| geneid | 166752 |
|---|---|
| ensemblid | ENSG00000183090.5 |
| hgncid | 25172 |
| symbol | FREM3 |
| name | FRAS1 related extracellular matrix 3 |
| refseq_nuc | NM_001168235.2 |
| refseq_prot | NP_001161707.1 |
| ensembl_nuc | ENST00000329798.5 |
| ensembl_prot | ENSP00000332886.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 143577302 |
| end | 143700675 |
| strand | - |
| ver | v1.2 |
| region | chr4:143577302-143700675 |
| region5000 | chr4:143572302-143705675 |
| regionname0 | FREM3_chr4_143577302_143700675 |
| regionname5000 | FREM3_chr4_143572302_143705675 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2139 | 124 | 23 | 27 | 47 | 8 | 19 | 35 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002 | 0/0 | 2139 | 45 | 1 | 16 | 12 | 6 | 10 | 10 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0003 | 0/0 | 2139 | 22 | 7 | 0 | 15 | 0 | 0 | 13 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0004 | 0/0 | 2139 | 13 | 9 | 1 | 3 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0005 | 1/0 | 2139 | 11 | 9 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0006 | 0/0 | 2141 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0007 | 0/0 | 2139 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0008 | 0/0 | 2139 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0009 | 0/1 | 2139 | 3 | 0 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0010 | 0/0 | 2139 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0011 | 0/0 | 2139 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0012 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0013 | 0/0 | 2139 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0014 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0015 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0016 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0017 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0018 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0019 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0020 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0021 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0022 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0023 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0024 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0025 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0026 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0027 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 6420 | 116 | 23 | 27 | 39 | 8 | 19 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0002 | 0/0 | 6420 | 39 | 0 | 13 | 12 | 5 | 9 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0003 | 0/0 | 6420 | 22 | 7 | 0 | 15 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0004 | 0/0 | 6420 | 13 | 9 | 1 | 3 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0005 | 0/0 | 6420 | 9 | 8 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0006 | 0/0 | 6420 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0007 | 0/0 | 6426 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0008 | 0/0 | 6420 | 5 | 4 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0009 | 0/0 | 6420 | 3 | 0 | 3 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0010 | 0/0 | 6420 | 3 | 1 | 0 | 0 | 1 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0011 | 0/0 | 6420 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0012 | 0/0 | 6420 | 3 | 3 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0013 | 0/0 | 6420 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0014 | 0/0 | 6420 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0015 | 0/0 | 6420 | 2 | 0 | 0 | 0 | 2 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0016 | 0/0 | 6420 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0017 | 0/0 | 6420 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0018 | 0/0 | 6420 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0019 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0020 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0021 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0022 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0023 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0024 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0025 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0026 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0027 | 1/0 | 6420 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0028 | 0/0 | 6420 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0029 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0030 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0031 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0032 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0033 | 0/0 | 6420 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0034 | 0/1 | 6420 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| c0035 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 310 | 255 | 67 | 56 | 86 | 16 | 28 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| t0002 | 0/0 | 310 | 2 | 0 | 0 | 0 | 0 | 2 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| t0003 | 0/0 | 310 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| t0004 | 0/0 | 310 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 6420 | 116 | 23 | 27 | 39 | 8 | 19 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0001c0006 | 0/0 | 6420 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0001c0028 | 0/0 | 6420 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002c0002 | 0/0 | 6420 | 39 | 0 | 13 | 12 | 5 | 9 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002c0009 | 0/0 | 6420 | 3 | 0 | 3 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002c0010 | 0/0 | 6420 | 3 | 1 | 0 | 0 | 1 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0003c0003 | 0/0 | 6420 | 22 | 7 | 0 | 15 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0004c0004 | 0/0 | 6420 | 13 | 9 | 1 | 3 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0005c0005 | 0/0 | 6420 | 9 | 8 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0005c0022 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0005c0027 | 1/0 | 6420 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0006c0007 | 0/0 | 6426 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0007c0008 | 0/0 | 6420 | 5 | 4 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0007c0030 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0008c0012 | 0/0 | 6420 | 3 | 3 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0009c0015 | 0/0 | 6420 | 2 | 0 | 0 | 0 | 2 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0009c0034 | 0/1 | 6420 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0010c0013 | 0/0 | 6420 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0011c0011 | 0/0 | 6420 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0012c0016 | 0/0 | 6420 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0013c0017 | 0/0 | 6420 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0014c0018 | 0/0 | 6420 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0015c0014 | 0/0 | 6420 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0016c0019 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0017c0020 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0018c0024 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0019c0026 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0020c0033 | 0/0 | 6420 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0021c0032 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0022c0031 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0023c0029 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0024c0021 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0025c0035 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0026c0023 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0027c0025 | 0/0 | 6420 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6729 | 114 | 21 | 27 | 39 | 8 | 19 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0001c0001t0003 | 0/0 | 6729 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0001c0006t0001 | 0/0 | 6729 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0001c0028t0001 | 0/0 | 6729 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002c0002t0001 | 0/0 | 6729 | 37 | 0 | 13 | 12 | 5 | 7 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002c0002t0002 | 0/0 | 6729 | 2 | 0 | 0 | 0 | 0 | 2 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002c0009t0001 | 0/0 | 6729 | 3 | 0 | 3 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0002c0010t0001 | 0/0 | 6729 | 3 | 1 | 0 | 0 | 1 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0003c0003t0001 | 0/0 | 6729 | 22 | 7 | 0 | 15 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0004c0004t0001 | 0/0 | 6729 | 13 | 9 | 1 | 3 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0005c0005t0001 | 0/0 | 6729 | 9 | 8 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0005c0022t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0005c0027t0001 | 1/0 | 6729 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0006c0007t0001 | 0/0 | 6735 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0007c0008t0001 | 0/0 | 6729 | 5 | 4 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0007c0030t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0008c0012t0001 | 0/0 | 6729 | 3 | 3 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0009c0015t0001 | 0/0 | 6729 | 2 | 0 | 0 | 0 | 2 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0009c0034t0001 | 0/1 | 6729 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0010c0013t0001 | 0/0 | 6729 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0011c0011t0001 | 0/0 | 6729 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0012c0016t0001 | 0/0 | 6729 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0013c0017t0001 | 0/0 | 6729 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0014c0018t0001 | 0/0 | 6729 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0015c0014t0001 | 0/0 | 6729 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0016c0019t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0017c0020t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0018c0024t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0019c0026t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0020c0033t0001 | 0/0 | 6729 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0021c0032t0004 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0022c0031t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0023c0029t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0024c0021t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0025c0035t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0026c0023t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| a0027c0025t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | copy fasta | chr4 | 143572302 | 143705675 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0006t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0006t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0006t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0001c0028t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0009t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0009t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0009t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0010t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0010t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0002c0010t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0003c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0004c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0022t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0005c0027t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0006c0007t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0006c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0006c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0006c0007t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0006c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0006c0007t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0007c0008t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0007c0008t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0007c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0007c0008t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0007c0008t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0007c0030t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0008c0012t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0008c0012t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0009c0015t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0009c0015t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0009c0034t0001g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0010c0013t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0010c0013t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0010c0013t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0011c0011t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0011c0011t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0011c0011t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0012c0016t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0012c0016t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0013c0017t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0013c0017t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0014c0018t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0014c0018t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0015c0014t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0015c0014t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0016c0019t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0017c0020t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0018c0024t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0019c0026t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0020c0033t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0021c0032t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0022c0031t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0023c0029t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0024c0021t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0025c0035t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0026c0023t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| a0027c0025t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0033 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0029 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0019 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0088 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00558 | hp2 | a0004 | c0004 | t0001 | g0079 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0085 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01069 | hp1 | a0002 | c0009 | t0001 | g0010 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01070 | hp2 | a0014 | c0018 | t0001 | g0244 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01071 | hp1 | a0002 | c0009 | t0001 | g0009 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01071 | hp2 | a0014 | c0018 | t0001 | g0245 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01099 | hp2 | a0012 | c0016 | t0001 | g0074 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01106 | hp1 | a0005 | c0005 | t0001 | g0059 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01168 | hp1 | a0002 | c0009 | t0001 | g0008 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01192 | hp1 | a0011 | c0011 | t0001 | g0065 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01243 | hp1 | a0018 | c0024 | t0001 | g0070 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01243 | hp2 | a0010 | c0013 | t0001 | g0247 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01261 | hp2 | a0007 | c0008 | t0001 | g0157 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01361 | hp2 | a0027 | c0025 | t0001 | g0071 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01496 | hp2 | a0004 | c0004 | t0001 | g0098 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01515 | hp1 | a0009 | c0015 | t0001 | g0072 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01517 | hp2 | a0009 | c0015 | t0001 | g0073 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01884 | hp1 | a0025 | c0035 | t0001 | g0246 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0102 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01891 | hp1 | a0008 | c0012 | t0001 | g0069 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01943 | hp2 | a0016 | c0019 | t0001 | g0007 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01975 | hp2 | a0012 | c0016 | t0001 | g0075 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02004 | hp2 | a0019 | c0026 | t0001 | g0077 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02055 | hp1 | a0004 | c0004 | t0001 | g0097 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02055 | hp2 | a0005 | c0005 | t0001 | g0063 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02132 | hp1 | a0004 | c0004 | t0001 | g0080 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02132 | hp2 | a0006 | c0007 | t0001 | g0254 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02165 | hp2 | a0001 | c0028 | t0001 | g0111 | EAS | CDX | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02280 | hp1 | a0021 | c0032 | t0004 | g0153 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02451 | hp1 | a0007 | c0008 | t0001 | g0148 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02451 | hp2 | a0004 | c0004 | t0001 | g0103 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02572 | hp2 | a0005 | c0005 | t0001 | g0060 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02622 | hp1 | a0005 | c0005 | t0001 | g0057 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02622 | hp2 | a0007 | c0030 | t0001 | g0154 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02630 | hp1 | a0005 | c0022 | t0001 | g0064 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02647 | hp2 | a0005 | c0005 | t0001 | g0055 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02717 | hp1 | a0005 | c0005 | t0001 | g0058 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02922 | hp2 | a0022 | c0031 | t0001 | g0146 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02965 | hp1 | a0005 | c0005 | t0001 | g0061 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02970 | hp1 | a0008 | c0012 | t0001 | g0002 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02970 | hp2 | a0010 | c0013 | t0001 | g0248 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02976 | hp2 | a0004 | c0004 | t0001 | g0099 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03041 | hp1 | a0004 | c0004 | t0001 | g0091 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0108 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0109 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03098 | hp2 | a0007 | c0008 | t0001 | g0137 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03130 | hp1 | a0023 | c0029 | t0001 | g0232 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03130 | hp2 | a0004 | c0004 | t0001 | g0093 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03195 | hp1 | a0024 | c0021 | t0001 | g0054 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0105 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03209 | hp1 | a0010 | c0013 | t0001 | g0249 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03225 | hp2 | a0015 | c0014 | t0001 | g0051 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03453 | hp1 | a0026 | c0023 | t0001 | g0068 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03453 | hp2 | a0015 | c0014 | t0001 | g0052 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03540 | hp2 | a0005 | c0005 | t0001 | g0056 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03579 | hp1 | a0011 | c0011 | t0001 | g0066 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0092 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0045 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03710 | hp2 | a0002 | c0010 | t0001 | g0012 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG03834 | hp2 | a0020 | c0033 | t0001 | g0242 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18522 | hp1 | a0004 | c0004 | t0001 | g0101 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18612 | hp2 | a0013 | c0017 | t0001 | g0173 | EAS | CHB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18906 | hp1 | a0004 | c0004 | t0001 | g0094 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18906 | hp2 | a0005 | c0005 | t0001 | g0062 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18943 | hp2 | a0006 | c0007 | t0001 | g0006 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18946 | hp1 | a0001 | c0006 | t0001 | g0113 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18951 | hp1 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18953 | hp2 | a0001 | c0006 | t0001 | g0112 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0107 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18975 | hp2 | a0001 | c0006 | t0001 | g0116 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18978 | hp2 | a0006 | c0007 | t0001 | g0253 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18979 | hp2 | a0004 | c0004 | t0001 | g0106 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18986 | hp2 | a0013 | c0017 | t0001 | g0208 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18987 | hp1 | a0001 | c0006 | t0001 | g0114 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19010 | hp1 | a0006 | c0007 | t0001 | g0251 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19011 | hp2 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19030 | hp2 | a0017 | c0020 | t0001 | g0053 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19065 | hp2 | a0001 | c0006 | t0001 | g0115 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19082 | hp2 | a0006 | c0007 | t0001 | g0252 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19084 | hp1 | a0006 | c0007 | t0001 | g0006 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19089 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA19089 | hp2 | a0006 | c0007 | t0001 | g0250 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA20129 | hp1 | a0004 | c0004 | t0001 | g0100 | AFR | ASW | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA20129 | hp2 | a0011 | c0011 | t0001 | g0067 | AFR | ASW | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA20805 | hp1 | a0002 | c0010 | t0001 | g0011 | EUR | TSI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02109 | hp1 | a0008 | c0012 | t0001 | g0002 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02486 | hp1 | a0007 | c0008 | t0001 | g0239 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0096 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02559 | hp1 | a0002 | c0010 | t0001 | g0013 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| HG06807 | hp2 | a0007 | c0008 | t0001 | g0145 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0095 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| homoSapiens_chm13v2 | hp1 | a0009 | c0034 | t0001 | g0243 | REF | REF | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| homoSapiens_grch38 | hp1 | a0005 | c0027 | t0001 | g0110 | REF | REF | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143577615
|
T | C | 2 | a0010a0022 | 4 | HG01243.hp2 HG02922.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.6416A>G | p.Asp2139Gly | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6416/6729 | 6416/6420 | 2139/2139 | chr4 | 143577615 | ||
| chr4:143577712
|
T | A | 1 | a0021 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.6319A>T | p.Met2107Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6319/6729 | 6319/6420 | 2107/2139 | chr4 | 143577712 | ||
| chr4:143577729
|
A | G | 1 | a0013 | 2 | NA18612.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.6302T>C | p.Phe2101Ser | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6302/6729 | 6302/6420 | 2101/2139 | chr4 | 143577729 | ||
| chr4:143585880
|
C | T | 1 | a0008 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.6142G>A | p.Val2048Met | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/8 | 6142/6729 | 6142/6420 | 2048/2139 | chr4 | 143585880 | ||
| chr4:143611458
|
G | T | 1 | a0019 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.5849C>A | p.Thr1950Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/8 | 5849/6729 | 5849/6420 | 1950/2139 | chr4 | 143611458 | ||
| chr4:143611491
|
A | G | 3 | a0004a0023a0026 | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
missense_variant | MODERATE | c.5816T>C | p.Phe1939Ser | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/8 | 5816/6729 | 5816/6420 | 1939/2139 | chr4 | 143611491 | ||
| chr4:143621060
|
A | G | 6 | a0004a0007a0011others(3): Show | 26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
missense_variant | MODERATE | c.5756T>C | p.Ile1919Thr | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/8 | 5756/6729 | 5756/6420 | 1919/2139 | chr4 | 143621060 | ||
| chr4:143695685
|
G | C | 1 | a0020 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.4991C>G | p.Thr1664Ser | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4991/6729 | 4991/6420 | 1664/2139 | chr4 | 143695685 | ||
| chr4:143696163
|
C | T | 2 | a0008a0018 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
missense_variant | MODERATE | c.4513G>A | p.Glu1505Lys | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4513/6729 | 4513/6420 | 1505/2139 | chr4 | 143696163 | ||
| chr4:143696194
|
G | C | 2 | a0008a0018 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
missense_variant | MODERATE | c.4482C>G | p.Asn1494Lys | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4482/6729 | 4482/6420 | 1494/2139 | chr4 | 143696194 | ||
| chr4:143696244
|
A | T | 4 | a0003a0004a0012others(1): Show | 38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
missense_variant | MODERATE | c.4432T>A | p.Tyr1478Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4432/6729 | 4432/6420 | 1478/2139 | chr4 | 143696244 | ||
| chr4:143696966
|
C | T | 1 | a0012 | 2 | HG01099.hp2 HG01975.hp2 |
missense_variant | MODERATE | c.3710G>A | p.Arg1237Gln | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3710/6729 | 3710/6420 | 1237/2139 | chr4 | 143696966 | ||
| chr4:143697191
|
T | C | 1 | a0024 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.3485A>G | p.Gln1162Arg | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3485/6729 | 3485/6420 | 1162/2139 | chr4 | 143697191 | ||
| chr4:143697457
|
G | C | 26 | a0001a0002a0003others(23): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
missense_variant | MODERATE | c.3219C>G | p.Phe1073Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3219/6729 | 3219/6420 | 1073/2139 | chr4 | 143697457 | ||
| chr4:143697935
|
G | T | 2 | a0008a0018 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
missense_variant | MODERATE | c.2741C>A | p.Thr914Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2741/6729 | 2741/6420 | 914/2139 | chr4 | 143697935 | ||
| chr4:143698161
|
T | G | 1 | a0009 | 3 | HG01515.hp1 HG01517.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2515A>C | p.Ile839Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2515/6729 | 2515/6420 | 839/2139 | chr4 | 143698161 | ||
| chr4:143699177
|
G | T | 1 | a0016 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1499C>A | p.Ala500Glu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1499/6729 | 1499/6420 | 500/2139 | chr4 | 143699177 | ||
| chr4:143699189
|
G | A | 3 | a0010a0014a0025 | 6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
missense_variant | MODERATE | c.1487C>T | p.Ala496Val | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1487/6729 | 1487/6420 | 496/2139 | chr4 | 143699189 | ||
| chr4:143699290
|
T | G | 2 | a0011a0026 | 4 | HG01192.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.1386A>C | p.Lys462Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1386/6729 | 1386/6420 | 462/2139 | chr4 | 143699290 | ||
| chr4:143699849
|
C | T | 1 | a0017 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.827G>A | p.Gly276Asp | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 827/6729 | 827/6420 | 276/2139 | chr4 | 143699849 | ||
| chr4:143699853
|
C | T | 1 | a0027 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.823G>A | p.Glu275Lys | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 823/6729 | 823/6420 | 275/2139 | chr4 | 143699853 | ||
| chr4:143700104
|
C | G | 1 | a0015 | 2 | HG03225.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.572G>C | p.Arg191Thr | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 572/6729 | 572/6420 | 191/2139 | chr4 | 143700104 | ||
| chr4:143700251
|
T | TGCAGCA | 1 | a0006 | 7 | HG02132.hp2 NA18943.hp2 NA18978.hp2 others(4): Show |
conservative_inframe_insertion | MODERATE | c.419_424dupTGCTGC | p.Leu140_Leu141dup | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 424/6729 | 424/6420 | 142/2139 | chr4 | 143700251 | ||
| chr4:143700626
|
A | G | 2 | a0002a0016 | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
missense_variant | MODERATE | c.50T>C | p.Val17Ala | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 50/6729 | 50/6420 | 17/2139 | chr4 | 143700626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143577647
|
C | T | 1 | a0021c0032 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.6384G>A | p.Thr2128Thr | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6384/6729 | 6384/6420 | 2128/2139 | chr4 | 143577647 | ||
| chr4:143585881
|
G | A | 1 | a0007c0030 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.6141C>T | p.Ala2047Ala | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/8 | 6141/6729 | 6141/6420 | 2047/2139 | chr4 | 143585881 | ||
| chr4:143695753
|
C | T | 1 | a0002c0010 | 3 | HG02559.hp1 HG03710.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.4923G>A | p.Ala1641Ala | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4923/6729 | 4923/6420 | 1641/2139 | chr4 | 143695753 | ||
| chr4:143696401
|
G | T | 1 | a0002c0009 | 3 | HG01069.hp1 HG01071.hp1 HG01168.hp1 |
synonymous_variant | LOW | c.4275C>A | p.Val1425Val | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4275/6729 | 4275/6420 | 1425/2139 | chr4 | 143696401 | ||
| chr4:143696689
|
G | T | 13 | a0001c0006a0002c0002a0002c0009others(10): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
synonymous_variant | LOW | c.3987C>A | p.Ile1329Ile | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3987/6729 | 3987/6420 | 1329/2139 | chr4 | 143696689 | ||
| chr4:143697448
|
C | T | 1 | a0001c0028 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.3228G>A | p.Glu1076Glu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3228/6729 | 3228/6420 | 1076/2139 | chr4 | 143697448 | ||
| chr4:143697927
|
G | A | 1 | a0005c0022 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2749C>T | p.Leu917Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2749/6729 | 2749/6420 | 917/2139 | chr4 | 143697927 | ||
| chr4:143698135
|
G | A | 2 | a0005c0005a0005c0022 | 10 | HG01106.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
synonymous_variant | LOW | c.2541C>T | p.Leu847Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2541/6729 | 2541/6420 | 847/2139 | chr4 | 143698135 | ||
| chr4:143698624
|
A | G | 1 | a0024c0021 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2052T>C | p.Asn684Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2052/6729 | 2052/6420 | 684/2139 | chr4 | 143698624 | ||
| chr4:143698768
|
C | T | 4 | a0003c0003a0004c0004a0012c0016others(1): Show | 38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
synonymous_variant | LOW | c.1908G>A | p.Gly636Gly | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1908/6729 | 1908/6420 | 636/2139 | chr4 | 143698768 | ||
| chr4:143698981
|
A | G | 1 | a0009c0015 | 2 | HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.1695T>C | p.Phe565Phe | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1695/6729 | 1695/6420 | 565/2139 | chr4 | 143698981 | ||
| chr4:143699605
|
C | T | 12 | a0002c0002a0002c0009a0002c0010others(9): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
synonymous_variant | LOW | c.1071G>A | p.Pro357Pro | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1071/6729 | 1071/6420 | 357/2139 | chr4 | 143699605 | ||
| chr4:143699755
|
G | A | 2 | a0008c0012a0018c0024 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
synonymous_variant | LOW | c.921C>T | p.Pro307Pro | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 921/6729 | 921/6420 | 307/2139 | chr4 | 143699755 | ||
| chr4:143700046
|
A | G | 12 | a0002c0002a0002c0009a0002c0010others(9): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
synonymous_variant | LOW | c.630T>C | p.Leu210Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 630/6729 | 630/6420 | 210/2139 | chr4 | 143700046 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143577319
|
T | C | 1 | a0021c0032t0004 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 292 | chr4 | 143577319 | |||||
| chr4:143577522
|
T | C | 1 | a0001c0001t0003 | 2 | HG02559.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 89 | chr4 | 143577522 | |||||
| chr4:143577538
|
A | T | 1 | a0002c0002t0002 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*73T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 73 | chr4 | 143577538 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:143577859
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.6179-7T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143577859 | ||||||
| chr4:143577910
|
C | T | 4 | a0004c0004t0001g0093a0007c0030t0001g0154a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.6179-58G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143577910 | ||||||
| chr4:143578133
|
A | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0122a0001c0001t0001g0124others(115): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.6179-281T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143578133 | ||||||
| chr4:143578691
|
A | G | 93 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0126others(90): Show | 97 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.6179-839T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143578691 | ||||||
| chr4:143579015
|
T | C | 1 | a0004c0004t0001g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6179-1163A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579015 | ||||||
| chr4:143579043
|
AC | A | 4 | a0004c0004t0001g0093a0007c0030t0001g0154a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.6179-1192delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579043 | ||||||
| chr4:143579047
|
A | T | 4 | a0004c0004t0001g0093a0007c0030t0001g0154a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.6179-1195T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579047 | ||||||
| chr4:143579062
|
CA | C | 5 | a0001c0001t0003g0233a0001c0001t0003g0234a0007c0030t0001g0154others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.6179-1211delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579062 | ||||||
| chr4:143579078
|
C | T | 133 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(130): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.6179-1226G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579078 | ||||||
| chr4:143579703
|
G | A | 2 | a0003c0003t0001g0108a0004c0004t0001g0100 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6179-1851C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579703 | ||||||
| chr4:143579737
|
T | A | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6179-1885A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579737 | ||||||
| chr4:143579753
|
C | T | 250 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6179-1901G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579753 | ||||||
| chr4:143579801
|
G | A | 1 | a0015c0014t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6179-1949C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579801 | ||||||
| chr4:143579943
|
C | T | 3 | a0001c0001t0001g0121a0002c0002t0001g0014a0002c0002t0001g0016 | 3 | HG01192.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6179-2091G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579943 | ||||||
| chr4:143580053
|
T | G | 50 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0123others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.6179-2201A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580053 | ||||||
| chr4:143580063
|
C | T | 1 | a0003c0003t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6179-2211G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580063 | ||||||
| chr4:143580111
|
A | C | 2 | a0009c0015t0001g0072a0009c0015t0001g0073 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.6179-2259T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580111 | ||||||
| chr4:143580148
|
T | C | 248 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6179-2296A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580148 | ||||||
| chr4:143580707
|
C | G | 197 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(194): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.6179-2855G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580707 | ||||||
| chr4:143580711
|
C | A | 3 | a0004c0004t0001g0091a0020c0033t0001g0242a0023c0029t0001g0232 | 3 | HG03041.hp1 HG03130.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6179-2859G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580711 | ||||||
| chr4:143580932
|
G | A | 50 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0123others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.6179-3080C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580932 | ||||||
| chr4:143581007
|
A | G | 50 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0123others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.6179-3155T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581007 | ||||||
| chr4:143581047
|
A | G | 248 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6179-3195T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581047 | ||||||
| chr4:143581124
|
A | C | 248 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6179-3272T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581124 | ||||||
| chr4:143581326
|
C | T | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6179-3474G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581326 | ||||||
| chr4:143581329
|
C | T | 1 | a0002c0002t0001g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6179-3477G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581329 | ||||||
| chr4:143581387
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.6179-3535G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581387 | ||||||
| chr4:143581498
|
C | T | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6179-3646G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581498 | ||||||
| chr4:143581636
|
T | C | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6179-3784A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581636 | ||||||
| chr4:143581675
|
A | C | 1 | a0002c0002t0001g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.6179-3823T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581675 | ||||||
| chr4:143581828
|
C | A | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6179-3976G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581828 | ||||||
| chr4:143581933
|
AC | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0193 | 3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.6178+3910delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581933 | ||||||
| chr4:143582114
|
CA | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0135a0001c0001t0001g0136others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.6178+3729delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582114 | ||||||
| chr4:143582118
|
A | G | 1 | a0003c0003t0001g0081 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+3726T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582118 | ||||||
| chr4:143582119
|
G | C | 1 | a0003c0003t0001g0081 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+3725C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582119 | ||||||
| chr4:143582444
|
A | G | 1 | a0003c0003t0001g0081 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+3400T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582444 | ||||||
| chr4:143582494
|
G | A | 63 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0152others(60): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.6178+3350C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582494 | ||||||
| chr4:143582577
|
C | A | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6178+3267G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582577 | ||||||
| chr4:143582649
|
A | G | 1 | a0009c0034t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6178+3195T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582649 | ||||||
| chr4:143582748
|
A | G | 1 | a0022c0031t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6178+3096T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582748 | ||||||
| chr4:143582812
|
A | G | 1 | a0009c0034t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6178+3032T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582812 | ||||||
| chr4:143582839
|
A | C | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.6178+3005T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582839 | ||||||
| chr4:143582898
|
C | CT | 214 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(211): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.6178+2945dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582898 | ||||||
| chr4:143582915
|
T | C | 249 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(246): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.6178+2929A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582915 | ||||||
| chr4:143583041
|
G | T | 249 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(246): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.6178+2803C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583041 | ||||||
| chr4:143583042
|
G | T | 1 | a0003c0003t0001g0081 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+2802C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583042 | ||||||
| chr4:143583062
|
T | C | 38 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0160others(35): Show | 39 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.6178+2782A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583062 | ||||||
| chr4:143583130
|
A | G | 1 | a0020c0033t0001g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6178+2714T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583130 | ||||||
| chr4:143583163
|
C | T | 1 | a0024c0021t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6178+2681G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583163 | ||||||
| chr4:143583164
|
G | A | 3 | a0001c0001t0001g0122a0002c0002t0002g0001a0003c0003t0001g0082 | 4 | HG02976.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.6178+2680C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583164 | ||||||
| chr4:143583300
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0219 | 2 | HG02738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.6178+2544G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583300 | ||||||
| chr4:143583326
|
A | G | 3 | a0011c0011t0001g0065a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.6178+2518T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583326 | ||||||
| chr4:143583364
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6178+2480G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583364 | ||||||
| chr4:143583409
|
T | A | 64 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0152others(61): Show | 65 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.6178+2435A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583409 | ||||||
| chr4:143583439
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6178+2405T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583439 | ||||||
| chr4:143583453
|
C | T | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+2391G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583453 | ||||||
| chr4:143583454
|
A | G | 134 | a0001c0001t0001g0005a0001c0001t0001g0122a0001c0001t0001g0123others(131): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.6178+2390T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583454 | ||||||
| chr4:143583465
|
T | C | 250 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6178+2379A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583465 | ||||||
| chr4:143583653
|
A | C | 1 | a0002c0002t0001g0050 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6178+2191T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583653 | ||||||
| chr4:143583918
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6178+1926G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583918 | ||||||
| chr4:143583996
|
T | C | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6178+1848A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583996 | ||||||
| chr4:143584136
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6178+1708C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584136 | ||||||
| chr4:143584205
|
C | T | 2 | a0001c0001t0001g0155a0003c0003t0001g0084 | 2 | NA18941.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6178+1639G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584205 | ||||||
| chr4:143584266
|
G | A | 3 | a0011c0011t0001g0065a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.6178+1578C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584266 | ||||||
| chr4:143584272
|
G | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+1572C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584272 | ||||||
| chr4:143584353
|
A | G | 250 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6178+1491T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584353 | ||||||
| chr4:143584373
|
C | T | 5 | a0001c0001t0001g0136a0001c0001t0001g0199a0005c0005t0001g0058others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.6178+1471G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584373 | ||||||
| chr4:143584379
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6178+1465C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584379 | ||||||
| chr4:143584383
|
T | A | 1 | a0003c0003t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6178+1461A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584383 | ||||||
| chr4:143584395
|
G | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+1449C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584395 | ||||||
| chr4:143584415
|
CA | C | 82 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(79): Show | 82 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.6178+1428delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584415 | ||||||
| chr4:143584415
|
CAA | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0122a0001c0001t0001g0123others(118): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.6178+1427_6178+142 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584415 | ||||||
| chr4:143584492
|
C | T | 1 | a0004c0004t0001g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6178+1352G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584492 | ||||||
| chr4:143584540
|
T | C | 2 | a0011c0011t0001g0066a0011c0011t0001g0067 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.6178+1304A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584540 | ||||||
| chr4:143584620
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.6178+1224T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584620 | ||||||
| chr4:143584922
|
C | A | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6178+922G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584922 | ||||||
| chr4:143585201
|
A | C | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+643T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585201 | ||||||
| chr4:143585257
|
G | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.6178+587C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585257 | ||||||
| chr4:143585276
|
C | T | 1 | a0004c0004t0001g0079 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6178+568G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585276 | ||||||
| chr4:143585282
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6178+562C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585282 | ||||||
| chr4:143585510
|
G | A | 4 | a0002c0002t0001g0015a0002c0002t0001g0024a0002c0009t0001g0009others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+334C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585510 | ||||||
| chr4:143585561
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.6178+283G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585561 | ||||||
| chr4:143586117
|
G | GT | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(71): Show | 74 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.6029-125dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143586117 | ||||||
| chr4:143586553
|
G | A | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.6029-560C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143586553 | ||||||
| chr4:143586557
|
A | G | 65 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0132others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.6029-564T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143586557 | ||||||
| chr4:143587107
|
A | G | 1 | a0002c0010t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6029-1114T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587107 | ||||||
| chr4:143587235
|
A | AT | 32 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0161others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-1243dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587235 | ||||||
| chr4:143587247
|
C | T | 1 | a0022c0031t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-1254G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587247 | ||||||
| chr4:143587292
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-1299G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587292 | ||||||
| chr4:143587375
|
A | G | 1 | a0004c0004t0001g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6029-1382T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587375 | ||||||
| chr4:143587384
|
C | T | 108 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-1391G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587384 | ||||||
| chr4:143587401
|
G | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(137): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.6029-1408C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587401 | ||||||
| chr4:143587426
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0133others(2): Show | 5 | HG00673.hp2 NA18973.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-1433C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587426 | ||||||
| chr4:143587435
|
T | C | 108 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-1442A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587435 | ||||||
| chr4:143587655
|
C | G | 140 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(137): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.6029-1662G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587655 | ||||||
| chr4:143587749
|
C | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.6029-1756G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587749 | ||||||
| chr4:143587763
|
G | GA | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.6029-1771_6029-177 others(5): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587763 | ||||||
| chr4:143587854
|
C | T | 1 | a0021c0032t0004g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6029-1861G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587854 | ||||||
| chr4:143588148
|
G | T | 1 | a0006c0007t0001g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6029-2155C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588148 | ||||||
| chr4:143588239
|
G | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-2246C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588239 | ||||||
| chr4:143588249
|
T | A | 2 | a0003c0003t0001g0076a0003c0003t0001g0087 | 2 | NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.6029-2256A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588249 | ||||||
| chr4:143588359
|
C | A | 1 | a0004c0004t0001g0079 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6029-2366G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588359 | ||||||
| chr4:143588576
|
T | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(66): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.6029-2583A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588576 | ||||||
| chr4:143588599
|
C | T | 23 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0161others(20): Show | 24 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.6029-2606G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588599 | ||||||
| chr4:143588609
|
T | G | 1 | a0002c0002t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6029-2616A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588609 | ||||||
| chr4:143588705
|
C | T | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-2712G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588705 | ||||||
| chr4:143588740
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.6029-2747A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588740 | ||||||
| chr4:143588812
|
T | A | 138 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(135): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.6029-2819A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588812 | ||||||
| chr4:143588812
|
T | C | 107 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.6029-2819A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588812 | ||||||
| chr4:143588816
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6029-2823G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588816 | ||||||
| chr4:143588864
|
G | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.6029-2871C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588864 | ||||||
| chr4:143588870
|
A | G | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-2877T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588870 | ||||||
| chr4:143588888
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6029-2895G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588888 | ||||||
| chr4:143588896
|
C | T | 1 | a0020c0033t0001g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6029-2903G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588896 | ||||||
| chr4:143588906
|
T | A | 107 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.6029-2913A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588906 | ||||||
| chr4:143588907
|
C | T | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-2914G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588907 | ||||||
| chr4:143588929
|
C | T | 5 | a0002c0002t0001g0030a0010c0013t0001g0247a0010c0013t0001g0248others(2): Show | 5 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-2936G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588929 | ||||||
| chr4:143588930
|
A | G | 5 | a0002c0002t0001g0030a0010c0013t0001g0247a0010c0013t0001g0248others(2): Show | 5 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-2937T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588930 | ||||||
| chr4:143589162
|
T | G | 1 | a0010c0013t0001g0248 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6029-3169A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589162 | ||||||
| chr4:143589175
|
G | T | 1 | a0002c0002t0001g0031 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.6029-3182C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589175 | ||||||
| chr4:143589268
|
G | T | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-3275C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589268 | ||||||
| chr4:143589332
|
T | C | 1 | a0002c0002t0001g0049 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6029-3339A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589332 | ||||||
| chr4:143589334
|
G | A | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-3341C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589334 | ||||||
| chr4:143589339
|
G | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(66): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.6029-3346C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589339 | ||||||
| chr4:143589383
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0226 | 2 | HG00741.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.6029-3390C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589383 | ||||||
| chr4:143589384
|
TA | T | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-3392delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589384 | ||||||
| chr4:143589438
|
C | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-3445G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589438 | ||||||
| chr4:143589522
|
C | G | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.6029-3529G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589522 | ||||||
| chr4:143589580
|
C | G | 76 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.6029-3587G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589580 | ||||||
| chr4:143589686
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6029-3693G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589686 | ||||||
| chr4:143589707
|
T | A | 25 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0132others(22): Show | 26 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.6029-3714A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589707 | ||||||
| chr4:143589717
|
G | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-3724C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589717 | ||||||
| chr4:143589721
|
T | C | 216 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(213): Show | 221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.6029-3728A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589721 | ||||||
| chr4:143589769
|
T | G | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-3776A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589769 | ||||||
| chr4:143589848
|
C | A | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-3855G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589848 | ||||||
| chr4:143589957
|
C | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0003c0003t0001g0104 | 3 | HG02257.hp2 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6029-3964G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589957 | ||||||
| chr4:143590011
|
C | T | 220 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(217): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.6029-4018G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590011 | ||||||
| chr4:143590023
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(135): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.6029-4030G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590023 | ||||||
| chr4:143590145
|
G | A | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-4152C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590145 | ||||||
| chr4:143590246
|
C | T | 1 | a0003c0003t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6029-4253G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590246 | ||||||
| chr4:143590265
|
C | T | 2 | a0001c0001t0001g0199a0005c0005t0001g0058 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6029-4272G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590265 | ||||||
| chr4:143590281
|
A | G | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-4288T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590281 | ||||||
| chr4:143590332
|
G | A | 73 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(70): Show | 73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-4339C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590332 | ||||||
| chr4:143590333
|
T | C | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-4340A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590333 | ||||||
| chr4:143590376
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6029-4383C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590376 | ||||||
| chr4:143590496
|
C | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(66): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.6029-4503G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590496 | ||||||
| chr4:143590509
|
T | C | 4 | a0007c0008t0001g0145a0007c0008t0001g0148a0011c0011t0001g0066others(1): Show | 4 | HG02451.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.6029-4516A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590509 | ||||||
| chr4:143590664
|
A | T | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-4671T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590664 | ||||||
| chr4:143590682
|
T | C | 3 | a0011c0011t0001g0065a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.6029-4689A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590682 | ||||||
| chr4:143590692
|
A | G | 1 | a0004c0004t0001g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.6029-4699T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590692 | ||||||
| chr4:143590721
|
A | C | 1 | a0022c0031t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-4728T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590721 | ||||||
| chr4:143590723
|
G | C | 1 | a0022c0031t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-4730C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590723 | ||||||
| chr4:143590795
|
A | G | 68 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0132others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.6029-4802T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590795 | ||||||
| chr4:143590808
|
A | G | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.6029-4815T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590808 | ||||||
| chr4:143590847
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0178a0001c0001t0001g0179others(2): Show | 5 | HG01257.hp1 HG01496.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-4854C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590847 | ||||||
| chr4:143590995
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6029-5002T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590995 | ||||||
| chr4:143591098
|
T | G | 108 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-5105A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591098 | ||||||
| chr4:143591123
|
C | G | 1 | a0026c0023t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6029-5130G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591123 | ||||||
| chr4:143591278
|
C | T | 1 | a0002c0002t0001g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6029-5285G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591278 | ||||||
| chr4:143591290
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6029-5297A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591290 | ||||||
| chr4:143591545
|
C | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0178a0001c0001t0001g0179others(2): Show | 5 | HG01257.hp1 HG01496.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-5552G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591545 | ||||||
| chr4:143591546
|
G | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(137): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.6029-5553C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591546 | ||||||
| chr4:143591635
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0163 | 2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.6029-5642A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591635 | ||||||
| chr4:143591637
|
T | G | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.6029-5644A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591637 | ||||||
| chr4:143591751
|
G | T | 79 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.6029-5758C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591751 | ||||||
| chr4:143591813
|
C | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(216): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.6029-5820G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591813 | ||||||
| chr4:143591836
|
C | T | 1 | a0022c0031t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-5843G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591836 | ||||||
| chr4:143591855
|
T | G | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-5862A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591855 | ||||||
| chr4:143591895
|
A | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(66): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.6029-5902T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591895 | ||||||
| chr4:143591918
|
A | G | 1 | a0020c0033t0001g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6029-5925T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591918 | ||||||
| chr4:143591966
|
G | A | 1 | a0004c0004t0001g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6029-5973C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591966 | ||||||
| chr4:143592037
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6029-6044C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592037 | ||||||
| chr4:143592236
|
T | C | 3 | a0001c0001t0001g0204a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG00673.hp1 NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.6029-6243A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592236 | ||||||
| chr4:143592348
|
C | CAATTTGG others(1412): Show |
2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-6356_6029-635 others(1423): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592348 | ||||||
| chr4:143592436
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6029-6443C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592436 | ||||||
| chr4:143592441
|
G | A | 65 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0132others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.6029-6448C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592441 | ||||||
| chr4:143592441
|
G | C | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-6448C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592441 | ||||||
| chr4:143592445
|
A | G | 1 | a0026c0023t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6029-6452T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592445 | ||||||
| chr4:143592519
|
T | G | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-6526A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592519 | ||||||
| chr4:143592565
|
G | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-6572C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592565 | ||||||
| chr4:143592566
|
G | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(66): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.6029-6573C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592566 | ||||||
| chr4:143592567
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6029-6574G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592567 | ||||||
| chr4:143592610
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6029-6617C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592610 | ||||||
| chr4:143592613
|
G | T | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-6620C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592613 | ||||||
| chr4:143592626
|
G | C | 32 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0161others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-6633C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592626 | ||||||
| chr4:143592647
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.6029-6654C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592647 | ||||||
| chr4:143592822
|
C | T | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-6829G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592822 | ||||||
| chr4:143592824
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6029-6831A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592824 | ||||||
| chr4:143592858
|
C | A | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-6865G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592858 | ||||||
| chr4:143592859
|
G | A | 7 | a0007c0008t0001g0145a0007c0008t0001g0148a0011c0011t0001g0065others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.6029-6866C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592859 | ||||||
| chr4:143592934
|
G | A | 1 | a0022c0031t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-6941C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592934 | ||||||
| chr4:143592997
|
C | G | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-7004G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592997 | ||||||
| chr4:143593000
|
C | T | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(71): Show | 74 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.6029-7007G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593000 | ||||||
| chr4:143593031
|
C | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-7038G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593031 | ||||||
| chr4:143593064
|
C | T | 73 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(70): Show | 73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-7071G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593064 | ||||||
| chr4:143593065
|
G | A | 65 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0132others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.6029-7072C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593065 | ||||||
| chr4:143593177
|
C | T | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-7184G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593177 | ||||||
| chr4:143593187
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.6029-7194G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593187 | ||||||
| chr4:143593213
|
T | C | 2 | a0002c0009t0001g0009a0002c0009t0001g0010 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.6029-7220A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593213 | ||||||
| chr4:143593267
|
G | A | 136 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(133): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.6029-7274C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593267 | ||||||
| chr4:143593301
|
G | A | 6 | a0003c0003t0001g0102a0005c0005t0001g0062a0005c0022t0001g0064others(3): Show | 6 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.6029-7308C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593301 | ||||||
| chr4:143593359
|
T | A | 1 | a0022c0031t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-7366A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593359 | ||||||
| chr4:143593396
|
C | T | 73 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(70): Show | 73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-7403G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593396 | ||||||
| chr4:143593456
|
C | T | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-7463G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593456 | ||||||
| chr4:143593532
|
G | A | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-7539C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593532 | ||||||
| chr4:143593549
|
G | A | 32 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0161others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-7556C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593549 | ||||||
| chr4:143593584
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-7591C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593584 | ||||||
| chr4:143593646
|
C | G | 1 | a0002c0002t0001g0049 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6029-7653G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593646 | ||||||
| chr4:143593675
|
G | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-7682C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593675 | ||||||
| chr4:143593693
|
T | A | 136 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(133): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.6029-7700A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593693 | ||||||
| chr4:143593702
|
A | C | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-7709T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593702 | ||||||
| chr4:143593736
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0224 | 3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.6029-7743C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593736 | ||||||
| chr4:143594016
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6029-8023T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594016 | ||||||
| chr4:143594033
|
C | T | 2 | a0008c0012t0001g0002a0008c0012t0001g0069 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-8040G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594033 | ||||||
| chr4:143594063
|
G | T | 76 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.6029-8070C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594063 | ||||||
| chr4:143594210
|
C | G | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-8217G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594210 | ||||||
| chr4:143594211
|
A | G | 32 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0161others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-8218T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594211 | ||||||
| chr4:143594214
|
C | T | 1 | a0002c0002t0001g0031 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.6029-8221G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594214 | ||||||
| chr4:143594215
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6029-8222C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594215 | ||||||
| chr4:143594304
|
C | T | 73 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(70): Show | 73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-8311G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594304 | ||||||
| chr4:143594354
|
T | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(137): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.6029-8361A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594354 | ||||||
| chr4:143594381
|
C | T | 73 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(70): Show | 73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-8388G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594381 | ||||||
| chr4:143594447
|
A | G | 1 | a0012c0016t0001g0075 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6029-8454T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594447 | ||||||
| chr4:143594480
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-8487T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594480 | ||||||
| chr4:143594480
|
A | T | 7 | a0007c0008t0001g0145a0007c0008t0001g0148a0011c0011t0001g0065others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.6029-8487T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594480 | ||||||
| chr4:143594611
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-8618G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594611 | ||||||
| chr4:143594661
|
G | A | 250 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-8668C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594661 | ||||||
| chr4:143594710
|
C | G | 1 | a0004c0004t0001g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6029-8717G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594710 | ||||||
| chr4:143594735
|
G | A | 108 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-8742C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594735 | ||||||
| chr4:143594743
|
A | C | 35 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0161others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.6029-8750T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594743 | ||||||
| chr4:143595009
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6029-9016C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595009 | ||||||
| chr4:143595430
|
G | A | 1 | a0007c0008t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6029-9437C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595430 | ||||||
| chr4:143595438
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0193 | 3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.6029-9445T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595438 | ||||||
| chr4:143595468
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0168 | 2 | HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.6029-9475C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595468 | ||||||
| chr4:143595470
|
G | C | 4 | a0007c0008t0001g0145a0007c0008t0001g0148a0011c0011t0001g0066others(1): Show | 4 | HG02451.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.6029-9477C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595470 | ||||||
| chr4:143595637
|
C | T | 155 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(152): Show | 159 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.6029-9644G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595637 | ||||||
| chr4:143595662
|
C | T | 139 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(136): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.6029-9669G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595662 | ||||||
| chr4:143595684
|
A | G | 9 | a0001c0001t0001g0180a0001c0001t0001g0191a0001c0001t0001g0228others(6): Show | 9 | HG01243.hp2 HG01981.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.6029-9691T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595684 | ||||||
| chr4:143595694
|
T | C | 5 | a0001c0001t0001g0147a0007c0008t0001g0137a0007c0008t0001g0239others(2): Show | 5 | HG00741.hp1 HG01192.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-9701A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595694 | ||||||
| chr4:143595698
|
T | C | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-9705A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595698 | ||||||
| chr4:143595744
|
C | T | 1 | a0003c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6029-9751G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595744 | ||||||
| chr4:143595745
|
A | G | 1 | a0003c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6029-9752T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595745 | ||||||
| chr4:143595757
|
A | G | 20 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(17): Show | 20 | HG01496.hp2 HG01981.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.6029-9764T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595757 | ||||||
| chr4:143595761
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6029-9768A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595761 | ||||||
| chr4:143595771
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-9778G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595771 | ||||||
| chr4:143595775
|
T | C | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-9782A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595775 | ||||||
| chr4:143595777
|
A | G | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-9784T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595777 | ||||||
| chr4:143595804
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6029-9811G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595804 | ||||||
| chr4:143595805
|
G | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-9812C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595805 | ||||||
| chr4:143595859
|
G | A | 3 | a0003c0003t0001g0108a0021c0032t0004g0153a0022c0031t0001g0146 | 3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6029-9866C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595859 | ||||||
| chr4:143595860
|
T | C | 3 | a0003c0003t0001g0108a0021c0032t0004g0153a0022c0031t0001g0146 | 3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6029-9867A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595860 | ||||||
| chr4:143595866
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6029-9873G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595866 | ||||||
| chr4:143595875
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(67): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-9882C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595875 | ||||||
| chr4:143595889
|
G | GAAAAAAA others(6): Show |
18 | a0001c0001t0001g0165a0004c0004t0001g0091a0004c0004t0001g0093others(15): Show | 18 | HG01496.hp2 HG01981.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.6029-9909_6029-989 others(17): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | ||||||
| chr4:143595889
|
G | GAAAAAAA others(7): Show |
2 | a0004c0004t0001g0097a0007c0030t0001g0154 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.6029-9910_6029-989 others(18): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | ||||||
| chr4:143595889
|
G | GAAAAAAA others(8): Show |
1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-9911_6029-989 others(19): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | ||||||
| chr4:143595889
|
G | GAAAAAAA others(9): Show |
4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(20): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | ||||||
| chr4:143595889
|
G | GGAAAAAA others(4): Show |
2 | a0001c0006t0001g0113a0002c0002t0001g0026 | 2 | HG01167.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(15): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | ||||||
| chr4:143595889
|
G | GGAAAAAA others(5): Show |
57 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(54): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(16): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | ||||||
| chr4:143595889
|
G | GGAAAAAA others(6): Show |
11 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0001t0001g0172others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(17): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | ||||||
| chr4:143595961
|
T | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(81): Show | 87 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.6029-9968A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595961 | ||||||
| chr4:143596018
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.6029-10025C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596018 | ||||||
| chr4:143596063
|
G | A | 1 | a0002c0002t0001g0050 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6029-10070C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596063 | ||||||
| chr4:143596196
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.6029-10203C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596196 | ||||||
| chr4:143596454
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.6029-10461G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596454 | ||||||
| chr4:143596558
|
T | C | 9 | a0004c0004t0001g0091a0004c0004t0001g0094a0004c0004t0001g0095others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.6029-10565A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596558 | ||||||
| chr4:143596700
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6029-10707G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596700 | ||||||
| chr4:143596771
|
TA | T | 92 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.6029-10779delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596771 | ||||||
| chr4:143596869
|
T | C | 1 | a0004c0004t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6029-10876A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596869 | ||||||
| chr4:143597127
|
AACAG | A | 3 | a0001c0001t0001g0156a0001c0001t0003g0233a0001c0001t0003g0234 | 3 | HG02559.hp2 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6029-11138_6029-11 others(10): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597127 | ||||||
| chr4:143597135
|
G | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0224 | 3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.6029-11142C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597135 | ||||||
| chr4:143597151
|
A | T | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-11158T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597151 | ||||||
| chr4:143597181
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-11188G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597181 | ||||||
| chr4:143597268
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6029-11275G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597268 | ||||||
| chr4:143597269
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6029-11276C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597269 | ||||||
| chr4:143597370
|
A | G | 1 | a0005c0005t0001g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6029-11377T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597370 | ||||||
| chr4:143597371
|
T | C | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6029-11378A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597371 | ||||||
| chr4:143597580
|
A | G | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-11587T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597580 | ||||||
| chr4:143597724
|
A | T | 1 | a0007c0008t0001g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6029-11731T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597724 | ||||||
| chr4:143597740
|
G | A | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-11747C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597740 | ||||||
| chr4:143597971
|
T | C | 17 | a0001c0001t0001g0147a0004c0004t0001g0079a0004c0004t0001g0091others(14): Show | 17 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.6029-11978A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597971 | ||||||
| chr4:143598260
|
C | A | 4 | a0007c0008t0001g0157a0011c0011t0001g0065a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-12267G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598260 | ||||||
| chr4:143598278
|
T | C | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.6029-12285A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598278 | ||||||
| chr4:143598598
|
GTA | G | 4 | a0007c0008t0001g0157a0011c0011t0001g0065a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-12607_6029-12 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598598 | ||||||
| chr4:143598631
|
G | A | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-12638C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598631 | ||||||
| chr4:143599424
|
T | C | 15 | a0001c0001t0001g0147a0004c0004t0001g0079a0004c0004t0001g0091others(12): Show | 15 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.6028+11855A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599424 | ||||||
| chr4:143599484
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.6028+11795T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599484 | ||||||
| chr4:143599629
|
A | G | 94 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.6028+11650T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599629 | ||||||
| chr4:143599692
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6028+11587T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599692 | ||||||
| chr4:143599695
|
A | C | 15 | a0001c0001t0001g0147a0004c0004t0001g0079a0004c0004t0001g0091others(12): Show | 15 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.6028+11584T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599695 | ||||||
| chr4:143599729
|
G | A | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+11550C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599729 | ||||||
| chr4:143599766
|
T | TGGGCTAG others(5): Show |
184 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(181): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.6028+11501_6028+11 others(18): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599766 | ||||||
| chr4:143599803
|
G | A | 4 | a0007c0008t0001g0157a0011c0011t0001g0065a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+11476C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599803 | ||||||
| chr4:143599938
|
G | T | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6028+11341C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599938 | ||||||
| chr4:143599998
|
G | A | 5 | a0007c0008t0001g0145a0007c0008t0001g0148a0007c0030t0001g0154others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6028+11281C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599998 | ||||||
| chr4:143600070
|
C | T | 4 | a0007c0008t0001g0157a0011c0011t0001g0065a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+11209G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600070 | ||||||
| chr4:143600078
|
T | C | 2 | a0001c0001t0001g0167a0003c0003t0001g0107 | 2 | NA18968.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.6028+11201A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600078 | ||||||
| chr4:143600222
|
TA | T | 76 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.6028+11056delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600222 | ||||||
| chr4:143600460
|
C | A | 4 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0241others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+10819G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600460 | ||||||
| chr4:143600590
|
T | C | 1 | a0027c0025t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6028+10689A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600590 | ||||||
| chr4:143600705
|
G | A | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.6028+10574C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600705 | ||||||
| chr4:143600950
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6028+10329G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600950 | ||||||
| chr4:143600963
|
CT | C | 92 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.6028+10315delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600963 | ||||||
| chr4:143601016
|
G | A | 1 | a0027c0025t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6028+10263C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601016 | ||||||
| chr4:143601092
|
T | TA | 21 | a0001c0001t0001g0147a0004c0004t0001g0079a0004c0004t0001g0091others(18): Show | 21 | HG00558.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.6028+10186dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601092 | ||||||
| chr4:143601135
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6028+10144G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601135 | ||||||
| chr4:143601429
|
C | T | 6 | a0007c0008t0001g0137a0007c0008t0001g0157a0007c0008t0001g0239others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+9850G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601429 | ||||||
| chr4:143601474
|
C | T | 94 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.6028+9805G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601474 | ||||||
| chr4:143601544
|
T | C | 15 | a0001c0001t0001g0147a0004c0004t0001g0079a0004c0004t0001g0091others(12): Show | 15 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.6028+9735A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601544 | ||||||
| chr4:143601572
|
C | T | 21 | a0001c0001t0001g0147a0004c0004t0001g0079a0004c0004t0001g0091others(18): Show | 21 | HG00558.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.6028+9707G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601572 | ||||||
| chr4:143601714
|
G | A | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+9565C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601714 | ||||||
| chr4:143601750
|
G | T | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.6028+9529C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601750 | ||||||
| chr4:143602017
|
C | T | 93 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(90): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.6028+9262G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602017 | ||||||
| chr4:143602173
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0186a0001c0001t0001g0188 | 3 | NA18979.hp1 NA19056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.6028+9106G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602173 | ||||||
| chr4:143602379
|
T | A | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+8900A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602379 | ||||||
| chr4:143602554
|
C | T | 6 | a0007c0008t0001g0137a0007c0008t0001g0157a0007c0008t0001g0239others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+8725G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602554 | ||||||
| chr4:143602609
|
AGGAGATT others(27): Show |
A | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+8636_6028+866 others(38): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602609 | ||||||
| chr4:143603041
|
T | A | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.6028+8238A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603041 | ||||||
| chr4:143603047
|
G | A | 2 | a0001c0001t0001g0185a0004c0004t0001g0080 | 2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.6028+8232C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603047 | ||||||
| chr4:143603429
|
G | A | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.6028+7850C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603429 | ||||||
| chr4:143603519
|
C | A | 96 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(93): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.6028+7760G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603519 | ||||||
| chr4:143603587
|
C | T | 1 | a0003c0003t0001g0086 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6028+7692G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603587 | ||||||
| chr4:143603599
|
A | G | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.6028+7680T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603599 | ||||||
| chr4:143603650
|
A | G | 1 | a0003c0003t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6028+7629T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603650 | ||||||
| chr4:143603670
|
A | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+7609T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603670 | ||||||
| chr4:143603787
|
C | T | 10 | a0001c0001t0001g0159a0001c0001t0001g0197a0001c0001t0001g0203others(7): Show | 10 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.6028+7492G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603787 | ||||||
| chr4:143604211
|
C | T | 6 | a0007c0008t0001g0137a0007c0008t0001g0157a0007c0008t0001g0239others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+7068G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604211 | ||||||
| chr4:143604323
|
C | T | 9 | a0001c0001t0001g0121a0002c0002t0001g0014a0002c0002t0001g0016others(6): Show | 9 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.6028+6956G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604323 | ||||||
| chr4:143604327
|
A | G | 20 | a0004c0004t0001g0079a0004c0004t0001g0091a0004c0004t0001g0093others(17): Show | 20 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.6028+6952T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604327 | ||||||
| chr4:143604779
|
T | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01952.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.6028+6500A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604779 | ||||||
| chr4:143604833
|
C | T | 2 | a0001c0001t0001g0200a0003c0003t0001g0092 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6028+6446G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604833 | ||||||
| chr4:143604986
|
A | C | 4 | a0001c0001t0001g0181a0002c0002t0001g0018a0002c0002t0001g0026others(1): Show | 4 | HG01167.hp1 HG01943.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.6028+6293T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604986 | ||||||
| chr4:143605046
|
G | A | 84 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.6028+6233C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605046 | ||||||
| chr4:143605173
|
T | A | 84 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.6028+6106A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605173 | ||||||
| chr4:143605297
|
C | G | 32 | a0001c0001t0001g0005a0001c0001t0001g0159a0001c0001t0001g0197others(29): Show | 33 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.6028+5982G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605297 | ||||||
| chr4:143605356
|
C | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6028+5923G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605356 | ||||||
| chr4:143605360
|
CTCCT | C | 9 | a0007c0008t0001g0137a0007c0008t0001g0157a0007c0008t0001g0239others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.6028+5915_6028+591 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605360 | ||||||
| chr4:143605410
|
T | A | 1 | a0001c0001t0001g0127 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6028+5869A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605410 | ||||||
| chr4:143605630
|
C | T | 1 | a0005c0005t0001g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6028+5649G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605630 | ||||||
| chr4:143605680
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+5599G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605680 | ||||||
| chr4:143605847
|
G | A | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6028+5432C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605847 | ||||||
| chr4:143606022
|
G | A | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+5257C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606022 | ||||||
| chr4:143606077
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6028+5202G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606077 | ||||||
| chr4:143606340
|
T | C | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+4939A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606340 | ||||||
| chr4:143606371
|
C | CT | 101 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.6028+4907dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606371 | ||||||
| chr4:143606568
|
T | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+4711A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606568 | ||||||
| chr4:143606630
|
C | T | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+4649G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606630 | ||||||
| chr4:143606703
|
C | A | 1 | a0003c0003t0001g0084 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6028+4576G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606703 | ||||||
| chr4:143606793
|
AT | A | 99 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.6028+4485delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606793 | ||||||
| chr4:143606950
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6028+4329G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606950 | ||||||
| chr4:143607219
|
C | G | 5 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+4060G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607219 | ||||||
| chr4:143607355
|
T | C | 217 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(214): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.6028+3924A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607355 | ||||||
| chr4:143607475
|
C | A | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.6028+3804G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607475 | ||||||
| chr4:143607830
|
C | T | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.6028+3449G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607830 | ||||||
| chr4:143608232
|
A | G | 15 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.6028+3047T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608232 | ||||||
| chr4:143608234
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG00741.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.6028+3045C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608234 | ||||||
| chr4:143608237
|
A | C | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+3042T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608237 | ||||||
| chr4:143608325
|
G | C | 102 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.6028+2954C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608325 | ||||||
| chr4:143608364
|
G | C | 20 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(17): Show | 20 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.6028+2915C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608364 | ||||||
| chr4:143608400
|
T | C | 3 | a0003c0003t0001g0108a0021c0032t0004g0153a0022c0031t0001g0146 | 3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6028+2879A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608400 | ||||||
| chr4:143608660
|
T | C | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6028+2619A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608660 | ||||||
| chr4:143608746
|
T | G | 1 | a0003c0003t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6028+2533A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608746 | ||||||
| chr4:143609072
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01952.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.6028+2207G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609072 | ||||||
| chr4:143609083
|
T | C | 102 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.6028+2196A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609083 | ||||||
| chr4:143609096
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.6028+2183T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609096 | ||||||
| chr4:143609253
|
G | A | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6028+2026C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609253 | ||||||
| chr4:143609454
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6028+1825G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609454 | ||||||
| chr4:143609480
|
TAA | T | 34 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0128others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.6028+1797_6028+179 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609480 | ||||||
| chr4:143609502
|
G | A | 102 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.6028+1777C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609502 | ||||||
| chr4:143609688
|
G | A | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6028+1591C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609688 | ||||||
| chr4:143609694
|
AT | A | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6028+1584delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609694 | ||||||
| chr4:143609734
|
T | A | 4 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.6028+1545A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609734 | ||||||
| chr4:143609754
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6028+1525T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609754 | ||||||
| chr4:143609846
|
T | C | 2 | a0001c0001t0001g0231a0002c0002t0001g0049 | 2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.6028+1433A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609846 | ||||||
| chr4:143610050
|
A | T | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6028+1229T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610050 | ||||||
| chr4:143610055
|
A | G | 2 | a0001c0001t0001g0231a0002c0002t0001g0049 | 2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.6028+1224T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610055 | ||||||
| chr4:143610333
|
G | A | 26 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(23): Show | 26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.6028+946C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610333 | ||||||
| chr4:143610582
|
A | G | 3 | a0003c0003t0001g0108a0021c0032t0004g0153a0022c0031t0001g0146 | 3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6028+697T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610582 | ||||||
| chr4:143610778
|
T | C | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+501A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610778 | ||||||
| chr4:143610838
|
A | G | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6028+441T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610838 | ||||||
| chr4:143611009
|
C | T | 1 | a0004c0004t0001g0079 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6028+270G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143611009 | ||||||
| chr4:143611056
|
CAAGTA | C | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.6028+218_6028+222d others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143611056 | ||||||
| chr4:143611111
|
T | A | 26 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(23): Show | 26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.6028+168A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143611111 | ||||||
| chr4:143611540
|
G | A | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-13C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143611540 | ||||||
| chr4:143611543
|
A | G | 4 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0241others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5780-16T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143611543 | ||||||
| chr4:143611786
|
C | T | 4 | a0007c0008t0001g0145a0007c0008t0001g0148a0011c0011t0001g0066others(1): Show | 4 | HG02451.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.5780-259G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143611786 | ||||||
| chr4:143612001
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0193 | 3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.5780-474T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612001 | ||||||
| chr4:143612181
|
C | G | 5 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5780-654G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612181 | ||||||
| chr4:143612221
|
C | T | 102 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.5780-694G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612221 | ||||||
| chr4:143612235
|
A | G | 4 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-708T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612235 | ||||||
| chr4:143612334
|
G | A | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5780-807C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612334 | ||||||
| chr4:143612483
|
T | G | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5780-956A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612483 | ||||||
| chr4:143612562
|
G | C | 4 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-1035C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612562 | ||||||
| chr4:143612563
|
T | G | 102 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(99): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.5780-1036A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612563 | ||||||
| chr4:143612658
|
T | G | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5780-1131A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612658 | ||||||
| chr4:143612794
|
A | T | 26 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(23): Show | 26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.5780-1267T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612794 | ||||||
| chr4:143613167
|
C | T | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5780-1640G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613167 | ||||||
| chr4:143613247
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5780-1720C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613247 | ||||||
| chr4:143613465
|
C | A | 67 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.5780-1938G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613465 | ||||||
| chr4:143613641
|
T | C | 1 | a0026c0023t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5780-2114A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613641 | ||||||
| chr4:143613866
|
C | G | 1 | a0003c0003t0001g0078 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5780-2339G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613866 | ||||||
| chr4:143614234
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.5780-2707A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614234 | ||||||
| chr4:143614414
|
A | G | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5780-2887T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614414 | ||||||
| chr4:143614502
|
C | A | 5 | a0007c0008t0001g0145a0007c0008t0001g0148a0007c0030t0001g0154others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-2975G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614502 | ||||||
| chr4:143614522
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.5780-2995A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614522 | ||||||
| chr4:143614631
|
T | C | 5 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5780-3104A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614631 | ||||||
| chr4:143614681
|
C | A | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5780-3154G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614681 | ||||||
| chr4:143614824
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5780-3297G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614824 | ||||||
| chr4:143614851
|
G | A | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-3324C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614851 | ||||||
| chr4:143615022
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5780-3495C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615022 | ||||||
| chr4:143615180
|
G | A | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5780-3653C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615180 | ||||||
| chr4:143615191
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5780-3664C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615191 | ||||||
| chr4:143615258
|
C | T | 15 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5780-3731G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615258 | ||||||
| chr4:143615299
|
T | G | 15 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5780-3772A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615299 | ||||||
| chr4:143615540
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02109.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5780-4013A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615540 | ||||||
| chr4:143615679
|
G | A | 5 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5780-4152C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615679 | ||||||
| chr4:143615698
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5780-4171C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615698 | ||||||
| chr4:143615707
|
C | CA | 77 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(74): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.5780-4181dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615707 | ||||||
| chr4:143615716
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5780-4189T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615716 | ||||||
| chr4:143615716
|
AAC | A | 4 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-4191_5780-419 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615716 | ||||||
| chr4:143615717
|
AC | A | 11 | a0004c0004t0001g0091a0004c0004t0001g0093a0004c0004t0001g0094others(8): Show | 11 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.5780-4191delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615717 | ||||||
| chr4:143615718
|
C | A | 12 | a0002c0009t0001g0008a0004c0004t0001g0079a0004c0004t0001g0080others(9): Show | 12 | HG00558.hp2 HG01168.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.5780-4191G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615718 | ||||||
| chr4:143615718
|
CA | C | 4 | a0007c0008t0001g0157a0011c0011t0001g0065a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.5780-4192delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615718 | ||||||
| chr4:143615841
|
G | T | 1 | a0001c0001t0001g0005 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.5780-4314C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615841 | ||||||
| chr4:143615844
|
TC | T | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-4318delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615844 | ||||||
| chr4:143616096
|
A | C | 2 | a0001c0001t0001g0167a0003c0003t0001g0107 | 2 | NA18968.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.5780-4569T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616096 | ||||||
| chr4:143616142
|
G | T | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-4615C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616142 | ||||||
| chr4:143616187
|
T | C | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5780-4660A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616187 | ||||||
| chr4:143616197
|
G | C | 1 | a0015c0014t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5780-4670C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616197 | ||||||
| chr4:143616205
|
A | G | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-4678T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616205 | ||||||
| chr4:143616278
|
G | A | 1 | a0005c0022t0001g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5780-4751C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616278 | ||||||
| chr4:143616446
|
G | C | 1 | a0004c0004t0001g0079 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5779+4591C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616446 | ||||||
| chr4:143616515
|
A | G | 103 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.5779+4522T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616515 | ||||||
| chr4:143616543
|
T | C | 15 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5779+4494A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616543 | ||||||
| chr4:143616547
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0193 | 3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.5779+4490C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616547 | ||||||
| chr4:143616561
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5779+4476G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616561 | ||||||
| chr4:143616746
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5779+4291G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616746 | ||||||
| chr4:143616753
|
A | C | 4 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5779+4284T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616753 | ||||||
| chr4:143616792
|
C | CAAAAA | 5 | a0005c0005t0001g0062a0008c0012t0001g0002a0008c0012t0001g0069others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5779+4240_5779+424 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616792 | ||||||
| chr4:143616792
|
C | CAAAAAAA others(1): Show |
19 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(16): Show | 19 | HG00558.hp2 HG01496.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.5779+4237_5779+424 others(12): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616792 | ||||||
| chr4:143616792
|
C | CAAAAAAA others(3): Show |
2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5779+4235_5779+424 others(14): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616792 | ||||||
| chr4:143616804
|
G | A | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.5779+4233C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616804 | ||||||
| chr4:143616891
|
G | T | 1 | a0016c0019t0001g0007 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5779+4146C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616891 | ||||||
| chr4:143616934
|
A | G | 3 | a0004c0004t0001g0098a0004c0004t0001g0099a0004c0004t0001g0101 | 3 | HG01496.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5779+4103T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616934 | ||||||
| chr4:143617163
|
TCTTTA | T | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5779+3869_5779+387 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617163 | ||||||
| chr4:143617262
|
G | C | 5 | a0007c0008t0001g0145a0007c0008t0001g0148a0007c0030t0001g0154others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5779+3775C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617262 | ||||||
| chr4:143617561
|
G | A | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5779+3476C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617561 | ||||||
| chr4:143617665
|
G | GGGTTTAA others(96): Show |
1 | a0007c0008t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5779+3371_5779+337 others(107): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617665 | ||||||
| chr4:143617665
|
G | GGGTTTAA others(97): Show |
1 | a0007c0008t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5779+3371_5779+337 others(108): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617665 | ||||||
| chr4:143617704
|
AGAG | A | 5 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5779+3330_5779+333 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617704 | ||||||
| chr4:143617855
|
C | T | 4 | a0001c0001t0001g0181a0002c0002t0001g0018a0002c0002t0001g0026others(1): Show | 4 | HG01167.hp1 HG01943.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.5779+3182G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617855 | ||||||
| chr4:143617985
|
C | A | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5779+3052G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617985 | ||||||
| chr4:143618295
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5779+2742G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618295 | ||||||
| chr4:143618349
|
C | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5779+2688G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618349 | ||||||
| chr4:143618369
|
C | G | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5779+2668G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618369 | ||||||
| chr4:143618504
|
C | G | 1 | a0002c0002t0001g0020 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5779+2533G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618504 | ||||||
| chr4:143618621
|
T | C | 103 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.5779+2416A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618621 | ||||||
| chr4:143618626
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5779+2411C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618626 | ||||||
| chr4:143618682
|
T | C | 103 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.5779+2355A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618682 | ||||||
| chr4:143618793
|
G | A | 26 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(23): Show | 26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.5779+2244C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618793 | ||||||
| chr4:143618869
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5779+2168G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618869 | ||||||
| chr4:143618931
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5779+2106T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618931 | ||||||
| chr4:143619089
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5779+1948G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619089 | ||||||
| chr4:143619179
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5779+1858C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619179 | ||||||
| chr4:143619348
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5779+1689G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619348 | ||||||
| chr4:143619433
|
G | A | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.5779+1604C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619433 | ||||||
| chr4:143619525
|
C | T | 1 | a0024c0021t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5779+1512G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619525 | ||||||
| chr4:143619562
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5779+1475A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619562 | ||||||
| chr4:143619563
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5779+1474G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619563 | ||||||
| chr4:143619843
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5779+1194C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619843 | ||||||
| chr4:143620204
|
G | A | 1 | a0003c0003t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5779+833C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620204 | ||||||
| chr4:143620426
|
C | T | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5779+611G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620426 | ||||||
| chr4:143620434
|
G | A | 31 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(28): Show | 32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5779+603C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620434 | ||||||
| chr4:143620436
|
A | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5779+601T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620436 | ||||||
| chr4:143620657
|
G | C | 1 | a0006c0007t0001g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5779+380C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620657 | ||||||
| chr4:143620781
|
G | A | 1 | a0009c0034t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5779+256C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620781 | ||||||
| chr4:143620895
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5779+142C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620895 | ||||||
| chr4:143620974
|
C | A | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5779+63G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620974 | ||||||
| chr4:143621021
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5779+16G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143621021 | ||||||
| chr4:143621183
|
C | G | 1 | a0002c0010t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5654-21G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621183 | ||||||
| chr4:143621738
|
G | C | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5654-576C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621738 | ||||||
| chr4:143621795
|
G | A | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.5654-633C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621795 | ||||||
| chr4:143621923
|
A | G | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5654-761T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621923 | ||||||
| chr4:143621946
|
G | A | 105 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(102): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.5654-784C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621946 | ||||||
| chr4:143622078
|
T | C | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5654-916A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622078 | ||||||
| chr4:143622091
|
C | CT | 15 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0226others(12): Show | 16 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.5654-930dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622091 | ||||||
| chr4:143622203
|
C | T | 1 | a0002c0002t0001g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5654-1041G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622203 | ||||||
| chr4:143622290
|
C | T | 5 | a0007c0008t0001g0145a0007c0008t0001g0148a0007c0030t0001g0154others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5654-1128G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622290 | ||||||
| chr4:143622313
|
C | T | 1 | a0027c0025t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5654-1151G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622313 | ||||||
| chr4:143622403
|
C | CT | 40 | a0001c0001t0001g0005a0001c0001t0001g0147a0001c0001t0001g0174others(37): Show | 41 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.5654-1242dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | ||||||
| chr4:143622403
|
CT | C | 10 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0161others(7): Show | 10 | HG00558.hp2 HG01099.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.5654-1242delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | ||||||
| chr4:143622403
|
CTT | C | 89 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.5654-1243_5654-124 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | ||||||
| chr4:143622403
|
CTTT | C | 5 | a0007c0008t0001g0145a0007c0008t0001g0148a0007c0030t0001g0154others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5654-1244_5654-124 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | ||||||
| chr4:143622625
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0163 | 2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5654-1463C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622625 | ||||||
| chr4:143622722
|
T | C | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5653+1386A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622722 | ||||||
| chr4:143622797
|
A | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5653+1311T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622797 | ||||||
| chr4:143623410
|
A | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG00438.hp2 NA18962.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.5653+698T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623410 | ||||||
| chr4:143623493
|
T | TC | 43 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0132others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.5653+614dupG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | ||||||
| chr4:143623493
|
T | TCC | 16 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0162others(13): Show | 17 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.5653+613_5653+614d others(4): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | ||||||
| chr4:143623493
|
TC | T | 71 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0124others(68): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.5653+614delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | ||||||
| chr4:143623493
|
TCCC | T | 19 | a0004c0004t0001g0079a0004c0004t0001g0080a0004c0004t0001g0091others(16): Show | 19 | HG00558.hp2 HG01261.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.5653+612_5653+614d others(5): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | ||||||
| chr4:143623498
|
C | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0225 | 2 | HG01168.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.5653+610G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623498 | ||||||
| chr4:143623554
|
C | T | 1 | a0004c0004t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5653+554G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623554 | ||||||
| chr4:143623573
|
A | AT | 32 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(29): Show | 33 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5653+534dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623573 | ||||||
| chr4:143623794
|
G | T | 1 | a0009c0034t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5653+314C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623794 | ||||||
| chr4:143623986
|
T | G | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5653+122A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623986 | ||||||
| chr4:143624574
|
G | A | 104 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(101): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.5423-236C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624574 | ||||||
| chr4:143624601
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5423-263C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624601 | ||||||
| chr4:143624844
|
C | A | 1 | a0002c0002t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5423-506G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624844 | ||||||
| chr4:143624879
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5423-541C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624879 | ||||||
| chr4:143625122
|
A | G | 30 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(27): Show | 31 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.5423-784T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625122 | ||||||
| chr4:143625331
|
C | T | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5423-993G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625331 | ||||||
| chr4:143625380
|
C | T | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.5423-1042G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625380 | ||||||
| chr4:143625551
|
A | G | 32 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(29): Show | 33 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5423-1213T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625551 | ||||||
| chr4:143625649
|
A | C | 104 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(101): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.5423-1311T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625649 | ||||||
| chr4:143625696
|
G | T | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5423-1358C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625696 | ||||||
| chr4:143625902
|
CATT | C | 6 | a0007c0008t0001g0137a0007c0008t0001g0157a0007c0008t0001g0239others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.5423-1567_5423-156 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625902 | ||||||
| chr4:143625982
|
C | CA | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5422+1631dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625982 | ||||||
| chr4:143625984
|
C | A | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5422+1630G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625984 | ||||||
| chr4:143626185
|
A | G | 4 | a0007c0008t0001g0157a0011c0011t0001g0065a0014c0018t0001g0244others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.5422+1429T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626185 | ||||||
| chr4:143626204
|
T | G | 2 | a0003c0003t0001g0109a0005c0005t0001g0061 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5422+1410A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626204 | ||||||
| chr4:143626434
|
A | G | 7 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG00140.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.5422+1180T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626434 | ||||||
| chr4:143626455
|
A | G | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5422+1159T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626455 | ||||||
| chr4:143626619
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5422+995G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626619 | ||||||
| chr4:143626680
|
G | C | 32 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(29): Show | 33 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5422+934C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626680 | ||||||
| chr4:143626699
|
G | T | 2 | a0007c0008t0001g0137a0007c0008t0001g0239 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5422+915C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626699 | ||||||
| chr4:143626870
|
A | C | 2 | a0005c0005t0001g0062a0015c0014t0001g0052 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5422+744T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626870 | ||||||
| chr4:143626999
|
A | G | 104 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(101): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.5422+615T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626999 | ||||||
| chr4:143627170
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01069.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.5422+444C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627170 | ||||||
| chr4:143627302
|
T | C | 1 | a0004c0004t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5422+312A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627302 | ||||||
| chr4:143627472
|
G | A | 1 | a0005c0005t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5422+142C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627472 | ||||||
| chr4:143627526
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5422+88G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627526 | ||||||
| chr4:143627999
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5276-239T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143627999 | ||||||
| chr4:143628057
|
T | C | 1 | a0002c0002t0001g0017 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5276-297A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628057 | ||||||
| chr4:143628092
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02109.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5276-332C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628092 | ||||||
| chr4:143628250
|
T | A | 2 | a0005c0005t0001g0061a0015c0014t0001g0052 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5276-490A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628250 | ||||||
| chr4:143628301
|
A | G | 4 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(1): Show | 4 | HG00558.hp2 HG02132.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-541T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628301 | ||||||
| chr4:143628357
|
G | A | 3 | a0003c0003t0001g0108a0021c0032t0004g0153a0022c0031t0001g0146 | 3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5276-597C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628357 | ||||||
| chr4:143628394
|
C | A | 16 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.5276-634G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628394 | ||||||
| chr4:143628478
|
C | T | 241 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(238): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.5276-718G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628478 | ||||||
| chr4:143628507
|
A | G | 16 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.5276-747T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628507 | ||||||
| chr4:143628893
|
G | A | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-1133C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628893 | ||||||
| chr4:143628984
|
A | T | 4 | a0001c0001t0001g0200a0003c0003t0001g0092a0005c0005t0001g0055others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-1224T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628984 | ||||||
| chr4:143629029
|
A | G | 242 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(239): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.5276-1269T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629029 | ||||||
| chr4:143629058
|
C | T | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(71): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.5276-1298G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629058 | ||||||
| chr4:143629418
|
T | C | 248 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.5276-1658A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629418 | ||||||
| chr4:143629785
|
T | G | 14 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.5276-2025A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629785 | ||||||
| chr4:143629835
|
A | T | 59 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(56): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-2075T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629835 | ||||||
| chr4:143629910
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5276-2150C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629910 | ||||||
| chr4:143629987
|
A | G | 19 | a0001c0001t0001g0132a0001c0001t0001g0210a0001c0001t0001g0211others(16): Show | 20 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.5276-2227T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629987 | ||||||
| chr4:143630143
|
C | T | 1 | a0008c0012t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5276-2383G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630143 | ||||||
| chr4:143630280
|
A | G | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(71): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.5276-2520T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630280 | ||||||
| chr4:143630306
|
C | T | 1 | a0005c0005t0001g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5276-2546G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630306 | ||||||
| chr4:143630451
|
A | G | 1 | a0002c0002t0001g0043 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5276-2691T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630451 | ||||||
| chr4:143630767
|
T | C | 59 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(56): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-3007A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630767 | ||||||
| chr4:143630780
|
A | G | 9 | a0004c0004t0001g0091a0004c0004t0001g0093a0004c0004t0001g0094others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.5276-3020T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630780 | ||||||
| chr4:143630934
|
C | T | 152 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(149): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.5276-3174G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630934 | ||||||
| chr4:143631292
|
G | A | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-3532C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631292 | ||||||
| chr4:143631329
|
G | GTATT | 3 | a0001c0001t0001g0123a0001c0001t0001g0134a0002c0002t0001g0015 | 3 | HG01099.hp1 HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.5276-3573_5276-357 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631329 | ||||||
| chr4:143631329
|
G | GTATTTAT others(5): Show |
3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5276-3581_5276-357 others(16): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631329 | ||||||
| chr4:143631329
|
GTATT | G | 18 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(15): Show | 19 | HG00558.hp2 HG01243.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.5276-3573_5276-357 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631329 | ||||||
| chr4:143631355
|
A | G | 5 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0213others(2): Show | 5 | HG03492.hp1 HG03688.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-3595T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631355 | ||||||
| chr4:143631378
|
T | C | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(71): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.5276-3618A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631378 | ||||||
| chr4:143631638
|
A | T | 1 | a0001c0001t0001g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5276-3878T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631638 | ||||||
| chr4:143631694
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5276-3934C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631694 | ||||||
| chr4:143632033
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5276-4273G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632033 | ||||||
| chr4:143632188
|
G | T | 1 | a0003c0003t0001g0078 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5276-4428C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632188 | ||||||
| chr4:143632205
|
C | CA | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(71): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.5276-4446dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632205 | ||||||
| chr4:143632393
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-4633T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632393 | ||||||
| chr4:143632634
|
T | C | 15 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-4874A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632634 | ||||||
| chr4:143632810
|
T | TA | 15 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-5051dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632810 | ||||||
| chr4:143632810
|
TA | T | 15 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(12): Show | 15 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.5276-5051delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632810 | ||||||
| chr4:143632854
|
C | T | 59 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(56): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-5094G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632854 | ||||||
| chr4:143632954
|
T | C | 1 | a0003c0003t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5276-5194A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632954 | ||||||
| chr4:143632962
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-5202G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632962 | ||||||
| chr4:143633010
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5276-5250T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633010 | ||||||
| chr4:143633418
|
G | A | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-5658C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633418 | ||||||
| chr4:143633544
|
G | A | 15 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(12): Show | 15 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.5276-5784C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633544 | ||||||
| chr4:143633668
|
T | C | 59 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(56): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-5908A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633668 | ||||||
| chr4:143633798
|
C | A | 1 | a0003c0003t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5276-6038G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633798 | ||||||
| chr4:143633825
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5276-6065C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633825 | ||||||
| chr4:143633871
|
G | A | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5276-6111C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633871 | ||||||
| chr4:143633889
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(140): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-6129T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633889 | ||||||
| chr4:143634098
|
T | G | 1 | a0004c0004t0001g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5276-6338A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634098 | ||||||
| chr4:143634165
|
A | G | 39 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.5276-6405T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634165 | ||||||
| chr4:143634326
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5276-6566T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634326 | ||||||
| chr4:143634334
|
T | G | 59 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(56): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-6574A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634334 | ||||||
| chr4:143634586
|
T | G | 1 | a0001c0001t0001g0133 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5276-6826A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634586 | ||||||
| chr4:143634636
|
T | A | 15 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-6876A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634636 | ||||||
| chr4:143634639
|
C | G | 3 | a0004c0004t0001g0098a0004c0004t0001g0099a0004c0004t0001g0101 | 3 | HG01496.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5276-6879G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634639 | ||||||
| chr4:143634732
|
A | ACT | 245 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(242): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.5276-6974_5276-697 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634732 | ||||||
| chr4:143634770
|
C | T | 10 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0214others(7): Show | 10 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.5276-7010G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634770 | ||||||
| chr4:143634806
|
G | A | 1 | a0009c0034t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5276-7046C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634806 | ||||||
| chr4:143634850
|
A | G | 2 | a0003c0003t0001g0085a0003c0003t0001g0089 | 2 | HG00609.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.5276-7090T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634850 | ||||||
| chr4:143635682
|
C | T | 1 | a0004c0004t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5276-7922G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143635682 | ||||||
| chr4:143636169
|
T | G | 15 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-8409A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636169 | ||||||
| chr4:143636235
|
A | G | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-8475T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636235 | ||||||
| chr4:143636333
|
C | CA | 10 | a0001c0001t0001g0120a0001c0001t0001g0175a0001c0001t0001g0219others(7): Show | 10 | HG00280.hp2 HG01433.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.5276-8574dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636333 | ||||||
| chr4:143636333
|
CA | C | 88 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(85): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.5276-8574delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636333 | ||||||
| chr4:143636591
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5276-8831T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636591 | ||||||
| chr4:143636858
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5276-9098C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636858 | ||||||
| chr4:143636860
|
A | G | 14 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.5276-9100T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636860 | ||||||
| chr4:143637251
|
TA | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0120a0001c0001t0001g0125others(59): Show | 63 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.5276-9492delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637251 | ||||||
| chr4:143637547
|
C | T | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5276-9787G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637547 | ||||||
| chr4:143637732
|
G | C | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5276-9972C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637732 | ||||||
| chr4:143637806
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0175a0001c0001t0001g0197others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.5276-10046C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637806 | ||||||
| chr4:143637806
|
G | T | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-10046C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637806 | ||||||
| chr4:143638069
|
T | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(140): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-10309A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638069 | ||||||
| chr4:143638138
|
C | T | 4 | a0001c0001t0001g0200a0003c0003t0001g0092a0005c0005t0001g0055others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-10378G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638138 | ||||||
| chr4:143638313
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5276-10553C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638313 | ||||||
| chr4:143638377
|
G | A | 143 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(140): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-10617C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638377 | ||||||
| chr4:143638485
|
A | C | 1 | a0002c0002t0001g0018 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5276-10725T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638485 | ||||||
| chr4:143638553
|
C | T | 4 | a0001c0001t0001g0181a0002c0002t0001g0018a0002c0002t0001g0026others(1): Show | 4 | HG01167.hp1 HG01943.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-10793G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638553 | ||||||
| chr4:143638719
|
C | A | 15 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-10959G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638719 | ||||||
| chr4:143638994
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0197a0001c0001t0001g0203others(21): Show | 25 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.5276-11234C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638994 | ||||||
| chr4:143639163
|
A | C | 4 | a0001c0001t0001g0200a0003c0003t0001g0092a0005c0005t0001g0055others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-11403T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639163 | ||||||
| chr4:143639327
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5276-11567C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639327 | ||||||
| chr4:143639395
|
G | C | 1 | a0003c0003t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5276-11635C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639395 | ||||||
| chr4:143639407
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5276-11647C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639407 | ||||||
| chr4:143639499
|
G | A | 97 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.5276-11739C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639499 | ||||||
| chr4:143639795
|
T | A | 59 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(56): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-12035A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639795 | ||||||
| chr4:143639813
|
A | C | 1 | a0001c0001t0001g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5276-12053T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639813 | ||||||
| chr4:143640162
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5276-12402T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640162 | ||||||
| chr4:143640293
|
G | T | 1 | a0002c0002t0001g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5276-12533C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640293 | ||||||
| chr4:143640316
|
A | T | 147 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(144): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.5276-12556T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640316 | ||||||
| chr4:143640394
|
C | T | 98 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.5276-12634G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640394 | ||||||
| chr4:143640395
|
A | G | 60 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(57): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.5276-12635T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640395 | ||||||
| chr4:143640775
|
C | T | 248 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.5276-13015G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640775 | ||||||
| chr4:143641073
|
A | G | 8 | a0001c0001t0001g0200a0003c0003t0001g0092a0005c0005t0001g0055others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-13313T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641073 | ||||||
| chr4:143641164
|
T | G | 8 | a0001c0001t0001g0200a0003c0003t0001g0092a0005c0005t0001g0055others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-13404A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641164 | ||||||
| chr4:143641320
|
TAAA | T | 143 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(140): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-13563_5276-13 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641320 | ||||||
| chr4:143641364
|
A | C | 245 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(242): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.5276-13604T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641364 | ||||||
| chr4:143641778
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5276-14018G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641778 | ||||||
| chr4:143641972
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0161 | 2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.5276-14212A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641972 | ||||||
| chr4:143642300
|
C | T | 15 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-14540G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642300 | ||||||
| chr4:143642604
|
C | A | 15 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(12): Show | 15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-14844G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642604 | ||||||
| chr4:143642620
|
T | G | 1 | a0004c0004t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5276-14860A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642620 | ||||||
| chr4:143642705
|
C | A | 1 | a0002c0002t0001g0037 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.5276-14945G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642705 | ||||||
| chr4:143642705
|
C | G | 4 | a0001c0001t0001g0200a0003c0003t0001g0092a0005c0005t0001g0055others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-14945G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642705 | ||||||
| chr4:143643024
|
T | C | 2 | a0004c0004t0001g0091a0004c0004t0001g0093 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5276-15264A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643024 | ||||||
| chr4:143643266
|
G | A | 59 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126others(56): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-15506C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643266 | ||||||
| chr4:143643352
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5276-15592T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643352 | ||||||
| chr4:143643423
|
T | TA | 248 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.5276-15664_5276-15 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643423 | ||||||
| chr4:143643514
|
A | C | 1 | a0002c0002t0001g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5276-15754T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643514 | ||||||
| chr4:143643662
|
G | A | 13 | a0003c0003t0001g0107a0004c0004t0001g0079a0004c0004t0001g0080others(10): Show | 13 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.5276-15902C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643662 | ||||||
| chr4:143643864
|
C | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-16104G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643864 | ||||||
| chr4:143643865
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG00673.hp1 NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.5276-16105C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643865 | ||||||
| chr4:143644056
|
A | G | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-16296T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644056 | ||||||
| chr4:143644096
|
G | A | 1 | a0026c0023t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5276-16336C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644096 | ||||||
| chr4:143644177
|
A | ATG | 3 | a0001c0001t0001g0144a0011c0011t0001g0065a0015c0014t0001g0052 | 3 | HG01192.hp1 HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5276-16419_5276-16 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644177 | ||||||
| chr4:143644177
|
ATG | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(109): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.5276-16419_5276-16 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644177 | ||||||
| chr4:143644178
|
T | G | 1 | a0005c0005t0001g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5276-16418A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644178 | ||||||
| chr4:143644401
|
A | G | 1 | a0019c0026t0001g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5276-16641T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644401 | ||||||
| chr4:143644420
|
C | T | 3 | a0003c0003t0001g0102a0005c0005t0001g0059a0017c0020t0001g0053 | 3 | HG01106.hp1 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5276-16660G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644420 | ||||||
| chr4:143644456
|
T | C | 2 | a0011c0011t0001g0066a0011c0011t0001g0067 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5276-16696A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644456 | ||||||
| chr4:143644472
|
C | T | 3 | a0003c0003t0001g0102a0005c0005t0001g0059a0017c0020t0001g0053 | 3 | HG01106.hp1 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5276-16712G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644472 | ||||||
| chr4:143644639
|
T | C | 116 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(113): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-16879A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644639 | ||||||
| chr4:143644766
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5276-17006G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644766 | ||||||
| chr4:143644891
|
A | T | 3 | a0007c0008t0001g0137a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-17131T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644891 | ||||||
| chr4:143644990
|
G | A | 116 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(113): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-17230C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644990 | ||||||
| chr4:143645228
|
T | C | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-17468A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645228 | ||||||
| chr4:143645229
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5276-17469G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645229 | ||||||
| chr4:143645288
|
T | C | 113 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.5276-17528A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645288 | ||||||
| chr4:143645358
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5276-17598C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645358 | ||||||
| chr4:143645436
|
C | T | 2 | a0002c0002t0001g0021a0002c0002t0001g0022 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5276-17676G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645436 | ||||||
| chr4:143645541
|
T | A | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-17781A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645541 | ||||||
| chr4:143645544
|
C | T | 1 | a0027c0025t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5276-17784G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645544 | ||||||
| chr4:143645844
|
T | G | 1 | a0002c0002t0001g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5276-18084A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645844 | ||||||
| chr4:143646001
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.5276-18241T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646001 | ||||||
| chr4:143646037
|
G | A | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-18277C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646037 | ||||||
| chr4:143646184
|
A | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(188): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.5276-18424T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646184 | ||||||
| chr4:143646184
|
A | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-18424T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646184 | ||||||
| chr4:143646189
|
A | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-18429T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646189 | ||||||
| chr4:143646223
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5276-18463T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646223 | ||||||
| chr4:143646339
|
C | T | 3 | a0005c0005t0001g0055a0005c0005t0001g0058a0005c0022t0001g0064 | 3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5276-18579G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646339 | ||||||
| chr4:143646530
|
T | C | 2 | a0007c0030t0001g0154a0011c0011t0001g0065 | 2 | HG01192.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.5276-18770A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646530 | ||||||
| chr4:143646591
|
T | C | 1 | a0007c0008t0001g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5276-18831A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646591 | ||||||
| chr4:143646710
|
G | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-18950C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646710 | ||||||
| chr4:143646766
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5276-19006C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646766 | ||||||
| chr4:143646772
|
T | C | 7 | a0005c0005t0001g0055a0005c0005t0001g0058a0005c0022t0001g0064others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.5276-19012A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646772 | ||||||
| chr4:143646781
|
C | T | 1 | a0026c0023t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5276-19021G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646781 | ||||||
| chr4:143646800
|
A | T | 30 | a0001c0001t0001g0175a0001c0001t0001g0227a0003c0003t0001g0003others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.5276-19040T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646800 | ||||||
| chr4:143647078
|
G | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19318C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647078 | ||||||
| chr4:143647122
|
C | T | 1 | a0004c0004t0001g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5276-19362G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647122 | ||||||
| chr4:143647249
|
AT | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19490delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647249 | ||||||
| chr4:143647250
|
T | A | 1 | a0009c0034t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5276-19490A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647250 | ||||||
| chr4:143647337
|
T | C | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19577A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647337 | ||||||
| chr4:143647345
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5276-19585C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647345 | ||||||
| chr4:143647382
|
G | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-19622C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647382 | ||||||
| chr4:143647698
|
T | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-19938A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647698 | ||||||
| chr4:143647737
|
A | G | 1 | a0006c0007t0001g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5276-19977T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647737 | ||||||
| chr4:143647746
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5276-19986G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647746 | ||||||
| chr4:143647753
|
G | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19993C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647753 | ||||||
| chr4:143647876
|
A | G | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.5276-20116T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647876 | ||||||
| chr4:143647896
|
A | G | 1 | a0003c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5276-20136T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647896 | ||||||
| chr4:143647921
|
A | T | 192 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(189): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.5276-20161T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647921 | ||||||
| chr4:143647939
|
C | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-20179G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647939 | ||||||
| chr4:143647955
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-20195G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647955 | ||||||
| chr4:143648022
|
G | A | 1 | a0002c0002t0001g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5276-20262C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648022 | ||||||
| chr4:143648274
|
G | C | 1 | a0001c0001t0003g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5276-20514C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648274 | ||||||
| chr4:143648295
|
T | C | 1 | a0001c0001t0003g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5276-20535A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648295 | ||||||
| chr4:143648482
|
A | C | 1 | a0001c0028t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5276-20722T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648482 | ||||||
| chr4:143648600
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5276-20840A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648600 | ||||||
| chr4:143648784
|
G | A | 1 | a0002c0002t0001g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5276-21024C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648784 | ||||||
| chr4:143648791
|
C | T | 1 | a0013c0017t0001g0208 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5276-21031G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648791 | ||||||
| chr4:143648803
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5276-21043G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648803 | ||||||
| chr4:143648804
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0163 | 2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5276-21044C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648804 | ||||||
| chr4:143648824
|
A | G | 192 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(189): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.5276-21064T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648824 | ||||||
| chr4:143648838
|
A | G | 1 | a0002c0002t0001g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5276-21078T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648838 | ||||||
| chr4:143649583
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5276-21823C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649583 | ||||||
| chr4:143649734
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0163 | 2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5276-21974C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649734 | ||||||
| chr4:143649797
|
A | G | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5276-22037T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649797 | ||||||
| chr4:143649874
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5276-22114G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649874 | ||||||
| chr4:143649892
|
G | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-22132C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649892 | ||||||
| chr4:143649985
|
G | A | 1 | a0005c0005t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5276-22225C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649985 | ||||||
| chr4:143650347
|
C | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-22587G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650347 | ||||||
| chr4:143650405
|
A | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0224 | 3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.5276-22645T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650405 | ||||||
| chr4:143650451
|
T | G | 1 | a0002c0002t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5276-22691A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650451 | ||||||
| chr4:143650483
|
T | C | 116 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(113): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-22723A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650483 | ||||||
| chr4:143651389
|
G | A | 248 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.5276-23629C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651389 | ||||||
| chr4:143651497
|
A | C | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5276-23737T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651497 | ||||||
| chr4:143651550
|
A | G | 116 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(113): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-23790T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651550 | ||||||
| chr4:143651714
|
T | C | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5276-23954A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651714 | ||||||
| chr4:143651801
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5276-24041T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651801 | ||||||
| chr4:143652099
|
T | G | 253 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.5276-24339A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652099 | ||||||
| chr4:143652115
|
T | TAACTC | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-24356_5276-24 others(11): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652115 | ||||||
| chr4:143652134
|
TCTTTTTC others(320): Show |
T | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-24701_5276-24 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652134 | ||||||
| chr4:143652146
|
C | CT | 6 | a0001c0001t0001g0126a0002c0002t0001g0032a0002c0010t0001g0013others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.5276-24387dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | ||||||
| chr4:143652146
|
C | CTT | 25 | a0001c0001t0001g0175a0001c0001t0001g0227a0003c0003t0001g0003others(22): Show | 26 | HG00438.hp1 HG00558.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.5276-24388_5276-24 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | ||||||
| chr4:143652146
|
C | CTTT | 5 | a0003c0003t0001g0085a0003c0003t0001g0089a0003c0003t0001g0090others(2): Show | 5 | HG00609.hp1 HG02055.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-24389_5276-24 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | ||||||
| chr4:143652146
|
CT | C | 10 | a0002c0002t0001g0017a0002c0002t0001g0022a0003c0003t0001g0109others(7): Show | 10 | HG01070.hp1 HG01106.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.5276-24387delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | ||||||
| chr4:143652146
|
CTT | C | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.5276-24388_5276-24 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | ||||||
| chr4:143652215
|
T | C | 1 | a0002c0002t0001g0043 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5276-24455A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652215 | ||||||
| chr4:143652231
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5276-24471G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652231 | ||||||
| chr4:143652281
|
G | A | 1 | a0003c0003t0001g0089 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5276-24521C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652281 | ||||||
| chr4:143652307
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5276-24547G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652307 | ||||||
| chr4:143652444
|
G | A | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5276-24684C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652444 | ||||||
| chr4:143652835
|
G | A | 5 | a0005c0005t0001g0055a0005c0005t0001g0058a0005c0022t0001g0064others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-25075C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652835 | ||||||
| chr4:143652986
|
G | T | 192 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(189): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.5276-25226C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652986 | ||||||
| chr4:143653013
|
T | G | 2 | a0011c0011t0001g0066a0011c0011t0001g0067 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5276-25253A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653013 | ||||||
| chr4:143653169
|
A | G | 1 | a0005c0005t0001g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5276-25409T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653169 | ||||||
| chr4:143653179
|
G | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0038 | 3 | HG01074.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5276-25419C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653179 | ||||||
| chr4:143653219
|
C | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-25459G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653219 | ||||||
| chr4:143653229
|
G | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-25469C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653229 | ||||||
| chr4:143653242
|
C | T | 1 | a0001c0006t0001g0112 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5276-25482G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653242 | ||||||
| chr4:143653282
|
A | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-25522T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653282 | ||||||
| chr4:143653288
|
A | C | 5 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.5276-25528T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653288 | ||||||
| chr4:143653747
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5276-25987T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653747 | ||||||
| chr4:143653791
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG00140.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.5276-26031C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653791 | ||||||
| chr4:143653947
|
G | A | 192 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(189): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.5276-26187C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653947 | ||||||
| chr4:143653997
|
T | A | 47 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(44): Show | 48 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.5276-26237A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653997 | ||||||
| chr4:143654107
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-26347T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654107 | ||||||
| chr4:143654304
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5276-26544A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654304 | ||||||
| chr4:143654562
|
C | T | 30 | a0001c0001t0001g0175a0001c0001t0001g0227a0003c0003t0001g0003others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.5276-26802G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654562 | ||||||
| chr4:143654588
|
A | G | 1 | a0005c0005t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5276-26828T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654588 | ||||||
| chr4:143654656
|
A | G | 1 | a0026c0023t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5276-26896T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654656 | ||||||
| chr4:143654720
|
G | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-26960C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654720 | ||||||
| chr4:143654823
|
T | TA | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5276-27064dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654823 | ||||||
| chr4:143655021
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5276-27261T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655021 | ||||||
| chr4:143655151
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5276-27391A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655151 | ||||||
| chr4:143655174
|
C | T | 3 | a0005c0005t0001g0055a0005c0005t0001g0058a0005c0022t0001g0064 | 3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5276-27414G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655174 | ||||||
| chr4:143655359
|
C | T | 253 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.5276-27599G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655359 | ||||||
| chr4:143655541
|
T | C | 124 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(121): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.5276-27781A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655541 | ||||||
| chr4:143655575
|
C | T | 1 | a0009c0034t0001g0243 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5276-27815G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655575 | ||||||
| chr4:143655589
|
G | A | 34 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.5276-27829C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655589 | ||||||
| chr4:143655795
|
C | T | 3 | a0007c0008t0001g0137a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-28035G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655795 | ||||||
| chr4:143655858
|
A | G | 1 | a0003c0003t0001g0090 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5276-28098T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655858 | ||||||
| chr4:143655970
|
C | T | 3 | a0005c0005t0001g0055a0005c0005t0001g0058a0005c0022t0001g0064 | 3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5276-28210G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655970 | ||||||
| chr4:143656507
|
A | T | 29 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5276-28747T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656507 | ||||||
| chr4:143656516
|
C | A | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-28756G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656516 | ||||||
| chr4:143656805
|
A | G | 3 | a0007c0008t0001g0137a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-29045T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656805 | ||||||
| chr4:143656931
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(119): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5276-29171T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656931 | ||||||
| chr4:143657021
|
A | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-29261T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657021 | ||||||
| chr4:143657030
|
G | GA | 28 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.5276-29271dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657030 | ||||||
| chr4:143657322
|
A | G | 1 | a0007c0008t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5276-29562T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657322 | ||||||
| chr4:143657630
|
T | C | 1 | a0002c0002t0001g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5276-29870A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657630 | ||||||
| chr4:143657779
|
T | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(195): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.5276-30019A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657779 | ||||||
| chr4:143657887
|
T | C | 8 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-30127A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657887 | ||||||
| chr4:143657996
|
C | T | 3 | a0001c0001t0001g0199a0003c0003t0001g0109a0005c0005t0001g0061 | 3 | HG02965.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5276-30236G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657996 | ||||||
| chr4:143658228
|
G | A | 160 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(157): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.5276-30468C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658228 | ||||||
| chr4:143658540
|
C | A | 2 | a0011c0011t0001g0066a0011c0011t0001g0067 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5276-30780G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658540 | ||||||
| chr4:143658578
|
T | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(119): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5276-30818A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658578 | ||||||
| chr4:143658783
|
G | A | 29 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5276-31023C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658783 | ||||||
| chr4:143658899
|
C | T | 29 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5276-31139G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658899 | ||||||
| chr4:143658948
|
C | T | 3 | a0007c0008t0001g0137a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-31188G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658948 | ||||||
| chr4:143659032
|
CT | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5276-31273delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659032 | ||||||
| chr4:143659089
|
T | TTTA | 32 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(29): Show | 33 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.5276-31332_5276-31 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659089 | ||||||
| chr4:143659089
|
TTTA | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5276-31332_5276-31 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659089 | ||||||
| chr4:143659089
|
TTTATTA | T | 3 | a0003c0003t0001g0108a0007c0030t0001g0154a0011c0011t0001g0065 | 3 | HG01192.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5276-31335_5276-31 others(12): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659089 | ||||||
| chr4:143659090
|
T | TTATTATT others(5): Show |
1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-31331_5276-31 others(18): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659090 | ||||||
| chr4:143659178
|
G | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0132a0001c0001t0001g0171others(5): Show | 8 | HG00423.hp1 HG01515.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.5276-31418C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659178 | ||||||
| chr4:143659199
|
C | T | 2 | a0012c0016t0001g0074a0012c0016t0001g0075 | 2 | HG01099.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.5276-31439G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659199 | ||||||
| chr4:143659357
|
C | G | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5276-31597G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659357 | ||||||
| chr4:143659394
|
C | T | 1 | a0004c0004t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5276-31634G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659394 | ||||||
| chr4:143659530
|
C | T | 35 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.5276-31770G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659530 | ||||||
| chr4:143659531
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5276-31771C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659531 | ||||||
| chr4:143659562
|
A | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-31802T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659562 | ||||||
| chr4:143659578
|
T | G | 197 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(194): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5276-31818A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659578 | ||||||
| chr4:143659652
|
A | G | 76 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(73): Show | 78 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.5276-31892T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659652 | ||||||
| chr4:143659655
|
C | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(194): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5276-31895G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659655 | ||||||
| chr4:143659687
|
CA | C | 35 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.5276-31928delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659687 | ||||||
| chr4:143659688
|
A | AGTC | 121 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5276-31931_5276-31 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659688 | ||||||
| chr4:143659748
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-31988G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659748 | ||||||
| chr4:143659786
|
A | C | 1 | a0007c0008t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5276-32026T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659786 | ||||||
| chr4:143659837
|
G | T | 1 | a0002c0002t0001g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5276-32077C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659837 | ||||||
| chr4:143659967
|
A | C | 1 | a0005c0005t0001g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5276-32207T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659967 | ||||||
| chr4:143660048
|
T | C | 8 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-32288A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660048 | ||||||
| chr4:143660079
|
T | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-32319A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660079 | ||||||
| chr4:143660114
|
T | C | 28 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.5276-32354A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660114 | ||||||
| chr4:143660160
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5276-32400C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660160 | ||||||
| chr4:143660164
|
A | G | 3 | a0007c0008t0001g0137a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-32404T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660164 | ||||||
| chr4:143660205
|
TA | T | 41 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(38): Show | 42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5276-32446delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660205 | ||||||
| chr4:143660224
|
A | C | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5276-32464T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660224 | ||||||
| chr4:143660247
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0161 | 2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.5276-32487T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660247 | ||||||
| chr4:143660247
|
A | T | 1 | a0001c0001t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5276-32487T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660247 | ||||||
| chr4:143660300
|
A | G | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-32540T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660300 | ||||||
| chr4:143660380
|
G | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5276-32620C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660380 | ||||||
| chr4:143660437
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0211 | 2 | NA18612.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.5275+32676T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660437 | ||||||
| chr4:143660560
|
G | A | 1 | a0023c0029t0001g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5275+32553C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660560 | ||||||
| chr4:143660564
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5275+32549G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660564 | ||||||
| chr4:143660585
|
G | A | 2 | a0011c0011t0001g0066a0011c0011t0001g0067 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5275+32528C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660585 | ||||||
| chr4:143660644
|
C | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5275+32469G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660644 | ||||||
| chr4:143660737
|
T | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5275+32376A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660737 | ||||||
| chr4:143660800
|
G | A | 1 | a0007c0008t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+32313C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660800 | ||||||
| chr4:143660807
|
G | A | 41 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(38): Show | 42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5275+32306C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660807 | ||||||
| chr4:143660835
|
T | G | 1 | a0003c0003t0001g0090 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5275+32278A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660835 | ||||||
| chr4:143660897
|
G | A | 1 | a0002c0002t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5275+32216C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660897 | ||||||
| chr4:143660910
|
T | C | 4 | a0005c0005t0001g0057a0010c0013t0001g0247a0010c0013t0001g0248others(1): Show | 4 | HG01243.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+32203A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660910 | ||||||
| chr4:143660930
|
A | C | 1 | a0001c0001t0001g0184 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5275+32183T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660930 | ||||||
| chr4:143660935
|
G | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5275+32178C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660935 | ||||||
| chr4:143660985
|
T | C | 1 | a0003c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+32128A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660985 | ||||||
| chr4:143661152
|
G | C | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5275+31961C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661152 | ||||||
| chr4:143661251
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5275+31862T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661251 | ||||||
| chr4:143661252
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5275+31861G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661252 | ||||||
| chr4:143661254
|
T | C | 3 | a0007c0008t0001g0137a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5275+31859A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661254 | ||||||
| chr4:143661263
|
T | A | 1 | a0023c0029t0001g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5275+31850A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661263 | ||||||
| chr4:143661286
|
A | C | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+31827T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661286 | ||||||
| chr4:143661359
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5275+31754C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661359 | ||||||
| chr4:143661425
|
C | T | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31688G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661425 | ||||||
| chr4:143661515
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31598C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661515 | ||||||
| chr4:143661573
|
G | A | 1 | a0007c0008t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5275+31540C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661573 | ||||||
| chr4:143661601
|
T | C | 252 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(249): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.5275+31512A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661601 | ||||||
| chr4:143661712
|
C | T | 8 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+31401G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661712 | ||||||
| chr4:143661746
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31367C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661746 | ||||||
| chr4:143661832
|
G | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31281C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661832 | ||||||
| chr4:143661926
|
A | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31187T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661926 | ||||||
| chr4:143661963
|
A | G | 29 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+31150T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661963 | ||||||
| chr4:143662050
|
T | C | 9 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(6): Show | 9 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.5275+31063A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662050 | ||||||
| chr4:143662068
|
G | T | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31045C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662068 | ||||||
| chr4:143662128
|
C | A | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+30985G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662128 | ||||||
| chr4:143662168
|
T | C | 3 | a0005c0005t0001g0055a0005c0005t0001g0058a0005c0022t0001g0064 | 3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5275+30945A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662168 | ||||||
| chr4:143662202
|
T | C | 2 | a0011c0011t0001g0066a0011c0011t0001g0067 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5275+30911A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662202 | ||||||
| chr4:143662252
|
T | A | 3 | a0005c0005t0001g0055a0005c0005t0001g0058a0005c0022t0001g0064 | 3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5275+30861A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662252 | ||||||
| chr4:143662258
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30855C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662258 | ||||||
| chr4:143662279
|
G | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30834C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662279 | ||||||
| chr4:143662314
|
A | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30799T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662314 | ||||||
| chr4:143662407
|
T | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0171others(1): Show | 4 | HG01099.hp1 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+30706A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662407 | ||||||
| chr4:143662529
|
A | AGGTGT | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30579_5275+30 others(11): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662529 | ||||||
| chr4:143662549
|
T | G | 1 | a0019c0026t0001g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+30564A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662549 | ||||||
| chr4:143662617
|
A | T | 41 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(38): Show | 42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5275+30496T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662617 | ||||||
| chr4:143662942
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+30171G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662942 | ||||||
| chr4:143663007
|
A | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+30106T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663007 | ||||||
| chr4:143663021
|
T | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30092A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663021 | ||||||
| chr4:143663046
|
C | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30067G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663046 | ||||||
| chr4:143663052
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5275+30061C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663052 | ||||||
| chr4:143663082
|
C | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG00741.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5275+30031G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663082 | ||||||
| chr4:143663106
|
C | G | 35 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0135others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.5275+30007G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663106 | ||||||
| chr4:143663123
|
A | G | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5275+29990T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663123 | ||||||
| chr4:143663151
|
G | C | 1 | a0015c0014t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5275+29962C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663151 | ||||||
| chr4:143663244
|
G | A | 1 | a0002c0002t0001g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5275+29869C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663244 | ||||||
| chr4:143663276
|
C | T | 8 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+29837G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663276 | ||||||
| chr4:143663294
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5275+29819G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663294 | ||||||
| chr4:143663403
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5275+29710T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663403 | ||||||
| chr4:143663418
|
C | G | 1 | a0003c0003t0001g0084 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5275+29695G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663418 | ||||||
| chr4:143663452
|
T | C | 196 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(193): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.5275+29661A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663452 | ||||||
| chr4:143663568
|
G | A | 49 | a0001c0001t0001g0126a0001c0001t0001g0139a0001c0001t0001g0183others(46): Show | 51 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.5275+29545C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663568 | ||||||
| chr4:143663584
|
C | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+29529G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663584 | ||||||
| chr4:143663598
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5275+29515T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663598 | ||||||
| chr4:143663701
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5275+29412T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663701 | ||||||
| chr4:143663807
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG00099.hp2 HG00323.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.5275+29306G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663807 | ||||||
| chr4:143663817
|
C | T | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+29296G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663817 | ||||||
| chr4:143663818
|
G | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+29295C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663818 | ||||||
| chr4:143663870
|
A | G | 3 | a0007c0008t0001g0137a0014c0018t0001g0244a0014c0018t0001g0245 | 3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5275+29243T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663870 | ||||||
| chr4:143663872
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+29241G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663872 | ||||||
| chr4:143663914
|
G | A | 1 | a0003c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+29199C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663914 | ||||||
| chr4:143664061
|
G | A | 2 | a0007c0008t0001g0145a0007c0008t0001g0148 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5275+29052C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664061 | ||||||
| chr4:143664080
|
C | T | 3 | a0003c0003t0001g0081a0003c0003t0001g0082a0003c0003t0001g0083 | 3 | NA18957.hp2 NA19079.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.5275+29033G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664080 | ||||||
| chr4:143664146
|
A | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+28967T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664146 | ||||||
| chr4:143664283
|
T | C | 19 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0132others(16): Show | 19 | HG00423.hp1 HG00741.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.5275+28830A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664283 | ||||||
| chr4:143664293
|
T | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+28820A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664293 | ||||||
| chr4:143664305
|
A | T | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5275+28808T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664305 | ||||||
| chr4:143664451
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0224 | 3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.5275+28662C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664451 | ||||||
| chr4:143664567
|
C | T | 41 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(38): Show | 42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5275+28546G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664567 | ||||||
| chr4:143664575
|
G | C | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+28538C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664575 | ||||||
| chr4:143664701
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5275+28412G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664701 | ||||||
| chr4:143664705
|
G | A | 1 | a0005c0005t0001g0060 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5275+28408C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664705 | ||||||
| chr4:143664780
|
G | A | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5275+28333C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664780 | ||||||
| chr4:143664810
|
A | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+28303T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664810 | ||||||
| chr4:143664894
|
G | T | 126 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(123): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.5275+28219C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664894 | ||||||
| chr4:143664895
|
G | T | 4 | a0006c0007t0001g0006a0006c0007t0001g0252a0006c0007t0001g0253others(1): Show | 5 | HG02132.hp2 NA18943.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.5275+28218C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664895 | ||||||
| chr4:143664934
|
C | T | 1 | a0015c0014t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5275+28179G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664934 | ||||||
| chr4:143665009
|
G | A | 1 | a0001c0028t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5275+28104C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665009 | ||||||
| chr4:143665129
|
A | T | 1 | a0001c0001t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5275+27984T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665129 | ||||||
| chr4:143665136
|
T | C | 199 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(196): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.5275+27977A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665136 | ||||||
| chr4:143665169
|
C | T | 1 | a0004c0004t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5275+27944G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665169 | ||||||
| chr4:143665188
|
G | A | 3 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016 | 3 | HG01433.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5275+27925C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665188 | ||||||
| chr4:143665211
|
G | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+27902C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665211 | ||||||
| chr4:143665264
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5275+27849G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665264 | ||||||
| chr4:143665264
|
C | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(119): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5275+27849G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665264 | ||||||
| chr4:143665358
|
T | G | 1 | a0001c0001t0001g0133 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5275+27755A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665358 | ||||||
| chr4:143665467
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+27646C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665467 | ||||||
| chr4:143665524
|
T | A | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.5275+27589A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665524 | ||||||
| chr4:143665526
|
C | A | 2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.5275+27587G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665526 | ||||||
| chr4:143665526
|
C | T | 1 | a0003c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+27587G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665526 | ||||||
| chr4:143665748
|
G | C | 199 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(196): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.5275+27365C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665748 | ||||||
| chr4:143665903
|
T | C | 8 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+27210A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665903 | ||||||
| chr4:143666078
|
C | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+27035G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666078 | ||||||
| chr4:143666203
|
A | G | 6 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+26910T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666203 | ||||||
| chr4:143666217
|
C | T | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+26896G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666217 | ||||||
| chr4:143666536
|
G | A | 8 | a0003c0003t0001g0108a0005c0005t0001g0055a0005c0005t0001g0058others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+26577C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666536 | ||||||
| chr4:143666555
|
A | G | 1 | a0003c0003t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+26558T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666555 | ||||||
| chr4:143666698
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5275+26415A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666698 | ||||||
| chr4:143666841
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+26272C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666841 | ||||||
| chr4:143666962
|
G | T | 1 | a0007c0008t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+26151C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666962 | ||||||
| chr4:143667053
|
T | C | 29 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+26060A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667053 | ||||||
| chr4:143667441
|
T | A | 1 | a0005c0005t0001g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5275+25672A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667441 | ||||||
| chr4:143667484
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5275+25629G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667484 | ||||||
| chr4:143667657
|
A | C | 29 | a0001c0001t0001g0175a0003c0003t0001g0003a0003c0003t0001g0076others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+25456T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667657 | ||||||
| chr4:143667908
|
A | G | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+25205T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667908 | ||||||
| chr4:143668892
|
G | A | 32 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(29): Show | 33 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.5275+24221C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143668892 | ||||||
| chr4:143668927
|
A | G | 247 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(244): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5275+24186T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143668927 | ||||||
| chr4:143668972
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+24141G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143668972 | ||||||
| chr4:143669056
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0134 | 2 | HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.5275+24057C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669056 | ||||||
| chr4:143669217
|
C | T | 1 | a0003c0003t0001g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5275+23896G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669217 | ||||||
| chr4:143669332
|
G | T | 19 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.5275+23781C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669332 | ||||||
| chr4:143669422
|
G | A | 1 | a0003c0003t0001g0078 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5275+23691C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669422 | ||||||
| chr4:143669433
|
C | T | 3 | a0002c0010t0001g0011a0002c0010t0001g0012a0002c0010t0001g0013 | 3 | HG02559.hp1 HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.5275+23680G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669433 | ||||||
| chr4:143669656
|
G | GA | 11 | a0001c0001t0001g0144a0001c0001t0001g0194a0001c0001t0001g0238others(8): Show | 11 | HG01069.hp1 HG01106.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.5275+23456dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669656 | ||||||
| chr4:143669927
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5275+23186G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669927 | ||||||
| chr4:143669928
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5275+23185G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669928 | ||||||
| chr4:143670062
|
C | T | 38 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(35): Show | 39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+23051G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670062 | ||||||
| chr4:143670074
|
C | A | 38 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(35): Show | 39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+23039G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670074 | ||||||
| chr4:143670115
|
C | CA | 38 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(35): Show | 39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+22997dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670115 | ||||||
| chr4:143670354
|
C | T | 38 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(35): Show | 39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+22759G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670354 | ||||||
| chr4:143670901
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5275+22212C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670901 | ||||||
| chr4:143671120
|
C | T | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+21993G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671120 | ||||||
| chr4:143671301
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5275+21812G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671301 | ||||||
| chr4:143671320
|
C | T | 1 | a0005c0005t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5275+21793G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671320 | ||||||
| chr4:143671586
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5275+21527A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671586 | ||||||
| chr4:143671901
|
A | G | 1 | a0027c0025t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5275+21212T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671901 | ||||||
| chr4:143671992
|
C | T | 1 | a0007c0008t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5275+21121G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671992 | ||||||
| chr4:143672009
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+21104T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672009 | ||||||
| chr4:143672069
|
C | T | 1 | a0025c0035t0001g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5275+21044G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672069 | ||||||
| chr4:143672137
|
A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5275+20976T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672137 | ||||||
| chr4:143672300
|
T | C | 1 | a0003c0003t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5275+20813A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672300 | ||||||
| chr4:143672549
|
T | C | 7 | a0001c0001t0001g0119a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG01257.hp1 HG01496.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.5275+20564A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672549 | ||||||
| chr4:143672680
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+20433T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672680 | ||||||
| chr4:143672740
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5275+20373T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672740 | ||||||
| chr4:143672835
|
G | A | 2 | a0003c0003t0001g0107a0004c0004t0001g0106 | 2 | NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.5275+20278C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672835 | ||||||
| chr4:143672995
|
T | A | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+20118A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672995 | ||||||
| chr4:143673034
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5275+20079G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673034 | ||||||
| chr4:143673068
|
G | A | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+20045C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673068 | ||||||
| chr4:143673138
|
G | A | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+19975C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673138 | ||||||
| chr4:143673158
|
G | A | 38 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(35): Show | 39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+19955C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673158 | ||||||
| chr4:143673270
|
G | A | 10 | a0005c0005t0001g0055a0005c0005t0001g0056a0005c0005t0001g0057others(7): Show | 10 | HG01106.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.5275+19843C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673270 | ||||||
| chr4:143673370
|
T | C | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+19743A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673370 | ||||||
| chr4:143673384
|
C | T | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+19729G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673384 | ||||||
| chr4:143673428
|
T | C | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5275+19685A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673428 | ||||||
| chr4:143673475
|
G | A | 1 | a0007c0030t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5275+19638C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673475 | ||||||
| chr4:143673499
|
C | T | 1 | a0003c0003t0001g0078 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5275+19614G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673499 | ||||||
| chr4:143673568
|
G | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+19545C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673568 | ||||||
| chr4:143673664
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5275+19449G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673664 | ||||||
| chr4:143673673
|
A | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+19440T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673673 | ||||||
| chr4:143673710
|
C | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+19403G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673710 | ||||||
| chr4:143673760
|
G | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+19353C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673760 | ||||||
| chr4:143673871
|
G | C | 1 | a0002c0002t0001g0020 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5275+19242C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673871 | ||||||
| chr4:143673881
|
C | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+19232G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673881 | ||||||
| chr4:143674022
|
C | T | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+19091G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674022 | ||||||
| chr4:143674049
|
C | T | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00423.hp1 HG00609.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.5275+19064G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674049 | ||||||
| chr4:143674074
|
C | T | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+19039G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674074 | ||||||
| chr4:143674138
|
G | A | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+18975C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674138 | ||||||
| chr4:143674154
|
ATGCAGAA others(13): Show |
A | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5275+18939_5275+18 others(26): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674154 | ||||||
| chr4:143674169
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18944T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674169 | ||||||
| chr4:143674213
|
C | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+18900G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674213 | ||||||
| chr4:143674284
|
C | A | 1 | a0002c0002t0001g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5275+18829G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674284 | ||||||
| chr4:143674355
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18758T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674355 | ||||||
| chr4:143674375
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG00673.hp1 NA18963.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+18738T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674375 | ||||||
| chr4:143674415
|
C | T | 36 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(33): Show | 37 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.5275+18698G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674415 | ||||||
| chr4:143674510
|
C | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02257.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5275+18603G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674510 | ||||||
| chr4:143674653
|
T | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5275+18460A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674653 | ||||||
| chr4:143674707
|
C | A | 120 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(117): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.5275+18406G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674707 | ||||||
| chr4:143674770
|
C | A | 35 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(32): Show | 36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+18343G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674770 | ||||||
| chr4:143674789
|
A | C | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18324T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674789 | ||||||
| chr4:143674801
|
C | T | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18312G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674801 | ||||||
| chr4:143674859
|
T | A | 3 | a0003c0003t0001g0108a0003c0003t0001g0109a0024c0021t0001g0054 | 3 | HG03041.hp2 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5275+18254A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674859 | ||||||
| chr4:143674886
|
A | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0209 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.5275+18227T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674886 | ||||||
| chr4:143675248
|
G | A | 1 | a0005c0005t0001g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5275+17865C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675248 | ||||||
| chr4:143675304
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5275+17809C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675304 | ||||||
| chr4:143675306
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5275+17807T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675306 | ||||||
| chr4:143675312
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17801T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675312 | ||||||
| chr4:143675321
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17792T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675321 | ||||||
| chr4:143675343
|
G | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17770C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675343 | ||||||
| chr4:143675354
|
C | A | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+17759G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675354 | ||||||
| chr4:143675384
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5275+17729A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675384 | ||||||
| chr4:143675533
|
C | T | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+17580G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675533 | ||||||
| chr4:143675593
|
G | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17520C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675593 | ||||||
| chr4:143675647
|
G | A | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+17466C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675647 | ||||||
| chr4:143675704
|
G | A | 2 | a0005c0005t0001g0060a0005c0005t0001g0061 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5275+17409C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675704 | ||||||
| chr4:143675707
|
A | C | 1 | a0002c0002t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5275+17406T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675707 | ||||||
| chr4:143675788
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+17325A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675788 | ||||||
| chr4:143675811
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+17302G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675811 | ||||||
| chr4:143675816
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+17297C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675816 | ||||||
| chr4:143675861
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5275+17252A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675861 | ||||||
| chr4:143675866
|
C | A | 2 | a0003c0003t0001g0108a0003c0003t0001g0109 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5275+17247G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675866 | ||||||
| chr4:143675876
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5275+17237G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675876 | ||||||
| chr4:143675884
|
C | T | 239 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5275+17229G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675884 | ||||||
| chr4:143676018
|
T | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17095A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676018 | ||||||
| chr4:143676070
|
C | T | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+17043G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676070 | ||||||
| chr4:143676126
|
G | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02257.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5275+16987C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676126 | ||||||
| chr4:143676159
|
T | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+16954A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676159 | ||||||
| chr4:143676200
|
A | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+16913T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676200 | ||||||
| chr4:143676255
|
T | G | 239 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5275+16858A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676255 | ||||||
| chr4:143676323
|
C | T | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+16790G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676323 | ||||||
| chr4:143676331
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16782T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676331 | ||||||
| chr4:143676343
|
C | G | 8 | a0001c0001t0001g0119a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01257.hp1 HG01496.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.5275+16770G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676343 | ||||||
| chr4:143676386
|
G | T | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+16727C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676386 | ||||||
| chr4:143676421
|
T | C | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16692A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676421 | ||||||
| chr4:143676499
|
T | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16614A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676499 | ||||||
| chr4:143676560
|
T | C | 40 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(37): Show | 41 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.5275+16553A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676560 | ||||||
| chr4:143676784
|
T | C | 2 | a0003c0003t0001g0108a0003c0003t0001g0109 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5275+16329A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676784 | ||||||
| chr4:143676809
|
A | C | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16304T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676809 | ||||||
| chr4:143676819
|
A | G | 243 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(240): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.5275+16294T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676819 | ||||||
| chr4:143676844
|
A | C | 238 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(235): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.5275+16269T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676844 | ||||||
| chr4:143676868
|
AACC | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16242_5275+16 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676868 | ||||||
| chr4:143676923
|
G | C | 1 | a0019c0026t0001g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+16190C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676923 | ||||||
| chr4:143676929
|
A | G | 1 | a0019c0026t0001g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+16184T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676929 | ||||||
| chr4:143676930
|
A | G | 1 | a0019c0026t0001g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+16183T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676930 | ||||||
| chr4:143676999
|
A | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+16114T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676999 | ||||||
| chr4:143677213
|
G | T | 18 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(15): Show | 18 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.5275+15900C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677213 | ||||||
| chr4:143677411
|
T | G | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+15702A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677411 | ||||||
| chr4:143677461
|
A | C | 1 | a0024c0021t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5275+15652T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677461 | ||||||
| chr4:143677571
|
G | C | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+15542C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677571 | ||||||
| chr4:143677590
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5275+15523C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677590 | ||||||
| chr4:143677617
|
T | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+15496A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677617 | ||||||
| chr4:143677627
|
A | T | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+15486T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677627 | ||||||
| chr4:143677652
|
A | G | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG00423.hp1 HG00609.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.5275+15461T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677652 | ||||||
| chr4:143677700
|
A | T | 1 | a0013c0017t0001g0208 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5275+15413T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677700 | ||||||
| chr4:143677740
|
G | A | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+15373C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677740 | ||||||
| chr4:143677901
|
A | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+15212T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677901 | ||||||
| chr4:143677922
|
A | G | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+15191T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677922 | ||||||
| chr4:143677942
|
G | A | 1 | a0007c0008t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5275+15171C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677942 | ||||||
| chr4:143678128
|
T | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14985A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678128 | ||||||
| chr4:143678233
|
C | G | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+14880G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678233 | ||||||
| chr4:143678308
|
G | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14805C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678308 | ||||||
| chr4:143678443
|
T | G | 1 | a0013c0017t0001g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5275+14670A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678443 | ||||||
| chr4:143678543
|
A | AAT | 5 | a0005c0005t0001g0055a0008c0012t0001g0002a0008c0012t0001g0069others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+14568_5275+14 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678543 | ||||||
| chr4:143678545
|
T | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14568A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678545 | ||||||
| chr4:143678575
|
C | A | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+14538G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678575 | ||||||
| chr4:143678761
|
T | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14352A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678761 | ||||||
| chr4:143678851
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5275+14262T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678851 | ||||||
| chr4:143678882
|
A | ATATGT | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14230_5275+14 others(11): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678882 | ||||||
| chr4:143679071
|
C | T | 1 | a0006c0007t0001g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5275+14042G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679071 | ||||||
| chr4:143679158
|
C | T | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+13955G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679158 | ||||||
| chr4:143679161
|
A | C | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+13952T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679161 | ||||||
| chr4:143679244
|
A | G | 5 | a0004c0004t0001g0097a0004c0004t0001g0098a0004c0004t0001g0099others(2): Show | 5 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5275+13869T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679244 | ||||||
| chr4:143679246
|
G | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG00438.hp2 NA18962.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.5275+13867C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679246 | ||||||
| chr4:143679313
|
G | A | 14 | a0005c0005t0001g0055a0005c0005t0001g0056a0005c0005t0001g0057others(11): Show | 14 | HG01106.hp1 HG01192.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.5275+13800C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679313 | ||||||
| chr4:143679425
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5275+13688C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679425 | ||||||
| chr4:143679476
|
A | G | 2 | a0003c0003t0001g0108a0003c0003t0001g0109 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5275+13637T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679476 | ||||||
| chr4:143679506
|
T | C | 6 | a0001c0001t0001g0152a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01261.hp2 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5275+13607A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679506 | ||||||
| chr4:143679525
|
C | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+13588G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679525 | ||||||
| chr4:143679715
|
A | T | 35 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(32): Show | 36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+13398T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679715 | ||||||
| chr4:143679999
|
A | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+13114T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679999 | ||||||
| chr4:143680038
|
T | C | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+13075A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680038 | ||||||
| chr4:143680118
|
A | G | 44 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(41): Show | 46 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.5275+12995T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680118 | ||||||
| chr4:143680140
|
T | C | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+12973A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680140 | ||||||
| chr4:143680150
|
T | G | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+12963A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680150 | ||||||
| chr4:143680216
|
CTA | C | 35 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(32): Show | 36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+12895_5275+12 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680216 | ||||||
| chr4:143680250
|
A | G | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+12863T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680250 | ||||||
| chr4:143680256
|
C | CAT | 42 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(39): Show | 43 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.5275+12855_5275+12 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680256 | ||||||
| chr4:143680323
|
T | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0195 | 2 | NA18953.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.5275+12790A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680323 | ||||||
| chr4:143680430
|
A | G | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+12683T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680430 | ||||||
| chr4:143680484
|
G | C | 3 | a0003c0003t0001g0108a0003c0003t0001g0109a0024c0021t0001g0054 | 3 | HG03041.hp2 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5275+12629C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680484 | ||||||
| chr4:143680625
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5275+12488T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680625 | ||||||
| chr4:143680677
|
C | A | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+12436G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680677 | ||||||
| chr4:143680691
|
G | T | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+12422C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680691 | ||||||
| chr4:143680693
|
G | A | 55 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(52): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.5275+12420C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680693 | ||||||
| chr4:143680732
|
T | C | 49 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(46): Show | 51 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.5275+12381A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680732 | ||||||
| chr4:143680788
|
T | C | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+12325A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680788 | ||||||
| chr4:143680836
|
A | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+12277T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680836 | ||||||
| chr4:143681293
|
T | C | 1 | a0002c0002t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5275+11820A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143681293 | ||||||
| chr4:143681847
|
A | T | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+11266T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143681847 | ||||||
| chr4:143681975
|
G | A | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+11138C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143681975 | ||||||
| chr4:143682050
|
C | A | 44 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(41): Show | 46 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.5275+11063G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682050 | ||||||
| chr4:143682151
|
A | G | 1 | a0004c0004t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5275+10962T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682151 | ||||||
| chr4:143682167
|
A | C | 1 | a0002c0002t0001g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5275+10946T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682167 | ||||||
| chr4:143682342
|
A | G | 6 | a0003c0003t0001g0092a0003c0003t0001g0096a0004c0004t0001g0091others(3): Show | 6 | HG02486.hp2 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.5275+10771T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682342 | ||||||
| chr4:143682402
|
G | A | 1 | a0024c0021t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5275+10711C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682402 | ||||||
| chr4:143682426
|
C | T | 18 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(15): Show | 19 | HG00280.hp1 HG01167.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.5275+10687G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682426 | ||||||
| chr4:143682541
|
T | C | 49 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(46): Show | 51 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.5275+10572A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682541 | ||||||
| chr4:143682602
|
G | A | 1 | a0015c0014t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5275+10511C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682602 | ||||||
| chr4:143682614
|
A | G | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+10499T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682614 | ||||||
| chr4:143682744
|
A | G | 1 | a0015c0014t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+10369T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682744 | ||||||
| chr4:143682753
|
G | A | 1 | a0002c0002t0001g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5275+10360C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682753 | ||||||
| chr4:143682990
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+10123T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682990 | ||||||
| chr4:143683066
|
C | G | 1 | a0001c0001t0001g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5275+10047G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683066 | ||||||
| chr4:143683131
|
T | C | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+9982A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683131 | ||||||
| chr4:143683229
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG00673.hp1 NA18963.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+9884A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683229 | ||||||
| chr4:143683335
|
C | A | 5 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+9778G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683335 | ||||||
| chr4:143683450
|
A | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.5275+9663T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683450 | ||||||
| chr4:143683855
|
C | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+9258G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683855 | ||||||
| chr4:143683884
|
C | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+9229G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683884 | ||||||
| chr4:143683985
|
A | G | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+9128T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683985 | ||||||
| chr4:143684069
|
C | A | 1 | a0024c0021t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5275+9044G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684069 | ||||||
| chr4:143684392
|
T | C | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+8721A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684392 | ||||||
| chr4:143684509
|
C | A | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+8604G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684509 | ||||||
| chr4:143684721
|
C | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+8392G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684721 | ||||||
| chr4:143684948
|
A | AACAAAG | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+8164_5275+816 others(10): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684948 | ||||||
| chr4:143684950
|
G | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5275+8163C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684950 | ||||||
| chr4:143685113
|
G | A | 3 | a0011c0011t0001g0066a0011c0011t0001g0067a0026c0023t0001g0068 | 3 | HG03453.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5275+8000C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685113 | ||||||
| chr4:143685211
|
C | T | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+7902G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685211 | ||||||
| chr4:143685371
|
G | T | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+7742C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685371 | ||||||
| chr4:143685478
|
T | G | 35 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(32): Show | 36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+7635A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685478 | ||||||
| chr4:143685727
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5275+7386T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685727 | ||||||
| chr4:143685862
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+7251T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685862 | ||||||
| chr4:143685957
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5275+7156G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685957 | ||||||
| chr4:143686508
|
C | T | 1 | a0007c0008t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+6605G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686508 | ||||||
| chr4:143686789
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+6324T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686789 | ||||||
| chr4:143686811
|
G | A | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+6302C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686811 | ||||||
| chr4:143686927
|
C | A | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+6186G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686927 | ||||||
| chr4:143686997
|
C | T | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+6116G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686997 | ||||||
| chr4:143687190
|
C | T | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+5923G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687190 | ||||||
| chr4:143687209
|
G | A | 4 | a0011c0011t0001g0065a0011c0011t0001g0066a0011c0011t0001g0067others(1): Show | 4 | HG01192.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+5904C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687209 | ||||||
| chr4:143687213
|
C | T | 43 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(40): Show | 44 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.5275+5900G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687213 | ||||||
| chr4:143687214
|
G | A | 24 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(21): Show | 25 | HG00140.hp1 HG00738.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.5275+5899C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687214 | ||||||
| chr4:143687229
|
C | T | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+5884G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687229 | ||||||
| chr4:143687283
|
C | T | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+5830G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687283 | ||||||
| chr4:143687314
|
G | T | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+5799C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687314 | ||||||
| chr4:143687348
|
G | GTAA | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+5764_5275+576 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687348 | ||||||
| chr4:143687860
|
C | T | 1 | a0002c0010t0001g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5275+5253G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687860 | ||||||
| chr4:143687886
|
ACAAACCC others(5): Show |
A | 1 | a0002c0010t0001g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5275+5215_5275+522 others(16): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687886 | ||||||
| chr4:143687990
|
A | C | 1 | a0002c0002t0001g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5275+5123T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687990 | ||||||
| chr4:143688029
|
G | A | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+5084C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688029 | ||||||
| chr4:143688180
|
G | A | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+4933C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688180 | ||||||
| chr4:143688197
|
G | A | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+4916C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688197 | ||||||
| chr4:143688357
|
A | G | 39 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(36): Show | 40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+4756T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688357 | ||||||
| chr4:143688715
|
G | A | 63 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(60): Show | 65 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.5275+4398C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688715 | ||||||
| chr4:143688917
|
A | G | 1 | a0007c0008t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+4196T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688917 | ||||||
| chr4:143688946
|
C | G | 35 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(32): Show | 36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+4167G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688946 | ||||||
| chr4:143688997
|
A | G | 2 | a0002c0002t0001g0021a0002c0002t0001g0022 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5275+4116T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688997 | ||||||
| chr4:143689187
|
A | C | 1 | a0011c0011t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5275+3926T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689187 | ||||||
| chr4:143689372
|
A | T | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+3741T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689372 | ||||||
| chr4:143689583
|
C | T | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+3530G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689583 | ||||||
| chr4:143689669
|
G | GAT | 5 | a0002c0002t0001g0020a0008c0012t0001g0002a0008c0012t0001g0069others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+3442_5275+344 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689669 | ||||||
| chr4:143690017
|
TA | T | 148 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.5275+3095delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | ||||||
| chr4:143690017
|
TAA | T | 21 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.5275+3094_5275+309 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | ||||||
| chr4:143690017
|
TAAA | T | 37 | a0001c0001t0001g0123a0001c0001t0001g0206a0003c0003t0001g0003others(34): Show | 38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.5275+3093_5275+309 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | ||||||
| chr4:143690017
|
TAAAA | T | 7 | a0003c0003t0001g0076a0010c0013t0001g0247a0010c0013t0001g0248others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.5275+3092_5275+309 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | ||||||
| chr4:143690104
|
G | A | 243 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(240): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.5275+3009C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690104 | ||||||
| chr4:143690106
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5275+3007A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690106 | ||||||
| chr4:143690420
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+2693G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690420 | ||||||
| chr4:143690436
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5275+2677G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690436 | ||||||
| chr4:143690470
|
G | A | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+2643C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690470 | ||||||
| chr4:143690753
|
A | G | 1 | a0008c0012t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5275+2360T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690753 | ||||||
| chr4:143690784
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5275+2329T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690784 | ||||||
| chr4:143690903
|
C | T | 3 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016 | 3 | HG01433.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5275+2210G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690903 | ||||||
| chr4:143690951
|
T | C | 71 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(68): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+2162A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690951 | ||||||
| chr4:143690953
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5275+2160C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690953 | ||||||
| chr4:143691099
|
G | A | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+2014C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691099 | ||||||
| chr4:143691127
|
G | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+1986C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691127 | ||||||
| chr4:143691172
|
C | G | 1 | a0025c0035t0001g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5275+1941G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691172 | ||||||
| chr4:143691323
|
G | A | 139 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(136): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.5275+1790C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691323 | ||||||
| chr4:143691384
|
C | T | 71 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(68): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1729G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691384 | ||||||
| chr4:143691418
|
TA | T | 71 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(68): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1694delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691418 | ||||||
| chr4:143691501
|
G | A | 30 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0174others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+1612C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691501 | ||||||
| chr4:143691504
|
A | G | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+1609T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691504 | ||||||
| chr4:143691519
|
G | A | 66 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(63): Show | 68 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.5275+1594C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691519 | ||||||
| chr4:143691585
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5275+1528T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691585 | ||||||
| chr4:143691717
|
G | A | 1 | a0003c0003t0001g0003 | 2 | NA18969.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.5275+1396C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691717 | ||||||
| chr4:143691747
|
T | A | 71 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(68): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1366A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691747 | ||||||
| chr4:143691776
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5275+1337T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691776 | ||||||
| chr4:143691825
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5275+1288C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691825 | ||||||
| chr4:143691870
|
AT | A | 71 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(68): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1242delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691870 | ||||||
| chr4:143691920
|
T | A | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+1193A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691920 | ||||||
| chr4:143691943
|
T | A | 6 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.5275+1170A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691943 | ||||||
| chr4:143691952
|
T | G | 3 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5275+1161A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691952 | ||||||
| chr4:143692103
|
T | A | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+1010A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692103 | ||||||
| chr4:143692663
|
C | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.5275+450G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692663 | ||||||
| chr4:143692709
|
G | A | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02109.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+404C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692709 | ||||||
| chr4:143692752
|
T | A | 4 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+361A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692752 | ||||||
| chr4:143692897
|
G | T | 1 | a0027c0025t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5275+216C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692897 | ||||||
| chr4:143693019
|
C | A | 4 | a0008c0012t0001g0002a0008c0012t0001g0069a0015c0014t0001g0051others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+94G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143693019 | ||||||
| chr4:143693290
|
G | T | 14 | a0005c0005t0001g0055a0005c0005t0001g0056a0005c0005t0001g0057others(11): Show | 14 | HG01106.hp1 HG01192.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.5186-88C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693290 | ||||||
| chr4:143693377
|
T | A | 71 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(68): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5186-175A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693377 | ||||||
| chr4:143693430
|
T | A | 6 | a0010c0013t0001g0247a0010c0013t0001g0248a0010c0013t0001g0249others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.5186-228A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693430 | ||||||
| chr4:143693496
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0203a0001c0001t0001g0204others(29): Show | 33 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.5186-294C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693496 | ||||||
| chr4:143693518
|
A | G | 71 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(68): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5186-316T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693518 | ||||||
| chr4:143693954
|
C | A | 3 | a0008c0012t0001g0002a0008c0012t0001g0069a0018c0024t0001g0070 | 4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5186-752G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693954 | ||||||
| chr4:143693955
|
A | C | 1 | a0024c0021t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5186-753T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693955 | ||||||
| chr4:143694268
|
T | C | 37 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(34): Show | 38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.5186-1066A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694268 | ||||||
| chr4:143694302
|
G | A | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5186-1100C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694302 | ||||||
| chr4:143694363
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5185+1128T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694363 | ||||||
| chr4:143694369
|
G | A | 3 | a0001c0001t0003g0233a0001c0001t0003g0234a0023c0029t0001g0232 | 3 | HG02559.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5185+1122C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694369 | ||||||
| chr4:143694452
|
AT | A | 15 | a0001c0001t0001g0235a0005c0005t0001g0055a0005c0005t0001g0056others(12): Show | 15 | HG01106.hp1 HG01192.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.5185+1038delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694452 | ||||||
| chr4:143694565
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5185+926C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694565 | ||||||
| chr4:143694595
|
A | C | 1 | a0017c0020t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5185+896T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694595 | ||||||
| chr4:143694611
|
A | G | 2 | a0014c0018t0001g0244a0014c0018t0001g0245 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5185+880T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694611 | ||||||
| chr4:143694683
|
C | T | 18 | a0003c0003t0001g0003a0003c0003t0001g0076a0003c0003t0001g0078others(15): Show | 19 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.5185+808G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694683 | ||||||
| chr4:143694940
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5185+551G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694940 | ||||||
| chr4:143695008
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5185+483A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695008 | ||||||
| chr4:143695022
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5185+469C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695022 | ||||||
| chr4:143695167
|
A | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG00673.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.5185+324T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695167 | ||||||
| chr4:143695213
|
A | G | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5185+278T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695213 | ||||||
| chr4:143695248
|
T | C | 51 | a0001c0006t0001g0004a0001c0006t0001g0112a0001c0006t0001g0113others(48): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5185+243A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695248 |