | chr3 | 14819359 | ||
chr3:14819448 | C | T | 1 | a0012 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.377C>T | p.Pro126Leu | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 487/5903 | 377/4389 | 126/1462 | chr3 | 14819448 | |||
chr3:14819596 | G | T | 1 | a0015 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.525G>T | p.Glu175Asp | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 635/5903 | 525/4389 | 175/1462 | chr3 | 14819596 | |||
chr3:14819606 | G | C | 1 | a0016 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.535G>C | p.Glu179Gln | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 645/5903 | 535/4389 | 179/1462 | chr3 | 14819606 | |||
chr3:14819670 | A | G | 1 | a0017 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.599A>G | p.His200Arg | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 709/5903 | 599/4389 | 200/1462 | chr3 | 14819670 | |||
chr3:14819683 | G | C | 4 | a0003 a0015 a0017 others(1): Show |
15 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
missense_variant | MODERATE | c.612G>C | p.Gln204His | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 722/5903 | 612/4389 | 204/1462 | chr3 | 14819683 | |||
chr3:14819843 | G | A | 1 | a0011 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.772G>A | p.Glu258Lys | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 882/5903 | 772/4389 | 258/1462 | chr3 | 14819843 | |||
chr3:14819906 | T | C | 1 | a0025 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.835T>C | p.Cys279Arg | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 945/5903 | 835/4389 | 279/1462 | chr3 | 14819906 | |||
chr3:14820278 | G | A | 1 | a0005 | 8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
missense_variant | MODERATE | c.1207G>A | p.Gly403Arg | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 1317/5903 | 1207/4389 | 403/1462 | chr3 | 14820278 | |||
chr3:14820614 | G | A | 3 | a0004 a0012 a0020 |
11 | HG01081.hp2 HG01106.hp1 HG01975.hp2 others(8): Show |
missense_variant | MODERATE | c.1543G>A | p.Ala515Thr | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 1653/5903 | 1543/4389 | 515/1462 | chr3 | 14820614 | |||
chr3:14820686 | G | A | 1 | a0021 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.1615G>A | p.Ala539Thr | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 1725/5903 | 1615/4389 | 539/1462 | chr3 | 14820686 | |||
chr3:14820728 | G | A | 1 | a0010 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1657G>A | p.Val553Met | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 1767/5903 | 1657/4389 | 553/1462 | chr3 | 14820728 | |||
chr3:14820869 | C | T | 1 | a0008 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1798C>T | p.His600Tyr | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 1908/5903 | 1798/4389 | 600/1462 | chr3 | 14820869 | |||
chr3:14820971 | C | G | 1 | a0024 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.1900C>G | p.Pro634Ala | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 2010/5903 | 1900/4389 | 634/1462 | chr3 | 14820971 | |||
chr3:14821553 | G | A | 2 | a0006 a0022 |
4 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.2482G>A | p.Ala828Thr | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 2592/5903 | 2482/4389 | 828/1462 | chr3 | 14821553 | |||
chr3:14821589 | G | A | 1 | a0019 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.2518G>A | p.Ala840Thr | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 2628/5903 | 2518/4389 | 840/1462 | chr3 | 14821589 | |||
chr3:14897581 | G | A | 4 | a0002 a0024 a0025 others(1): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
missense_variant | MODERATE | c.2821G>A | p.Glu941Lys | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 5/20 | 2931/5903 | 2821/4389 | 941/1462 | chr3 | 14897581 | |||
chr3:14897582 | A | T | 4 | a0002 a0024 a0025 others(1): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
missense_variant | MODERATE | c.2822A>T | p.Glu941Val | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 5/20 | 2932/5903 | 2822/4389 | 941/1462 | chr3 | 14897582 | |||
chr3:14897955 | G | A | 1 | a0015 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2926G>A | p.Val976Ile | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/20 | 3036/5903 | 2926/4389 | 976/1462 | chr3 | 14897955 | |||
chr3:14898046 | A | G | 1 | a0009 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.3017A>G | p.Glu1006Gly | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/20 | 3127/5903 | 3017/4389 | 1006/1462 | chr3 | 14898046 | |||
chr3:14901035 | C | T | 1 | a0013 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.3238C>T | p.Arg1080Cys | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/20 | 3348/5903 | 3238/4389 | 1080/1462 | chr3 | 14901035 | |||
chr3:14901044 | G | A | 1 | a0023 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.3247G>A | p.Asp1083Asn | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/20 | 3357/5903 | 3247/4389 | 1083/1462 | chr3 | 14901044 | |||
chr3:14924040 | T | A | 1 | a0020 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.3970T>A | p.Ser1324Thr | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/20 | 4080/5903 | 3970/4389 | 1324/1462 | chr3 | 14924040 | |||
chr3:14924073 | G | A | 3 | a0007 a0022 a0026 |
4 | HG03540.hp2 NA18991.hp1 NA19074.hp1 others(1): Show |
missense_variant | MODERATE | c.4003G>A | p.Val1335Ile | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/20 | 4113/5903 | 4003/4389 | 1335/1462 | chr3 | 14924073 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:14819158 | C | T | 1 | a0001c0014 | 2 | HG02615.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.87C>T | p.Asp29Asp | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 197/5903 | 87/4389 | 29/1462 | chr3 | 14819158 | |||
chr3:14819326 | G | C | 1 | a0001c0008 | 3 | HG03209.hp1 HG03516.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.255G>C | p.Gly85Gly | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 365/5903 | 255/4389 | 85/1462 | chr3 | 14819326 | |||
chr3:14820223 | G | A | 1 | a0001c0022 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.1152G>A | p.Ala384Ala | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 1262/5903 | 1152/4389 | 384/1462 | chr3 | 14820223 | |||
chr3:14820295 | C | T | 1 | a0019c0036 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1224C>T | p.Pro408Pro | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 1334/5903 | 1224/4389 | 408/1462 | chr3 | 14820295 | |||
chr3:14821516 | C | T | 1 | a0002c0007 | 4 | NA18939.hp1 NA18953.hp2 NA18980.hp1 others(1): Show |
synonymous_variant | LOW | c.2445C>T | p.Asn815Asn | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 2555/5903 | 2445/4389 | 815/1462 | chr3 | 14821516 | |||
chr3:14821531 | C | T | 1 | a0006c0033 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.2460C>T | p.Tyr820Tyr | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 2570/5903 | 2460/4389 | 820/1462 | chr3 | 14821531 | |||
chr3:14897972 | G | T | 20 | a0001c0001 a0001c0008 a0001c0013 others(17): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
synonymous_variant | LOW | c.2943G>T | p.Leu981Leu | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/20 | 3053/5903 | 2943/4389 | 981/1462 | chr3 | 14897972 | |||
chr3:14897999 | C | T | 4 | a0001c0030 a0003c0009 a0003c0018 others(1): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
synonymous_variant | LOW | c.2970C>T | p.His990His | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/20 | 3080/5903 | 2970/4389 | 990/1462 | chr3 | 14897999 | |||
chr3:14918819 | G | A | 1 | a0001c0031 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.3555G>A | p.Leu1185Leu | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/20 | 3665/5903 | 3555/4389 | 1185/1462 | chr3 | 14918819 | |||
chr3:14922527 | T | C | 2 | a0003c0018 a0003c0019 |
2 | HG02258.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.3786T>C | p.His1262His | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 15/20 | 3896/5903 | 3786/4389 | 1262/1462 | chr3 | 14922527 | |||
chr3:14922536 | C | T | 1 | a0001c0013 | 2 | HG03834.hp1 HG04184.hp2 |
synonymous_variant | LOW | c.3795C>T | p.His1265His | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 15/20 | 3905/5903 | 3795/4389 | 1265/1462 | chr3 | 14922536 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:14819017 | C | G | 1 | a0001c0002t0018 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 55 | chr3 | 14819017 | ||||||
chr3:14819046 | C | T | 1 | a0001c0001t0017 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 26 | chr3 | 14819046 | ||||||
chr3:14819048 | G | A | 1 | a0001c0002t0007 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/20 | 24 | chr3 | 14819048 | ||||||
chr3:14933403 | C | G | 1 | a0001c0001t0016 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 236 | chr3 | 14933403 | ||||||
chr3:14933437 | G | T | 1 | a0001c0001t0015 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*270G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 270 | chr3 | 14933437 | ||||||
chr3:14933545 | A | G | 1 | a0001c0002t0014 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 378 | chr3 | 14933545 | ||||||
chr3:14933622 | G | A | 2 | a0001c0001t0003 a0002c0003t0003 |
6 | NA18942.hp1 NA18995.hp1 NA18998.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 455 | chr3 | 14933622 | ||||||
chr3:14933643 | G | A | 2 | a0001c0001t0005 a0001c0002t0005 |
3 | HG01261.hp1 HG03654.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*476G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 476 | chr3 | 14933643 | ||||||
chr3:14933886 | C | G | 1 | a0024c0034t0013 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*719C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 719 | chr3 | 14933886 | ||||||
chr3:14933931 | CTA | C | 4 | a0001c0001t0002 a0001c0002t0002 a0002c0003t0002 others(1): Show |
15 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*766_*767delAT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 766 | INFO_REALIGN_3_PRIME | chr3 | 14933931 | |||||
chr3:14933951 | C | T | 2 | a0001c0001t0004 a0001c0008t0004 |
4 | HG02809.hp1 HG03209.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*784C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 784 | chr3 | 14933951 | ||||||
chr3:14933985 | C | T | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 818 | chr3 | 14933985 | ||||||
chr3:14934023 | T | A | 1 | a0001c0001t0008 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*856T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 856 | chr3 | 14934023 | ||||||
chr3:14934318 | C | T | 1 | a0001c0001t0011 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1151C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 1151 | chr3 | 14934318 | ||||||
chr3:14934379 | A | G | 1 | a0001c0002t0010 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 1212 | chr3 | 14934379 | ||||||
chr3:14934448 | C | T | 1 | a0003c0005t0006 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1281C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 1281 | chr3 | 14934448 | ||||||
chr3:14934489 | A | G | 1 | a0001c0002t0009 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1322A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 20/20 | 1322 | chr3 | 14934489 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:14821631 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2525+35G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14821631 | |||||||
chr3:14821667 | A | G | 1 | a0001c0001t0011g0340 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2525+71A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14821667 | |||||||
chr3:14821753 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+157G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14821753 | |||||||
chr3:14821839 | T | C | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+243T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14821839 | |||||||
chr3:14821994 | G | C | 4 | a0006c0011t0001g0006 a0006c0011t0001g0007 a0006c0033t0001g0008 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2525+398G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14821994 | |||||||
chr3:14822127 | A | C | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+531A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14822127 | |||||||
chr3:14822129 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0279 a0001c0001t0001g0282 others(79): Show |
84 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2525+533A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14822129 | |||||||
chr3:14822214 | A | G | 10 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+618A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14822214 | |||||||
chr3:14822354 | T | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(8): Show |
11 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2525+758T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14822354 | |||||||
chr3:14822489 | G | GT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(67): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.2525+908dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14822489 | ||||||
chr3:14822489 | GT | G | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(20): Show |
23 | HG01109.hp2 HG01168.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.2525+908delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14822489 | ||||||
chr3:14822654 | G | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(8): Show |
11 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2525+1058G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14822654 | |||||||
chr3:14822899 | A | G | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2525+1303A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14822899 | |||||||
chr3:14823079 | G | A | 23 | a0001c0001t0001g0279 a0001c0002t0001g0259 a0001c0002t0001g0260 others(20): Show |
23 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.2525+1483G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823079 | |||||||
chr3:14823400 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2525+1804A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823400 | |||||||
chr3:14823485 | A | G | 4 | a0002c0007t0001g0240 a0002c0007t0001g0241 a0002c0007t0001g0242 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+1889A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823485 | |||||||
chr3:14823528 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+1932G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823528 | |||||||
chr3:14823853 | CA | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG02055.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2525+2264delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14823853 | ||||||
chr3:14823860 | A | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0279 a0001c0001t0001g0282 others(79): Show |
84 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2525+2264A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823860 | |||||||
chr3:14823861 | C | A | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2525+2265C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823861 | |||||||
chr3:14823889 | A | G | 1 | a0003c0005t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2525+2293A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823889 | |||||||
chr3:14823956 | C | T | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+2360C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823956 | |||||||
chr3:14823964 | G | A | 2 | a0002c0003t0001g0034 a0002c0003t0001g0035 |
2 | NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2525+2368G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14823964 | |||||||
chr3:14824131 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2525+2535A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824131 | |||||||
chr3:14824138 | C | T | 1 | a0002c0003t0001g0234 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2525+2542C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824138 | |||||||
chr3:14824181 | C | G | 2 | a0001c0002t0001g0232 a0001c0002t0001g0233 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2525+2585C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824181 | |||||||
chr3:14824251 | G | A | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2525+2655G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824251 | |||||||
chr3:14824432 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2525+2836C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824432 | |||||||
chr3:14824617 | A | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+3021A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824617 | |||||||
chr3:14824729 | A | G | 1 | a0001c0030t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2525+3133A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824729 | |||||||
chr3:14824824 | T | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0279 a0001c0001t0001g0282 others(79): Show |
84 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2525+3228T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824824 | |||||||
chr3:14824959 | A | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+3363A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14824959 | |||||||
chr3:14825293 | T | C | 1 | a0001c0002t0001g0259 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2525+3697T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825293 | |||||||
chr3:14825411 | C | T | 1 | a0014c0015t0001g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2525+3815C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825411 | |||||||
chr3:14825428 | GACTCCCA others(13): Show |
G | 2 | a0001c0001t0001g0248 a0001c0001t0004g0247 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2525+3852_2525+387 others(24): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14825428 | ||||||
chr3:14825462 | C | CAT | 16 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0285 others(13): Show |
16 | HG01081.hp1 HG02129.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2525+3881_2525+388 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14825462 | ||||||
chr3:14825462 | C | CATAT | 4 | a0003c0005t0001g0252 a0003c0009t0001g0250 a0003c0009t0001g0251 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+3879_2525+388 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14825462 | ||||||
chr3:14825487 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+3891G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825487 | |||||||
chr3:14825495 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(212): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.2525+3899G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825495 | |||||||
chr3:14825515 | T | A | 1 | a0001c0001t0017g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2525+3919T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825515 | |||||||
chr3:14825563 | T | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2525+3967T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825563 | |||||||
chr3:14825601 | A | G | 1 | a0001c0001t0004g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2525+4005A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825601 | |||||||
chr3:14825893 | G | C | 1 | a0005c0004t0001g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2525+4297G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825893 | |||||||
chr3:14825917 | A | G | 1 | a0001c0002t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2525+4321A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825917 | |||||||
chr3:14825958 | A | ACACAGTG others(12): Show |
3 | a0001c0008t0001g0049 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG03209.hp1 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2525+4380_2525+438 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14825958 | ||||||
chr3:14825992 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2525+4396A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14825992 | |||||||
chr3:14826157 | A | ACTTGTTG others(2): Show |
3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+4561_2525+456 others(13): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826157 | |||||||
chr3:14826192 | C | T | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2525+4596C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826192 | |||||||
chr3:14826206 | T | G | 10 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+4610T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826206 | |||||||
chr3:14826209 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2525+4613C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826209 | |||||||
chr3:14826287 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2525+4691C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826287 | |||||||
chr3:14826313 | T | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(6): Show |
9 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2525+4717T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826313 | |||||||
chr3:14826339 | C | T | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+4743C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826339 | |||||||
chr3:14826367 | C | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2525+4771C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826367 | |||||||
chr3:14826406 | G | A | 1 | a0014c0015t0001g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2525+4810G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826406 | |||||||
chr3:14826486 | C | T | 3 | a0002c0003t0001g0226 a0002c0003t0003g0224 a0002c0003t0003g0225 |
3 | NA18995.hp1 NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2525+4890C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826486 | |||||||
chr3:14826519 | A | T | 2 | a0001c0002t0005g0118 a0001c0002t0005g0119 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2525+4923A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826519 | |||||||
chr3:14826671 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2525+5075G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826671 | |||||||
chr3:14826772 | T | TCA | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02083.hp1 HG02132.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.2525+5191_2525+519 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14826772 | ||||||
chr3:14826774 | A | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2525+5178A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826774 | |||||||
chr3:14826945 | G | C | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2525+5349G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826945 | |||||||
chr3:14826946 | C | A | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2525+5350C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826946 | |||||||
chr3:14826975 | C | T | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG00642.hp2 HG00733.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2525+5379C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14826975 | |||||||
chr3:14827205 | T | C | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+5609T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827205 | |||||||
chr3:14827271 | T | G | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2525+5675T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827271 | |||||||
chr3:14827278 | ATTC | A | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01934.hp1 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+5685_2525+568 others(7): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14827278 | ||||||
chr3:14827281 | C | CT | 11 | a0001c0001t0008g0170 a0001c0002t0001g0166 a0001c0002t0001g0174 others(8): Show |
11 | HG01109.hp1 HG02723.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2525+5710dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14827281 | ||||||
chr3:14827281 | CT | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0098 a0001c0001t0001g0099 others(7): Show |
10 | HG01069.hp2 HG01070.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+5710delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14827281 | ||||||
chr3:14827285 | T | TC | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0155 others(11): Show |
14 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.2525+5689_2525+569 others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827285 | |||||||
chr3:14827286 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2525+5690T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827286 | |||||||
chr3:14827287 | T | C | 8 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG01070.hp2 HG01256.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.2525+5691T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827287 | |||||||
chr3:14827293 | T | C | 3 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0023c0028t0001g0011 |
3 | HG02055.hp2 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2525+5697T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827293 | |||||||
chr3:14827439 | G | T | 2 | a0002c0003t0001g0216 a0002c0003t0001g0217 |
2 | NA19009.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2525+5843G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827439 | |||||||
chr3:14827442 | T | C | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+5846T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827442 | |||||||
chr3:14827655 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2525+6059G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827655 | |||||||
chr3:14827813 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0002t0001g0010 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.2525+6217G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827813 | |||||||
chr3:14827869 | G | C | 1 | a0001c0001t0016g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2525+6273G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827869 | |||||||
chr3:14827988 | G | A | 10 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+6392G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14827988 | |||||||
chr3:14828081 | T | C | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+6485T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14828081 | |||||||
chr3:14828115 | G | T | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2525+6519G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14828115 | |||||||
chr3:14828191 | G | T | 2 | a0001c0001t0001g0248 a0001c0001t0004g0247 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2525+6595G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14828191 | |||||||
chr3:14828364 | G | A | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+6768G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14828364 | |||||||
chr3:14828453 | G | T | 2 | a0001c0002t0005g0118 a0001c0002t0005g0119 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2525+6857G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14828453 | |||||||
chr3:14828483 | A | T | 1 | a0001c0001t0001g0337 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2525+6887A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14828483 | |||||||
chr3:14828820 | C | CT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0129 others(30): Show |
33 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.2525+7243dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14828820 | ||||||
chr3:14828820 | CT | C | 19 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0098 others(16): Show |
19 | HG01069.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2525+7243delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14828820 | ||||||
chr3:14828856 | C | T | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+7260C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14828856 | |||||||
chr3:14829027 | C | T | 4 | a0006c0011t0001g0006 a0006c0011t0001g0007 a0006c0033t0001g0008 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2525+7431C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829027 | |||||||
chr3:14829042 | C | T | 8 | a0002c0003t0001g0210 a0002c0003t0001g0211 a0002c0003t0001g0212 others(5): Show |
8 | NA18960.hp1 NA19009.hp1 NA19010.hp1 others(5): Show |
intron_variant | MODIFIER | c.2525+7446C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829042 | |||||||
chr3:14829094 | A | G | 9 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(6): Show |
9 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2525+7498A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829094 | |||||||
chr3:14829158 | C | T | 3 | a0004c0006t0001g0044 a0004c0010t0001g0091 a0012c0039t0001g0092 |
3 | HG02074.hp2 HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2525+7562C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829158 | |||||||
chr3:14829189 | G | A | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+7593G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829189 | |||||||
chr3:14829335 | C | T | 3 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0209 |
3 | HG01433.hp1 NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2525+7739C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829335 | |||||||
chr3:14829538 | T | C | 3 | a0001c0008t0001g0049 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG03209.hp1 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2525+7942T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829538 | |||||||
chr3:14829714 | G | C | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2525+8118G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829714 | |||||||
chr3:14829744 | C | T | 1 | a0002c0003t0001g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2525+8148C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829744 | |||||||
chr3:14829753 | C | T | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+8157C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14829753 | |||||||
chr3:14829908 | A | AT | 5 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | NA18946.hp1 NA18994.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.2525+8320dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14829908 | ||||||
chr3:14830175 | A | G | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2525+8579A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830175 | |||||||
chr3:14830200 | G | A | 9 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(6): Show |
9 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2525+8604G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830200 | |||||||
chr3:14830259 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0279 others(80): Show |
85 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2525+8663G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830259 | |||||||
chr3:14830463 | A | AT | 122 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.2525+8875dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14830463 | ||||||
chr3:14830558 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2525+8962C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830558 | |||||||
chr3:14830718 | C | T | 7 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2525+9122C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830718 | |||||||
chr3:14830783 | G | A | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+9187G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830783 | |||||||
chr3:14830923 | T | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0283 a0001c0001t0001g0294 others(1): Show |
4 | NA18957.hp1 NA18961.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+9327T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830923 | |||||||
chr3:14830936 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2525+9340C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14830936 | |||||||
chr3:14831232 | T | C | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+9636T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831232 | |||||||
chr3:14831398 | C | T | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+9802C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831398 | |||||||
chr3:14831503 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0154 |
2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2525+9907C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831503 | |||||||
chr3:14831638 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2525+10042T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831638 | |||||||
chr3:14831705 | C | T | 1 | a0001c0030t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2525+10109C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831705 | |||||||
chr3:14831707 | T | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.2525+10111T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831707 | |||||||
chr3:14831728 | A | G | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2525+10132A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831728 | |||||||
chr3:14831828 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0203 a0003c0005t0001g0003 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.2525+10232C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831828 | |||||||
chr3:14831875 | G | C | 10 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+10279G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14831875 | |||||||
chr3:14832105 | G | T | 4 | a0002c0007t0001g0240 a0002c0007t0001g0241 a0002c0007t0001g0242 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+10509G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832105 | |||||||
chr3:14832133 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.2525+10537C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832133 | |||||||
chr3:14832287 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2525+10691T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832287 | |||||||
chr3:14832318 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2525+10722G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832318 | |||||||
chr3:14832584 | T | G | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+10988T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832584 | |||||||
chr3:14832622 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2525+11026G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832622 | |||||||
chr3:14832703 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2525+11107A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832703 | |||||||
chr3:14832741 | C | T | 1 | a0001c0002t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2525+11145C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832741 | |||||||
chr3:14832892 | AC | A | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+11297delC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14832892 | |||||||
chr3:14833493 | T | C | 1 | a0001c0002t0001g0261 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2525+11897T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14833493 | |||||||
chr3:14833532 | A | T | 1 | a0001c0001t0001g0283 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2525+11936A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14833532 | |||||||
chr3:14833652 | A | G | 1 | a0002c0003t0001g0336 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2525+12056A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14833652 | |||||||
chr3:14833746 | C | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG00099.hp2 HG00639.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+12150C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14833746 | |||||||
chr3:14833903 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2525+12307T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14833903 | |||||||
chr3:14833950 | G | C | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+12354G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14833950 | |||||||
chr3:14833967 | C | G | 58 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(55): Show |
58 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2525+12371C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14833967 | |||||||
chr3:14834107 | A | C | 10 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+12511A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834107 | |||||||
chr3:14834249 | G | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(9): Show |
12 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2525+12653G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834249 | |||||||
chr3:14834401 | C | T | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+12805C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834401 | |||||||
chr3:14834504 | C | G | 1 | a0005c0004t0001g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2525+12908C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834504 | |||||||
chr3:14834601 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+13005C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834601 | |||||||
chr3:14834716 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0002t0001g0010 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.2525+13120T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834716 | |||||||
chr3:14834724 | G | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.2525+13128G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834724 | |||||||
chr3:14834873 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2525+13277T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834873 | |||||||
chr3:14834957 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0004g0247 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2525+13361C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14834957 | |||||||
chr3:14835105 | G | A | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2525+13509G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835105 | |||||||
chr3:14835136 | G | A | 10 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+13540G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835136 | |||||||
chr3:14835193 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2525+13597G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835193 | |||||||
chr3:14835305 | T | C | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+13709T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835305 | |||||||
chr3:14835355 | C | A | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2525+13759C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835355 | |||||||
chr3:14835499 | C | CA | 7 | a0001c0001t0001g0056 a0001c0001t0001g0298 a0001c0002t0001g0261 others(4): Show |
7 | HG00408.hp1 HG00544.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.2525+13914dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14835499 | ||||||
chr3:14835506 | AAAAAGAA others(3): Show |
A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0002t0001g0010 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.2525+13924_2525+13 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14835506 | ||||||
chr3:14835749 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2525+14153G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835749 | |||||||
chr3:14835797 | G | T | 24 | a0001c0001t0001g0279 a0001c0002t0001g0228 a0001c0002t0001g0259 others(21): Show |
24 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.2525+14201G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835797 | |||||||
chr3:14835921 | G | A | 1 | a0002c0003t0001g0176 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2525+14325G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835921 | |||||||
chr3:14835931 | G | C | 1 | a0017c0037t0001g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2525+14335G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14835931 | |||||||
chr3:14836028 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.2525+14432G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836028 | |||||||
chr3:14836067 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0279 others(83): Show |
88 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.2525+14471A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836067 | |||||||
chr3:14836081 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0002t0001g0010 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.2525+14485G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836081 | |||||||
chr3:14836118 | A | G | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2525+14522A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836118 | |||||||
chr3:14836138 | C | T | 10 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2525+14542C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836138 | |||||||
chr3:14836265 | G | A | 4 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2525+14669G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836265 | |||||||
chr3:14836422 | G | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.2525+14826G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836422 | |||||||
chr3:14836432 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.2525+14836T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836432 | |||||||
chr3:14836553 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.2525+14957T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836553 | |||||||
chr3:14836923 | C | A | 5 | a0001c0001t0001g0020 a0003c0005t0001g0003 a0003c0005t0001g0005 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2525+15327C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836923 | |||||||
chr3:14836990 | C | G | 1 | a0004c0006t0001g0044 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2525+15394C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14836990 | |||||||
chr3:14837022 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2525+15426A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837022 | |||||||
chr3:14837046 | C | A | 1 | a0001c0001t0001g0299 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2525+15450C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837046 | |||||||
chr3:14837146 | G | A | 1 | a0001c0001t0015g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2525+15550G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837146 | |||||||
chr3:14837222 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2525+15626C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837222 | |||||||
chr3:14837296 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2525+15700A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837296 | |||||||
chr3:14837323 | C | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.2525+15727C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837323 | |||||||
chr3:14837336 | C | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0030 others(99): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.2525+15740C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837336 | |||||||
chr3:14837339 | G | A | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2525+15743G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837339 | |||||||
chr3:14837550 | C | T | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2525+15954C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837550 | |||||||
chr3:14837571 | T | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0248 a0001c0001t0004g0247 others(11): Show |
14 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.2525+15975T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837571 | |||||||
chr3:14837575 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2525+15979G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837575 | |||||||
chr3:14837803 | T | A | 1 | a0001c0001t0001g0302 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2525+16207T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837803 | |||||||
chr3:14837809 | G | T | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2525+16213G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837809 | |||||||
chr3:14837820 | G | A | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2525+16224G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837820 | |||||||
chr3:14837866 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG01109.hp2 HG01168.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2525+16270G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837866 | |||||||
chr3:14837914 | C | T | 32 | a0001c0001t0001g0020 a0001c0001t0001g0279 a0001c0002t0001g0156 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2525+16318C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14837914 | |||||||
chr3:14838141 | C | T | 8 | a0002c0003t0001g0210 a0002c0003t0001g0211 a0002c0003t0001g0212 others(5): Show |
8 | NA18960.hp1 NA19009.hp1 NA19010.hp1 others(5): Show |
intron_variant | MODIFIER | c.2525+16545C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838141 | |||||||
chr3:14838144 | T | C | 2 | a0001c0002t0001g0259 a0011c0020t0002g0269 |
2 | HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.2525+16548T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838144 | |||||||
chr3:14838218 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2525+16622T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838218 | |||||||
chr3:14838237 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0056 others(92): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2525+16641C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838237 | |||||||
chr3:14838252 | CTCTT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(54): Show |
59 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2525+16660_2525+16 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14838252 | ||||||
chr3:14838273 | T | C | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2525+16677T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838273 | |||||||
chr3:14838346 | T | A | 62 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(59): Show |
62 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2525+16750T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838346 | |||||||
chr3:14838430 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0056 others(92): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2525+16834A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838430 | |||||||
chr3:14838929 | C | T | 8 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.2525+17333C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14838929 | |||||||
chr3:14839115 | T | A | 6 | a0001c0001t0017g0046 a0003c0005t0001g0252 a0003c0005t0001g0256 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2525+17519T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839115 | |||||||
chr3:14839166 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2525+17570C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839166 | |||||||
chr3:14839365 | G | A | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2525+17769G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839365 | |||||||
chr3:14839380 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(54): Show |
59 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2525+17784A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839380 | |||||||
chr3:14839444 | C | G | 1 | a0001c0002t0001g0334 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2525+17848C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839444 | |||||||
chr3:14839463 | C | G | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2525+17867C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839463 | |||||||
chr3:14839488 | C | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(320): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2525+17892C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839488 | |||||||
chr3:14839608 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2525+18012T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839608 | |||||||
chr3:14839654 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0056 others(84): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2525+18058C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839654 | |||||||
chr3:14839712 | C | G | 3 | a0002c0003t0001g0226 a0002c0003t0003g0224 a0002c0003t0003g0225 |
3 | NA18995.hp1 NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2525+18116C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839712 | |||||||
chr3:14839757 | C | T | 16 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(13): Show |
16 | HG00140.hp2 HG01099.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2525+18161C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839757 | |||||||
chr3:14839848 | G | A | 1 | a0005c0004t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2525+18252G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839848 | |||||||
chr3:14839933 | A | AAAAC | 52 | a0001c0001t0001g0130 a0001c0001t0001g0282 a0001c0001t0001g0283 others(49): Show |
52 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.2525+18367_2525+18 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14839933 | ||||||
chr3:14839933 | A | AAAACAAA others(1): Show |
9 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0096 others(6): Show |
9 | HG00140.hp2 HG02258.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.2525+18363_2525+18 others(14): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14839933 | ||||||
chr3:14839933 | A | AAAACAAA others(5): Show |
7 | a0005c0004t0001g0021 a0005c0004t0001g0037 a0005c0004t0001g0039 others(4): Show |
7 | HG02622.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2525+18359_2525+18 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14839933 | ||||||
chr3:14839933 | AAAAC | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2525+18367_2525+18 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14839933 | ||||||
chr3:14839933 | AAAACAAA others(1): Show |
A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG03516.hp1 HG03704.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.2525+18363_2525+18 others(14): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14839933 | ||||||
chr3:14839952 | A | G | 1 | a0002c0003t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2525+18356A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839952 | |||||||
chr3:14839963 | AACAG | A | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(4): Show |
7 | HG01081.hp1 HG02559.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2525+18368_2525+18 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839963 | |||||||
chr3:14839967 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0056 others(85): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2525+18371G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839967 | |||||||
chr3:14839969 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(54): Show |
59 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2525+18373G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14839969 | |||||||
chr3:14840034 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2525+18438C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14840034 | |||||||
chr3:14840050 | C | G | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2525+18454C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14840050 | |||||||
chr3:14840146 | CTT | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2525+18563_2525+18 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14840146 | ||||||
chr3:14840245 | A | G | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2525+18649A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14840245 | |||||||
chr3:14840247 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2525+18651C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14840247 | |||||||
chr3:14840364 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2525+18768C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14840364 | |||||||
chr3:14840752 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2525+19156A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14840752 | |||||||
chr3:14840952 | G | A | 1 | a0006c0033t0001g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2525+19356G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14840952 | |||||||
chr3:14841044 | T | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2525+19448T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841044 | |||||||
chr3:14841046 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2525+19450A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841046 | |||||||
chr3:14841068 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2525+19472A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841068 | |||||||
chr3:14841128 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(52): Show |
57 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2525+19532G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841128 | |||||||
chr3:14841279 | T | C | 1 | a0001c0002t0001g0297 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2525+19683T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841279 | |||||||
chr3:14841328 | A | G | 15 | a0001c0001t0001g0279 a0001c0002t0001g0260 a0001c0002t0001g0266 others(12): Show |
15 | HG00639.hp1 HG01975.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.2525+19732A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841328 | |||||||
chr3:14841330 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(52): Show |
57 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2525+19734T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841330 | |||||||
chr3:14841414 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0085 others(3): Show |
6 | HG02027.hp2 NA18960.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.2525+19818G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841414 | |||||||
chr3:14841561 | C | CT | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(269): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2525+19980dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14841561 | ||||||
chr3:14841618 | A | G | 2 | a0015c0038t0001g0258 a0017c0037t0001g0253 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2525+20022A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841618 | |||||||
chr3:14841933 | C | G | 27 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(24): Show |
27 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.2525+20337C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841933 | |||||||
chr3:14841945 | G | A | 1 | a0001c0001t0003g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2525+20349G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841945 | |||||||
chr3:14841955 | C | T | 1 | a0001c0002t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2525+20359C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14841955 | |||||||
chr3:14842063 | A | G | 101 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0123 others(98): Show |
101 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2525+20467A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14842063 | |||||||
chr3:14842353 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0004g0247 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2525+20757G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14842353 | |||||||
chr3:14842602 | C | T | 2 | a0004c0006t0001g0081 a0004c0006t0001g0082 |
2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2525+21006C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14842602 | |||||||
chr3:14842655 | G | A | 33 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2525+21059G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14842655 | |||||||
chr3:14842902 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2526-21226C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14842902 | |||||||
chr3:14842956 | G | A | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2526-21172G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14842956 | |||||||
chr3:14842963 | GCCT | G | 33 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2526-21157_2526-21 others(9): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14842963 | ||||||
chr3:14842981 | A | G | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2526-21147A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14842981 | |||||||
chr3:14843045 | T | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0105 others(10): Show |
13 | HG01192.hp1 HG01934.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2526-21083T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843045 | |||||||
chr3:14843073 | T | C | 1 | a0001c0002t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2526-21055T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843073 | |||||||
chr3:14843535 | C | CTGCTTGG others(12): Show |
1 | a0022c0026t0001g0009 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2526-20576_2526-20 others(25): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14843535 | ||||||
chr3:14843611 | A | C | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2526-20517A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843611 | |||||||
chr3:14843686 | C | CT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2526-20425dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14843686 | ||||||
chr3:14843686 | C | CTT | 45 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0090 others(42): Show |
45 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.2526-20426_2526-20 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14843686 | ||||||
chr3:14843686 | C | CTTT | 9 | a0001c0002t0001g0174 a0001c0002t0001g0261 a0001c0002t0001g0271 others(6): Show |
9 | HG01106.hp1 HG02135.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.2526-20427_2526-20 others(9): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14843686 | ||||||
chr3:14843703 | TG | T | 15 | a0001c0001t0001g0181 a0002c0003t0001g0159 a0002c0003t0001g0178 others(12): Show |
15 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.2526-20419delG | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14843703 | ||||||
chr3:14843704 | G | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(291): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2526-20424G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843704 | |||||||
chr3:14843705 | G | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-20423G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843705 | |||||||
chr3:14843746 | A | G | 1 | a0001c0001t0004g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2526-20382A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843746 | |||||||
chr3:14843761 | G | A | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2526-20367G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843761 | |||||||
chr3:14843792 | G | A | 1 | a0002c0003t0001g0178 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2526-20336G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843792 | |||||||
chr3:14843812 | T | C | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-20316T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843812 | |||||||
chr3:14843892 | G | C | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2526-20236G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843892 | |||||||
chr3:14843906 | G | A | 5 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 others(2): Show |
5 | HG00642.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2526-20222G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843906 | |||||||
chr3:14843941 | C | T | 6 | a0001c0001t0001g0013 a0001c0030t0001g0230 a0003c0009t0001g0250 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-20187C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843941 | |||||||
chr3:14843942 | G | A | 1 | a0001c0001t0011g0340 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2526-20186G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14843942 | |||||||
chr3:14844003 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2526-20125G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844003 | |||||||
chr3:14844004 | CTTTTCT | C | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-20123_2526-20 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844004 | |||||||
chr3:14844204 | T | TA | 7 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0106 others(4): Show |
7 | HG01256.hp1 HG01928.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2526-19910dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAA | 9 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0131 others(6): Show |
9 | HG01099.hp1 HG01255.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.2526-19911_2526-19 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAAAAAA | 6 | a0001c0001t0001g0133 a0001c0002t0001g0232 a0001c0002t0001g0233 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-19915_2526-19 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAAAAAAA others(3): Show |
1 | a0001c0002t0002g0268 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2526-19919_2526-19 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2526-19920_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAAAAAAA others(5): Show |
1 | a0001c0002t0001g0266 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2526-19921_2526-19 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAAAAAAA others(7): Show |
1 | a0001c0002t0001g0261 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2526-19923_2526-19 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAAAAAAA others(8): Show |
1 | a0001c0002t0010g0263 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | T | TAAAAAAA others(9): Show |
1 | a0001c0002t0002g0262 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(22): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844204 | TAA | T | 10 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 others(7): Show |
10 | HG00642.hp1 HG00741.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.2526-19911_2526-19 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844204 | ||||||
chr3:14844209 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0322 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2526-19918_2526-19 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844209 | ||||||
chr3:14844209 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0323 a0001c0001t0001g0333 |
3 | HG01168.hp2 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2526-19917_2526-19 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844209 | ||||||
chr3:14844210 | AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2526-19916_2526-19 others(33): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844210 | ||||||
chr3:14844211 | A | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0322 |
2 | HG00140.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2526-19917A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844211 | |||||||
chr3:14844211 | AAAAAAAA others(39): Show |
A | 14 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(11): Show |
14 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.2526-19915_2526-19 others(52): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844211 | ||||||
chr3:14844212 | AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0008g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2526-19914_2526-19 others(19): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844212 | ||||||
chr3:14844213 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0338 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2526-19915_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844213 | |||||||
chr3:14844213 | A | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0289 a0001c0001t0001g0303 others(4): Show |
7 | HG00140.hp1 HG00642.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.2526-19915A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844213 | |||||||
chr3:14844213 | AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0316 a0001c0002t0007g0157 |
2 | HG02735.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2526-19913_2526-19 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844213 | ||||||
chr3:14844213 | AAAAAATA others(23): Show |
A | 1 | a0001c0002t0001g0330 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2526-19913_2526-19 others(36): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844213 | ||||||
chr3:14844213 | AAAAAATA others(25): Show |
A | 1 | a0001c0001t0001g0309 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2526-19913_2526-19 others(38): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844213 | ||||||
chr3:14844213 | AAAAAATA others(27): Show |
A | 1 | a0001c0014t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2526-19913_2526-19 others(40): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844213 | ||||||
chr3:14844213 | AAAAAATA others(29): Show |
A | 1 | a0001c0014t0001g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2526-19913_2526-19 others(42): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844213 | ||||||
chr3:14844213 | AAAAAATA others(39): Show |
A | 12 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(9): Show |
12 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.2526-19913_2526-19 others(52): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844213 | ||||||
chr3:14844214 | AAAAATAT others(4): Show |
A | 1 | a0002c0003t0001g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2526-19912_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844214 | ||||||
chr3:14844214 | AAAAATAT others(6): Show |
A | 1 | a0002c0003t0001g0194 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2526-19912_2526-19 others(19): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844214 | ||||||
chr3:14844214 | AAAAATAT others(30): Show |
A | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2526-19912_2526-19 others(43): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844214 | ||||||
chr3:14844215 | A | ATATATAT others(8): Show |
1 | a0025c0021t0001g0191 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2526-19913_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844215 | |||||||
chr3:14844215 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0185 a0001c0001t0001g0289 others(14): Show |
17 | HG00140.hp1 HG00621.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.2526-19913A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844215 | |||||||
chr3:14844215 | AAAATATA others(1): Show |
A | 7 | a0001c0001t0001g0086 a0001c0001t0001g0130 a0001c0001t0001g0312 others(4): Show |
7 | HG02015.hp2 HG02055.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.2526-19911_2526-19 others(14): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844215 | ||||||
chr3:14844215 | AAAATATA others(3): Show |
A | 2 | a0001c0002t0014g0160 a0003c0009t0001g0250 |
2 | HG01257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2526-19911_2526-19 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844215 | ||||||
chr3:14844215 | AAAATATA others(7): Show |
A | 5 | a0001c0001t0001g0205 a0002c0003t0001g0159 a0002c0003t0001g0197 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.2526-19911_2526-19 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844215 | ||||||
chr3:14844215 | AAAATATA others(11): Show |
A | 1 | a0001c0001t0001g0325 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2526-19911_2526-19 others(24): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844215 | ||||||
chr3:14844216 | AAATATAT others(4): Show |
A | 3 | a0002c0003t0001g0178 a0002c0003t0001g0199 a0026c0027t0001g0201 |
3 | HG00558.hp2 NA18959.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2526-19910_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844216 | ||||||
chr3:14844216 | AAATATAT others(6): Show |
A | 3 | a0002c0003t0001g0192 a0002c0003t0001g0193 a0002c0003t0002g0189 |
3 | HG00597.hp2 NA18943.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2526-19910_2526-19 others(19): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844216 | ||||||
chr3:14844216 | AAATATAT others(8): Show |
A | 1 | a0002c0003t0001g0188 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844216 | ||||||
chr3:14844216 | AAATATAT others(10): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844216 | ||||||
chr3:14844216 | AAATATAT others(28): Show |
A | 3 | a0001c0001t0001g0123 a0002c0003t0001g0202 a0002c0007t0001g0243 |
3 | HG02071.hp1 NA18953.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2526-19910_2526-19 others(41): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844216 | ||||||
chr3:14844217 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(8): Show |
1 | a0001c0022t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(16): Show |
1 | a0001c0002t0002g0265 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(29): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(21): Show |
1 | a0001c0002t0002g0267 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(34): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0218 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0011g0340 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0137 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0149 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0219 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0129 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0231 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(35): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0114 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0143 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(22): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAAATA others(15): Show |
1 | a0001c0001t0001g0067 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(28): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0004g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(19): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AAATATAT others(8): Show |
1 | a0002c0003t0001g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2526-19910_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0308 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2526-19867_2526-19 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AATATATA others(7): Show |
1 | a0007c0012t0001g0059 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2526-19869_2526-19 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | AATATATA others(9): Show |
1 | a0007c0012t0001g0060 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2526-19871_2526-19 others(22): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0244 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2526-19911_2526-19 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844217 | |||||||
chr3:14844217 | A | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0185 a0001c0001t0001g0282 others(22): Show |
26 | HG00140.hp1 HG00621.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.2526-19911A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844217 | |||||||
chr3:14844217 | AAT | A | 12 | a0001c0001t0001g0288 a0001c0001t0001g0317 a0001c0001t0002g0107 others(9): Show |
12 | HG01109.hp1 HG01433.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2526-19857_2526-19 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATAT | A | 9 | a0001c0001t0001g0108 a0001c0001t0001g0313 a0001c0001t0001g0324 others(6): Show |
9 | HG00558.hp1 HG01975.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.2526-19859_2526-19 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(1): Show |
A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0098 others(6): Show |
9 | HG01069.hp1 HG01175.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.2526-19863_2526-19 others(14): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(3): Show |
A | 6 | a0001c0001t0001g0030 a0001c0002t0001g0012 a0002c0003t0001g0200 others(3): Show |
6 | HG02055.hp2 NA18960.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-19865_2526-19 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(5): Show |
A | 7 | a0001c0001t0001g0203 a0001c0002t0001g0010 a0001c0002t0001g0173 others(4): Show |
7 | HG01934.hp2 HG02040.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2526-19867_2526-19 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(7): Show |
A | 11 | a0001c0001t0001g0111 a0001c0001t0001g0223 a0002c0003t0001g0034 others(8): Show |
11 | HG01081.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.2526-19869_2526-19 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(9): Show |
A | 1 | a0001c0001t0017g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2526-19871_2526-19 others(22): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(11): Show |
A | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2526-19873_2526-19 others(24): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2526-19877_2526-19 others(28): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(17): Show |
A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0024 others(1): Show |
4 | HG01175.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2526-19879_2526-19 others(30): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(19): Show |
A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0248 others(1): Show |
4 | HG01168.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2526-19881_2526-19 others(32): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(23): Show |
A | 2 | a0001c0001t0002g0031 a0017c0037t0001g0253 |
2 | HG01943.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2526-19885_2526-19 others(36): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844217 | AATATATA others(27): Show |
A | 1 | a0002c0003t0001g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2526-19889_2526-19 others(40): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14844217 | ||||||
chr3:14844218 | AT | A | 6 | a0001c0001t0001g0071 a0001c0002t0001g0228 a0001c0002t0001g0259 others(3): Show |
6 | HG01928.hp2 HG02148.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-19909delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATAT | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0279 others(2): Show |
5 | HG01943.hp1 NA18967.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(9): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATAT | A | 9 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0001g0076 others(6): Show |
9 | HG00099.hp1 HG02132.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(11): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0124 a0016c0016t0001g0068 |
3 | HG01243.hp2 HG01981.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(13): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(2): Show |
A | 7 | a0001c0001t0001g0085 a0001c0001t0001g0121 a0001c0001t0001g0128 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(15): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(4): Show |
A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0181 a0001c0001t0005g0125 others(5): Show |
8 | HG00735.hp1 HG01261.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(6): Show |
A | 5 | a0001c0001t0001g0168 a0001c0002t0001g0156 a0002c0003t0001g0210 others(2): Show |
5 | HG02027.hp1 HG03471.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(19): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(8): Show |
A | 2 | a0001c0030t0001g0230 a0023c0028t0001g0011 |
2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0001g0150 a0001c0001t0002g0141 |
2 | HG03831.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0058 a0001c0002t0001g0297 |
2 | HG02027.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(25): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(18): Show |
A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0142 |
3 | HG01109.hp2 HG02155.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(31): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(22): Show |
A | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2526-19909_2526-19 others(35): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844218 | ATATATAT others(28): Show |
A | 3 | a0002c0007t0001g0240 a0002c0007t0001g0241 a0002c0007t0001g0242 |
3 | NA18939.hp1 NA18980.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2526-19909_2526-19 others(41): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844218 | |||||||
chr3:14844219 | T | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0105 others(29): Show |
32 | HG00642.hp2 HG00735.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.2526-19909T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844219 | |||||||
chr3:14844221 | T | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0105 others(28): Show |
31 | HG00735.hp2 HG01192.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.2526-19907T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844221 | |||||||
chr3:14844223 | T | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0108 others(27): Show |
30 | HG01192.hp2 HG01433.hp1 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.2526-19905T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844223 | |||||||
chr3:14844225 | T | A | 25 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0109 others(22): Show |
25 | HG01928.hp2 HG01943.hp1 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.2526-19903T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844225 | |||||||
chr3:14844227 | T | A | 30 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0065 others(27): Show |
30 | HG01243.hp2 HG01928.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.2526-19901T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844227 | |||||||
chr3:14844229 | T | A | 23 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0121 others(20): Show |
23 | HG01069.hp2 HG01071.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.2526-19899T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844229 | |||||||
chr3:14844231 | T | A | 34 | a0001c0001t0001g0045 a0001c0001t0001g0126 a0001c0001t0001g0128 others(31): Show |
34 | HG00735.hp1 HG01261.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.2526-19897T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844231 | |||||||
chr3:14844233 | T | A | 29 | a0001c0001t0001g0045 a0001c0001t0001g0140 a0001c0001t0001g0168 others(26): Show |
29 | HG01261.hp1 HG01943.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.2526-19895T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844233 | |||||||
chr3:14844235 | T | A | 19 | a0001c0001t0001g0045 a0001c0001t0001g0140 a0001c0001t0001g0223 others(16): Show |
19 | HG02132.hp2 HG02257.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.2526-19893T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844235 | |||||||
chr3:14844237 | T | A | 11 | a0001c0001t0001g0140 a0001c0001t0001g0150 a0001c0001t0001g0223 others(8): Show |
11 | HG02132.hp2 HG02622.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2526-19891T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844237 | |||||||
chr3:14844239 | T | A | 10 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0002g0141 others(7): Show |
10 | HG02622.hp2 HG02738.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.2526-19889T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844239 | |||||||
chr3:14844241 | T | A | 7 | a0001c0001t0001g0223 a0001c0002t0001g0156 a0001c0002t0001g0173 others(4): Show |
7 | HG02622.hp2 HG02738.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.2526-19887T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844241 | |||||||
chr3:14844243 | T | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0012g0032 others(4): Show |
7 | HG01175.hp1 HG02723.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2526-19885T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844243 | |||||||
chr3:14844243 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2526-19885T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844243 | |||||||
chr3:14844245 | T | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
10 | HG01109.hp2 HG01168.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.2526-19883T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844245 | |||||||
chr3:14844247 | T | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0142 a0001c0001t0004g0247 others(1): Show |
4 | HG02155.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2526-19881T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844247 | |||||||
chr3:14844249 | T | A | 2 | a0001c0001t0002g0031 a0017c0037t0001g0253 |
2 | HG01943.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2526-19879T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844249 | |||||||
chr3:14844251 | T | A | 1 | a0001c0001t0002g0031 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2526-19877T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844251 | |||||||
chr3:14844253 | T | A | 2 | a0001c0001t0002g0031 a0002c0003t0001g0035 |
2 | HG01943.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2526-19875T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844253 | |||||||
chr3:14844255 | T | A | 1 | a0002c0003t0001g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2526-19873T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844255 | |||||||
chr3:14844271 | T | A | 7 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0067 others(4): Show |
7 | HG01358.hp1 HG02738.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2526-19857T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844271 | |||||||
chr3:14844306 | G | A | 1 | a0004c0006t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2526-19822G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844306 | |||||||
chr3:14844373 | T | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-19755T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844373 | |||||||
chr3:14844404 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2526-19724G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844404 | |||||||
chr3:14844570 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-19558A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844570 | |||||||
chr3:14844717 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-19411A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844717 | |||||||
chr3:14844851 | C | A | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2526-19277C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844851 | |||||||
chr3:14844855 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0033 others(38): Show |
41 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.2526-19273T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14844855 | |||||||
chr3:14845066 | C | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-19062C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845066 | |||||||
chr3:14845145 | A | T | 18 | a0001c0001t0001g0181 a0002c0003t0001g0159 a0002c0003t0001g0178 others(15): Show |
18 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.2526-18983A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845145 | |||||||
chr3:14845180 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2526-18948G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845180 | |||||||
chr3:14845212 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2526-18916C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845212 | |||||||
chr3:14845289 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2526-18839A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845289 | |||||||
chr3:14845320 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0004g0247 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2526-18808G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845320 | |||||||
chr3:14845522 | G | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-18606G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845522 | |||||||
chr3:14845583 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2526-18545G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845583 | |||||||
chr3:14845675 | T | C | 2 | a0015c0038t0001g0258 a0017c0037t0001g0253 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2526-18453T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845675 | |||||||
chr3:14845675 | T | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2526-18453T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845675 | |||||||
chr3:14845729 | C | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-18399C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845729 | |||||||
chr3:14845789 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-18339C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845789 | |||||||
chr3:14845934 | G | A | 13 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(10): Show |
13 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.2526-18194G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845934 | |||||||
chr3:14845935 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2526-18193A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14845935 | |||||||
chr3:14846020 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-18108C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846020 | |||||||
chr3:14846039 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2526-18089A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846039 | |||||||
chr3:14846136 | T | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2526-17992T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846136 | |||||||
chr3:14846155 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0004g0247 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2526-17973G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846155 | |||||||
chr3:14846169 | A | G | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2526-17959A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846169 | |||||||
chr3:14846323 | T | C | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2526-17805T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846323 | |||||||
chr3:14846337 | A | G | 1 | a0001c0030t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2526-17791A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846337 | |||||||
chr3:14846421 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2526-17707T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846421 | |||||||
chr3:14846823 | C | T | 30 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(27): Show |
30 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.2526-17305C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846823 | |||||||
chr3:14846856 | G | A | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2526-17272G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14846856 | |||||||
chr3:14847062 | C | G | 26 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(23): Show |
26 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.2526-17066C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847062 | |||||||
chr3:14847156 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2526-16972C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847156 | |||||||
chr3:14847220 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2526-16908T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847220 | |||||||
chr3:14847581 | A | T | 2 | a0005c0004t0001g0037 a0005c0004t0001g0040 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2526-16547A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847581 | |||||||
chr3:14847621 | T | G | 1 | a0002c0003t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2526-16507T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847621 | |||||||
chr3:14847738 | A | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2526-16390A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847738 | |||||||
chr3:14847785 | T | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(333): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2526-16343T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847785 | |||||||
chr3:14847801 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2526-16327C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847801 | |||||||
chr3:14847812 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0011g0340 |
2 | HG00673.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2526-16316A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847812 | |||||||
chr3:14847881 | C | T | 1 | a0001c0002t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2526-16247C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847881 | |||||||
chr3:14847945 | A | T | 1 | a0001c0002t0001g0260 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2526-16183A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14847945 | |||||||
chr3:14848011 | C | A | 1 | a0001c0002t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2526-16117C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848011 | |||||||
chr3:14848040 | G | A | 1 | a0001c0002t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2526-16088G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848040 | |||||||
chr3:14848071 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2526-16057C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848071 | |||||||
chr3:14848233 | C | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2526-15895C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848233 | |||||||
chr3:14848249 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(282): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2526-15879T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848249 | |||||||
chr3:14848270 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-15858G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848270 | |||||||
chr3:14848271 | C | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2526-15857C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848271 | |||||||
chr3:14848304 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0056 others(85): Show |
90 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2526-15824C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848304 | |||||||
chr3:14848389 | CT | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2526-15738delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848389 | |||||||
chr3:14848425 | TTGC | T | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-15699_2526-15 others(9): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14848425 | ||||||
chr3:14848507 | A | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01109.hp2 HG01168.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-15621A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848507 | |||||||
chr3:14848675 | A | T | 1 | a0001c0001t0001g0302 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2526-15453A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848675 | |||||||
chr3:14848748 | C | A | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2526-15380C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848748 | |||||||
chr3:14848764 | A | C | 1 | a0026c0027t0001g0201 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2526-15364A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848764 | |||||||
chr3:14848954 | G | A | 2 | a0015c0038t0001g0258 a0017c0037t0001g0253 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2526-15174G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848954 | |||||||
chr3:14848982 | C | T | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2526-15146C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14848982 | |||||||
chr3:14849122 | G | A | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2526-15006G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849122 | |||||||
chr3:14849148 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2526-14980C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849148 | |||||||
chr3:14849155 | G | C | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2526-14973G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849155 | |||||||
chr3:14849386 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2526-14742G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849386 | |||||||
chr3:14849432 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2526-14696G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849432 | |||||||
chr3:14849640 | A | G | 3 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0097 |
3 | NA18942.hp1 NA19077.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2526-14488A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849640 | |||||||
chr3:14849671 | T | C | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-14457T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849671 | |||||||
chr3:14849827 | T | C | 27 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(24): Show |
27 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.2526-14301T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14849827 | |||||||
chr3:14850121 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2526-14007G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850121 | |||||||
chr3:14850162 | G | A | 2 | a0001c0002t0001g0010 a0001c0002t0001g0012 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2526-13966G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850162 | |||||||
chr3:14850248 | G | A | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-13880G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850248 | |||||||
chr3:14850291 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2526-13837T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850291 | |||||||
chr3:14850332 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2526-13796G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850332 | |||||||
chr3:14850381 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2526-13747G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850381 | |||||||
chr3:14850612 | A | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0147 a0001c0001t0001g0235 |
3 | NA19004.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2526-13516A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850612 | |||||||
chr3:14850699 | C | T | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2526-13429C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850699 | |||||||
chr3:14850894 | A | G | 2 | a0001c0002t0005g0118 a0001c0002t0005g0119 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2526-13234A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850894 | |||||||
chr3:14850953 | G | T | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-13175G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850953 | |||||||
chr3:14850995 | A | G | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2526-13133A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14850995 | |||||||
chr3:14851121 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2526-13007A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851121 | |||||||
chr3:14851133 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2526-12995G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851133 | |||||||
chr3:14851163 | T | TG | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(282): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2526-12964dupG | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14851163 | ||||||
chr3:14851199 | C | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(52): Show |
57 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2526-12929C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851199 | |||||||
chr3:14851262 | A | G | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2526-12866A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851262 | |||||||
chr3:14851365 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2526-12763T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851365 | |||||||
chr3:14851453 | C | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2526-12675C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851453 | |||||||
chr3:14851454 | C | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2526-12674C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851454 | |||||||
chr3:14851638 | G | C | 1 | a0001c0001t0002g0031 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2526-12490G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851638 | |||||||
chr3:14851662 | A | T | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2526-12466A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851662 | |||||||
chr3:14851718 | C | T | 2 | a0001c0002t0001g0171 a0001c0002t0001g0172 |
2 | NA18995.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2526-12410C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851718 | |||||||
chr3:14851776 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2526-12352A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851776 | |||||||
chr3:14851848 | G | A | 39 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2526-12280G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851848 | |||||||
chr3:14851924 | T | TA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2526-12192dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14851924 | ||||||
chr3:14851924 | TA | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0123 others(109): Show |
114 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2526-12192delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14851924 | ||||||
chr3:14851960 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-12168A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851960 | |||||||
chr3:14851968 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2526-12160A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14851968 | |||||||
chr3:14852051 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(52): Show |
57 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2526-12077A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852051 | |||||||
chr3:14852140 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2526-11988G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852140 | |||||||
chr3:14852171 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-11957G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852171 | |||||||
chr3:14852296 | G | A | 100 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2526-11832G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852296 | |||||||
chr3:14852340 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2526-11788A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852340 | |||||||
chr3:14852392 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-11736G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852392 | |||||||
chr3:14852511 | C | G | 1 | a0001c0001t0001g0337 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2526-11617C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852511 | |||||||
chr3:14852614 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2526-11514G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852614 | |||||||
chr3:14852633 | C | T | 32 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0056 others(29): Show |
32 | HG00140.hp2 HG01081.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.2526-11495C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852633 | |||||||
chr3:14852645 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2526-11483C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852645 | |||||||
chr3:14852681 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2526-11447A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852681 | |||||||
chr3:14852756 | A | G | 2 | a0001c0013t0001g0304 a0001c0013t0001g0305 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2526-11372A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852756 | |||||||
chr3:14852856 | C | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2526-11272C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852856 | |||||||
chr3:14852876 | G | A | 2 | a0001c0002t0001g0015 a0001c0002t0001g0016 |
2 | HG00280.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.2526-11252G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852876 | |||||||
chr3:14852931 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0052 others(187): Show |
192 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.2526-11197A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852931 | |||||||
chr3:14852942 | T | C | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2526-11186T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14852942 | |||||||
chr3:14853045 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-11083G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853045 | |||||||
chr3:14853066 | AG | A | 132 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0056 others(129): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2526-11060delG | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853066 | ||||||
chr3:14853072 | C | G | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2526-11056C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853072 | |||||||
chr3:14853075 | AG | A | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-11052delG | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853075 | |||||||
chr3:14853113 | T | C | 1 | a0004c0006t0001g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2526-11015T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853113 | |||||||
chr3:14853127 | C | G | 132 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0056 others(129): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2526-11001C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853127 | |||||||
chr3:14853293 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-10835G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853293 | |||||||
chr3:14853457 | G | A | 1 | a0002c0003t0001g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2526-10671G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853457 | |||||||
chr3:14853502 | T | TC | 96 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0056 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2526-10623dupC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853502 | ||||||
chr3:14853550 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2526-10578C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853550 | |||||||
chr3:14853560 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-10568A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853560 | |||||||
chr3:14853564 | A | C | 1 | a0001c0001t0004g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2526-10564A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853564 | |||||||
chr3:14853598 | G | C | 96 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0056 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2526-10530G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853598 | |||||||
chr3:14853625 | G | C | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2526-10503G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853625 | |||||||
chr3:14853636 | C | CTTTTTTT others(1): Show |
8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02258.hp1 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2526-10468_2526-10 others(14): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0096 others(3): Show |
6 | HG00140.hp2 HG02622.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-10469_2526-10 others(15): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0056 a0001c0001t0001g0094 a0001c0001t0001g0300 others(2): Show |
5 | HG01099.hp2 HG01123.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2526-10470_2526-10 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2526-10471_2526-10 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0052 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2526-10473_2526-10 others(19): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0095 a0001c0001t0001g0203 a0001c0001t0003g0054 others(5): Show |
8 | HG00597.hp2 HG01258.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.2526-10474_2526-10 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(8): Show |
15 | a0001c0001t0003g0053 a0001c0002t0001g0186 a0002c0003t0001g0034 others(12): Show |
15 | HG01433.hp1 HG01515.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.2526-10475_2526-10 others(21): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(9): Show |
9 | a0001c0001t0001g0124 a0001c0002t0001g0187 a0002c0003t0001g0188 others(6): Show |
9 | HG00621.hp1 HG01106.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2526-10476_2526-10 others(22): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(10): Show |
4 | a0002c0003t0001g0176 a0002c0007t0001g0240 a0002c0007t0001g0241 others(1): Show |
4 | HG01175.hp2 NA18939.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.2526-10477_2526-10 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(12): Show |
2 | a0002c0003t0001g0197 a0002c0003t0001g0234 |
2 | HG02698.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2526-10479_2526-10 others(25): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(13): Show |
4 | a0002c0003t0001g0178 a0002c0003t0001g0198 a0002c0003t0001g0199 others(1): Show |
4 | HG00558.hp2 NA18959.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.2526-10480_2526-10 others(26): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(14): Show |
3 | a0001c0001t0001g0123 a0001c0001t0001g0181 a0002c0003t0001g0200 |
3 | HG02071.hp1 NA18961.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2526-10481_2526-10 others(27): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(15): Show |
2 | a0002c0003t0001g0213 a0002c0007t0001g0242 |
2 | NA18980.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2526-10482_2526-10 others(28): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(16): Show |
1 | a0002c0003t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2526-10483_2526-10 others(29): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(19): Show |
1 | a0002c0003t0001g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2526-10486_2526-10 others(32): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | C | CTTTTTTT others(20): Show |
1 | a0002c0007t0001g0243 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2526-10487_2526-10 others(33): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | CT | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0023 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.2526-10461delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | CTT | C | 92 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0043 others(89): Show |
92 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.2526-10462_2526-10 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | CTTT | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0106 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-10463_2526-10 others(9): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2526-10471_2526-10 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | CTTTTTTT others(5): Show |
C | 4 | a0002c0003t0001g0227 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG02559.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2526-10472_2526-10 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0051 a0001c0001t0002g0169 a0007c0012t0001g0060 |
3 | HG02129.hp1 NA18991.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2526-10473_2526-10 others(19): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853636 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2526-10474_2526-10 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853636 | ||||||
chr3:14853695 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-10433C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853695 | |||||||
chr3:14853790 | C | G | 1 | a0001c0002t0001g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2526-10338C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14853790 | |||||||
chr3:14853831 | AAAGGACT others(27): Show |
A | 129 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0056 others(126): Show |
129 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2526-10290_2526-10 others(40): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14853831 | ||||||
chr3:14854020 | GGCCA | G | 100 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2526-10106_2526-10 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854020 | ||||||
chr3:14854216 | A | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0123 others(155): Show |
160 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2526-9912A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854216 | |||||||
chr3:14854270 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-9858A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854270 | |||||||
chr3:14854387 | CTTTTTAT others(6): Show |
C | 3 | a0002c0003t0001g0193 a0002c0003t0001g0234 a0025c0021t0001g0191 |
3 | NA18943.hp1 NA19054.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2526-9740_2526-972 others(17): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854387 | |||||||
chr3:14854389 | T | A | 6 | a0004c0006t0001g0044 a0004c0006t0001g0078 a0004c0006t0001g0081 others(3): Show |
6 | HG02074.hp2 HG02129.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-9739T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854389 | |||||||
chr3:14854389 | T | TTTTA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0279 others(20): Show |
23 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2526-9696_2526-969 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854389 | ||||||
chr3:14854389 | T | TTTTATTT others(1): Show |
13 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0095 others(10): Show |
13 | HG01257.hp2 HG01258.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2526-9700_2526-969 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854389 | ||||||
chr3:14854389 | T | TTTTATTT others(5): Show |
3 | a0001c0001t0001g0094 a0001c0002t0002g0278 a0001c0014t0001g0018 |
3 | HG01099.hp2 HG02615.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2526-9704_2526-969 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854389 | ||||||
chr3:14854389 | TTTTA | T | 6 | a0002c0003t0001g0178 a0003c0009t0001g0250 a0003c0009t0001g0251 others(3): Show |
6 | HG00558.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-9696_2526-969 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854389 | ||||||
chr3:14854389 | TTTTATTT others(1): Show |
T | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2526-9700_2526-969 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854389 | ||||||
chr3:14854389 | TTTTATTT others(5): Show |
T | 4 | a0001c0030t0001g0230 a0003c0005t0001g0003 a0003c0005t0001g0005 others(1): Show |
4 | HG01081.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2526-9704_2526-969 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854389 | ||||||
chr3:14854420 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0086 |
2 | NA18945.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2526-9708T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854420 | |||||||
chr3:14854420 | T | TATTG | 5 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0114 others(2): Show |
5 | HG00673.hp1 HG01099.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-9705_2526-970 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854420 | ||||||
chr3:14854422 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(51): Show |
56 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2526-9706T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854422 | |||||||
chr3:14854424 | T | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0074 others(5): Show |
8 | HG00673.hp1 HG01099.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.2526-9704T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854424 | |||||||
chr3:14854424 | T | TATTG | 25 | a0001c0001t0001g0028 a0001c0001t0001g0045 a0001c0001t0001g0058 others(22): Show |
25 | HG00673.hp2 HG01069.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.2526-9701_2526-970 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854424 | ||||||
chr3:14854428 | T | G | 35 | a0001c0001t0001g0028 a0001c0001t0001g0045 a0001c0001t0001g0058 others(32): Show |
35 | HG00673.hp1 HG00673.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2526-9700T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854428 | |||||||
chr3:14854428 | T | TATTG | 42 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(39): Show |
42 | HG01175.hp1 HG01192.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.2526-9697_2526-969 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854428 | ||||||
chr3:14854428 | T | TATTGATT others(1): Show |
16 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0043 others(13): Show |
16 | HG01256.hp2 HG01258.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.2526-9697_2526-969 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854428 | ||||||
chr3:14854432 | T | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(90): Show |
93 | HG00673.hp1 HG00673.hp2 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.2526-9696T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854432 | |||||||
chr3:14854432 | T | TATTG | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01109.hp2 HG01168.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-9694_2526-969 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854432 | ||||||
chr3:14854432 | T | TATTGATT others(1): Show |
13 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0131 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.2526-9691_2526-969 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854432 | ||||||
chr3:14854432 | T | TATTGATT others(5): Show |
6 | a0001c0001t0001g0076 a0001c0001t0001g0149 a0001c0001t0001g0206 others(3): Show |
6 | HG00099.hp1 HG01255.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2526-9691_2526-969 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854432 | ||||||
chr3:14854432 | T | TATTTATT others(1): Show |
8 | a0001c0001t0001g0109 a0001c0001t0001g0220 a0001c0001t0001g0337 others(5): Show |
8 | HG00642.hp2 HG01070.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2526-9693_2526-969 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14854432 | ||||||
chr3:14854659 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-9469A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854659 | |||||||
chr3:14854680 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0033 others(45): Show |
48 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.2526-9448A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854680 | |||||||
chr3:14854700 | G | A | 2 | a0002c0003t0001g0034 a0002c0003t0001g0035 |
2 | NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2526-9428G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854700 | |||||||
chr3:14854714 | C | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(52): Show |
57 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2526-9414C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854714 | |||||||
chr3:14854772 | A | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0105 others(10): Show |
13 | HG01192.hp1 HG01934.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2526-9356A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14854772 | |||||||
chr3:14855406 | A | C | 2 | a0015c0038t0001g0258 a0017c0037t0001g0253 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2526-8722A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855406 | |||||||
chr3:14855452 | C | T | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-8676C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855452 | |||||||
chr3:14855530 | T | A | 1 | a0001c0002t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2526-8598T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855530 | |||||||
chr3:14855649 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2526-8479A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855649 | |||||||
chr3:14855651 | G | GT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0130 others(59): Show |
64 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2526-8467dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14855651 | ||||||
chr3:14855673 | A | G | 1 | a0001c0002t0007g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2526-8455A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855673 | |||||||
chr3:14855713 | T | G | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2526-8415T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855713 | |||||||
chr3:14855825 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-8303T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855825 | |||||||
chr3:14855946 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-8182T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14855946 | |||||||
chr3:14856003 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2526-8125G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14856003 | |||||||
chr3:14856029 | G | C | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2526-8099G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14856029 | |||||||
chr3:14856141 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0123 others(158): Show |
163 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2526-7987G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14856141 | |||||||
chr3:14856161 | T | C | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2526-7967T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14856161 | |||||||
chr3:14856183 | A | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-7945A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14856183 | |||||||
chr3:14856629 | A | C | 100 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2526-7499A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14856629 | |||||||
chr3:14856649 | AT | A | 99 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(96): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2526-7469delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14856649 | ||||||
chr3:14856991 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2526-7137G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14856991 | |||||||
chr3:14857155 | CT | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0123 others(153): Show |
158 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.2526-6961delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14857155 | ||||||
chr3:14857236 | A | AC | 21 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0056 others(18): Show |
21 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2526-6885dupC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14857236 | ||||||
chr3:14857239 | C | CG | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2526-6889_2526-688 others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14857239 | |||||||
chr3:14857619 | C | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-6509C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14857619 | |||||||
chr3:14857640 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2526-6488A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14857640 | |||||||
chr3:14857887 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2526-6241A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14857887 | |||||||
chr3:14858074 | G | C | 2 | a0001c0030t0001g0230 a0019c0036t0001g0245 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2526-6054G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858074 | |||||||
chr3:14858245 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2526-5883G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858245 | |||||||
chr3:14858271 | G | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2526-5857G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858271 | |||||||
chr3:14858344 | C | CGGGT | 68 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(65): Show |
68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.2526-5773_2526-577 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858344 | ||||||
chr3:14858355 | G | GTGGA | 160 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0020 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.2526-5735_2526-573 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858355 | ||||||
chr3:14858355 | G | GTGGATGG others(1): Show |
37 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0051 others(34): Show |
37 | HG00642.hp1 HG01106.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.2526-5739_2526-573 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858355 | ||||||
chr3:14858355 | G | GTGGATGG others(5): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0143 a0001c0001t0002g0107 |
3 | HG02015.hp1 HG02074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2526-5743_2526-573 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858355 | ||||||
chr3:14858355 | G | GTGGGTGG others(1): Show |
11 | a0001c0002t0001g0156 a0001c0002t0001g0171 a0001c0002t0001g0172 others(8): Show |
11 | HG01081.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2526-5770_2526-576 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858355 | ||||||
chr3:14858355 | G | GTGGGTGG others(5): Show |
6 | a0001c0002t0001g0261 a0001c0002t0001g0274 a0001c0002t0001g0275 others(3): Show |
6 | HG02135.hp1 HG02622.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.2526-5770_2526-576 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858355 | ||||||
chr3:14858355 | G | GTGGGTGG others(9): Show |
21 | a0001c0001t0001g0238 a0001c0001t0001g0279 a0001c0002t0001g0228 others(18): Show |
21 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.2526-5770_2526-576 others(20): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858355 | ||||||
chr3:14858355 | G | GTGGGTGG others(13): Show |
1 | a0001c0002t0001g0276 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2526-5770_2526-576 others(24): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14858355 | ||||||
chr3:14858359 | A | G | 3 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0018t0001g0249 |
3 | HG02630.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2526-5769A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858359 | |||||||
chr3:14858363 | A | G | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2526-5765A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858363 | |||||||
chr3:14858406 | A | G | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2526-5722A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858406 | |||||||
chr3:14858645 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2526-5483G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858645 | |||||||
chr3:14858767 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2526-5361A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858767 | |||||||
chr3:14858979 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-5149T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858979 | |||||||
chr3:14858988 | C | G | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2526-5140C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14858988 | |||||||
chr3:14859044 | T | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0123 others(158): Show |
163 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2526-5084T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859044 | |||||||
chr3:14859231 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-4897C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859231 | |||||||
chr3:14859306 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2526-4822C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859306 | |||||||
chr3:14859393 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0123 others(158): Show |
163 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2526-4735T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859393 | |||||||
chr3:14859443 | A | T | 1 | a0001c0002t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2526-4685A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859443 | |||||||
chr3:14859453 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2526-4675G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859453 | |||||||
chr3:14859517 | C | G | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526-4611C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859517 | |||||||
chr3:14859552 | C | T | 19 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(16): Show |
19 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2526-4576C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859552 | |||||||
chr3:14859560 | A | C | 4 | a0001c0002t0001g0162 a0001c0013t0001g0304 a0001c0013t0001g0305 others(1): Show |
4 | HG01981.hp2 HG02572.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.2526-4568A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859560 | |||||||
chr3:14859572 | T | TGAAA | 33 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2526-4556_2526-455 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859572 | |||||||
chr3:14859573 | A | AAAAGAAA others(1): Show |
70 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(67): Show |
70 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2526-4547_2526-454 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14859573 | ||||||
chr3:14859573 | A | G | 33 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2526-4555A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859573 | |||||||
chr3:14859651 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2526-4477A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859651 | |||||||
chr3:14859682 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-4446G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859682 | |||||||
chr3:14859687 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-4441G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859687 | |||||||
chr3:14859759 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-4369C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14859759 | |||||||
chr3:14859882 | TC | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0123 others(158): Show |
163 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2526-4238delC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14859882 | ||||||
chr3:14860004 | A | G | 1 | a0005c0004t0001g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2526-4124A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860004 | |||||||
chr3:14860008 | A | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.2526-4120A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860008 | |||||||
chr3:14860018 | C | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2526-4110C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860018 | |||||||
chr3:14860248 | A | G | 1 | a0001c0002t0001g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2526-3880A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860248 | |||||||
chr3:14860287 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2526-3841C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860287 | |||||||
chr3:14860486 | G | A | 15 | a0001c0001t0001g0279 a0001c0002t0001g0260 a0001c0002t0001g0266 others(12): Show |
15 | HG00639.hp1 HG01975.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.2526-3642G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860486 | |||||||
chr3:14860572 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2526-3556A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860572 | |||||||
chr3:14860621 | G | A | 5 | a0002c0003t0001g0190 a0002c0003t0001g0194 a0002c0003t0001g0195 others(2): Show |
5 | HG00408.hp2 HG00621.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2526-3507G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860621 | |||||||
chr3:14860644 | G | A | 64 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(61): Show |
64 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2526-3484G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860644 | |||||||
chr3:14860695 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2526-3433C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860695 | |||||||
chr3:14860696 | G | A | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2526-3432G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860696 | |||||||
chr3:14860766 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2526-3362G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860766 | |||||||
chr3:14860808 | T | A | 2 | a0001c0001t0001g0126 a0004c0006t0001g0078 |
2 | HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2526-3320T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860808 | |||||||
chr3:14860808 | T | TA | 93 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(90): Show |
93 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.2526-3308dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14860808 | ||||||
chr3:14860808 | T | TAA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0248 a0001c0001t0001g0282 others(52): Show |
57 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2526-3309_2526-330 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14860808 | ||||||
chr3:14860808 | TA | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0102 others(6): Show |
9 | HG01256.hp2 HG02258.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.2526-3308delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14860808 | ||||||
chr3:14860998 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0085 others(3): Show |
6 | HG02027.hp2 NA18960.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.2526-3130A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14860998 | |||||||
chr3:14861009 | G | A | 6 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0004c0006t0001g0077 others(3): Show |
6 | HG01106.hp1 HG01255.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2526-3119G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861009 | |||||||
chr3:14861071 | G | T | 1 | a0003c0009t0001g0250 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2526-3057G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861071 | |||||||
chr3:14861237 | C | T | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2526-2891C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861237 | |||||||
chr3:14861276 | G | T | 1 | a0001c0001t0001g0328 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2526-2852G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861276 | |||||||
chr3:14861292 | C | T | 1 | a0006c0033t0001g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2526-2836C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861292 | |||||||
chr3:14861421 | A | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(320): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2526-2707A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861421 | |||||||
chr3:14861473 | A | G | 1 | a0002c0003t0001g0234 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2526-2655A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861473 | |||||||
chr3:14861583 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2526-2545G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861583 | |||||||
chr3:14861643 | T | C | 100 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2526-2485T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861643 | |||||||
chr3:14861679 | C | G | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2526-2449C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861679 | |||||||
chr3:14861727 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0002g0107 a0014c0015t0001g0229 |
3 | HG02559.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2526-2401G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861727 | |||||||
chr3:14861746 | A | ACAG | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2526-2369_2526-236 others(7): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14861746 | ||||||
chr3:14861884 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2526-2244T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14861884 | |||||||
chr3:14862029 | A | G | 100 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2526-2099A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862029 | |||||||
chr3:14862123 | C | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2526-2005C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862123 | |||||||
chr3:14862184 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2526-1944G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862184 | |||||||
chr3:14862219 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2526-1909G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862219 | |||||||
chr3:14862453 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2526-1675A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862453 | |||||||
chr3:14862459 | C | G | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2526-1669C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862459 | |||||||
chr3:14862491 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2526-1637G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862491 | |||||||
chr3:14862670 | G | T | 1 | a0001c0001t0001g0322 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2526-1458G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862670 | |||||||
chr3:14862716 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2526-1412C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862716 | |||||||
chr3:14862806 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2526-1322C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862806 | |||||||
chr3:14862850 | A | G | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2526-1278A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862850 | |||||||
chr3:14862913 | A | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2526-1215A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862913 | |||||||
chr3:14862931 | G | A | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2526-1197G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862931 | |||||||
chr3:14862940 | G | A | 33 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2526-1188G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14862940 | |||||||
chr3:14863004 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2526-1124T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863004 | |||||||
chr3:14863054 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2526-1074G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863054 | |||||||
chr3:14863112 | C | G | 1 | a0004c0010t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2526-1016C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863112 | |||||||
chr3:14863128 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2526-1000C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863128 | |||||||
chr3:14863220 | G | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2526-908G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863220 | |||||||
chr3:14863238 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-890G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863238 | |||||||
chr3:14863283 | C | A | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2526-845C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863283 | |||||||
chr3:14863383 | A | AGTT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2526-744_2526-742d others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 14863383 | ||||||
chr3:14863466 | A | T | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2526-662A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863466 | |||||||
chr3:14863688 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526-440G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863688 | |||||||
chr3:14863919 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2526-209C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863919 | |||||||
chr3:14863920 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2526-208G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14863920 | |||||||
chr3:14864006 | T | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2526-122T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 1/19 | chr3 | 14864006 | |||||||
chr3:14864334 | CT | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0128 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2658+76delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14864334 | ||||||
chr3:14864440 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+180T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864440 | |||||||
chr3:14864473 | C | T | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2658+213C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864473 | |||||||
chr3:14864479 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+219T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864479 | |||||||
chr3:14864544 | C | G | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2658+284C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864544 | |||||||
chr3:14864626 | A | C | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2658+366A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864626 | |||||||
chr3:14864653 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+393C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864653 | |||||||
chr3:14864674 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2658+414A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864674 | |||||||
chr3:14864886 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+626T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864886 | |||||||
chr3:14864904 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+644C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864904 | |||||||
chr3:14864971 | G | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2658+711G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14864971 | |||||||
chr3:14865011 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+751G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865011 | |||||||
chr3:14865024 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+764G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865024 | |||||||
chr3:14865047 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+787T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865047 | |||||||
chr3:14865119 | A | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+859A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865119 | |||||||
chr3:14865131 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+871G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865131 | |||||||
chr3:14865227 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2658+967C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865227 | |||||||
chr3:14865315 | C | T | 3 | a0006c0011t0001g0006 a0006c0011t0001g0007 a0022c0026t0001g0009 |
3 | HG02622.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2658+1055C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865315 | |||||||
chr3:14865362 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+1102A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865362 | |||||||
chr3:14865533 | C | T | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2658+1273C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865533 | |||||||
chr3:14865545 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+1285C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865545 | |||||||
chr3:14865573 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+1313C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865573 | |||||||
chr3:14865600 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(66): Show |
71 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2658+1340G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865600 | |||||||
chr3:14865679 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0130 others(59): Show |
64 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2658+1419C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865679 | |||||||
chr3:14865680 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+1420T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865680 | |||||||
chr3:14865732 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0154 |
2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2658+1472C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865732 | |||||||
chr3:14865805 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+1545C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865805 | |||||||
chr3:14865808 | A | G | 1 | a0001c0002t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2658+1548A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865808 | |||||||
chr3:14865960 | G | A | 1 | a0001c0001t0017g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2658+1700G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14865960 | |||||||
chr3:14866075 | A | ACT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+1818_2658+181 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14866075 | ||||||
chr3:14866092 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.2658+1832C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866092 | |||||||
chr3:14866176 | C | T | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2658+1916C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866176 | |||||||
chr3:14866177 | G | A | 1 | a0001c0002t0002g0267 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2658+1917G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866177 | |||||||
chr3:14866181 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+1921A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866181 | |||||||
chr3:14866357 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2658+2097G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866357 | |||||||
chr3:14866418 | T | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2658+2158T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866418 | |||||||
chr3:14866423 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2658+2163A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866423 | |||||||
chr3:14866445 | G | A | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2658+2185G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866445 | |||||||
chr3:14866469 | A | T | 1 | a0003c0009t0001g0250 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2658+2209A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866469 | |||||||
chr3:14866470 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+2210C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866470 | |||||||
chr3:14866481 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2658+2221G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866481 | |||||||
chr3:14866523 | G | A | 1 | a0001c0031t0001g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2658+2263G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866523 | |||||||
chr3:14866598 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+2338T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866598 | |||||||
chr3:14866636 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+2376C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866636 | |||||||
chr3:14866669 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2658+2409A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866669 | |||||||
chr3:14866759 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+2499G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866759 | |||||||
chr3:14866778 | G | A | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2658+2518G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866778 | |||||||
chr3:14866838 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+2578T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866838 | |||||||
chr3:14866900 | GCATC | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+2646_2658+264 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14866900 | ||||||
chr3:14866931 | G | C | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2658+2671G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866931 | |||||||
chr3:14866931 | G | T | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2658+2671G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866931 | |||||||
chr3:14866970 | T | A | 5 | a0001c0002t0001g0156 a0001c0002t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG02738.hp1 HG03688.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.2658+2710T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866970 | |||||||
chr3:14866977 | A | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+2717A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14866977 | |||||||
chr3:14867000 | G | GCT | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2658+2741_2658+274 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14867000 | ||||||
chr3:14867083 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+2823C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867083 | |||||||
chr3:14867102 | A | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2658+2842A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867102 | |||||||
chr3:14867158 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2658+2898C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867158 | |||||||
chr3:14867168 | T | C | 8 | a0002c0003t0001g0210 a0002c0003t0001g0211 a0002c0003t0001g0212 others(5): Show |
8 | NA18960.hp1 NA19009.hp1 NA19010.hp1 others(5): Show |
intron_variant | MODIFIER | c.2658+2908T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867168 | |||||||
chr3:14867474 | G | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2658+3214G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867474 | |||||||
chr3:14867475 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+3215G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867475 | |||||||
chr3:14867493 | CCCAGAAG others(16): Show |
C | 1 | a0001c0001t0001g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2658+3234_2658+325 others(27): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867493 | |||||||
chr3:14867506 | C | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2658+3246C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867506 | |||||||
chr3:14867508 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2658+3248A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867508 | |||||||
chr3:14867517 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2658+3257A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867517 | |||||||
chr3:14867557 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+3297G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867557 | |||||||
chr3:14867587 | C | G | 8 | a0002c0003t0001g0210 a0002c0003t0001g0211 a0002c0003t0001g0212 others(5): Show |
8 | NA18960.hp1 NA19009.hp1 NA19010.hp1 others(5): Show |
intron_variant | MODIFIER | c.2658+3327C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867587 | |||||||
chr3:14867616 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2658+3356C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867616 | |||||||
chr3:14867857 | T | C | 5 | a0001c0001t0001g0185 a0001c0002t0001g0186 a0001c0002t0001g0187 others(2): Show |
5 | HG01106.hp2 HG01123.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.2658+3597T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867857 | |||||||
chr3:14867873 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2658+3613G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867873 | |||||||
chr3:14867942 | G | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+3682G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867942 | |||||||
chr3:14867999 | G | A | 1 | a0001c0002t0014g0160 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2658+3739G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14867999 | |||||||
chr3:14868122 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+3862G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868122 | |||||||
chr3:14868280 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+4020C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868280 | |||||||
chr3:14868322 | G | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0339 |
3 | NA18946.hp2 NA18950.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2658+4062G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868322 | |||||||
chr3:14868333 | A | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+4073A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868333 | |||||||
chr3:14868383 | A | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+4123A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868383 | |||||||
chr3:14868392 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2658+4132A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868392 | |||||||
chr3:14868420 | G | A | 2 | a0007c0012t0001g0059 a0007c0012t0001g0060 |
2 | NA18991.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2658+4160G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868420 | |||||||
chr3:14868436 | T | C | 1 | a0001c0002t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2658+4176T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868436 | |||||||
chr3:14868523 | C | T | 1 | a0021c0024t0001g0281 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2658+4263C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868523 | |||||||
chr3:14868561 | G | A | 1 | a0005c0004t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2658+4301G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868561 | |||||||
chr3:14868613 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+4353C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868613 | |||||||
chr3:14868614 | T | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+4354T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868614 | |||||||
chr3:14868684 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(52): Show |
57 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2658+4424T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868684 | |||||||
chr3:14868696 | A | G | 1 | a0011c0020t0002g0269 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2658+4436A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868696 | |||||||
chr3:14868813 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+4553T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868813 | |||||||
chr3:14868856 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG00642.hp2 HG00733.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2658+4596C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868856 | |||||||
chr3:14868938 | A | G | 1 | a0001c0002t0014g0160 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2658+4678A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14868938 | |||||||
chr3:14869011 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(58): Show |
63 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2658+4751G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869011 | |||||||
chr3:14869013 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+4753A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869013 | |||||||
chr3:14869165 | G | A | 1 | a0001c0002t0001g0172 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2658+4905G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869165 | |||||||
chr3:14869263 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+5003T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869263 | |||||||
chr3:14869310 | TACAA | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0143 others(59): Show |
64 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2658+5072_2658+507 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14869310 | ||||||
chr3:14869637 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+5377C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869637 | |||||||
chr3:14869693 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+5433A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869693 | |||||||
chr3:14869718 | A | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+5458A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869718 | |||||||
chr3:14869719 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+5459G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869719 | |||||||
chr3:14869756 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2658+5496A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869756 | |||||||
chr3:14869855 | G | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(56): Show |
61 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2658+5595G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869855 | |||||||
chr3:14869899 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2658+5639C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14869899 | |||||||
chr3:14870061 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2658+5801C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870061 | |||||||
chr3:14870103 | G | A | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2658+5843G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870103 | |||||||
chr3:14870125 | GGAATGGC others(12): Show |
G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2658+5886_2658+590 others(23): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14870125 | ||||||
chr3:14870164 | G | A | 8 | a0002c0003t0001g0210 a0002c0003t0001g0211 a0002c0003t0001g0212 others(5): Show |
8 | NA18960.hp1 NA19009.hp1 NA19010.hp1 others(5): Show |
intron_variant | MODIFIER | c.2658+5904G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870164 | |||||||
chr3:14870220 | G | A | 15 | a0001c0001t0001g0279 a0001c0002t0001g0260 a0001c0002t0001g0266 others(12): Show |
15 | HG00639.hp1 HG01975.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.2658+5960G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870220 | |||||||
chr3:14870229 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+5969A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870229 | |||||||
chr3:14870301 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+6041C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870301 | |||||||
chr3:14870439 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | NA18993.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2658+6179G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870439 | |||||||
chr3:14870581 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(56): Show |
61 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2658+6321A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870581 | |||||||
chr3:14870615 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG00642.hp2 HG00733.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2658+6355C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870615 | |||||||
chr3:14870619 | C | T | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2658+6359C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870619 | |||||||
chr3:14870630 | T | C | 19 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(16): Show |
19 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2658+6370T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870630 | |||||||
chr3:14870662 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+6402C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870662 | |||||||
chr3:14870803 | A | G | 98 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(95): Show |
98 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2658+6543A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870803 | |||||||
chr3:14870895 | G | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+6635G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870895 | |||||||
chr3:14870951 | C | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2658+6691C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14870951 | |||||||
chr3:14871059 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2658+6799C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871059 | |||||||
chr3:14871092 | A | G | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2658+6832A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871092 | |||||||
chr3:14871309 | A | G | 2 | a0001c0002t0001g0232 a0001c0002t0001g0233 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2658+7049A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871309 | |||||||
chr3:14871519 | T | C | 14 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(11): Show |
14 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658+7259T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871519 | |||||||
chr3:14871630 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2658+7370G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871630 | |||||||
chr3:14871655 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2658+7395G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871655 | |||||||
chr3:14871787 | A | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+7527A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871787 | |||||||
chr3:14871900 | G | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+7640G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871900 | |||||||
chr3:14871951 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2658+7691G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14871951 | |||||||
chr3:14872004 | C | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(56): Show |
61 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2658+7744C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872004 | |||||||
chr3:14872004 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2658+7744C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872004 | |||||||
chr3:14872041 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+7781C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872041 | |||||||
chr3:14872249 | TCTCTGAA others(7): Show |
T | 103 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(100): Show |
103 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2658+8004_2658+801 others(18): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14872249 | ||||||
chr3:14872308 | T | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+8048T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872308 | |||||||
chr3:14872375 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2658+8115A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872375 | |||||||
chr3:14872637 | C | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0168 |
3 | HG02027.hp1 HG02132.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2659-7935C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872637 | |||||||
chr3:14872642 | G | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-7930G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872642 | |||||||
chr3:14872662 | T | C | 1 | a0002c0003t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2659-7910T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872662 | |||||||
chr3:14872705 | T | A | 106 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0121 others(103): Show |
106 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2659-7867T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872705 | |||||||
chr3:14872819 | A | G | 19 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(16): Show |
19 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2659-7753A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872819 | |||||||
chr3:14872878 | C | T | 106 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0121 others(103): Show |
106 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2659-7694C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872878 | |||||||
chr3:14872902 | G | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-7670G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872902 | |||||||
chr3:14872999 | G | A | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2659-7573G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14872999 | |||||||
chr3:14873071 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-7501A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873071 | |||||||
chr3:14873150 | G | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-7422G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873150 | |||||||
chr3:14873155 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2659-7417G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873155 | |||||||
chr3:14873192 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-7380A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873192 | |||||||
chr3:14873217 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(313): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2659-7355A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873217 | |||||||
chr3:14873416 | A | G | 2 | a0001c0001t0001g0300 a0001c0001t0001g0327 |
2 | HG01123.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2659-7156A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873416 | |||||||
chr3:14873458 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-7114A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873458 | |||||||
chr3:14873539 | C | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-7033C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873539 | |||||||
chr3:14873581 | T | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6991T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873581 | |||||||
chr3:14873624 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6948C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873624 | |||||||
chr3:14873625 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6947A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873625 | |||||||
chr3:14873696 | G | T | 1 | a0006c0011t0001g0006 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2659-6876G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873696 | |||||||
chr3:14873723 | C | CT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0248 others(56): Show |
61 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2659-6839dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14873723 | ||||||
chr3:14873732 | T | TC | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2659-6840_2659-683 others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873732 | |||||||
chr3:14873733 | T | C | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2659-6839T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873733 | |||||||
chr3:14873734 | C | CT | 52 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(49): Show |
52 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.2659-6826dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14873734 | ||||||
chr3:14873734 | C | T | 65 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(62): Show |
65 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2659-6838C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873734 | |||||||
chr3:14873735 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2659-6837T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873735 | |||||||
chr3:14873996 | A | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2659-6576A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14873996 | |||||||
chr3:14874005 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6567A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874005 | |||||||
chr3:14874025 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6547C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874025 | |||||||
chr3:14874070 | G | A | 31 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2659-6502G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874070 | |||||||
chr3:14874089 | GAAT | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6481_2659-647 others(7): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14874089 | ||||||
chr3:14874093 | A | G | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6479A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874093 | |||||||
chr3:14874135 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0318 a0001c0001t0001g0319 |
3 | HG00621.hp2 NA19005.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2659-6437C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874135 | |||||||
chr3:14874155 | G | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6417G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874155 | |||||||
chr3:14874166 | G | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-6406G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874166 | |||||||
chr3:14874187 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2659-6385G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874187 | |||||||
chr3:14874388 | G | A | 4 | a0004c0006t0001g0044 a0004c0006t0001g0081 a0004c0006t0001g0082 others(1): Show |
4 | HG02129.hp2 HG02165.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2659-6184G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874388 | |||||||
chr3:14874418 | G | A | 1 | a0002c0003t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2659-6154G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874418 | |||||||
chr3:14874433 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2659-6139A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874433 | |||||||
chr3:14874541 | T | C | 103 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0121 others(100): Show |
103 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2659-6031T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874541 | |||||||
chr3:14874840 | A | C | 2 | a0015c0038t0001g0258 a0017c0037t0001g0253 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2659-5732A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874840 | |||||||
chr3:14874873 | G | A | 1 | a0010c0025t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2659-5699G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874873 | |||||||
chr3:14874930 | C | T | 3 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0002c0003t0001g0122 |
3 | HG01106.hp2 HG01515.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2659-5642C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14874930 | |||||||
chr3:14875028 | C | G | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2659-5544C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875028 | |||||||
chr3:14875130 | C | T | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2659-5442C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875130 | |||||||
chr3:14875139 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2659-5433C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875139 | |||||||
chr3:14875177 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-5395C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875177 | |||||||
chr3:14875306 | T | C | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-5266T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875306 | |||||||
chr3:14875323 | AG | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-5243delG | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14875323 | ||||||
chr3:14875351 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-5221C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875351 | |||||||
chr3:14875672 | C | T | 1 | a0006c0011t0001g0006 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2659-4900C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875672 | |||||||
chr3:14875673 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0238 others(3): Show |
6 | HG02717.hp2 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2659-4899A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875673 | |||||||
chr3:14875711 | C | A | 1 | a0001c0001t0017g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2659-4861C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875711 | |||||||
chr3:14875720 | G | C | 1 | a0005c0004t0001g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2659-4852G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875720 | |||||||
chr3:14875812 | A | G | 2 | a0002c0003t0003g0224 a0002c0003t0003g0225 |
2 | NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2659-4760A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14875812 | |||||||
chr3:14875875 | AC | A | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2659-4695delC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14875875 | ||||||
chr3:14876019 | T | C | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2659-4553T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876019 | |||||||
chr3:14876074 | C | T | 1 | a0002c0003t0001g0199 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2659-4498C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876074 | |||||||
chr3:14876321 | G | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0307 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2659-4251G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876321 | |||||||
chr3:14876447 | T | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG01109.hp2 HG01168.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2659-4125T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876447 | |||||||
chr3:14876518 | C | CA | 6 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0238 others(3): Show |
6 | HG02717.hp2 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2659-4048dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14876518 | ||||||
chr3:14876552 | C | T | 1 | a0001c0002t0001g0271 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2659-4020C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876552 | |||||||
chr3:14876556 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2659-4016G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876556 | |||||||
chr3:14876560 | T | C | 33 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2659-4012T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876560 | |||||||
chr3:14876619 | G | A | 2 | a0004c0006t0001g0077 a0020c0023t0001g0075 |
2 | HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2659-3953G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876619 | |||||||
chr3:14876662 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2659-3910C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876662 | |||||||
chr3:14876665 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0011g0340 |
2 | HG00673.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2659-3907C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876665 | |||||||
chr3:14876886 | G | A | 4 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0002t0001g0239 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2659-3686G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876886 | |||||||
chr3:14876916 | C | T | 33 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2659-3656C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876916 | |||||||
chr3:14876977 | A | G | 25 | a0001c0001t0001g0279 a0001c0002t0001g0228 a0001c0002t0001g0259 others(22): Show |
25 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2659-3595A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876977 | |||||||
chr3:14876999 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2659-3573C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14876999 | |||||||
chr3:14877184 | C | T | 8 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0001c0002t0001g0015 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.2659-3388C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877184 | |||||||
chr3:14877269 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG00642.hp2 HG00733.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2659-3303C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877269 | |||||||
chr3:14877345 | C | T | 1 | a0001c0002t0001g0015 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2659-3227C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877345 | |||||||
chr3:14877479 | G | A | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-3093G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877479 | |||||||
chr3:14877566 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2659-3006G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877566 | |||||||
chr3:14877602 | T | G | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2659-2970T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877602 | |||||||
chr3:14877652 | A | G | 4 | a0001c0002t0001g0261 a0001c0002t0002g0262 a0001c0002t0010g0263 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2659-2920A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877652 | |||||||
chr3:14877707 | G | T | 1 | a0001c0001t0002g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2659-2865G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877707 | |||||||
chr3:14877747 | A | G | 103 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(100): Show |
103 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2659-2825A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877747 | |||||||
chr3:14877790 | C | T | 1 | a0023c0028t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2659-2782C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877790 | |||||||
chr3:14877845 | A | G | 100 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2659-2727A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877845 | |||||||
chr3:14877871 | A | G | 100 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2659-2701A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877871 | |||||||
chr3:14877933 | G | T | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2659-2639G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14877933 | |||||||
chr3:14878113 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2659-2459C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878113 | |||||||
chr3:14878139 | G | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2659-2433G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878139 | |||||||
chr3:14878278 | G | GA | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2659-2291dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14878278 | ||||||
chr3:14878316 | G | A | 5 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(2): Show |
5 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2659-2256G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878316 | |||||||
chr3:14878329 | A | G | 1 | a0007c0012t0001g0060 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2659-2243A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878329 | |||||||
chr3:14878489 | C | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-2083C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878489 | |||||||
chr3:14878503 | G | T | 97 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2659-2069G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878503 | |||||||
chr3:14878548 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(53): Show |
58 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2659-2024G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878548 | |||||||
chr3:14878555 | A | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.2659-2017A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878555 | |||||||
chr3:14878598 | G | A | 98 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(95): Show |
98 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2659-1974G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878598 | |||||||
chr3:14878637 | G | A | 1 | a0001c0002t0001g0275 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2659-1935G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878637 | |||||||
chr3:14878673 | G | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0003c0005t0001g0061 |
3 | HG03130.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2659-1899G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878673 | |||||||
chr3:14878683 | TAA | T | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2659-1888_2659-188 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878683 | |||||||
chr3:14878725 | C | CT | 100 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0093 others(97): Show |
100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2659-1829dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14878725 | ||||||
chr3:14878725 | C | CTT | 7 | a0001c0002t0001g0173 a0001c0002t0001g0261 a0001c0002t0001g0275 others(4): Show |
7 | HG02135.hp1 HG03688.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.2659-1830_2659-182 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 14878725 | ||||||
chr3:14878769 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2659-1803A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878769 | |||||||
chr3:14878782 | A | G | 5 | a0001c0002t0001g0156 a0001c0002t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG02738.hp1 HG03688.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.2659-1790A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878782 | |||||||
chr3:14878856 | A | G | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2659-1716A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878856 | |||||||
chr3:14878898 | A | G | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2659-1674A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878898 | |||||||
chr3:14878927 | T | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0128 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2659-1645T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878927 | |||||||
chr3:14878946 | T | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2659-1626T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14878946 | |||||||
chr3:14879043 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2659-1529G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14879043 | |||||||
chr3:14879242 | C | T | 11 | a0001c0001t0001g0296 a0001c0001t0001g0309 a0001c0001t0001g0313 others(8): Show |
11 | HG02015.hp2 NA18940.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.2659-1330C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14879242 | |||||||
chr3:14879277 | C | T | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2659-1295C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14879277 | |||||||
chr3:14879307 | T | G | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2659-1265T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14879307 | |||||||
chr3:14879326 | C | T | 2 | a0015c0038t0001g0258 a0017c0037t0001g0253 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2659-1246C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14879326 | |||||||
chr3:14879795 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0031t0001g0066 others(2): Show |
5 | HG02738.hp2 HG03195.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.2659-777C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14879795 | |||||||
chr3:14879804 | G | A | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2659-768G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14879804 | |||||||
chr3:14880228 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2659-344C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14880228 | |||||||
chr3:14880423 | G | T | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2659-149G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14880423 | |||||||
chr3:14880484 | T | C | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2659-88T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14880484 | |||||||
chr3:14880500 | C | T | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2659-72C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14880500 | |||||||
chr3:14880542 | C | A | 1 | a0001c0002t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2659-30C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 2/19 | chr3 | 14880542 | |||||||
chr3:14880938 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2748+166G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14880938 | |||||||
chr3:14881103 | T | C | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2748+331T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881103 | |||||||
chr3:14881295 | A | ACAGCCTG others(5): Show |
316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(313): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2748+526_2748+527i others(14): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14881295 | ||||||
chr3:14881320 | C | G | 3 | a0001c0002t0001g0010 a0001c0002t0001g0012 a0023c0028t0001g0011 |
3 | HG02055.hp2 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2748+548C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881320 | |||||||
chr3:14881344 | C | G | 1 | a0006c0033t0001g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2748+572C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881344 | |||||||
chr3:14881723 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2748+951C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881723 | |||||||
chr3:14881755 | C | G | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2748+983C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881755 | |||||||
chr3:14881794 | C | G | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2748+1022C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881794 | |||||||
chr3:14881889 | A | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2748+1117A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881889 | |||||||
chr3:14881988 | A | G | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2748+1216A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881988 | |||||||
chr3:14881999 | G | A | 3 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 |
3 | HG02717.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2748+1227G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14881999 | |||||||
chr3:14882021 | G | A | 2 | a0015c0038t0001g0258 a0017c0037t0001g0253 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2748+1249G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882021 | |||||||
chr3:14882025 | A | G | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2748+1253A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882025 | |||||||
chr3:14882420 | A | G | 2 | a0002c0003t0001g0214 a0002c0003t0001g0217 |
2 | NA19009.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2748+1648A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882420 | |||||||
chr3:14882463 | C | T | 59 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2748+1691C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882463 | |||||||
chr3:14882524 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2748+1752C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882524 | |||||||
chr3:14882697 | G | GA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0154 others(59): Show |
64 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2748+1942dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14882697 | ||||||
chr3:14882697 | GA | G | 98 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(95): Show |
98 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2748+1942delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14882697 | ||||||
chr3:14882851 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0282 others(53): Show |
58 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2748+2079A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882851 | |||||||
chr3:14882887 | T | C | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2748+2115T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882887 | |||||||
chr3:14882997 | C | T | 3 | a0003c0005t0001g0003 a0003c0005t0001g0005 a0003c0017t0001g0004 |
3 | HG01081.hp1 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2748+2225C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14882997 | |||||||
chr3:14883010 | A | G | 1 | a0001c0001t0011g0340 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2748+2238A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883010 | |||||||
chr3:14883017 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0205 a0001c0001t0015g0022 |
3 | HG02572.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2748+2245C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883017 | |||||||
chr3:14883107 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2748+2335A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883107 | |||||||
chr3:14883114 | T | C | 6 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2748+2342T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883114 | |||||||
chr3:14883387 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2748+2615C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883387 | |||||||
chr3:14883451 | C | G | 2 | a0001c0001t0001g0134 a0004c0006t0001g0078 |
2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2748+2679C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883451 | |||||||
chr3:14883749 | G | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2748+2977G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883749 | |||||||
chr3:14883938 | G | A | 4 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(1): Show |
4 | HG02717.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2748+3166G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883938 | |||||||
chr3:14883948 | A | G | 1 | a0001c0002t0001g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2748+3176A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14883948 | |||||||
chr3:14884061 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0056 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.2748+3289A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884061 | |||||||
chr3:14884187 | CCTT | C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0326 |
3 | NA18982.hp1 NA18999.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2748+3418_2748+342 others(7): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14884187 | ||||||
chr3:14884252 | A | T | 1 | a0001c0001t0003g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2748+3480A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884252 | |||||||
chr3:14884314 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0153 others(56): Show |
61 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2748+3542A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884314 | |||||||
chr3:14884369 | G | A | 55 | a0001c0001t0001g0025 a0001c0001t0001g0130 a0001c0001t0001g0181 others(52): Show |
55 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2748+3597G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884369 | |||||||
chr3:14884548 | T | G | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2748+3776T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884548 | |||||||
chr3:14884686 | A | G | 1 | a0002c0003t0001g0200 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2748+3914A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884686 | |||||||
chr3:14884696 | G | A | 35 | a0001c0001t0001g0279 a0001c0002t0001g0156 a0001c0002t0001g0171 others(32): Show |
35 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2748+3924G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884696 | |||||||
chr3:14884722 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2748+3950C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884722 | |||||||
chr3:14884780 | C | T | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2748+4008C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884780 | |||||||
chr3:14884823 | C | G | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2748+4051C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884823 | |||||||
chr3:14884844 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.2748+4072T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884844 | |||||||
chr3:14884884 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG00735.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2748+4112C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884884 | |||||||
chr3:14884975 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(219): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2748+4203G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884975 | |||||||
chr3:14884997 | C | T | 35 | a0001c0002t0001g0156 a0001c0002t0001g0171 a0001c0002t0001g0172 others(32): Show |
35 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2748+4225C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14884997 | |||||||
chr3:14885328 | G | A | 1 | a0001c0002t0001g0204 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2748+4556G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885328 | |||||||
chr3:14885366 | T | C | 36 | a0001c0002t0001g0156 a0001c0002t0001g0171 a0001c0002t0001g0172 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.2748+4594T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885366 | |||||||
chr3:14885381 | T | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0130 others(51): Show |
56 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.2748+4609T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885381 | |||||||
chr3:14885448 | A | G | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2748+4676A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885448 | |||||||
chr3:14885476 | C | G | 13 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0084 others(10): Show |
13 | HG00140.hp2 HG01099.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.2748+4704C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885476 | |||||||
chr3:14885534 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2748+4762C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885534 | |||||||
chr3:14885722 | A | C | 6 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2748+4950A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885722 | |||||||
chr3:14885829 | A | G | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2748+5057A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14885829 | |||||||
chr3:14886140 | C | G | 8 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2748+5368C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886140 | |||||||
chr3:14886188 | C | T | 27 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0104 others(24): Show |
27 | HG01192.hp1 HG01934.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.2748+5416C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886188 | |||||||
chr3:14886296 | C | T | 11 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(8): Show |
11 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748+5524C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886296 | |||||||
chr3:14886374 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2748+5602T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886374 | |||||||
chr3:14886494 | C | T | 1 | a0001c0002t0001g0275 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2748+5722C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886494 | |||||||
chr3:14886522 | A | G | 11 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(8): Show |
11 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748+5750A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886522 | |||||||
chr3:14886570 | G | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2748+5798G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886570 | |||||||
chr3:14886625 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2748+5853C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886625 | |||||||
chr3:14886645 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2748+5873C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886645 | |||||||
chr3:14886804 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0003c0005t0001g0061 |
3 | HG03130.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2748+6032G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886804 | |||||||
chr3:14886828 | T | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2748+6056T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886828 | |||||||
chr3:14886901 | T | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2748+6129T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886901 | |||||||
chr3:14886936 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0302 |
2 | NA18947.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2748+6164A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14886936 | |||||||
chr3:14887150 | C | G | 50 | a0001c0001t0001g0185 a0002c0003t0001g0034 a0002c0003t0001g0035 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2748+6378C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887150 | |||||||
chr3:14887222 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0130 others(50): Show |
55 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2748+6450A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887222 | |||||||
chr3:14887264 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2748+6492G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887264 | |||||||
chr3:14887375 | C | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2748+6603C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887375 | |||||||
chr3:14887381 | A | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2748+6609A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887381 | |||||||
chr3:14887409 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2748+6637G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887409 | |||||||
chr3:14887484 | T | C | 2 | a0005c0004t0001g0037 a0005c0004t0001g0040 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2748+6712T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887484 | |||||||
chr3:14887616 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2748+6844T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887616 | |||||||
chr3:14887746 | G | A | 1 | a0002c0003t0001g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2748+6974G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887746 | |||||||
chr3:14887798 | G | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2748+7026G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887798 | |||||||
chr3:14887814 | A | G | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2748+7042A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14887814 | |||||||
chr3:14888002 | C | CA | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2748+7241dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14888002 | ||||||
chr3:14888154 | A | AGT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2748+7383_2748+738 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14888154 | ||||||
chr3:14888168 | G | GAA | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2748+7408_2748+740 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14888168 | ||||||
chr3:14888185 | A | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2748+7413A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888185 | |||||||
chr3:14888185 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0056 others(73): Show |
78 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.2748+7413A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888185 | |||||||
chr3:14888200 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2748+7428G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888200 | |||||||
chr3:14888268 | G | A | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2748+7496G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888268 | |||||||
chr3:14888299 | G | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2748+7527G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888299 | |||||||
chr3:14888357 | A | G | 5 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(2): Show |
5 | HG02717.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2748+7585A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888357 | |||||||
chr3:14888434 | G | C | 1 | a0002c0003t0001g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2748+7662G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888434 | |||||||
chr3:14888771 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2748+7999G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888771 | |||||||
chr3:14888875 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2748+8103A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888875 | |||||||
chr3:14888888 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2748+8116C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888888 | |||||||
chr3:14888899 | G | GA | 5 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(2): Show |
5 | HG02717.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2748+8131dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14888899 | ||||||
chr3:14888910 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2748+8138C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14888910 | |||||||
chr3:14889030 | C | T | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2748+8258C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889030 | |||||||
chr3:14889126 | C | A | 1 | a0017c0037t0001g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2748+8354C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889126 | |||||||
chr3:14889127 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2748+8355A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889127 | |||||||
chr3:14889160 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-8349A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889160 | |||||||
chr3:14889171 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2749-8338G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889171 | |||||||
chr3:14889175 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0338 |
2 | NA18940.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2749-8334G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889175 | |||||||
chr3:14889435 | G | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0339 |
3 | NA18946.hp2 NA18950.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2749-8074G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889435 | |||||||
chr3:14889446 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2749-8063T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889446 | |||||||
chr3:14889465 | C | T | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2749-8044C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889465 | |||||||
chr3:14889480 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2749-8029G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889480 | |||||||
chr3:14889611 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2749-7898T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889611 | |||||||
chr3:14889823 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2749-7686A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889823 | |||||||
chr3:14889857 | CT | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0147 others(2): Show |
5 | HG03130.hp2 HG03491.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.2749-7643delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14889857 | ||||||
chr3:14889866 | T | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(231): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2749-7643T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14889866 | |||||||
chr3:14890118 | C | T | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2749-7391C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890118 | |||||||
chr3:14890283 | A | G | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2749-7226A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890283 | |||||||
chr3:14890304 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2749-7205T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890304 | |||||||
chr3:14890338 | G | A | 1 | a0001c0001t0015g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2749-7171G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890338 | |||||||
chr3:14890378 | C | T | 1 | a0006c0033t0001g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2749-7131C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890378 | |||||||
chr3:14890649 | A | G | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2749-6860A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890649 | |||||||
chr3:14890832 | C | T | 6 | a0001c0001t0001g0185 a0001c0001t0001g0303 a0001c0001t0001g0306 others(3): Show |
6 | HG00642.hp1 HG01123.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2749-6677C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890832 | |||||||
chr3:14890900 | C | T | 1 | a0002c0003t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2749-6609C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890900 | |||||||
chr3:14890955 | A | T | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-6554A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890955 | |||||||
chr3:14890995 | A | G | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-6514A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14890995 | |||||||
chr3:14891038 | G | A | 1 | a0001c0002t0014g0160 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2749-6471G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891038 | |||||||
chr3:14891039 | T | G | 6 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0274 others(3): Show |
6 | NA18747.hp2 NA18945.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.2749-6470T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891039 | |||||||
chr3:14891197 | G | A | 1 | a0001c0022t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2749-6312G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891197 | |||||||
chr3:14891235 | C | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0084 |
2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2749-6274C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891235 | |||||||
chr3:14891356 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2749-6153T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891356 | |||||||
chr3:14891590 | G | A | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2749-5919G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891590 | |||||||
chr3:14891715 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.2749-5794T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891715 | |||||||
chr3:14891818 | G | A | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2749-5691G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891818 | |||||||
chr3:14891831 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2749-5678T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14891831 | |||||||
chr3:14891870 | GC | G | 6 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2749-5634delC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14891870 | ||||||
chr3:14892012 | T | C | 3 | a0002c0003t0001g0183 a0002c0003t0001g0184 a0002c0003t0002g0182 |
3 | NA18957.hp2 NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2749-5497T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892012 | |||||||
chr3:14892355 | C | G | 1 | a0002c0003t0001g0234 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2749-5154C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892355 | |||||||
chr3:14892406 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2749-5103G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892406 | |||||||
chr3:14892569 | G | A | 5 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(2): Show |
5 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2749-4940G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892569 | |||||||
chr3:14892633 | C | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2749-4876C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892633 | |||||||
chr3:14892734 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2749-4775A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892734 | |||||||
chr3:14892819 | CA | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2749-4678delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14892819 | ||||||
chr3:14892900 | A | G | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2749-4609A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892900 | |||||||
chr3:14892930 | A | G | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-4579A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14892930 | |||||||
chr3:14893169 | C | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2749-4340C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893169 | |||||||
chr3:14893294 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2749-4215G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893294 | |||||||
chr3:14893320 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2749-4189A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893320 | |||||||
chr3:14893330 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2749-4179G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893330 | |||||||
chr3:14893427 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2749-4082C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893427 | |||||||
chr3:14893489 | G | A | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-4020G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893489 | |||||||
chr3:14893682 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2749-3827C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893682 | |||||||
chr3:14893752 | C | CT | 60 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0045 others(57): Show |
60 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.2749-3737dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14893752 | ||||||
chr3:14893752 | C | CTT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2749-3738_2749-373 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14893752 | ||||||
chr3:14893752 | C | CTTT | 15 | a0001c0001t0001g0079 a0001c0001t0001g0123 a0001c0001t0001g0130 others(12): Show |
15 | HG00642.hp2 HG00673.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.2749-3739_2749-373 others(7): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14893752 | ||||||
chr3:14893810 | A | G | 24 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0104 others(21): Show |
24 | HG01192.hp1 HG01934.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2749-3699A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893810 | |||||||
chr3:14893891 | T | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2749-3618T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14893891 | |||||||
chr3:14894054 | G | T | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2749-3455G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894054 | |||||||
chr3:14894186 | A | G | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2749-3323A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894186 | |||||||
chr3:14894253 | A | T | 1 | a0001c0001t0002g0031 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2749-3256A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894253 | |||||||
chr3:14894274 | G | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0323 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2749-3235G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894274 | |||||||
chr3:14894341 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0031t0001g0066 others(1): Show |
4 | HG02738.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2749-3168T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894341 | |||||||
chr3:14894422 | G | T | 38 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2749-3087G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894422 | |||||||
chr3:14894505 | CT | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(239): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2749-2984delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14894505 | ||||||
chr3:14894523 | T | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(310): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2749-2986T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894523 | |||||||
chr3:14894589 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2749-2920C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894589 | |||||||
chr3:14894674 | AT | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2749-2816delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14894674 | ||||||
chr3:14894716 | G | A | 38 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2749-2793G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14894716 | |||||||
chr3:14894924 | C | CTTG | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2749-2583_2749-258 others(7): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14894924 | ||||||
chr3:14895021 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-2488T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895021 | |||||||
chr3:14895095 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2749-2414T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895095 | |||||||
chr3:14895231 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2749-2278C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895231 | |||||||
chr3:14895328 | A | G | 5 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(2): Show |
5 | HG02717.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2749-2181A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895328 | |||||||
chr3:14895375 | T | G | 37 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0043 others(34): Show |
37 | HG00099.hp1 HG00673.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.2749-2134T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895375 | |||||||
chr3:14895439 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-2070G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895439 | |||||||
chr3:14895519 | G | T | 5 | a0002c0003t0001g0202 a0002c0007t0001g0240 a0002c0007t0001g0241 others(2): Show |
5 | NA18939.hp1 NA18953.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.2749-1990G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895519 | |||||||
chr3:14895540 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-1969T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895540 | |||||||
chr3:14895559 | T | C | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2749-1950T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895559 | |||||||
chr3:14895583 | T | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
6 | HG00673.hp1 NA18612.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.2749-1926T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895583 | |||||||
chr3:14895588 | T | G | 1 | a0002c0003t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2749-1921T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895588 | |||||||
chr3:14895667 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-1842A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895667 | |||||||
chr3:14895753 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-1756A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895753 | |||||||
chr3:14895835 | A | T | 6 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2749-1674A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895835 | |||||||
chr3:14895893 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-1616G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895893 | |||||||
chr3:14895900 | A | G | 1 | a0001c0002t0001g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2749-1609A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895900 | |||||||
chr3:14895928 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2749-1581C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14895928 | |||||||
chr3:14896014 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2749-1495A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896014 | |||||||
chr3:14896034 | A | G | 1 | a0013c0032t0001g0222 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2749-1475A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896034 | |||||||
chr3:14896270 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0130 others(49): Show |
54 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2749-1239A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896270 | |||||||
chr3:14896301 | T | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2749-1208T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896301 | |||||||
chr3:14896336 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2749-1173C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896336 | |||||||
chr3:14896337 | G | A | 1 | a0001c0001t0016g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2749-1172G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896337 | |||||||
chr3:14896471 | CT | C | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-1022delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 14896471 | ||||||
chr3:14896483 | T | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2749-1026T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896483 | |||||||
chr3:14896484 | T | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2749-1025T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896484 | |||||||
chr3:14896493 | G | A | 2 | a0001c0001t0001g0013 a0018c0040t0001g0057 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2749-1016G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896493 | |||||||
chr3:14896517 | G | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2749-992G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896517 | |||||||
chr3:14896523 | T | C | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-986T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896523 | |||||||
chr3:14896540 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.2749-969G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896540 | |||||||
chr3:14896575 | A | T | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2749-934A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896575 | |||||||
chr3:14896643 | G | C | 3 | a0003c0009t0001g0250 a0003c0009t0001g0251 a0003c0018t0001g0249 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2749-866G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896643 | |||||||
chr3:14896703 | T | G | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-806T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896703 | |||||||
chr3:14896704 | C | T | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-805C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896704 | |||||||
chr3:14896887 | G | T | 1 | a0003c0005t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2749-622G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896887 | |||||||
chr3:14896950 | C | T | 1 | a0001c0001t0017g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2749-559C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14896950 | |||||||
chr3:14897280 | C | T | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2749-229C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14897280 | |||||||
chr3:14897333 | G | T | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2749-176G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14897333 | |||||||
chr3:14897439 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2749-70G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14897439 | |||||||
chr3:14897497 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2749-12T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 4/19 | chr3 | 14897497 | |||||||
chr3:14897691 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2909+22G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 5/19 | chr3 | 14897691 | |||||||
chr3:14897802 | T | C | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2909+133T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 5/19 | chr3 | 14897802 | |||||||
chr3:14897830 | G | A | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2910-109G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 5/19 | chr3 | 14897830 | |||||||
chr3:14897857 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2910-82G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 5/19 | chr3 | 14897857 | |||||||
chr3:14898172 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3066+77G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/19 | chr3 | 14898172 | |||||||
chr3:14898279 | G | T | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.3066+184G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/19 | chr3 | 14898279 | |||||||
chr3:14898307 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG01109.hp2 HG01168.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3066+212G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/19 | chr3 | 14898307 | |||||||
chr3:14898568 | G | A | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3067-171G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/19 | chr3 | 14898568 | |||||||
chr3:14898589 | G | A | 3 | a0002c0003t0001g0183 a0002c0003t0001g0184 a0002c0003t0002g0182 |
3 | NA18957.hp2 NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3067-150G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/19 | chr3 | 14898589 | |||||||
chr3:14898591 | A | G | 39 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.3067-148A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 6/19 | chr3 | 14898591 | |||||||
chr3:14899089 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3154+263C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899089 | |||||||
chr3:14899104 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3154+278T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899104 | |||||||
chr3:14899185 | C | T | 2 | a0001c0001t0001g0013 a0018c0040t0001g0057 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3154+359C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899185 | |||||||
chr3:14899248 | A | T | 5 | a0001c0001t0001g0282 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG00621.hp2 NA18943.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.3154+422A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899248 | |||||||
chr3:14899314 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3154+488C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899314 | |||||||
chr3:14899335 | G | A | 1 | a0001c0002t0001g0113 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3154+509G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899335 | |||||||
chr3:14899645 | G | T | 38 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.3155-758G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899645 | |||||||
chr3:14899940 | C | A | 95 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3155-463C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899940 | |||||||
chr3:14899977 | A | T | 50 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.3155-426A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14899977 | |||||||
chr3:14900041 | T | C | 1 | a0002c0003t0001g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3155-362T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14900041 | |||||||
chr3:14900060 | C | A | 2 | a0001c0002t0001g0175 a0001c0002t0001g0239 |
2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3155-343C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14900060 | |||||||
chr3:14900108 | T | C | 95 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3155-295T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14900108 | |||||||
chr3:14900135 | G | A | 1 | a0002c0003t0002g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3155-268G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14900135 | |||||||
chr3:14900286 | G | C | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3155-117G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14900286 | |||||||
chr3:14900291 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3155-112A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14900291 | |||||||
chr3:14900348 | G | A | 1 | a0001c0001t0001g0339 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3155-55G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 7/19 | chr3 | 14900348 | |||||||
chr3:14900517 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.3205+64T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 8/19 | chr3 | 14900517 | |||||||
chr3:14900851 | C | G | 1 | a0001c0013t0001g0304 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3206-152C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 8/19 | chr3 | 14900851 | |||||||
chr3:14900940 | A | G | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3206-63A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 8/19 | chr3 | 14900940 | |||||||
chr3:14900942 | A | G | 2 | a0001c0002t0005g0118 a0001c0002t0005g0119 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.3206-61A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 8/19 | chr3 | 14900942 | |||||||
chr3:14901128 | C | T | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3264+67C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14901128 | |||||||
chr3:14901168 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3264+107G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14901168 | |||||||
chr3:14901264 | T | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0147 a0001c0001t0001g0235 others(1): Show |
4 | NA18982.hp2 NA19004.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.3264+203T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14901264 | |||||||
chr3:14901546 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3264+485C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14901546 | |||||||
chr3:14901640 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3264+579C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14901640 | |||||||
chr3:14901876 | G | A | 1 | a0004c0006t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3264+815G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14901876 | |||||||
chr3:14902064 | T | A | 5 | a0001c0030t0001g0230 a0003c0009t0001g0250 a0003c0009t0001g0251 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3264+1003T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14902064 | |||||||
chr3:14902070 | T | G | 95 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3264+1009T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14902070 | |||||||
chr3:14902071 | C | T | 95 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3264+1010C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14902071 | |||||||
chr3:14902281 | T | TA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.3264+1239dupA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 14902281 | ||||||
chr3:14902281 | TA | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0114 a0001c0001t0001g0307 others(6): Show |
9 | HG01169.hp1 HG01517.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.3264+1239delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 14902281 | ||||||
chr3:14902458 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.3264+1397G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14902458 | |||||||
chr3:14902577 | C | T | 2 | a0001c0001t0001g0051 a0003c0005t0001g0061 |
2 | HG03486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3264+1516C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14902577 | |||||||
chr3:14902926 | T | C | 1 | a0023c0028t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3264+1865T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14902926 | |||||||
chr3:14902944 | G | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0084 others(9): Show |
12 | HG00140.hp2 HG01123.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.3264+1883G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14902944 | |||||||
chr3:14903039 | T | C | 1 | a0021c0024t0001g0281 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3264+1978T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903039 | |||||||
chr3:14903094 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3264+2033T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903094 | |||||||
chr3:14903104 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0293 a0001c0001t0001g0322 others(4): Show |
9 | HG00140.hp1 HG00733.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.3264+2043C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903104 | |||||||
chr3:14903267 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3264+2206G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903267 | |||||||
chr3:14903354 | T | TTTA | 7 | a0001c0001t0001g0083 a0001c0001t0001g0115 a0001c0001t0002g0158 others(4): Show |
7 | HG01978.hp2 HG03704.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.3264+2313_3264+231 others(7): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 14903354 | ||||||
chr3:14903354 | T | TTTATTA | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3264+2310_3264+231 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 14903354 | ||||||
chr3:14903443 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0205 a0001c0001t0015g0022 |
3 | HG02572.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3264+2382G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903443 | |||||||
chr3:14903477 | A | T | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3264+2416A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903477 | |||||||
chr3:14903525 | C | T | 25 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0104 others(22): Show |
25 | HG01192.hp1 HG01934.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.3264+2464C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903525 | |||||||
chr3:14903574 | T | A | 95 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3264+2513T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903574 | |||||||
chr3:14903651 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3264+2590G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903651 | |||||||
chr3:14903679 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3264+2618G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14903679 | |||||||
chr3:14904002 | G | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0084 others(9): Show |
12 | HG00140.hp2 HG01123.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.3264+2941G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904002 | |||||||
chr3:14904149 | T | G | 95 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3264+3088T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904149 | |||||||
chr3:14904218 | T | C | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3264+3157T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904218 | |||||||
chr3:14904237 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3264+3176C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904237 | |||||||
chr3:14904238 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | NA18946.hp1 NA18992.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264+3177G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904238 | |||||||
chr3:14904324 | C | T | 2 | a0001c0014t0001g0018 a0001c0014t0001g0019 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3264+3263C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904324 | |||||||
chr3:14904438 | G | A | 37 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0043 others(34): Show |
37 | HG00099.hp1 HG00673.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.3265-3202G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904438 | |||||||
chr3:14904450 | G | C | 29 | a0001c0002t0001g0228 a0001c0002t0001g0232 a0001c0002t0001g0233 others(26): Show |
29 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.3265-3190G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904450 | |||||||
chr3:14904505 | G | GGTGTGT | 95 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.3265-3126_3265-312 others(10): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 14904505 | ||||||
chr3:14904505 | G | GGTGTGTG others(1): Show |
219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3265-3128_3265-312 others(12): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 14904505 | ||||||
chr3:14904610 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3265-3030G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904610 | |||||||
chr3:14904612 | C | A | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3265-3028C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904612 | |||||||
chr3:14904746 | G | A | 2 | a0001c0002t0001g0259 a0011c0020t0002g0269 |
2 | HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.3265-2894G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904746 | |||||||
chr3:14904939 | C | T | 2 | a0001c0002t0001g0259 a0011c0020t0002g0269 |
2 | HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.3265-2701C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14904939 | |||||||
chr3:14905037 | A | G | 1 | a0021c0024t0001g0281 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3265-2603A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905037 | |||||||
chr3:14905075 | T | A | 3 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0014g0160 |
3 | HG01106.hp2 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3265-2565T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905075 | |||||||
chr3:14905086 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0002g0107 a0014c0015t0001g0229 |
3 | HG02559.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3265-2554G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905086 | |||||||
chr3:14905118 | T | G | 5 | a0002c0003t0001g0210 a0002c0003t0001g0211 a0002c0003t0001g0212 others(2): Show |
5 | NA18960.hp1 NA19010.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.3265-2522T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905118 | |||||||
chr3:14905344 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3265-2296G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905344 | |||||||
chr3:14905626 | C | G | 89 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(86): Show |
89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3265-2014C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905626 | |||||||
chr3:14905630 | C | T | 33 | a0001c0002t0001g0228 a0001c0002t0001g0259 a0001c0002t0001g0260 others(30): Show |
33 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.3265-2010C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905630 | |||||||
chr3:14905861 | C | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0085 others(3): Show |
6 | HG02027.hp2 NA18960.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.3265-1779C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905861 | |||||||
chr3:14905917 | A | G | 48 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(45): Show |
48 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3265-1723A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905917 | |||||||
chr3:14905958 | A | C | 29 | a0001c0002t0001g0228 a0001c0002t0001g0232 a0001c0002t0001g0233 others(26): Show |
29 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.3265-1682A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14905958 | |||||||
chr3:14906032 | T | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0052 others(15): Show |
18 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.3265-1608T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906032 | |||||||
chr3:14906046 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3265-1594G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906046 | |||||||
chr3:14906113 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3265-1527T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906113 | |||||||
chr3:14906148 | A | C | 1 | a0001c0001t0001g0312 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3265-1492A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906148 | |||||||
chr3:14906156 | G | C | 1 | a0001c0001t0004g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3265-1484G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906156 | |||||||
chr3:14906220 | A | G | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3265-1420A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906220 | |||||||
chr3:14906303 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3265-1337G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906303 | |||||||
chr3:14906632 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3265-1008G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906632 | |||||||
chr3:14906703 | G | A | 5 | a0001c0001t0001g0238 a0001c0008t0004g0047 a0001c0008t0004g0048 others(2): Show |
5 | HG02717.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3265-937G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906703 | |||||||
chr3:14906850 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3265-790C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14906850 | |||||||
chr3:14907195 | A | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.3265-445A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907195 | |||||||
chr3:14907370 | G | A | 2 | a0001c0001t0001g0013 a0018c0040t0001g0057 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3265-270G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907370 | |||||||
chr3:14907379 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.3265-261G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907379 | |||||||
chr3:14907429 | C | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0130 others(49): Show |
54 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.3265-211C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907429 | |||||||
chr3:14907433 | C | T | 89 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(86): Show |
89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3265-207C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907433 | |||||||
chr3:14907532 | C | T | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3265-108C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907532 | |||||||
chr3:14907583 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3265-57A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907583 | |||||||
chr3:14907595 | G | T | 89 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(86): Show |
89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3265-45G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 9/19 | chr3 | 14907595 | |||||||
chr3:14907761 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3336+50C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14907761 | |||||||
chr3:14908392 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.3336+681C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908392 | |||||||
chr3:14908393 | G | A | 89 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(86): Show |
89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3336+682G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908393 | |||||||
chr3:14908587 | T | C | 2 | a0001c0001t0001g0013 a0018c0040t0001g0057 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3336+876T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908587 | |||||||
chr3:14908625 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0130 others(49): Show |
54 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.3336+914G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908625 | |||||||
chr3:14908772 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0031t0001g0066 others(1): Show |
4 | HG02738.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3336+1061C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908772 | |||||||
chr3:14908854 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0325 |
2 | HG02135.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3336+1143C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908854 | |||||||
chr3:14908921 | A | AATTT | 10 | a0001c0001t0001g0056 a0001c0001t0001g0237 a0001c0001t0001g0327 others(7): Show |
10 | HG01081.hp1 HG01261.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.3336+1238_3336+124 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14908921 | ||||||
chr3:14908921 | AATTT | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0130 others(55): Show |
60 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.3336+1238_3336+124 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14908921 | ||||||
chr3:14908941 | T | C | 1 | a0001c0002t0018g0264 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3336+1230T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908941 | |||||||
chr3:14908945 | T | C | 42 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(39): Show |
42 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.3336+1234T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908945 | |||||||
chr3:14908945 | T | TATTC | 45 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(42): Show |
45 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.3336+1237_3336+123 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14908945 | ||||||
chr3:14908949 | T | C | 96 | a0001c0001t0001g0051 a0001c0001t0001g0074 a0001c0001t0001g0076 others(93): Show |
96 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.3336+1238T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908949 | |||||||
chr3:14908949 | T | TATTC | 33 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0043 others(30): Show |
33 | HG00673.hp2 HG01069.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.3336+1257_3336+126 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14908949 | ||||||
chr3:14908953 | C | T | 8 | a0005c0004t0001g0021 a0005c0004t0001g0036 a0005c0004t0001g0037 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3336+1242C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908953 | |||||||
chr3:14908960 | TCATTCAT others(5): Show |
T | 5 | a0003c0005t0001g0252 a0003c0005t0001g0256 a0003c0005t0006g0254 others(2): Show |
5 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3336+1261_3336+127 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14908960 | ||||||
chr3:14908992 | T | C | 40 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(37): Show |
40 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.3336+1281T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14908992 | |||||||
chr3:14909000 | G | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0322 a0001c0001t0001g0331 others(2): Show |
7 | HG00140.hp1 HG00733.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.3336+1289G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14909000 | |||||||
chr3:14909314 | C | A | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3337-1547C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14909314 | |||||||
chr3:14909761 | CT | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0083 a0001c0001t0001g0114 others(151): Show |
156 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.3337-1084delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14909761 | ||||||
chr3:14909761 | CTT | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0096 others(5): Show |
8 | HG00140.hp2 HG01123.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.3337-1085_3337-108 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14909761 | ||||||
chr3:14909767 | T | C | 2 | a0001c0001t0001g0013 a0018c0040t0001g0057 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3337-1094T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14909767 | |||||||
chr3:14909772 | T | C | 2 | a0001c0001t0001g0013 a0018c0040t0001g0057 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3337-1089T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14909772 | |||||||
chr3:14909972 | G | T | 1 | a0002c0003t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3337-889G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14909972 | |||||||
chr3:14909999 | T | C | 89 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(86): Show |
89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3337-862T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14909999 | |||||||
chr3:14910308 | C | T | 1 | a0004c0010t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3337-553C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14910308 | |||||||
chr3:14910698 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3337-163G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14910698 | |||||||
chr3:14910717 | ATGATTTA others(41): Show |
A | 9 | a0001c0001t0001g0111 a0005c0004t0001g0021 a0005c0004t0001g0036 others(6): Show |
9 | HG02723.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3337-94_3337-47del others(48): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr3 | 14910717 | ||||||
chr3:14910834 | C | T | 48 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0087 others(45): Show |
48 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3337-27C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 10/19 | chr3 | 14910834 | |||||||
chr3:14910940 | G | A | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3405+11G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14910940 | |||||||
chr3:14911019 | T | G | 88 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(85): Show |
88 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.3405+90T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911019 | |||||||
chr3:14911529 | C | G | 1 | a0002c0003t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3405+600C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911529 | |||||||
chr3:14911540 | T | C | 97 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0001c0002t0001g0113 others(94): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.3405+611T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911540 | |||||||
chr3:14911572 | C | T | 4 | a0002c0003t0001g0087 a0002c0003t0001g0226 a0002c0003t0003g0224 others(1): Show |
4 | NA18995.hp1 NA18998.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.3405+643C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911572 | |||||||
chr3:14911578 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0235 |
2 | NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3405+649A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911578 | |||||||
chr3:14911748 | G | A | 1 | a0002c0003t0001g0188 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3405+819G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911748 | |||||||
chr3:14911769 | C | T | 1 | a0023c0028t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3405+840C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911769 | |||||||
chr3:14911834 | AGAG | A | 4 | a0002c0003t0001g0087 a0002c0003t0001g0226 a0002c0003t0003g0224 others(1): Show |
4 | NA18995.hp1 NA18998.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.3405+909_3405+911d others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 14911834 | ||||||
chr3:14911857 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3405+928G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911857 | |||||||
chr3:14911891 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3405+962A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911891 | |||||||
chr3:14911933 | C | T | 91 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0001c0002t0001g0113 others(88): Show |
91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3405+1004C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911933 | |||||||
chr3:14911936 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3405+1007A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911936 | |||||||
chr3:14911954 | G | A | 1 | a0001c0002t0001g0277 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3405+1025G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14911954 | |||||||
chr3:14912139 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3405+1210C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912139 | |||||||
chr3:14912140 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3405+1211C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912140 | |||||||
chr3:14912175 | G | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.3405+1246G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912175 | |||||||
chr3:14912429 | CA | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0130 others(49): Show |
54 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.3405+1501delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912429 | |||||||
chr3:14912512 | A | C | 50 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0002c0003t0001g0034 others(47): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.3405+1583A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912512 | |||||||
chr3:14912539 | G | A | 91 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0001c0002t0001g0113 others(88): Show |
91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3405+1610G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912539 | |||||||
chr3:14912627 | T | C | 2 | a0002c0003t0001g0159 a0002c0003t0001g0197 |
2 | HG02698.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3405+1698T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912627 | |||||||
chr3:14912746 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3405+1817G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912746 | |||||||
chr3:14912894 | G | C | 12 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0084 others(9): Show |
12 | HG00140.hp2 HG01123.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.3405+1965G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912894 | |||||||
chr3:14912904 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.3405+1975C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14912904 | |||||||
chr3:14913042 | A | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.3405+2113A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913042 | |||||||
chr3:14913074 | A | G | 91 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0001c0002t0001g0113 others(88): Show |
91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3405+2145A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913074 | |||||||
chr3:14913076 | A | G | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3405+2147A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913076 | |||||||
chr3:14913121 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3405+2192T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913121 | |||||||
chr3:14913166 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.3405+2237A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913166 | |||||||
chr3:14913421 | T | C | 1 | a0001c0002t0002g0265 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3405+2492T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913421 | |||||||
chr3:14913458 | A | G | 60 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0001c0002t0001g0113 others(57): Show |
60 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.3405+2529A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913458 | |||||||
chr3:14913839 | C | G | 1 | a0001c0001t0012g0032 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3405+2910C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913839 | |||||||
chr3:14913892 | C | T | 4 | a0001c0002t0001g0261 a0001c0002t0002g0262 a0001c0002t0010g0263 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.3405+2963C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913892 | |||||||
chr3:14913945 | T | TC | 41 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.3405+3022dupC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 14913945 | ||||||
chr3:14913950 | C | G | 12 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0002c0003t0001g0177 others(9): Show |
12 | HG01934.hp2 NA18747.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.3405+3021C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14913950 | |||||||
chr3:14914098 | A | C | 25 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0104 others(22): Show |
25 | HG01192.hp1 HG01934.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.3406-3151A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914098 | |||||||
chr3:14914108 | A | T | 41 | a0001c0002t0001g0113 a0001c0002t0001g0156 a0001c0002t0001g0171 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.3406-3141A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914108 | |||||||
chr3:14914144 | G | A | 1 | a0010c0025t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3406-3105G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914144 | |||||||
chr3:14914167 | G | A | 1 | a0018c0040t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3406-3082G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914167 | |||||||
chr3:14914194 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.3406-3055A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914194 | |||||||
chr3:14914380 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3406-2869C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914380 | |||||||
chr3:14914477 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3406-2772C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914477 | |||||||
chr3:14914732 | C | T | 1 | a0001c0001t0016g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3406-2517C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914732 | |||||||
chr3:14914824 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0004g0120 a0001c0001t0004g0247 |
3 | HG02486.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3406-2425G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14914824 | |||||||
chr3:14915002 | T | C | 1 | a0006c0011t0001g0006 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3406-2247T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14915002 | |||||||
chr3:14915316 | GCT | G | 29 | a0001c0002t0001g0228 a0001c0002t0001g0232 a0001c0002t0001g0233 others(26): Show |
29 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.3406-1930_3406-192 others(6): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 14915316 | ||||||
chr3:14915358 | C | T | 1 | a0001c0001t0016g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3406-1891C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14915358 | |||||||
chr3:14915553 | C | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0043 others(35): Show |
38 | HG00099.hp1 HG00673.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.3406-1696C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14915553 | |||||||
chr3:14915556 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0331 a0001c0001t0001g0332 others(1): Show |
6 | HG00140.hp1 HG00733.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.3406-1693T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14915556 | |||||||
chr3:14915698 | C | T | 10 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0096 others(7): Show |
10 | HG01123.hp2 HG01978.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.3406-1551C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14915698 | |||||||
chr3:14915870 | G | A | 11 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0084 others(8): Show |
11 | HG00140.hp2 HG01123.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.3406-1379G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14915870 | |||||||
chr3:14916161 | A | G | 91 | a0001c0001t0001g0140 a0001c0001t0001g0279 a0001c0002t0001g0113 others(88): Show |
91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3406-1088A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916161 | |||||||
chr3:14916215 | T | C | 1 | a0007c0012t0001g0059 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3406-1034T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916215 | |||||||
chr3:14916269 | C | T | 2 | a0003c0005t0001g0003 a0003c0005t0001g0005 |
2 | HG01081.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3406-980C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916269 | |||||||
chr3:14916278 | A | G | 1 | a0004c0006t0001g0044 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3406-971A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916278 | |||||||
chr3:14916335 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0295 |
2 | NA18957.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.3406-914C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916335 | |||||||
chr3:14916336 | G | A | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3406-913G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916336 | |||||||
chr3:14916456 | C | T | 91 | a0001c0001t0001g0070 a0001c0001t0001g0140 a0001c0001t0001g0279 others(88): Show |
91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3406-793C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916456 | |||||||
chr3:14916473 | C | T | 1 | a0002c0003t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3406-776C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916473 | |||||||
chr3:14916512 | G | C | 89 | a0001c0001t0001g0070 a0001c0001t0001g0140 a0001c0001t0001g0279 others(86): Show |
89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3406-737G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916512 | |||||||
chr3:14916567 | T | G | 94 | a0001c0001t0001g0070 a0001c0001t0001g0140 a0001c0001t0001g0279 others(91): Show |
94 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.3406-682T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916567 | |||||||
chr3:14916619 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.3406-630G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916619 | |||||||
chr3:14916829 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | NA18946.hp1 NA18992.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.3406-420G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14916829 | |||||||
chr3:14917024 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3406-225C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14917024 | |||||||
chr3:14917038 | C | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(42): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.3406-211C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14917038 | |||||||
chr3:14917055 | C | G | 2 | a0001c0002t0001g0284 a0003c0005t0001g0256 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3406-194C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14917055 | |||||||
chr3:14917112 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0106 a0001c0001t0001g0110 others(6): Show |
9 | HG01934.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3406-137C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 11/19 | chr3 | 14917112 | |||||||
chr3:14917358 | C | T | 29 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(26): Show |
29 | HG00741.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.3489+26C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917358 | |||||||
chr3:14917420 | C | G | 3 | a0001c0001t0001g0105 a0001c0001t0017g0046 a0006c0011t0001g0006 |
3 | HG02615.hp2 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3489+88C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917420 | |||||||
chr3:14917446 | G | A | 2 | a0001c0002t0001g0010 a0001c0002t0001g0012 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3489+114G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917446 | |||||||
chr3:14917448 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.3489+116G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917448 | |||||||
chr3:14917452 | A | G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.3489+120A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917452 | |||||||
chr3:14917564 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3489+232G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917564 | |||||||
chr3:14917684 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3489+352T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917684 | |||||||
chr3:14917702 | T | C | 7 | a0001c0001t0001g0105 a0003c0009t0001g0251 a0003c0017t0001g0004 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3489+370T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917702 | |||||||
chr3:14917858 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3489+526A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917858 | |||||||
chr3:14917894 | A | G | 3 | a0001c0001t0004g0120 a0001c0001t0004g0247 a0001c0001t0012g0032 |
3 | HG02809.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3489+562A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14917894 | |||||||
chr3:14918086 | A | G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0143 others(4): Show |
7 | HG00597.hp2 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.3490-668A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918086 | |||||||
chr3:14918229 | T | C | 98 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): Show |
98 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.3490-525T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918229 | |||||||
chr3:14918317 | A | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0051 others(72): Show |
75 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.3490-437A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918317 | |||||||
chr3:14918521 | G | T | 17 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0106 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3490-233G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918521 | |||||||
chr3:14918536 | G | A | 3 | a0001c0001t0016g0050 a0012c0039t0001g0092 a0018c0040t0001g0057 |
3 | HG01261.hp2 HG02165.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3490-218G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918536 | |||||||
chr3:14918555 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.3490-199G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918555 | |||||||
chr3:14918641 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3490-113A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918641 | |||||||
chr3:14918663 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.3490-91T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918663 | |||||||
chr3:14918697 | G | T | 76 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0051 others(73): Show |
76 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.3490-57G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918697 | |||||||
chr3:14918715 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3490-39C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 12/19 | chr3 | 14918715 | |||||||
chr3:14918970 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3569+137T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14918970 | |||||||
chr3:14919109 | T | C | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3569+276T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919109 | |||||||
chr3:14919160 | C | T | 2 | a0001c0002t0001g0174 a0002c0003t0001g0227 |
2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3569+327C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919160 | |||||||
chr3:14919175 | A | T | 2 | a0001c0001t0001g0083 a0001c0001t0003g0053 |
2 | HG03704.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.3569+342A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919175 | |||||||
chr3:14919253 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0223 |
2 | HG02027.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3569+420A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919253 | |||||||
chr3:14919344 | C | T | 1 | a0005c0004t0001g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3569+511C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919344 | |||||||
chr3:14919415 | G | A | 1 | a0020c0023t0001g0075 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3569+582G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919415 | |||||||
chr3:14919487 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.3569+654A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919487 | |||||||
chr3:14919490 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.3569+657C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919490 | |||||||
chr3:14919491 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.3569+658A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919491 | |||||||
chr3:14919586 | C | A | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3569+753C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919586 | |||||||
chr3:14919617 | CAAAACA | C | 3 | a0001c0001t0002g0169 a0001c0002t0002g0262 a0001c0002t0010g0263 |
3 | HG00408.hp1 HG00544.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.3569+807_3569+812d others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 14919617 | ||||||
chr3:14919624 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3569+791A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919624 | |||||||
chr3:14919889 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3569+1056C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14919889 | |||||||
chr3:14920121 | G | T | 1 | a0001c0022t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3569+1288G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14920121 | |||||||
chr3:14920425 | G | A | 59 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(56): Show |
59 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.3570-1493G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14920425 | |||||||
chr3:14920498 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0003c0009t0001g0251 |
3 | HG02257.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3570-1420A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14920498 | |||||||
chr3:14920505 | T | A | 1 | a0001c0022t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3570-1413T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14920505 | |||||||
chr3:14920658 | G | A | 97 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0023 others(94): Show |
97 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.3570-1260G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14920658 | |||||||
chr3:14920958 | C | T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0106 others(15): Show |
18 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.3570-960C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14920958 | |||||||
chr3:14921101 | A | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0045 others(18): Show |
21 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.3570-817A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14921101 | |||||||
chr3:14921125 | C | T | 76 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0051 others(73): Show |
76 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.3570-793C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14921125 | |||||||
chr3:14921170 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3570-748C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14921170 | |||||||
chr3:14921441 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.3570-477T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14921441 | |||||||
chr3:14921781 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3570-137C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14921781 | |||||||
chr3:14921830 | C | T | 76 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0051 others(73): Show |
76 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.3570-88C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14921830 | |||||||
chr3:14921831 | A | T | 1 | a0001c0001t0001g0327 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3570-87A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 13/19 | chr3 | 14921831 | |||||||
chr3:14922111 | G | A | 1 | a0001c0001t0012g0032 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3669+94G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 14/19 | chr3 | 14922111 | |||||||
chr3:14922140 | C | A | 40 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(37): Show |
40 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.3669+123C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 14/19 | chr3 | 14922140 | |||||||
chr3:14922168 | T | C | 1 | a0002c0003t0001g0034 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3669+151T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 14/19 | chr3 | 14922168 | |||||||
chr3:14922264 | G | A | 3 | a0001c0001t0016g0050 a0012c0039t0001g0092 a0018c0040t0001g0057 |
3 | HG01261.hp2 HG02165.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3670-147G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 14/19 | chr3 | 14922264 | |||||||
chr3:14922319 | G | A | 3 | a0001c0001t0016g0050 a0012c0039t0001g0092 a0018c0040t0001g0057 |
3 | HG01261.hp2 HG02165.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3670-92G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 14/19 | chr3 | 14922319 | |||||||
chr3:14922789 | G | A | 94 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0023 others(91): Show |
94 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.3807+241G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 15/19 | chr3 | 14922789 | |||||||
chr3:14922876 | C | G | 3 | a0001c0001t0016g0050 a0012c0039t0001g0092 a0018c0040t0001g0057 |
3 | HG01261.hp2 HG02165.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3808-170C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 15/19 | chr3 | 14922876 | |||||||
chr3:14922972 | G | A | 57 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(54): Show |
57 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.3808-74G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 15/19 | chr3 | 14922972 | |||||||
chr3:14923229 | G | A | 1 | a0002c0007t0001g0243 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3937+54G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923229 | |||||||
chr3:14923307 | G | T | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.3937+132G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923307 | |||||||
chr3:14923314 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.3937+139C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923314 | |||||||
chr3:14923352 | T | C | 1 | a0001c0002t0001g0261 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3937+177T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923352 | |||||||
chr3:14923420 | G | A | 3 | a0003c0017t0001g0004 a0003c0018t0001g0249 a0003c0019t0001g0255 |
3 | HG02258.hp2 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3937+245G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923420 | |||||||
chr3:14923461 | A | G | 3 | a0003c0017t0001g0004 a0003c0018t0001g0249 a0003c0019t0001g0255 |
3 | HG02258.hp2 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3937+286A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923461 | |||||||
chr3:14923540 | C | T | 1 | a0001c0002t0001g0266 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3937+365C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923540 | |||||||
chr3:14923600 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3938-408G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923600 | |||||||
chr3:14923699 | C | G | 1 | a0001c0002t0001g0266 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3938-309C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923699 | |||||||
chr3:14923919 | C | G | 1 | a0002c0003t0001g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3938-89C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923919 | |||||||
chr3:14923959 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(224): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.3938-49C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14923959 | |||||||
chr3:14924000 | A | G | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(331): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
splice_region_variant&intron_variant | LOW | c.3938-8A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 16/19 | chr3 | 14924000 | |||||||
chr3:14924208 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0302 |
2 | NA18947.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4068+70G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924208 | |||||||
chr3:14924267 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4068+129T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924267 | |||||||
chr3:14924535 | T | C | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4068+397T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924535 | |||||||
chr3:14924716 | C | A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0001g0136 others(3): Show |
6 | HG01123.hp2 HG03540.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.4068+578C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924716 | |||||||
chr3:14924811 | C | A | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(329): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.4068+673C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924811 | |||||||
chr3:14924816 | A | C | 1 | a0002c0003t0001g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4068+678A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924816 | |||||||
chr3:14924864 | G | A | 1 | a0005c0004t0001g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4068+726G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924864 | |||||||
chr3:14924872 | T | C | 1 | a0001c0002t0001g0016 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4068+734T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924872 | |||||||
chr3:14924898 | C | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.4068+760C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924898 | |||||||
chr3:14924974 | G | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(329): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.4068+836G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14924974 | |||||||
chr3:14925086 | G | A | 4 | a0002c0007t0001g0240 a0002c0007t0001g0241 a0002c0007t0001g0242 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.4068+948G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925086 | |||||||
chr3:14925100 | CA | C | 89 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0051 others(86): Show |
89 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.4069-942delA | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr3 | 14925100 | ||||||
chr3:14925100 | CAA | C | 74 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0024 others(71): Show |
74 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.4069-943_4069-942d others(4): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr3 | 14925100 | ||||||
chr3:14925100 | CAAA | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(114): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.4069-944_4069-942d others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr3 | 14925100 | ||||||
chr3:14925100 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0001g0136 others(3): Show |
6 | HG01123.hp2 HG03540.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.4069-950_4069-942d others(11): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr3 | 14925100 | ||||||
chr3:14925126 | A | AAAC | 20 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0126 others(17): Show |
20 | HG00621.hp2 HG00735.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.4069-942_4069-940d others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr3 | 14925126 | ||||||
chr3:14925126 | A | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(273): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.4069-944A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925126 | |||||||
chr3:14925251 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4069-819G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925251 | |||||||
chr3:14925302 | T | A | 28 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(25): Show |
28 | HG00621.hp2 HG00735.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.4069-768T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925302 | |||||||
chr3:14925390 | T | C | 2 | a0001c0001t0001g0102 a0001c0002t0001g0171 |
2 | NA18946.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.4069-680T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925390 | |||||||
chr3:14925399 | A | ACCT | 3 | a0003c0017t0001g0004 a0003c0018t0001g0249 a0003c0019t0001g0255 |
3 | HG02258.hp2 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.4069-669_4069-667d others(5): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr3 | 14925399 | ||||||
chr3:14925466 | A | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0085 others(2): Show |
5 | HG00673.hp2 NA18960.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.4069-604A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925466 | |||||||
chr3:14925488 | T | C | 76 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0051 others(73): Show |
76 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.4069-582T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925488 | |||||||
chr3:14925596 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4069-474C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925596 | |||||||
chr3:14925623 | C | G | 1 | a0015c0038t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4069-447C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925623 | |||||||
chr3:14925762 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4069-308G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925762 | |||||||
chr3:14925871 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG01109.hp2 HG01168.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.4069-199C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 17/19 | chr3 | 14925871 | |||||||
chr3:14926341 | A | G | 1 | a0004c0006t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4197+143A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14926341 | |||||||
chr3:14926386 | T | C | 17 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0106 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.4197+188T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14926386 | |||||||
chr3:14926421 | T | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.4197+223T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14926421 | |||||||
chr3:14926422 | A | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0106 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.4197+224A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14926422 | |||||||
chr3:14926455 | A | G | 3 | a0005c0004t0001g0037 a0005c0004t0001g0040 a0022c0026t0001g0009 |
3 | HG02896.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4197+257A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14926455 | |||||||
chr3:14927091 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0143 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.4197+893T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927091 | |||||||
chr3:14927157 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4197+959G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927157 | |||||||
chr3:14927242 | G | A | 1 | a0019c0036t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4197+1044G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927242 | |||||||
chr3:14927248 | T | C | 2 | a0003c0018t0001g0249 a0003c0019t0001g0255 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.4197+1050T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927248 | |||||||
chr3:14927377 | G | T | 16 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0106 others(13): Show |
16 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.4197+1179G>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927377 | |||||||
chr3:14927464 | AAATGAAT others(5): Show |
A | 3 | a0003c0017t0001g0004 a0003c0018t0001g0249 a0003c0019t0001g0255 |
3 | HG02258.hp2 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.4197+1284_4197+129 others(16): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 14927464 | ||||||
chr3:14927469 | A | C | 1 | a0003c0009t0001g0250 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4197+1271A>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927469 | |||||||
chr3:14927553 | C | CAATA | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(331): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.4197+1357_4197+135 others(8): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 14927553 | ||||||
chr3:14927624 | G | C | 1 | a0002c0003t0001g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4197+1426G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927624 | |||||||
chr3:14927690 | G | A | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.4197+1492G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927690 | |||||||
chr3:14927763 | A | T | 15 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0237 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4197+1565A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927763 | |||||||
chr3:14927875 | C | A | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.4197+1677C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927875 | |||||||
chr3:14927931 | A | AT | 64 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(61): Show |
64 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.4197+1749dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 14927931 | ||||||
chr3:14927931 | AT | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0123 others(36): Show |
39 | HG00621.hp2 HG00735.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.4197+1749delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 14927931 | ||||||
chr3:14927946 | T | A | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4197+1748T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927946 | |||||||
chr3:14927947 | T | A | 1 | a0003c0017t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4197+1749T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927947 | |||||||
chr3:14927949 | A | T | 1 | a0016c0016t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4197+1751A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927949 | |||||||
chr3:14927968 | A | T | 39 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.4197+1770A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14927968 | |||||||
chr3:14928035 | G | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG01109.hp2 HG01168.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.4197+1837G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14928035 | |||||||
chr3:14928088 | C | A | 1 | a0022c0026t0001g0009 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4197+1890C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14928088 | |||||||
chr3:14928132 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.4197+1934A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14928132 | |||||||
chr3:14928240 | A | AT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.4197+2049dupT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 14928240 | ||||||
chr3:14928414 | T | C | 2 | a0001c0002t0001g0329 a0002c0003t0001g0208 |
2 | NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.4197+2216T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14928414 | |||||||
chr3:14928755 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4197+2557T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14928755 | |||||||
chr3:14928887 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4197+2689A>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14928887 | |||||||
chr3:14928948 | A | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0106 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.4197+2750A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14928948 | |||||||
chr3:14929491 | C | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.4198-3086C>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14929491 | |||||||
chr3:14929495 | A | G | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.4198-3082A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14929495 | |||||||
chr3:14929566 | C | A | 14 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0237 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.4198-3011C>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14929566 | |||||||
chr3:14929571 | T | C | 1 | a0001c0002t0001g0266 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4198-3006T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14929571 | |||||||
chr3:14929822 | A | G | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG01081.hp1 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.4198-2755A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14929822 | |||||||
chr3:14929904 | GC | G | 4 | a0002c0007t0001g0240 a0002c0007t0001g0241 a0002c0007t0001g0242 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.4198-2672delC | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14929904 | |||||||
chr3:14929921 | G | C | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.4198-2656G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14929921 | |||||||
chr3:14930540 | T | A | 1 | a0001c0001t0002g0107 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4198-2037T>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14930540 | |||||||
chr3:14930545 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4198-2032C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14930545 | |||||||
chr3:14930574 | CT | C | 13 | a0001c0001t0001g0109 a0001c0001t0001g0237 a0001c0001t0012g0032 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.4198-1995delT | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 14930574 | ||||||
chr3:14930582 | T | C | 1 | a0002c0003t0002g0189 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4198-1995T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14930582 | |||||||
chr3:14931074 | T | C | 1 | a0001c0030t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4198-1503T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931074 | |||||||
chr3:14931293 | A | G | 1 | a0003c0005t0001g0003 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4198-1284A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931293 | |||||||
chr3:14931473 | G | A | 75 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0051 others(72): Show |
75 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.4198-1104G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931473 | |||||||
chr3:14931511 | C | T | 1 | a0004c0010t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4198-1066C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931511 | |||||||
chr3:14931645 | A | G | 2 | a0015c0038t0001g0258 a0019c0036t0001g0245 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4198-932A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931645 | |||||||
chr3:14931669 | A | G | 3 | a0001c0001t0001g0181 a0001c0002t0001g0166 a0004c0010t0001g0161 |
3 | HG01081.hp2 HG01109.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.4198-908A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931669 | |||||||
chr3:14931685 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4198-892G>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931685 | |||||||
chr3:14931813 | A | G | 39 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.4198-764A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931813 | |||||||
chr3:14931926 | T | C | 3 | a0001c0001t0001g0181 a0001c0002t0001g0166 a0004c0010t0001g0161 |
3 | HG01081.hp2 HG01109.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.4198-651T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14931926 | |||||||
chr3:14932002 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0172 |
2 | NA19068.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.4198-575A>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14932002 | |||||||
chr3:14932005 | T | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(332): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.4198-572T>G | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14932005 | |||||||
chr3:14932047 | A | AATATGTT others(27): Show |
1 | a0004c0006t0001g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4198-516_4198-483d others(36): Show |
FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 14932047 | ||||||
chr3:14932175 | C | T | 1 | a0001c0001t0005g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4198-402C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14932175 | |||||||
chr3:14932232 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0235 |
2 | NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4198-345G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14932232 | |||||||
chr3:14932314 | C | T | 3 | a0001c0002t0001g0272 a0001c0002t0001g0273 a0001c0002t0001g0301 |
3 | NA18747.hp2 NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.4198-263C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14932314 | |||||||
chr3:14932346 | G | A | 3 | a0003c0017t0001g0004 a0003c0018t0001g0249 a0003c0019t0001g0255 |
3 | HG02258.hp2 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.4198-231G>A | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14932346 | |||||||
chr3:14932388 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4198-189C>T | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 18/19 | chr3 | 14932388 | |||||||
chr3:14932815 | T | C | 2 | a0001c0001t0001g0105 a0006c0011t0001g0006 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4352+84T>C | FGD5 | ENSG00000154783.12 | transcript | ENST00000285046.10 | protein_coding | 19/19 | chr3 | 14932815 |