| geneid | 124989 |
|---|---|
| ensemblid | ENSG00000178852.16 |
| hgncid | 26864 |
| symbol | EFCAB13 |
| name | EF-hand calcium binding domain 13 |
| refseq_nuc | NM_152347.5 |
| refseq_prot | NP_689560.3 |
| ensembl_nuc | ENST00000331493.7 |
| ensembl_prot | ENSP00000332111.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 47323955 |
| end | 47441312 |
| strand | + |
| ver | v1.2 |
| region | chr17:47323955-47441312 |
| region5000 | chr17:47318955-47446312 |
| regionname0 | EFCAB13_chr17_47323955_47441312 |
| regionname5000 | EFCAB13_chr17_47318955_47446312 |
| 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 | 0/1 | 281 | 138 | 36 | 30 | 48 | 6 | 17 | 41 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002 | 1/0 | 973 | 82 | 21 | 16 | 31 | 4 | 9 | 24 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003 | 0/0 | 973 | 39 | 7 | 4 | 27 | 1 | 0 | 23 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0004 | 0/0 | 973 | 38 | 3 | 7 | 22 | 1 | 5 | 18 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0005 | 0/0 | 210 | 27 | 0 | 1 | 20 | 0 | 6 | 13 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0006 | 0/0 | 973 | 9 | 0 | 0 | 9 | 0 | 0 | 6 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0007 | 0/0 | 973 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0008 | 0/0 | 973 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0009 | 0/0 | 973 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0010 | 0/0 | 973 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0011 | 0/0 | 210 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0012 | 0/0 | 281 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0013 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0014 | 0/0 | 973 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0015 | 0/0 | 973 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0016 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0017 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| 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 | 2921 | 116 | 34 | 19 | 44 | 4 | 15 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0002 | 1/0 | 2922 | 76 | 15 | 16 | 31 | 4 | 9 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0003 | 0/0 | 2922 | 38 | 3 | 7 | 22 | 1 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0004 | 0/0 | 2922 | 29 | 2 | 0 | 26 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0005 | 0/0 | 2922 | 27 | 0 | 1 | 20 | 0 | 6 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0006 | 0/0 | 2921 | 13 | 2 | 8 | 0 | 2 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0007 | 0/0 | 2922 | 9 | 0 | 0 | 9 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0008 | 0/0 | 2922 | 9 | 5 | 3 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0009 | 0/0 | 2922 | 6 | 0 | 0 | 6 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0010 | 0/0 | 2922 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0011 | 0/0 | 2922 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0012 | 0/0 | 2922 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0013 | 0/1 | 2921 | 3 | 0 | 2 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0014 | 0/0 | 2922 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0015 | 0/0 | 2921 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0016 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0017 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0018 | 0/0 | 2922 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0019 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0020 | 0/0 | 2922 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0021 | 0/0 | 2922 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0022 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0023 | 0/0 | 2921 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0024 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0025 | 0/0 | 2921 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0026 | 0/0 | 2921 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| c0027 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| 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 | 1036 | 277 | 59 | 46 | 130 | 9 | 31 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0002 | 0/0 | 1036 | 47 | 2 | 4 | 38 | 2 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0003 | 0/0 | 1036 | 17 | 3 | 9 | 0 | 1 | 4 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0004 | 0/0 | 1036 | 6 | 5 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0005 | 0/0 | 1036 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0006 | 0/0 | 1036 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0007 | 0/0 | 1036 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0008 | 0/0 | 1036 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0009 | 0/0 | 1036 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| t0010 | 0/0 | 1036 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| 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 | 2921 | 116 | 34 | 19 | 44 | 4 | 15 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0006 | 0/0 | 2921 | 13 | 2 | 8 | 0 | 2 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0013 | 0/1 | 2921 | 3 | 0 | 2 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0015 | 0/0 | 2921 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0022 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0023 | 0/0 | 2921 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0024 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0025 | 0/0 | 2921 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002c0002 | 1/0 | 2922 | 76 | 15 | 16 | 31 | 4 | 9 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002c0010 | 0/0 | 2922 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0004 | 0/0 | 2922 | 29 | 2 | 0 | 26 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0008 | 0/0 | 2922 | 9 | 5 | 3 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0016 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0004c0003 | 0/0 | 2922 | 38 | 3 | 7 | 22 | 1 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0005c0005 | 0/0 | 2922 | 27 | 0 | 1 | 20 | 0 | 6 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0006c0007 | 0/0 | 2922 | 9 | 0 | 0 | 9 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0007c0009 | 0/0 | 2922 | 6 | 0 | 0 | 6 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0008c0011 | 0/0 | 2922 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0009c0012 | 0/0 | 2922 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0010c0014 | 0/0 | 2922 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0011c0027 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0012c0026 | 0/0 | 2921 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0013c0017 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0014c0019 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0015c0018 | 0/0 | 2922 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0016c0020 | 0/0 | 2922 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0017c0021 | 0/0 | 2922 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3956 | 111 | 31 | 19 | 42 | 4 | 15 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0001t0002 | 0/0 | 3956 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0001t0005 | 0/0 | 3956 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0006t0001 | 0/0 | 3956 | 6 | 0 | 4 | 0 | 1 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0006t0002 | 0/0 | 3956 | 5 | 1 | 3 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0006t0003 | 0/0 | 3956 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0013t0001 | 0/1 | 3956 | 3 | 0 | 2 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0015t0001 | 0/0 | 3956 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0022t0001 | 0/0 | 3956 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0023t0002 | 0/0 | 3956 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0024t0001 | 0/0 | 3956 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0001c0025t0001 | 0/0 | 3956 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002c0002t0001 | 1/0 | 3957 | 62 | 13 | 10 | 30 | 3 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002c0002t0003 | 0/0 | 3957 | 12 | 2 | 6 | 0 | 1 | 3 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002c0002t0008 | 0/0 | 3957 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002c0002t0009 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0002c0010t0001 | 0/0 | 3957 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0004t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0004t0002 | 0/0 | 3957 | 28 | 1 | 0 | 26 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0008t0001 | 0/0 | 3957 | 2 | 0 | 1 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0008t0003 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0008t0004 | 0/0 | 3957 | 6 | 5 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0003c0016t0002 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0004c0003t0001 | 0/0 | 3957 | 37 | 2 | 7 | 22 | 1 | 5 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0004c0003t0006 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0005c0005t0001 | 0/0 | 3957 | 23 | 0 | 0 | 19 | 0 | 4 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0005c0005t0002 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0005c0005t0003 | 0/0 | 3957 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0005c0005t0007 | 0/0 | 3957 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0006c0007t0001 | 0/0 | 3957 | 8 | 0 | 0 | 8 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0006c0007t0010 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0007c0009t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0007c0009t0002 | 0/0 | 3957 | 5 | 0 | 0 | 5 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0008c0011t0001 | 0/0 | 3957 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0009c0012t0002 | 0/0 | 3957 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0010c0014t0001 | 0/0 | 3957 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0011c0027t0001 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0012c0026t0001 | 0/0 | 3956 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0013c0017t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0014c0019t0001 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0015c0018t0001 | 0/0 | 3957 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0016c0020t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| a0017c0021t0006 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | copy fasta | chr17 | 47318955 | 47446312 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0006t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0013t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0013t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0013t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0015t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0015t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0022t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0023t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0024t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0001c0025t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0008g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0002t0009g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0010t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0010t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0010t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0010t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0010t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0002c0010t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0004t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0008t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0003c0016t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0004c0003t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0005c0005t0007g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0006c0007t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0007c0009t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0007c0009t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0007c0009t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0007c0009t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0007c0009t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0007c0009t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0008c0011t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0008c0011t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0008c0011t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0008c0011t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0009c0012t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0009c0012t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0009c0012t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0010c0014t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0010c0014t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0011c0027t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0012c0026t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0013c0017t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0014c0019t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0015c0018t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0016c0020t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| a0017c0021t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0006 | t0001 | g0095 | EUR | GBR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0316 | EUR | GBR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00280 | hp2 | a0004 | c0003 | t0001 | g0035 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00323 | hp2 | a0002 | c0002 | t0003 | g0315 | EUR | FIN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00408 | hp1 | a0006 | c0007 | t0001 | g0062 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00408 | hp2 | a0005 | c0005 | t0001 | g0074 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00423 | hp1 | a0005 | c0005 | t0001 | g0071 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00423 | hp2 | a0006 | c0007 | t0001 | g0340 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00438 | hp1 | a0005 | c0005 | t0001 | g0008 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00438 | hp2 | a0003 | c0004 | t0002 | g0244 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00544 | hp1 | a0003 | c0004 | t0002 | g0227 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00544 | hp2 | a0005 | c0005 | t0001 | g0211 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00558 | hp1 | a0007 | c0009 | t0002 | g0218 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00558 | hp2 | a0005 | c0005 | t0001 | g0068 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00642 | hp1 | a0001 | c0006 | t0003 | g0096 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00735 | hp1 | a0001 | c0006 | t0001 | g0097 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0317 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00738 | hp1 | a0004 | c0003 | t0001 | g0020 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0284 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0338 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01070 | hp1 | a0001 | c0013 | t0001 | g0196 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01071 | hp1 | a0001 | c0013 | t0001 | g0197 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0324 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01081 | hp1 | a0001 | c0006 | t0002 | g0102 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01099 | hp1 | a0001 | c0025 | t0001 | g0144 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01099 | hp2 | a0001 | c0006 | t0001 | g0098 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01106 | hp1 | a0003 | c0008 | t0004 | g0012 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0319 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01109 | hp1 | a0004 | c0003 | t0001 | g0022 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01168 | hp1 | a0001 | c0006 | t0001 | g0093 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01169 | hp1 | a0001 | c0006 | t0001 | g0094 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01175 | hp1 | a0001 | c0006 | t0002 | g0099 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01243 | hp2 | a0003 | c0008 | t0001 | g0006 | AMR | PUR | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0057 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0336 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01261 | hp1 | a0004 | c0003 | t0001 | g0021 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01261 | hp2 | a0001 | c0006 | t0002 | g0073 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01346 | hp1 | a0004 | c0003 | t0001 | g0003 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01346 | hp2 | a0003 | c0016 | t0002 | g0223 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01358 | hp1 | a0004 | c0003 | t0001 | g0033 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0320 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01361 | hp2 | a0002 | c0002 | t0003 | g0055 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01433 | hp2 | a0014 | c0019 | t0001 | g0280 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0318 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0281 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01515 | hp2 | a0003 | c0004 | t0002 | g0247 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0282 | EUR | IBS | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0331 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01975 | hp1 | a0004 | c0003 | t0001 | g0023 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01993 | hp2 | a0004 | c0003 | t0001 | g0034 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02004 | hp2 | a0005 | c0005 | t0003 | g0118 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02015 | hp2 | a0004 | c0003 | t0001 | g0047 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02027 | hp1 | a0001 | c0022 | t0001 | g0194 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02027 | hp2 | a0005 | c0005 | t0001 | g0115 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02055 | hp1 | a0001 | c0006 | t0002 | g0072 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02056 | hp1 | a0004 | c0003 | t0001 | g0046 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02056 | hp2 | a0013 | c0017 | t0001 | g0205 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02083 | hp1 | a0004 | c0003 | t0001 | g0045 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02135 | hp2 | a0006 | c0007 | t0001 | g0060 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02148 | hp1 | a0003 | c0008 | t0003 | g0276 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02155 | hp2 | a0005 | c0005 | t0001 | g0208 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | CDX | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02523 | hp1 | a0004 | c0003 | t0001 | g0032 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0335 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02602 | hp1 | a0001 | c0006 | t0001 | g0100 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02602 | hp2 | a0005 | c0005 | t0001 | g0069 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02615 | hp1 | a0002 | c0010 | t0001 | g0267 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02647 | hp2 | a0008 | c0011 | t0001 | g0049 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0333 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02698 | hp2 | a0002 | c0002 | t0003 | g0328 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02717 | hp2 | a0002 | c0010 | t0001 | g0265 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02735 | hp2 | a0004 | c0003 | t0001 | g0044 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02738 | hp2 | a0005 | c0005 | t0001 | g0274 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02809 | hp2 | a0003 | c0008 | t0004 | g0053 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02818 | hp1 | a0001 | c0006 | t0003 | g0101 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0350 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0140 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02976 | hp2 | a0008 | c0011 | t0001 | g0050 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03017 | hp1 | a0015 | c0018 | t0001 | g0337 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0347 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03041 | hp2 | a0003 | c0008 | t0004 | g0011 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03130 | hp1 | a0017 | c0021 | t0006 | g0261 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03139 | hp2 | a0002 | c0010 | t0001 | g0268 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0326 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03486 | hp1 | a0008 | c0011 | t0001 | g0054 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03492 | hp2 | a0004 | c0003 | t0001 | g0036 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0348 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0349 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03654 | hp1 | a0005 | c0005 | t0003 | g0327 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03669 | hp1 | a0002 | c0002 | t0008 | g0323 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03688 | hp1 | a0004 | c0003 | t0001 | g0038 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03704 | hp2 | a0005 | c0005 | t0007 | g0213 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03710 | hp2 | a0004 | c0003 | t0001 | g0037 | SAS | PJL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03834 | hp1 | a0005 | c0005 | t0001 | g0202 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03834 | hp2 | a0004 | c0003 | t0001 | g0039 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03927 | hp2 | a0005 | c0005 | t0001 | g0075 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0058 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG04228 | hp1 | a0001 | c0023 | t0002 | g0228 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0301 | SAS | STU | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18522 | hp1 | a0003 | c0008 | t0004 | g0005 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18612 | hp1 | a0003 | c0004 | t0002 | g0231 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18747 | hp1 | a0003 | c0004 | t0002 | g0219 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18906 | hp1 | a0008 | c0011 | t0001 | g0273 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18906 | hp2 | a0003 | c0008 | t0004 | g0162 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18941 | hp2 | a0009 | c0012 | t0002 | g0216 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18942 | hp1 | a0003 | c0004 | t0002 | g0232 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18943 | hp2 | a0003 | c0004 | t0002 | g0250 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18944 | hp2 | a0004 | c0003 | t0001 | g0001 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18945 | hp1 | a0003 | c0004 | t0002 | g0225 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18946 | hp1 | a0003 | c0004 | t0002 | g0222 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18948 | hp1 | a0003 | c0004 | t0002 | g0230 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18952 | hp1 | a0003 | c0004 | t0002 | g0241 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18956 | hp1 | a0004 | c0003 | t0001 | g0031 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18957 | hp1 | a0005 | c0005 | t0001 | g0342 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18961 | hp2 | a0007 | c0009 | t0002 | g0252 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18963 | hp1 | a0006 | c0007 | t0001 | g0059 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18963 | hp2 | a0004 | c0003 | t0001 | g0028 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18964 | hp1 | a0003 | c0004 | t0002 | g0251 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18964 | hp2 | a0004 | c0003 | t0001 | g0025 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18965 | hp1 | a0005 | c0005 | t0001 | g0204 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18965 | hp2 | a0006 | c0007 | t0001 | g0339 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18969 | hp2 | a0009 | c0012 | t0002 | g0004 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18971 | hp1 | a0004 | c0003 | t0001 | g0001 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18974 | hp2 | a0004 | c0003 | t0001 | g0026 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18975 | hp1 | a0007 | c0009 | t0002 | g0248 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18975 | hp2 | a0004 | c0003 | t0001 | g0024 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18977 | hp2 | a0005 | c0005 | t0001 | g0212 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18979 | hp2 | a0004 | c0003 | t0001 | g0030 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18981 | hp1 | a0001 | c0015 | t0001 | g0192 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18981 | hp2 | a0005 | c0005 | t0001 | g0207 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18982 | hp2 | a0010 | c0014 | t0001 | g0288 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18983 | hp2 | a0003 | c0004 | t0002 | g0243 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18984 | hp1 | a0004 | c0003 | t0001 | g0001 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18984 | hp2 | a0003 | c0004 | t0002 | g0226 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18985 | hp1 | a0004 | c0003 | t0001 | g0067 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18985 | hp2 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18988 | hp1 | a0007 | c0009 | t0001 | g0221 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18990 | hp1 | a0003 | c0004 | t0002 | g0236 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18993 | hp2 | a0009 | c0012 | t0002 | g0004 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18997 | hp1 | a0006 | c0007 | t0010 | g0061 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18998 | hp1 | a0004 | c0003 | t0001 | g0066 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18998 | hp2 | a0003 | c0008 | t0001 | g0141 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18999 | hp1 | a0004 | c0003 | t0001 | g0029 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19000 | hp1 | a0005 | c0005 | t0001 | g0116 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19000 | hp2 | a0007 | c0009 | t0002 | g0246 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19003 | hp1 | a0003 | c0004 | t0002 | g0233 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19003 | hp2 | a0005 | c0005 | t0001 | g0206 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19004 | hp1 | a0005 | c0005 | t0001 | g0203 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19004 | hp2 | a0003 | c0004 | t0002 | g0217 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19005 | hp2 | a0006 | c0007 | t0001 | g0063 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19007 | hp1 | a0001 | c0024 | t0001 | g0191 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19007 | hp2 | a0005 | c0005 | t0001 | g0110 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19009 | hp2 | a0003 | c0004 | t0002 | g0253 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19010 | hp1 | a0004 | c0003 | t0001 | g0048 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19011 | hp2 | a0003 | c0004 | t0002 | g0249 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19030 | hp1 | a0004 | c0003 | t0006 | g0260 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19055 | hp1 | a0003 | c0004 | t0002 | g0220 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19055 | hp2 | a0001 | c0015 | t0001 | g0106 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19056 | hp1 | a0003 | c0004 | t0002 | g0237 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19056 | hp2 | a0002 | c0002 | t0009 | g0313 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19057 | hp2 | a0004 | c0003 | t0001 | g0065 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19062 | hp1 | a0004 | c0003 | t0001 | g0042 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19063 | hp1 | a0003 | c0004 | t0002 | g0245 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19063 | hp2 | a0005 | c0005 | t0001 | g0200 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19065 | hp1 | a0006 | c0007 | t0001 | g0341 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19065 | hp2 | a0003 | c0004 | t0002 | g0235 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19066 | hp1 | a0009 | c0012 | t0002 | g0242 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19067 | hp2 | a0004 | c0003 | t0001 | g0043 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19070 | hp1 | a0007 | c0009 | t0002 | g0234 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19075 | hp1 | a0005 | c0005 | t0001 | g0210 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19076 | hp1 | a0003 | c0004 | t0002 | g0239 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19079 | hp1 | a0004 | c0003 | t0001 | g0027 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19081 | hp1 | a0005 | c0005 | t0001 | g0209 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19081 | hp2 | a0004 | c0003 | t0001 | g0040 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19084 | hp1 | a0003 | c0004 | t0002 | g0224 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19085 | hp1 | a0006 | c0007 | t0001 | g0064 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19085 | hp2 | a0003 | c0004 | t0002 | g0229 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19088 | hp1 | a0003 | c0004 | t0002 | g0214 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19091 | hp2 | a0010 | c0014 | t0001 | g0287 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA19240 | hp2 | a0002 | c0010 | t0001 | g0269 | AFR | YRI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20129 | hp1 | a0003 | c0008 | t0004 | g0258 | AFR | ASW | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | ASW | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20752 | hp2 | a0001 | c0006 | t0002 | g0092 | EUR | TSI | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | GIH | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0334 | SAS | GIH | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG01123 | hp2 | a0011 | c0027 | t0001 | g0121 | AMR | CLM | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG02559 | hp2 | a0004 | c0003 | t0001 | g0041 | AFR | ACB | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03471 | hp1 | a0016 | c0020 | t0001 | g0346 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG03471 | hp2 | a0002 | c0010 | t0001 | g0271 | AFR | MSL | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0325 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| HG06807 | hp2 | a0012 | c0026 | t0001 | g0164 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA18955 | hp2 | a0005 | c0005 | t0002 | g0238 | EAS | JPT | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20300 | hp1 | a0004 | c0003 | t0001 | g0003 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA20300 | hp2 | a0002 | c0010 | t0001 | g0270 | AFR | USA | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA21309 | hp1 | a0003 | c0004 | t0002 | g0109 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | LWK | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0013 | t0001 | g0117 | REF | REF | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0264 | REF | REF | EFCAB13_chr17_47318955_47446312 | EFCAB13 | chr17 | 47318955 | 47446312 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47335263
|
C | T | 1 | a0011 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.98C>T | p.Thr33Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/25 | 535/3957 | 98/2922 | 33/973 | chr17 | 47335263 | ||
| chr17:47347921
|
C | T | 2 | a0005a0011 | 28 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(25): Show |
stop_gained | HIGH | c.631C>T | p.Arg211* | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/25 | 1068/3957 | 631/2922 | 211/973 | chr17 | 47347921 | ||
| chr17:47361398
|
A | G | 1 | a0009 | 4 | NA18941.hp2 NA18969.hp2 NA18993.hp2 others(1): Show |
missense_variant | MODERATE | c.682A>G | p.Ile228Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/25 | 1119/3957 | 682/2922 | 228/973 | chr17 | 47361398 | ||
| chr17:47361479
|
C | T | 1 | a0012 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.763C>T | p.Arg255Cys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/25 | 1200/3957 | 763/2922 | 255/973 | chr17 | 47361479 | ||
| chr17:47370466
|
A | G | 3 | a0004a0016a0017 | 40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
missense_variant | MODERATE | c.835A>G | p.Ile279Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/25 | 1272/3957 | 835/2922 | 279/973 | chr17 | 47370466 | ||
| chr17:47374528
|
G | A | 11 | a0001a0003a0004others(8): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
missense_variant | MODERATE | c.934G>A | p.Val312Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1371/3957 | 934/2922 | 312/973 | chr17 | 47374528 | ||
| chr17:47374871
|
C | G | 1 | a0001 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1277C>G | p.Ser426Cys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1714/3957 | 1277/2922 | 426/973 | chr17 | 47374871 | ||
| chr17:47374891
|
A | T | 1 | a0001 | 3 | HG01070.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
stop_gained | HIGH | c.1297A>T | p.Lys433* | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1734/3957 | 1297/2922 | 433/973 | chr17 | 47374891 | ||
| chr17:47374952
|
C | T | 1 | a0010 | 2 | NA18982.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.1358C>T | p.Ala453Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1795/3957 | 1358/2922 | 453/973 | chr17 | 47374952 | ||
| chr17:47377817
|
A | C | 1 | a0013 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1424A>C | p.Glu475Ala | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/25 | 1861/3957 | 1424/2922 | 475/973 | chr17 | 47377817 | ||
| chr17:47391476
|
A | T | 4 | a0004a0006a0008others(1): Show | 52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
missense_variant | MODERATE | c.1622A>T | p.Asp541Val | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2059/3957 | 1622/2922 | 541/973 | chr17 | 47391476 | ||
| chr17:47391492
|
T | G | 1 | a0001 | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
stop_gained | HIGH | c.1638T>G | p.Tyr546* | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2075/3957 | 1638/2922 | 546/973 | chr17 | 47391492 | ||
| chr17:47391505
|
A | G | 1 | a0006 | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
missense_variant | MODERATE | c.1651A>G | p.Thr551Ala | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2088/3957 | 1651/2922 | 551/973 | chr17 | 47391505 | ||
| chr17:47391532
|
C | T | 1 | a0014 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1678C>T | p.Leu560Phe | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/25 | 2115/3957 | 1678/2922 | 560/973 | chr17 | 47391532 | ||
| chr17:47395863
|
G | A | 1 | a0007 | 6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
missense_variant | MODERATE | c.1831G>A | p.Asp611Asn | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/25 | 2268/3957 | 1831/2922 | 611/973 | chr17 | 47395863 | ||
| chr17:47409691
|
G | A | 1 | a0015 | 1 | HG03017.hp1 | missense_variant&splice_region_variant | MODERATE | c.2278G>A | p.Glu760Lys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/25 | 2715/3957 | 2278/2922 | 760/973 | chr17 | 47409691 | ||
| chr17:47414888
|
G | T | 1 | a0017 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.2463G>T | p.Met821Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/25 | 2900/3957 | 2463/2922 | 821/973 | chr17 | 47414888 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47344197
|
G | A | 2 | a0006c0007a0008c0011 | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
synonymous_variant | LOW | c.339G>A | p.Lys113Lys | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 7/25 | 776/3957 | 339/2922 | 113/973 | chr17 | 47344197 | ||
| chr17:47374567
|
T | C | 1 | a0003c0016 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.973T>C | p.Leu325Leu | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1410/3957 | 973/2922 | 325/973 | chr17 | 47374567 | ||
| chr17:47374878
|
C | A | 1 | a0001c0022 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1284C>A | p.Ile428Ile | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1721/3957 | 1284/2922 | 428/973 | chr17 | 47374878 | ||
| chr17:47374935
|
G | A | 1 | a0001c0023 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1341G>A | p.Ser447Ser | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/25 | 1778/3957 | 1341/2922 | 447/973 | chr17 | 47374935 | ||
| chr17:47394077
|
G | A | 1 | a0002c0010 | 6 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(3): Show |
synonymous_variant | LOW | c.1779G>A | p.Thr593Thr | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/25 | 2216/3957 | 1779/2922 | 593/973 | chr17 | 47394077 | ||
| chr17:47412885
|
C | T | 10 | a0003c0004a0003c0016a0004c0003others(7): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
synonymous_variant | LOW | c.2391C>T | p.Phe797Phe | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/25 | 2828/3957 | 2391/2922 | 797/973 | chr17 | 47412885 | ||
| chr17:47412909
|
C | T | 2 | a0001c0015a0001c0024 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
synonymous_variant | LOW | c.2415C>T | p.Asn805Asn | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/25 | 2852/3957 | 2415/2922 | 805/973 | chr17 | 47412909 | ||
| chr17:47440579
|
G | A | 1 | a0001c0024 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.2787G>A | p.Gln929Gln | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 3224/3957 | 2787/2922 | 929/973 | chr17 | 47440579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47323969
|
T | C | 8 | a0001c0001t0002a0001c0006t0002a0001c0023t0002others(5): Show | 47 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-423T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/25 | 4385 | chr17 | 47323969 | |||||
| chr17:47324048
|
G | A | 1 | a0001c0001t0005 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-344G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/25 | 4306 | chr17 | 47324048 | |||||
| chr17:47326340
|
C | T | 2 | a0004c0003t0006a0017c0021t0006 | 2 | HG03130.hp1 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-133C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/25 | chr17 | 47326340 | ||||||
| chr17:47326350
|
C | A | 1 | a0005c0005t0007 | 1 | HG03704.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-123C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/25 | chr17 | 47326350 | ||||||
| chr17:47328318
|
A | C | 1 | a0006c0007t0010 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/25 | 36 | chr17 | 47328318 | |||||
| chr17:47440827
|
A | G | 1 | a0003c0008t0004 | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*113A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 113 | chr17 | 47440827 | |||||
| chr17:47440839
|
A | G | 1 | a0002c0002t0009 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*125A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 125 | chr17 | 47440839 | |||||
| chr17:47440846
|
G | A | 1 | a0002c0002t0008 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 132 | chr17 | 47440846 | |||||
| chr17:47441217
|
T | G | 4 | a0001c0006t0003a0002c0002t0003a0003c0008t0003others(1): Show | 17 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*503T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 25/25 | 503 | chr17 | 47441217 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47324135
|
G | T | 5 | a0002c0002t0001g0347a0002c0002t0001g0348a0002c0002t0001g0349others(2): Show | 5 | HG02922.hp2 HG03041.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-318+61G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324135 | ||||||
| chr17:47324314
|
T | G | 2 | a0003c0008t0001g0006a0003c0008t0004g0005 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-317-140T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324314 | ||||||
| chr17:47324345
|
T | G | 262 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(259): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-317-109T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324345 | ||||||
| chr17:47324351
|
T | C | 1 | a0002c0002t0001g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-317-103T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324351 | ||||||
| chr17:47324391
|
A | G | 262 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(259): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-317-63A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324391 | ||||||
| chr17:47324415
|
G | T | 1 | a0003c0008t0004g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-317-39G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324415 | ||||||
| chr17:47324426
|
A | G | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-317-28A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324426 | ||||||
| chr17:47324435
|
G | C | 2 | a0005c0005t0001g0007a0005c0005t0001g0008 | 2 | HG00438.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-317-19G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 1/24 | chr17 | 47324435 | ||||||
| chr17:47324630
|
T | C | 4 | a0002c0002t0001g0009a0002c0002t0001g0010a0003c0008t0004g0011others(1): Show | 4 | HG01106.hp1 HG02109.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-248+107T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324630 | ||||||
| chr17:47324644
|
G | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-248+121G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324644 | ||||||
| chr17:47324842
|
C | T | 204 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(201): Show | 205 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.-248+319C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324842 | ||||||
| chr17:47324913
|
C | G | 297 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(294): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.-248+390C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324913 | ||||||
| chr17:47324919
|
T | TGTCTCCT others(19): Show |
1 | a0001c0001t0001g0254 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-248+397_-248+422d others(28): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47324919 | |||||
| chr17:47324974
|
T | A | 1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-248+451T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47324974 | ||||||
| chr17:47325025
|
C | CCCCCCCC others(257): Show |
1 | a0005c0005t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(266): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325025 | |||||
| chr17:47325025
|
C | CCCCCCCC others(264): Show |
1 | a0001c0025t0001g0144 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(273): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325025 | |||||
| chr17:47325025
|
C | CCCCCCCC others(249): Show |
1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(258): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325025 | |||||
| chr17:47325026
|
C | CCCACCCC others(275): Show |
1 | a0005c0005t0001g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-248+505_-248+506i others(284): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCACCCC others(276): Show |
1 | a0005c0005t0001g0342 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-248+505_-248+506i others(285): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(277): Show |
1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(286): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(278): Show |
1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(287): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(245): Show |
2 | a0001c0006t0002g0072a0001c0006t0002g0073 | 2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(254): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(250): Show |
1 | a0005c0005t0001g0074 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(259): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(251): Show |
1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(260): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(263): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00323.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(272): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(264): Show |
3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG01361.hp1 NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(273): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(265): Show |
8 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG00741.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(274): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(268): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(277): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(270): Show |
1 | a0002c0002t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(279): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(273): Show |
1 | a0001c0001t0001g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(282): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(274): Show |
1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(283): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(279): Show |
1 | a0001c0001t0001g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(288): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(244): Show |
9 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(6): Show | 9 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(253): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(245): Show |
2 | a0001c0006t0002g0102a0001c0006t0003g0101 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(254): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(246): Show |
3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(255): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(248): Show |
5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG01169.hp2 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(257): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(249): Show |
2 | a0001c0001t0001g0108a0003c0004t0002g0109 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(258): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(250): Show |
1 | a0005c0005t0001g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(259): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(251): Show |
1 | a0001c0001t0001g0111 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(260): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(252): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG01175.hp2 NA18944.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(261): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(253): Show |
1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(262): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(253): Show |
1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(262): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(258): Show |
1 | a0005c0005t0001g0116 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(267): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(259): Show |
2 | a0001c0013t0001g0117a0005c0005t0003g0118 | 2 | HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(268): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(260): Show |
1 | a0005c0005t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(269): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(262): Show |
3 | a0001c0001t0001g0119a0001c0001t0001g0120a0011c0027t0001g0121 | 3 | HG01123.hp2 HG01168.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(271): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(263): Show |
22 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(19): Show | 22 | HG01074.hp2 HG01123.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(272): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(264): Show |
20 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(17): Show | 20 | HG00642.hp2 HG01069.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(273): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(265): Show |
7 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | HG01070.hp2 HG02257.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(274): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(266): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(275): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(267): Show |
7 | a0001c0001t0001g0019a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG00673.hp2 HG01496.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(276): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(268): Show |
3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0275 | 3 | HG02647.hp1 HG02735.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(277): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(269): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG00280.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(278): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(270): Show |
10 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(7): Show | 10 | HG01192.hp1 HG01884.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(279): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(271): Show |
1 | a0001c0013t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(280): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(272): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0198a0001c0013t0001g0197 | 3 | HG01071.hp1 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-248+507_-248+508i others(281): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(273): Show |
7 | a0001c0001t0001g0199a0001c0001t0001g0201a0005c0005t0001g0007others(4): Show | 7 | HG01517.hp1 HG02683.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(282): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(274): Show |
8 | a0005c0005t0001g0008a0005c0005t0001g0206a0005c0005t0001g0207others(5): Show | 8 | HG00438.hp1 HG00544.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(283): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(275): Show |
1 | a0001c0001t0001g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(284): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(276): Show |
1 | a0005c0005t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(285): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(280): Show |
1 | a0005c0005t0007g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(289): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCC others(282): Show |
1 | a0001c0001t0001g0345 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-248+507_-248+508i others(291): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCT others(247): Show |
1 | a0003c0004t0002g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(256): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCT others(248): Show |
25 | a0001c0001t0002g0215a0001c0023t0002g0228a0003c0004t0002g0217others(22): Show | 26 | HG00544.hp1 HG00558.hp1 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(257): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCT others(249): Show |
15 | a0001c0001t0002g0240a0003c0004t0002g0241a0003c0004t0002g0243others(12): Show | 15 | HG00438.hp2 HG01515.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.-248+507_-248+508i others(258): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325026
|
C | CCCCCCCT others(262): Show |
1 | a0001c0001t0001g0254 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-248+507_-248+508i others(271): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325026 | |||||
| chr17:47325031
|
T | C | 211 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(208): Show | 212 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-248+508T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325031 | ||||||
| chr17:47325161
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-248+638A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325161 | ||||||
| chr17:47325222
|
C | A | 1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-248+699C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325222 | ||||||
| chr17:47325224
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-248+701A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325224 | ||||||
| chr17:47325511
|
C | T | 2 | a0005c0005t0001g0210a0005c0005t0001g0211 | 2 | HG00544.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-247-715C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325511 | ||||||
| chr17:47325534
|
A | G | 17 | a0001c0001t0001g0107a0003c0008t0004g0011a0003c0008t0004g0012others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.-247-692A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325534 | ||||||
| chr17:47325691
|
T | C | 266 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(263): Show | 270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-247-535T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325691 | ||||||
| chr17:47325803
|
CT | C | 5 | a0004c0003t0001g0003a0004c0003t0001g0020a0004c0003t0001g0021others(2): Show | 6 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-247-413delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325803 | |||||
| chr17:47325846
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-247-380A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325846 | ||||||
| chr17:47325862
|
A | AT | 67 | a0002c0002t0001g0002a0002c0002t0001g0056a0002c0002t0001g0259others(64): Show | 69 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.-247-361dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325862 | |||||
| chr17:47325920
|
CAA | C | 3 | a0002c0010t0001g0267a0002c0010t0001g0268a0002c0010t0001g0269 | 3 | HG02615.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-247-303_-247-302d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325920 | |||||
| chr17:47325921
|
AAAATATA others(25): Show |
A | 37 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(34): Show | 40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-247-303_-247-272d others(34): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325921 | |||||
| chr17:47325923
|
A | AAT | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0169others(13): Show | 16 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-247-265_-247-264d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATAT | 13 | a0001c0001t0001g0014a0001c0001t0001g0113a0002c0002t0001g0278others(10): Show | 13 | HG01074.hp1 HG01175.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-247-267_-247-264d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATATAT | 27 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0107others(24): Show | 27 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.-247-269_-247-264d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATATATA others(1): Show |
28 | a0001c0001t0001g0019a0001c0001t0001g0105a0001c0001t0001g0108others(25): Show | 28 | HG00544.hp2 HG01243.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.-247-271_-247-264d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATATATA others(3): Show |
24 | a0001c0001t0001g0051a0001c0001t0001g0173a0001c0001t0001g0180others(21): Show | 24 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-247-273_-247-264d others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATATATA others(5): Show |
10 | a0001c0001t0001g0201a0002c0002t0003g0338a0003c0004t0002g0229others(7): Show | 10 | HG01069.hp1 HG02056.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.-247-275_-247-264d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATATATA others(7): Show |
10 | a0001c0001t0001g0174a0001c0001t0001g0345a0003c0004t0002g0109others(7): Show | 10 | HG01123.hp2 HG02738.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-247-277_-247-264d others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATATATA others(9): Show |
3 | a0003c0004t0002g0236a0003c0004t0002g0237a0005c0005t0001g0202 | 3 | HG03834.hp1 NA18990.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-247-279_-247-264d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-247-281_-247-264d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
A | T | 2 | a0002c0010t0001g0270a0002c0010t0001g0271 | 2 | HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-247-303A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325923 | ||||||
| chr17:47325923
|
AAT | A | 27 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0070others(24): Show | 27 | HG01192.hp2 HG01255.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-247-265_-247-264d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATAT | A | 10 | a0002c0002t0001g0009a0002c0002t0001g0272a0002c0002t0001g0281others(7): Show | 11 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.-247-267_-247-264d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(1): Show |
A | 5 | a0001c0001t0001g0187a0002c0002t0001g0262a0003c0008t0004g0162others(2): Show | 5 | HG00408.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-247-271_-247-264d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(3): Show |
A | 9 | a0001c0006t0001g0100a0001c0006t0002g0102a0006c0007t0001g0059others(6): Show | 9 | HG00423.hp2 HG01081.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-247-273_-247-264d others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(5): Show |
A | 10 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(7): Show | 10 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-247-275_-247-264d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(7): Show |
A | 2 | a0001c0006t0002g0072a0001c0006t0002g0092 | 2 | HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-247-277_-247-264d others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(9): Show |
A | 8 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0184others(5): Show | 8 | HG01256.hp2 HG01517.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-247-279_-247-264d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(11): Show |
A | 49 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(46): Show | 49 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-247-281_-247-264d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(13): Show |
A | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-247-283_-247-264d others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(15): Show |
A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-247-285_-247-264d others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325923
|
AATATATA others(17): Show |
A | 6 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-247-287_-247-264d others(26): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325923 | |||||
| chr17:47325937
|
T | TATATATA others(24): Show |
1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-247-264_-247-263i others(33): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325937 | |||||
| chr17:47325941
|
T | TAAACAAA | 16 | a0001c0001t0001g0081a0001c0001t0001g0111a0001c0001t0001g0122others(13): Show | 16 | NA18943.hp1 NA18946.hp2 NA18962.hp2 others(13): Show |
intron_variant | MODIFIER | c.-247-284_-247-283i others(9): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325941 | |||||
| chr17:47325943
|
TATATATA others(14): Show |
T | 1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-247-272_-247-252d others(23): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | 47325943 | |||||
| chr17:47325960
|
A | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-247-266A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325960 | ||||||
| chr17:47325963
|
G | A | 3 | a0005c0005t0001g0007a0005c0005t0001g0008a0005c0005t0001g0200 | 3 | HG00438.hp1 NA18985.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-247-263G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325963 | ||||||
| chr17:47325963
|
G | T | 23 | a0002c0002t0001g0089a0005c0005t0001g0069a0005c0005t0001g0074others(20): Show | 23 | HG00408.hp2 HG00544.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.-247-263G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325963 | ||||||
| chr17:47325964
|
C | T | 3 | a0005c0005t0001g0007a0005c0005t0001g0008a0005c0005t0001g0200 | 3 | HG00438.hp1 NA18985.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-247-262C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47325964 | ||||||
| chr17:47326079
|
A | T | 1 | a0002c0002t0001g0311 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-247-147A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47326079 | ||||||
| chr17:47326105
|
C | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-247-121C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 2/24 | chr17 | 47326105 | ||||||
| chr17:47326404
|
G | A | 56 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-86+17G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47326404 | ||||||
| chr17:47326607
|
A | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-86+220A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47326607 | ||||||
| chr17:47326683
|
C | CAGT | 35 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(32): Show | 38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-86+300_-86+302dup others(3): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr17 | 47326683 | |||||
| chr17:47326744
|
G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-86+357G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47326744 | ||||||
| chr17:47327026
|
C | T | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86+639C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327026 | ||||||
| chr17:47327060
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-86+673A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327060 | ||||||
| chr17:47327119
|
G | T | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-86+732G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327119 | ||||||
| chr17:47327156
|
A | C | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-86+769A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327156 | ||||||
| chr17:47327166
|
GTTTTC | G | 56 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-86+784_-86+788del others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr17 | 47327166 | |||||
| chr17:47327171
|
C | G | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-86+784C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327171 | ||||||
| chr17:47327325
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-86+938C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327325 | ||||||
| chr17:47327358
|
T | A | 3 | a0004c0003t0006g0260a0016c0020t0001g0346a0017c0021t0006g0261 | 3 | HG03130.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-85-911T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327358 | ||||||
| chr17:47327398
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-85-871C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327398 | ||||||
| chr17:47327479
|
A | C | 1 | a0002c0002t0003g0338 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-85-790A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327479 | ||||||
| chr17:47327495
|
T | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-774T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327495 | ||||||
| chr17:47327543
|
C | T | 2 | a0002c0002t0001g0334a0015c0018t0001g0337 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-85-726C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327543 | ||||||
| chr17:47327550
|
C | T | 19 | a0002c0002t0001g0056a0002c0002t0001g0272a0002c0002t0001g0285others(16): Show | 19 | HG00673.hp1 HG01106.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-85-719C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327550 | ||||||
| chr17:47327571
|
C | T | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-85-698C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327571 | ||||||
| chr17:47327645
|
C | T | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-85-624C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327645 | ||||||
| chr17:47327691
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-85-578A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327691 | ||||||
| chr17:47327697
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-85-572C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327697 | ||||||
| chr17:47327778
|
G | A | 167 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(164): Show | 167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-85-491G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327778 | ||||||
| chr17:47327919
|
T | C | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-85-350T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327919 | ||||||
| chr17:47327935
|
C | T | 1 | a0002c0002t0003g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-85-334C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47327935 | ||||||
| chr17:47328082
|
G | A | 1 | a0002c0002t0003g0331 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-85-187G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47328082 | ||||||
| chr17:47328191
|
A | G | 1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-85-78A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 3/24 | chr17 | 47328191 | ||||||
| chr17:47328509
|
A | G | 1 | a0004c0003t0001g0023 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.30+126A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328509 | ||||||
| chr17:47328543
|
T | A | 2 | a0003c0008t0004g0162a0003c0008t0004g0258 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.30+160T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328543 | ||||||
| chr17:47328622
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+239T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328622 | ||||||
| chr17:47328793
|
A | G | 1 | a0004c0003t0001g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.30+410A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328793 | ||||||
| chr17:47328801
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.30+418A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328801 | ||||||
| chr17:47328864
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.30+481T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328864 | ||||||
| chr17:47328933
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.30+550G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328933 | ||||||
| chr17:47328979
|
T | C | 267 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(264): Show | 271 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.30+596T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47328979 | ||||||
| chr17:47329084
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+701T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329084 | ||||||
| chr17:47329241
|
G | C | 1 | a0005c0005t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.30+858G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329241 | ||||||
| chr17:47329362
|
A | G | 42 | a0003c0008t0001g0006a0003c0008t0001g0141a0003c0008t0004g0005others(39): Show | 45 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.30+979A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329362 | ||||||
| chr17:47329489
|
T | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+1106T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329489 | ||||||
| chr17:47329689
|
G | C | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+1306G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329689 | ||||||
| chr17:47329705
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+1322T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329705 | ||||||
| chr17:47329985
|
C | T | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+1602C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47329985 | ||||||
| chr17:47330147
|
A | T | 42 | a0003c0008t0001g0006a0003c0008t0001g0141a0003c0008t0004g0005others(39): Show | 45 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.30+1764A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330147 | ||||||
| chr17:47330242
|
C | A | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+1859C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330242 | ||||||
| chr17:47330251
|
T | A | 58 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(55): Show | 59 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.30+1868T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330251 | ||||||
| chr17:47330279
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+1896T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330279 | ||||||
| chr17:47330287
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+1904G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330287 | ||||||
| chr17:47330290
|
G | A | 1 | a0001c0015t0001g0106 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.30+1907G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330290 | ||||||
| chr17:47330489
|
C | A | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+2106C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330489 | ||||||
| chr17:47330649
|
G | T | 2 | a0002c0002t0001g0316a0002c0002t0001g0317 | 2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.30+2266G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330649 | ||||||
| chr17:47330788
|
C | T | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+2405C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330788 | ||||||
| chr17:47330802
|
C | T | 1 | a0005c0005t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.30+2419C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47330802 | ||||||
| chr17:47331019
|
T | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+2636T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331019 | ||||||
| chr17:47331102
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.30+2719A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331102 | ||||||
| chr17:47331489
|
C | T | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+3106C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331489 | ||||||
| chr17:47331508
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+3125G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331508 | ||||||
| chr17:47331803
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.31-3393T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331803 | ||||||
| chr17:47331905
|
A | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-3291A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331905 | ||||||
| chr17:47331947
|
G | A | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.31-3249G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47331947 | ||||||
| chr17:47332020
|
T | A | 168 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(165): Show | 168 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.31-3176T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332020 | ||||||
| chr17:47332077
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0173a0001c0001t0001g0182others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3119A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332077 | ||||||
| chr17:47332639
|
A | T | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.31-2557A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332639 | ||||||
| chr17:47332768
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-2428G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332768 | ||||||
| chr17:47332778
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.31-2418G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332778 | ||||||
| chr17:47332793
|
AT | A | 3 | a0004c0003t0006g0260a0016c0020t0001g0346a0017c0021t0006g0261 | 3 | HG03130.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.31-2399delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr17 | 47332793 | |||||
| chr17:47332823
|
C | T | 1 | a0002c0002t0001g0272 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.31-2373C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47332823 | ||||||
| chr17:47333020
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.31-2176C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333020 | ||||||
| chr17:47333100
|
G | A | 98 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(95): Show | 102 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.31-2096G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333100 | ||||||
| chr17:47333213
|
A | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.31-1983A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333213 | ||||||
| chr17:47333324
|
G | T | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.31-1872G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333324 | ||||||
| chr17:47333398
|
A | C | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.31-1798A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333398 | ||||||
| chr17:47333653
|
A | T | 3 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053 | 3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.31-1543A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333653 | ||||||
| chr17:47333718
|
C | T | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.31-1478C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333718 | ||||||
| chr17:47333977
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-1219A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333977 | ||||||
| chr17:47333993
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0193 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.31-1203G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47333993 | ||||||
| chr17:47334029
|
T | C | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-1167T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334029 | ||||||
| chr17:47334047
|
T | C | 3 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345 | 3 | HG03654.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-1149T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334047 | ||||||
| chr17:47334121
|
T | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-1075T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334121 | ||||||
| chr17:47334126
|
G | GT | 105 | a0001c0001t0001g0104a0001c0006t0001g0093a0001c0006t0001g0094others(102): Show | 109 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.31-1060dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr17 | 47334126 | |||||
| chr17:47334477
|
A | G | 38 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(35): Show | 41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-719A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334477 | ||||||
| chr17:47334653
|
T | C | 51 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(48): Show | 54 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.31-543T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334653 | ||||||
| chr17:47334788
|
G | C | 3 | a0004c0003t0006g0260a0016c0020t0001g0346a0017c0021t0006g0261 | 3 | HG03130.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.31-408G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334788 | ||||||
| chr17:47334876
|
C | T | 1 | a0004c0003t0001g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.31-320C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334876 | ||||||
| chr17:47334965
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.31-231A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334965 | ||||||
| chr17:47334981
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-215G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 4/24 | chr17 | 47334981 | ||||||
| chr17:47335676
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0161a0001c0025t0001g0144 | 3 | HG01099.hp1 NA18948.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.191+320C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47335676 | ||||||
| chr17:47335975
|
T | C | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.191+619T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47335975 | ||||||
| chr17:47336018
|
G | A | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.191+662G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336018 | ||||||
| chr17:47336087
|
G | C | 50 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.191+731G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336087 | ||||||
| chr17:47336129
|
GT | G | 92 | a0001c0001t0001g0122a0002c0002t0001g0303a0003c0004t0001g0140others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.191+788delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336129 | |||||
| chr17:47336240
|
C | T | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+884C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336240 | ||||||
| chr17:47336292
|
A | AT | 6 | a0004c0003t0001g0022a0004c0003t0001g0046a0008c0011t0001g0049others(3): Show | 6 | HG01109.hp1 HG02056.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+953dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336292 | |||||
| chr17:47336292
|
AT | A | 153 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(150): Show | 153 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.191+953delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336292 | |||||
| chr17:47336292
|
ATTT | A | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.191+951_191+953del others(3): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336292 | |||||
| chr17:47336581
|
G | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.191+1225G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47336581 | ||||||
| chr17:47336592
|
AT | A | 31 | a0001c0001t0001g0103a0001c0001t0001g0113a0001c0001t0001g0127others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.191+1256delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336592 | |||||
| chr17:47336592
|
ATT | A | 197 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(194): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.191+1255_191+1256d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336592 | |||||
| chr17:47336592
|
ATTT | A | 43 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(40): Show | 44 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.191+1254_191+1256d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47336592 | |||||
| chr17:47337256
|
C | G | 1 | a0002c0002t0003g0336 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.191+1900C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337256 | ||||||
| chr17:47337299
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+1943T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337299 | ||||||
| chr17:47337304
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.191+1948G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337304 | ||||||
| chr17:47337460
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.191+2104T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337460 | ||||||
| chr17:47337609
|
A | G | 5 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053others(2): Show | 5 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+2253A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337609 | ||||||
| chr17:47337641
|
T | C | 37 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(34): Show | 40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.191+2285T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337641 | ||||||
| chr17:47337775
|
G | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.191+2419G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337775 | ||||||
| chr17:47337886
|
T | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.191+2530T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47337886 | ||||||
| chr17:47338243
|
GT | G | 207 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(204): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.191+2904delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47338243 | |||||
| chr17:47338411
|
G | A | 38 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(35): Show | 41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.191+3055G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47338411 | ||||||
| chr17:47338558
|
G | GTT | 89 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(86): Show | 92 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.191+3212_191+3213d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47338558 | |||||
| chr17:47338570
|
A | T | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.191+3214A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47338570 | ||||||
| chr17:47338631
|
C | A | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.191+3275C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47338631 | ||||||
| chr17:47338895
|
T | TA | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.192-3020dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47338895 | |||||
| chr17:47339172
|
T | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.192-2749T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339172 | ||||||
| chr17:47339436
|
G | A | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.192-2485G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339436 | ||||||
| chr17:47339517
|
C | T | 1 | a0005c0005t0001g0207 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.192-2404C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339517 | ||||||
| chr17:47339631
|
A | G | 335 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.192-2290A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339631 | ||||||
| chr17:47339699
|
C | CA | 63 | a0001c0001t0001g0129a0002c0002t0001g0002a0002c0002t0001g0056others(60): Show | 65 | HG00099.hp2 HG00673.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.192-2206dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47339699 | |||||
| chr17:47339699
|
C | CAAA | 6 | a0004c0003t0001g0023a0004c0003t0001g0025a0008c0011t0001g0049others(3): Show | 6 | HG01975.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-2208_192-2206d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47339699 | |||||
| chr17:47339699
|
C | CAAAA | 44 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(41): Show | 47 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.192-2209_192-2206d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47339699 | |||||
| chr17:47339848
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-2073A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339848 | ||||||
| chr17:47339959
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.192-1962A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47339959 | ||||||
| chr17:47340189
|
A | G | 2 | a0004c0003t0006g0260a0017c0021t0006g0261 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.192-1732A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340189 | ||||||
| chr17:47340276
|
A | G | 1 | a0004c0003t0001g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.192-1645A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340276 | ||||||
| chr17:47340366
|
T | G | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.192-1555T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340366 | ||||||
| chr17:47340448
|
C | T | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-1473C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340448 | ||||||
| chr17:47340552
|
T | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.192-1369T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340552 | ||||||
| chr17:47340564
|
A | G | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.192-1357A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340564 | ||||||
| chr17:47340745
|
G | A | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.192-1176G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340745 | ||||||
| chr17:47340766
|
A | AT | 10 | a0002c0002t0001g0010a0002c0002t0001g0294a0002c0002t0001g0308others(7): Show | 10 | HG00423.hp1 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.192-1126dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | |||||
| chr17:47340766
|
AT | A | 127 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(124): Show |
intron_variant | MODIFIER | c.192-1126delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | |||||
| chr17:47340766
|
ATT | A | 22 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0122others(19): Show | 22 | HG00323.hp1 HG01069.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.192-1127_192-1126d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | |||||
| chr17:47340766
|
ATTT | A | 43 | a0003c0004t0002g0239a0003c0008t0001g0141a0004c0003t0001g0001others(40): Show | 46 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.192-1128_192-1126d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | |||||
| chr17:47340766
|
ATTTT | A | 42 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(39): Show | 43 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.192-1129_192-1126d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | |||||
| chr17:47340766
|
ATTTTTTT others(5): Show |
A | 1 | a0005c0005t0001g0202 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.192-1137_192-1126d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47340766 | |||||
| chr17:47340804
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192-1117C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47340804 | ||||||
| chr17:47341088
|
G | A | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.192-833G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341088 | ||||||
| chr17:47341464
|
T | TC | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.192-457_192-456ins others(1): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341464 | ||||||
| chr17:47341576
|
G | A | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.192-345G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341576 | ||||||
| chr17:47341670
|
C | CA | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.192-244dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr17 | 47341670 | |||||
| chr17:47341695
|
T | G | 96 | a0002c0002t0001g0002a0002c0002t0001g0056a0002c0002t0001g0089others(93): Show | 98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.192-226T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341695 | ||||||
| chr17:47341743
|
A | G | 42 | a0003c0008t0001g0006a0003c0008t0001g0141a0003c0008t0004g0005others(39): Show | 45 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.192-178A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341743 | ||||||
| chr17:47341773
|
A | G | 30 | a0001c0001t0001g0070a0001c0001t0001g0090a0001c0001t0001g0091others(27): Show | 30 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.192-148A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 5/24 | chr17 | 47341773 | ||||||
| chr17:47342082
|
G | A | 1 | a0005c0005t0003g0118 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.303+50G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342082 | ||||||
| chr17:47342101
|
A | T | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.303+69A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342101 | ||||||
| chr17:47342260
|
A | G | 1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.303+228A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342260 | ||||||
| chr17:47342480
|
A | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+448A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342480 | ||||||
| chr17:47342558
|
C | A | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.303+526C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47342558 | ||||||
| chr17:47343064
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.303+1032G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343064 | ||||||
| chr17:47343133
|
A | G | 1 | a0002c0002t0008g0323 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.304-1029A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343133 | ||||||
| chr17:47343167
|
C | G | 1 | a0001c0001t0001g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.304-995C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343167 | ||||||
| chr17:47343579
|
G | C | 2 | a0005c0005t0001g0007a0005c0005t0001g0008 | 2 | HG00438.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.304-583G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343579 | ||||||
| chr17:47343590
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.304-572C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343590 | ||||||
| chr17:47343626
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-536C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343626 | ||||||
| chr17:47343636
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.304-526A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343636 | ||||||
| chr17:47343666
|
T | A | 2 | a0006c0007t0001g0059a0006c0007t0001g0062 | 2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.304-496T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343666 | ||||||
| chr17:47343763
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.304-399C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343763 | ||||||
| chr17:47343869
|
A | G | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.304-293A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343869 | ||||||
| chr17:47343907
|
G | T | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.304-255G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 6/24 | chr17 | 47343907 | ||||||
| chr17:47344824
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.435-192T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 7/24 | chr17 | 47344824 | ||||||
| chr17:47344919
|
C | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.435-97C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 7/24 | chr17 | 47344919 | ||||||
| chr17:47345239
|
G | A | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.517+141G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345239 | ||||||
| chr17:47345262
|
A | G | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.517+164A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345262 | ||||||
| chr17:47345319
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.517+221G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345319 | ||||||
| chr17:47345367
|
T | G | 52 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(49): Show | 55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.517+269T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345367 | ||||||
| chr17:47345567
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.517+469G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345567 | ||||||
| chr17:47345650
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+552C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345650 | ||||||
| chr17:47345694
|
C | T | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.517+596C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345694 | ||||||
| chr17:47345912
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.517+814A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47345912 | ||||||
| chr17:47346004
|
G | T | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.517+906G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346004 | ||||||
| chr17:47346018
|
T | C | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.517+920T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346018 | ||||||
| chr17:47346105
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.517+1007G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346105 | ||||||
| chr17:47346131
|
T | C | 1 | a0008c0011t0001g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517+1033T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346131 | ||||||
| chr17:47346203
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517+1105A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346203 | ||||||
| chr17:47346256
|
A | T | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+1158A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346256 | ||||||
| chr17:47346353
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517+1255A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346353 | ||||||
| chr17:47346433
|
A | AC | 93 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(90): Show | 95 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.517+1346dupC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | |||||
| chr17:47346433
|
A | ACC | 91 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.517+1345_517+1346d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | |||||
| chr17:47346433
|
A | ACCC | 36 | a0001c0001t0001g0014a0001c0001t0001g0070a0001c0001t0001g0080others(33): Show | 36 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+1344_517+1346d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | |||||
| chr17:47346433
|
AC | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.517+1346delC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346433 | |||||
| chr17:47346435
|
C | CCG | 18 | a0001c0001t0001g0111a0001c0001t0001g0122a0001c0001t0001g0123others(15): Show | 18 | HG02135.hp1 HG02257.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.517+1338_517+1339i others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47346435 | |||||
| chr17:47346440
|
C | CG | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.517+1342_517+1343i others(3): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346440 | ||||||
| chr17:47346526
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.518-1282A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346526 | ||||||
| chr17:47346661
|
C | G | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.518-1147C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346661 | ||||||
| chr17:47346661
|
C | T | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.518-1147C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346661 | ||||||
| chr17:47346871
|
A | C | 5 | a0003c0004t0002g0224a0003c0004t0002g0231a0003c0004t0002g0235others(2): Show | 5 | NA18612.hp1 NA18964.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-937A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47346871 | ||||||
| chr17:47347017
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-791G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347017 | ||||||
| chr17:47347033
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.518-775A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347033 | ||||||
| chr17:47347048
|
T | C | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-760T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347048 | ||||||
| chr17:47347178
|
G | A | 1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518-630G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347178 | ||||||
| chr17:47347180
|
T | G | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518-628T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347180 | ||||||
| chr17:47347191
|
C | T | 44 | a0002c0002t0001g0307a0002c0002t0001g0314a0002c0002t0009g0313others(41): Show | 45 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.518-617C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347191 | ||||||
| chr17:47347200
|
G | A | 3 | a0007c0009t0001g0221a0007c0009t0002g0248a0007c0009t0002g0252 | 3 | NA18961.hp2 NA18975.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.518-608G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347200 | ||||||
| chr17:47347296
|
T | C | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-512T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347296 | ||||||
| chr17:47347417
|
GA | G | 57 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-385delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr17 | 47347417 | |||||
| chr17:47347423
|
A | C | 1 | a0002c0002t0001g0306 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.518-385A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347423 | ||||||
| chr17:47347508
|
A | C | 19 | a0003c0004t0002g0214a0003c0004t0002g0217a0003c0004t0002g0219others(16): Show | 20 | HG00438.hp2 HG00544.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.518-300A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347508 | ||||||
| chr17:47347531
|
G | A | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.518-277G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347531 | ||||||
| chr17:47347650
|
A | G | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.518-158A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347650 | ||||||
| chr17:47347749
|
G | A | 121 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.518-59G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347749 | ||||||
| chr17:47347778
|
C | T | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.518-30C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347778 | ||||||
| chr17:47347788
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.518-20G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 8/24 | chr17 | 47347788 | ||||||
| chr17:47348162
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.661+211G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348162 | ||||||
| chr17:47348183
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.661+232G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348183 | ||||||
| chr17:47348190
|
G | A | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.661+239G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348190 | ||||||
| chr17:47348213
|
C | T | 17 | a0001c0001t0001g0052a0001c0006t0001g0093a0001c0006t0001g0094others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.661+262C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348213 | ||||||
| chr17:47348238
|
C | T | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.661+287C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348238 | ||||||
| chr17:47348331
|
T | G | 50 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.661+380T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348331 | ||||||
| chr17:47348390
|
T | A | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+439T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348390 | ||||||
| chr17:47348414
|
T | G | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.661+463T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348414 | ||||||
| chr17:47348555
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.661+604A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348555 | ||||||
| chr17:47348755
|
T | TGAAAAAT others(321): Show |
1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+815_661+816ins others(328): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47348755 | |||||
| chr17:47348755
|
T | TGAAAAAT others(325): Show |
1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.661+815_661+816ins others(332): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47348755 | |||||
| chr17:47348774
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.661+823T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348774 | ||||||
| chr17:47348904
|
A | G | 1 | a0002c0002t0001g0311 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.661+953A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47348904 | ||||||
| chr17:47349554
|
G | A | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.661+1603G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349554 | ||||||
| chr17:47349759
|
C | CT | 7 | a0002c0002t0001g0314a0002c0002t0001g0332a0002c0002t0001g0333others(4): Show | 7 | HG00438.hp1 HG02572.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+1834dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | |||||
| chr17:47349759
|
CT | C | 56 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0070others(53): Show | 56 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.661+1834delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | |||||
| chr17:47349759
|
CTT | C | 89 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(86): Show | 89 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.661+1833_661+1834d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | |||||
| chr17:47349759
|
CTTTTTT | C | 49 | a0003c0004t0001g0140a0004c0003t0001g0001a0004c0003t0001g0003others(46): Show | 52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.661+1829_661+1834d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | |||||
| chr17:47349759
|
CTTTTTTT | C | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.661+1828_661+1834d others(9): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47349759 | |||||
| chr17:47349768
|
T | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+1817T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349768 | ||||||
| chr17:47349812
|
G | T | 1 | a0006c0007t0001g0059 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.661+1861G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349812 | ||||||
| chr17:47349815
|
T | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.661+1864T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349815 | ||||||
| chr17:47349822
|
C | T | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661+1871C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349822 | ||||||
| chr17:47349932
|
G | A | 25 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(22): Show | 28 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.661+1981G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349932 | ||||||
| chr17:47349935
|
T | C | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.661+1984T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349935 | ||||||
| chr17:47349996
|
G | A | 1 | a0003c0004t0002g0229 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.661+2045G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47349996 | ||||||
| chr17:47350054
|
G | A | 95 | a0002c0002t0001g0002a0002c0002t0001g0056a0002c0002t0001g0089others(92): Show | 97 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.661+2103G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350054 | ||||||
| chr17:47350063
|
C | T | 2 | a0006c0007t0001g0059a0006c0007t0001g0062 | 2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.661+2112C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350063 | ||||||
| chr17:47350142
|
C | A | 28 | a0005c0005t0001g0007a0005c0005t0001g0008a0005c0005t0001g0068others(25): Show | 28 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.661+2191C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350142 | ||||||
| chr17:47350533
|
T | G | 29 | a0002c0002t0003g0328a0005c0005t0001g0007a0005c0005t0001g0008others(26): Show | 29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+2582T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350533 | ||||||
| chr17:47350585
|
T | G | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.661+2634T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350585 | ||||||
| chr17:47350601
|
G | GT | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.661+2659dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47350601 | |||||
| chr17:47350603
|
T | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.661+2652T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350603 | ||||||
| chr17:47350783
|
G | A | 17 | a0001c0001t0001g0081a0001c0001t0001g0111a0001c0001t0001g0122others(14): Show | 17 | NA18943.hp1 NA18946.hp2 NA18962.hp2 others(14): Show |
intron_variant | MODIFIER | c.661+2832G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350783 | ||||||
| chr17:47350847
|
G | A | 1 | a0004c0003t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.661+2896G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350847 | ||||||
| chr17:47350873
|
G | A | 1 | a0004c0003t0001g0046 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.661+2922G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47350873 | ||||||
| chr17:47351051
|
C | G | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.661+3100C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351051 | ||||||
| chr17:47351118
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.661+3167C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351118 | ||||||
| chr17:47351140
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.661+3189A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351140 | ||||||
| chr17:47351279
|
C | CTG | 28 | a0001c0022t0001g0194a0002c0002t0001g0266a0002c0002t0003g0336others(25): Show | 29 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+3353_661+3354d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTG | 29 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0125others(26): Show | 29 | HG00673.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+3351_661+3354d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTG | 49 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0080others(46): Show | 52 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.661+3349_661+3354d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTGT others(1): Show |
42 | a0001c0001t0001g0016a0001c0001t0001g0084a0001c0001t0001g0087others(39): Show | 42 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.661+3347_661+3354d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTGT others(3): Show |
36 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(33): Show | 36 | HG01243.hp1 HG01433.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.661+3345_661+3354d others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTGT others(5): Show |
26 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0052others(23): Show | 26 | HG00280.hp2 HG01081.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.661+3343_661+3354d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTGT others(7): Show |
10 | a0001c0001t0001g0013a0001c0001t0001g0138a0001c0001t0001g0142others(7): Show | 10 | HG02109.hp1 HG02135.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.661+3341_661+3354d others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTGT others(9): Show |
2 | a0006c0007t0001g0339a0006c0007t0001g0340 | 2 | HG00423.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.661+3339_661+3354d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTGT others(11): Show |
5 | a0001c0001t0001g0143a0002c0002t0003g0055a0006c0007t0001g0063others(2): Show | 5 | HG01361.hp2 HG02647.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+3337_661+3354d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
C | CTGTGTGT others(13): Show |
1 | a0002c0002t0003g0315 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.661+3335_661+3354d others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
CTGTG | C | 7 | a0002c0002t0001g0089a0002c0002t0001g0283a0002c0002t0001g0307others(4): Show | 7 | HG02486.hp2 NA18612.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+3351_661+3354d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351279
|
CTGTGTG | C | 21 | a0002c0002t0001g0281a0002c0002t0001g0282a0002c0002t0001g0285others(18): Show | 21 | HG01358.hp2 HG01515.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.661+3349_661+3354d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351279 | |||||
| chr17:47351296
|
T | C | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.661+3345T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351296 | ||||||
| chr17:47351296
|
TGTGTGTG others(11): Show |
T | 29 | a0002c0002t0003g0328a0005c0005t0001g0007a0005c0005t0001g0008others(26): Show | 29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+3347_661+3364d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351296 | |||||
| chr17:47351298
|
T | C | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.661+3347T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351298 | ||||||
| chr17:47351298
|
TGTGTGTG others(9): Show |
T | 5 | a0002c0002t0001g0002a0002c0002t0001g0303a0002c0002t0001g0304others(2): Show | 7 | HG02083.hp2 NA18945.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+3349_661+3364d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351298 | |||||
| chr17:47351298
|
TGTGTGTG others(11): Show |
T | 1 | a0002c0002t0001g0272 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.661+3349_661+3366d others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351298 | |||||
| chr17:47351298
|
TGTGTGTG others(15): Show |
T | 8 | a0002c0002t0001g0056a0002c0002t0001g0297a0002c0002t0001g0309others(5): Show | 8 | HG00673.hp1 HG01106.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.661+3349_661+3370d others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351298 | |||||
| chr17:47351300
|
T | C | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.661+3349T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351300 | ||||||
| chr17:47351300
|
TGTGTGCG others(9): Show |
T | 6 | a0002c0002t0001g0259a0002c0002t0001g0294a0002c0002t0001g0312others(3): Show | 6 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.661+3351_661+3366d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351300 | |||||
| chr17:47351302
|
T | C | 3 | a0002c0002t0001g0290a0002c0002t0001g0293a0002c0002t0001g0325 | 3 | HG01192.hp2 HG03492.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.661+3351T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351302 | ||||||
| chr17:47351302
|
TGTGCGCG others(9): Show |
T | 2 | a0002c0002t0001g0279a0002c0002t0001g0347 | 2 | HG02004.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.661+3353_661+3368d others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351302 | |||||
| chr17:47351304
|
T | C | 12 | a0002c0002t0001g0262a0002c0002t0001g0283a0002c0002t0001g0290others(9): Show | 12 | HG01192.hp2 HG02895.hp2 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+3353T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351304 | ||||||
| chr17:47351304
|
T | TGCGC | 3 | a0002c0002t0001g0010a0002c0002t0001g0349a0002c0010t0001g0269 | 3 | HG03540.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.661+3374_661+3377d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
T | TGTGTGTG others(7): Show |
1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
T | TGTGTGTG others(21): Show |
1 | a0002c0002t0003g0338 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(30): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
T | TGTGTGTG others(11): Show |
1 | a0002c0002t0003g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.661+3354_661+3355i others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
T | TGTGTGTG others(13): Show |
1 | a0002c0002t0003g0057 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
T | TGTGTGTG others(15): Show |
2 | a0002c0002t0003g0284a0002c0002t0003g0331 | 2 | HG00741.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.661+3354_661+3355i others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
T | TGTGTGTG others(25): Show |
1 | a0002c0002t0003g0335 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.661+3354_661+3355i others(34): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
T | TGTGTGTG others(19): Show |
1 | a0002c0002t0003g0324 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.661+3354_661+3355i others(28): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351304
|
TGCGCGCG others(5): Show |
T | 2 | a0002c0002t0001g0263a0002c0002t0001g0278 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.661+3366_661+3377d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351304 | |||||
| chr17:47351306
|
C | T | 202 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(199): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.661+3355C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351306 | ||||||
| chr17:47351308
|
C | CGT | 5 | a0003c0004t0002g0222a0003c0004t0002g0232a0003c0004t0002g0233others(2): Show | 5 | NA18942.hp1 NA18946.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+3358_661+3359i others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351308 | |||||
| chr17:47351308
|
C | CGTGT | 5 | a0003c0004t0001g0140a0003c0004t0002g0229a0003c0004t0002g0245others(2): Show | 5 | HG01515.hp2 HG02056.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+3358_661+3359i others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351308 | |||||
| chr17:47351308
|
C | T | 228 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 232 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.661+3357C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351308 | ||||||
| chr17:47351310
|
C | T | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.661+3359C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351310 | ||||||
| chr17:47351312
|
C | T | 215 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 219 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.661+3361C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351312 | ||||||
| chr17:47351313
|
G | T | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.661+3362G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351313 | ||||||
| chr17:47351314
|
C | A | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.661+3363C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351314 | ||||||
| chr17:47351314
|
C | T | 146 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(143): Show | 146 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.661+3363C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351314 | ||||||
| chr17:47351316
|
C | T | 97 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 97 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.661+3365C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351316 | ||||||
| chr17:47351317
|
G | A | 2 | a0002c0002t0003g0335a0002c0002t0003g0338 | 2 | HG01069.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.661+3366G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351317 | ||||||
| chr17:47351318
|
C | T | 4 | a0001c0001t0001g0130a0002c0002t0001g0278a0003c0008t0001g0006others(1): Show | 4 | HG01243.hp2 HG03195.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+3367C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351318 | ||||||
| chr17:47351323
|
G | A | 1 | a0005c0005t0001g0207 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.661+3372G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351323 | ||||||
| chr17:47351327
|
G | A | 7 | a0001c0022t0001g0194a0002c0002t0003g0055a0002c0002t0003g0057others(4): Show | 7 | HG00323.hp2 HG00741.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+3376G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351327 | ||||||
| chr17:47351591
|
T | C | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.661+3640T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351591 | ||||||
| chr17:47351659
|
T | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.661+3708T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351659 | ||||||
| chr17:47351808
|
T | G | 1 | a0002c0002t0001g0322 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.661+3857T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351808 | ||||||
| chr17:47351848
|
A | ATTCTTTG others(20): Show |
1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+3919_661+3920i others(29): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351848 | |||||
| chr17:47351895
|
T | C | 1 | a0002c0002t0001g0304 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.661+3944T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351895 | ||||||
| chr17:47351899
|
G | GT | 78 | a0001c0001t0001g0081a0001c0001t0001g0126a0001c0001t0001g0146others(75): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.661+3969dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351899 | |||||
| chr17:47351899
|
GT | G | 6 | a0001c0001t0001g0120a0001c0001t0005g0256a0001c0013t0001g0196others(3): Show | 6 | HG01070.hp1 HG02056.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+3969delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351899 | |||||
| chr17:47351899
|
GTT | G | 38 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(35): Show | 39 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+3968_661+3969d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47351899 | |||||
| chr17:47351902
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.661+3951T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47351902 | ||||||
| chr17:47352058
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.661+4107C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352058 | ||||||
| chr17:47352065
|
C | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+4114C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352065 | ||||||
| chr17:47352096
|
G | C | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+4145G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352096 | ||||||
| chr17:47352104
|
G | A | 1 | a0002c0002t0003g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.661+4153G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352104 | ||||||
| chr17:47352181
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+4230C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352181 | ||||||
| chr17:47352183
|
C | T | 43 | a0001c0001t0001g0085a0001c0001t0001g0176a0003c0004t0001g0140others(40): Show | 44 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.661+4232C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352183 | ||||||
| chr17:47352248
|
C | T | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.661+4297C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352248 | ||||||
| chr17:47352359
|
C | T | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.661+4408C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352359 | ||||||
| chr17:47352365
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661+4414A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352365 | ||||||
| chr17:47352410
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.661+4459A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352410 | ||||||
| chr17:47352411
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.661+4460G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352411 | ||||||
| chr17:47352449
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.661+4498A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352449 | ||||||
| chr17:47352569
|
G | T | 1 | a0002c0002t0001g0330 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.661+4618G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352569 | ||||||
| chr17:47352722
|
A | G | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+4771A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352722 | ||||||
| chr17:47352797
|
A | C | 37 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(34): Show | 40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.661+4846A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47352797 | ||||||
| chr17:47353168
|
A | G | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.661+5217A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353168 | ||||||
| chr17:47353200
|
G | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.661+5249G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353200 | ||||||
| chr17:47353296
|
A | T | 1 | a0005c0005t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.661+5345A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353296 | ||||||
| chr17:47353389
|
G | A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.661+5438G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353389 | ||||||
| chr17:47353497
|
T | G | 3 | a0002c0002t0003g0331a0002c0002t0003g0335a0002c0002t0003g0338 | 3 | HG01069.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.661+5546T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353497 | ||||||
| chr17:47353539
|
G | A | 8 | a0002c0002t0001g0259a0002c0002t0001g0279a0002c0002t0001g0294others(5): Show | 8 | HG00738.hp2 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+5588G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353539 | ||||||
| chr17:47353632
|
G | A | 1 | a0002c0002t0001g0318 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.661+5681G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353632 | ||||||
| chr17:47353696
|
A | G | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+5745A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353696 | ||||||
| chr17:47353868
|
A | G | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.661+5917A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353868 | ||||||
| chr17:47353877
|
T | C | 1 | a0002c0002t0001g0314 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.661+5926T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47353877 | ||||||
| chr17:47354188
|
G | A | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.661+6237G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354188 | ||||||
| chr17:47354483
|
C | T | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661+6532C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354483 | ||||||
| chr17:47354534
|
A | T | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+6583A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354534 | ||||||
| chr17:47354535
|
T | A | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+6584T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354535 | ||||||
| chr17:47354535
|
T | G | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.661+6584T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354535 | ||||||
| chr17:47354536
|
A | T | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661+6585A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354536 | ||||||
| chr17:47354550
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.661+6599C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354550 | ||||||
| chr17:47354569
|
G | A | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.661+6618G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354569 | ||||||
| chr17:47354580
|
C | T | 1 | a0007c0009t0002g0246 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.661+6629C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354580 | ||||||
| chr17:47354640
|
C | A | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.661+6689C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354640 | ||||||
| chr17:47354705
|
C | T | 1 | a0005c0005t0003g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.662-6673C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354705 | ||||||
| chr17:47354775
|
G | C | 1 | a0002c0002t0001g0325 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.662-6603G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354775 | ||||||
| chr17:47354847
|
G | A | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.662-6531G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354847 | ||||||
| chr17:47354859
|
C | A | 1 | a0006c0007t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.662-6519C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47354859 | ||||||
| chr17:47355087
|
A | T | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.662-6291A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355087 | ||||||
| chr17:47355112
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.662-6266G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355112 | ||||||
| chr17:47355226
|
G | C | 1 | a0001c0006t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.662-6152G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355226 | ||||||
| chr17:47355252
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.662-6126A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355252 | ||||||
| chr17:47355314
|
G | T | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-6064G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355314 | ||||||
| chr17:47355512
|
C | T | 2 | a0003c0004t0002g0224a0003c0004t0002g0251 | 2 | NA18964.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.662-5866C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355512 | ||||||
| chr17:47355517
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-5861A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355517 | ||||||
| chr17:47355539
|
C | G | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.662-5839C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355539 | ||||||
| chr17:47355540
|
G | C | 1 | a0002c0002t0001g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.662-5838G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355540 | ||||||
| chr17:47355554
|
C | T | 3 | a0002c0002t0003g0284a0002c0002t0003g0315a0002c0002t0003g0324 | 3 | HG00323.hp2 HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.662-5824C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355554 | ||||||
| chr17:47355570
|
A | AT | 49 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(46): Show | 52 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.662-5787dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47355570 | |||||
| chr17:47355570
|
AT | A | 49 | a0001c0001t0001g0083a0001c0015t0001g0106a0002c0002t0001g0303others(46): Show | 50 | HG00438.hp2 HG00544.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.662-5787delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47355570 | |||||
| chr17:47355605
|
G | A | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.662-5773G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355605 | ||||||
| chr17:47355728
|
A | G | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-5650A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355728 | ||||||
| chr17:47355856
|
C | G | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-5522C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47355856 | ||||||
| chr17:47356104
|
CT | C | 41 | a0002c0002t0001g0303a0003c0004t0001g0140a0003c0004t0002g0109others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-5263delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47356104 | |||||
| chr17:47356141
|
G | A | 1 | a0006c0007t0001g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.662-5237G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356141 | ||||||
| chr17:47356300
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-5078A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356300 | ||||||
| chr17:47356594
|
G | A | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.662-4784G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356594 | ||||||
| chr17:47356605
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.662-4773C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356605 | ||||||
| chr17:47356631
|
G | A | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-4747G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356631 | ||||||
| chr17:47356722
|
A | G | 3 | a0001c0013t0001g0117a0001c0013t0001g0196a0001c0013t0001g0197 | 3 | HG01070.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.662-4656A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47356722 | ||||||
| chr17:47357043
|
C | T | 2 | a0002c0002t0001g0283a0002c0002t0008g0323 | 2 | HG03669.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.662-4335C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357043 | ||||||
| chr17:47357082
|
C | T | 7 | a0001c0001t0001g0128a0002c0010t0001g0265a0002c0010t0001g0267others(4): Show | 7 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-4296C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357082 | ||||||
| chr17:47357104
|
T | C | 1 | a0002c0002t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.662-4274T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357104 | ||||||
| chr17:47357196
|
C | CTGTT | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-4179_662-4178i others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47357196 | |||||
| chr17:47357405
|
C | T | 1 | a0002c0002t0001g0296 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.662-3973C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357405 | ||||||
| chr17:47357667
|
G | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-3711G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357667 | ||||||
| chr17:47357882
|
C | T | 1 | a0004c0003t0001g0027 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.662-3496C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357882 | ||||||
| chr17:47357989
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.662-3389G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47357989 | ||||||
| chr17:47358193
|
T | A | 1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.662-3185T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358193 | ||||||
| chr17:47358209
|
A | G | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-3169A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358209 | ||||||
| chr17:47358884
|
A | G | 2 | a0003c0008t0001g0006a0003c0008t0004g0005 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.662-2494A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358884 | ||||||
| chr17:47358941
|
T | C | 2 | a0003c0008t0004g0162a0003c0008t0004g0258 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662-2437T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358941 | ||||||
| chr17:47358956
|
T | G | 2 | a0001c0013t0001g0196a0001c0013t0001g0197 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.662-2422T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47358956 | ||||||
| chr17:47359119
|
G | A | 1 | a0002c0002t0001g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.662-2259G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359119 | ||||||
| chr17:47359149
|
A | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.662-2229A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359149 | ||||||
| chr17:47359190
|
G | A | 7 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257others(4): Show | 7 | HG02647.hp2 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-2188G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359190 | ||||||
| chr17:47359283
|
G | A | 8 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(5): Show | 8 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.662-2095G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359283 | ||||||
| chr17:47359492
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0052 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.662-1886G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359492 | ||||||
| chr17:47359517
|
G | GT | 95 | a0001c0001t0001g0123a0002c0002t0001g0002a0002c0002t0001g0056others(92): Show | 97 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.662-1846dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47359517 | |||||
| chr17:47359517
|
GT | G | 91 | a0001c0001t0001g0152a0003c0004t0001g0140a0003c0004t0002g0109others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.662-1846delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47359517 | |||||
| chr17:47359575
|
A | C | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.662-1803A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359575 | ||||||
| chr17:47359591
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.662-1787C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359591 | ||||||
| chr17:47359621
|
AT | A | 92 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-1747delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47359621 | |||||
| chr17:47359751
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-1627A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359751 | ||||||
| chr17:47359880
|
G | A | 1 | a0002c0002t0003g0336 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.662-1498G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47359880 | ||||||
| chr17:47360050
|
G | A | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-1328G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360050 | ||||||
| chr17:47360107
|
G | A | 1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.662-1271G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360107 | ||||||
| chr17:47360145
|
A | G | 2 | a0003c0008t0004g0162a0003c0008t0004g0258 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662-1233A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360145 | ||||||
| chr17:47360178
|
C | G | 2 | a0007c0009t0002g0218a0007c0009t0002g0246 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.662-1200C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360178 | ||||||
| chr17:47360255
|
G | A | 17 | a0001c0001t0001g0052a0001c0001t0005g0255a0001c0001t0005g0256others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.662-1123G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360255 | ||||||
| chr17:47360360
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-1018A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360360 | ||||||
| chr17:47360381
|
T | G | 100 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(97): Show | 104 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.662-997T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360381 | ||||||
| chr17:47360617
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662-761C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360617 | ||||||
| chr17:47360623
|
A | G | 1 | a0002c0002t0001g0320 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.662-755A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360623 | ||||||
| chr17:47360645
|
C | A | 50 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.662-733C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360645 | ||||||
| chr17:47360696
|
C | T | 1 | a0002c0002t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.662-682C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360696 | ||||||
| chr17:47360971
|
T | A | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-407T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47360971 | ||||||
| chr17:47361000
|
GTTTAA | G | 17 | a0001c0001t0001g0052a0001c0001t0005g0255a0001c0001t0005g0256others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.662-373_662-369del others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr17 | 47361000 | |||||
| chr17:47361047
|
T | C | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.662-331T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361047 | ||||||
| chr17:47361051
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-327A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361051 | ||||||
| chr17:47361149
|
T | C | 38 | a0003c0008t0001g0141a0004c0003t0001g0001a0004c0003t0001g0003others(35): Show | 41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.662-229T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361149 | ||||||
| chr17:47361216
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.662-162T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361216 | ||||||
| chr17:47361231
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.662-147A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361231 | ||||||
| chr17:47361324
|
G | C | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.662-54G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 9/24 | chr17 | 47361324 | ||||||
| chr17:47361520
|
CAGTG | C | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
splice_region_variant&intron_variant | LOW | c.805+3_805+6delGAGT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47361520 | |||||
| chr17:47361586
|
C | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 121 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.805+65C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47361586 | ||||||
| chr17:47361916
|
C | T | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.805+395C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47361916 | ||||||
| chr17:47362195
|
A | C | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+674A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362195 | ||||||
| chr17:47362389
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.805+868C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362389 | ||||||
| chr17:47362510
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.805+989C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362510 | ||||||
| chr17:47362674
|
G | A | 1 | a0008c0011t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.805+1153G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362674 | ||||||
| chr17:47362707
|
C | A | 1 | a0001c0001t0001g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.805+1186C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362707 | ||||||
| chr17:47362801
|
C | A | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+1280C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362801 | ||||||
| chr17:47362857
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.805+1336C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362857 | ||||||
| chr17:47362891
|
A | G | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.805+1370A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362891 | ||||||
| chr17:47362903
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.805+1382C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362903 | ||||||
| chr17:47362929
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+1408C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362929 | ||||||
| chr17:47362930
|
A | G | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+1409A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362930 | ||||||
| chr17:47362937
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+1416G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362937 | ||||||
| chr17:47362961
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.805+1440G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47362961 | ||||||
| chr17:47363019
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.805+1498C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363019 | ||||||
| chr17:47363025
|
C | T | 1 | a0002c0002t0001g0309 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.805+1504C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363025 | ||||||
| chr17:47363035
|
G | C | 2 | a0003c0004t0002g0222a0003c0004t0002g0229 | 2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.805+1514G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363035 | ||||||
| chr17:47363126
|
C | T | 5 | a0001c0001t0001g0082a0003c0008t0001g0141a0004c0003t0001g0065others(2): Show | 5 | HG02559.hp1 NA18985.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+1605C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363126 | ||||||
| chr17:47363261
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.805+1740C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363261 | ||||||
| chr17:47363462
|
C | CT | 11 | a0001c0001t0001g0122a0001c0001t0001g0190a0003c0008t0001g0006others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.805+1957dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47363462 | |||||
| chr17:47363462
|
CT | C | 56 | a0001c0001t0001g0119a0002c0002t0001g0281a0002c0002t0001g0295others(53): Show | 57 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.805+1957delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47363462 | |||||
| chr17:47363490
|
C | T | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+1969C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363490 | ||||||
| chr17:47363520
|
G | A | 1 | a0002c0002t0001g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.805+1999G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363520 | ||||||
| chr17:47363535
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.805+2014C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363535 | ||||||
| chr17:47363537
|
A | T | 6 | a0004c0003t0001g0001a0004c0003t0001g0025a0004c0003t0001g0026others(3): Show | 8 | NA18944.hp2 NA18964.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+2016A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363537 | ||||||
| chr17:47363582
|
T | C | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.805+2061T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363582 | ||||||
| chr17:47363754
|
A | T | 2 | a0003c0008t0004g0162a0003c0008t0004g0258 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.805+2233A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363754 | ||||||
| chr17:47363799
|
A | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.805+2278A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363799 | ||||||
| chr17:47363858
|
C | T | 14 | a0003c0004t0002g0214a0003c0004t0002g0217a0003c0004t0002g0219others(11): Show | 15 | HG00438.hp2 HG00544.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.805+2337C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363858 | ||||||
| chr17:47363956
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.805+2435A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47363956 | ||||||
| chr17:47364120
|
G | A | 92 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.805+2599G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364120 | ||||||
| chr17:47364349
|
C | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.805+2828C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364349 | ||||||
| chr17:47364409
|
G | A | 5 | a0002c0002t0001g0259a0002c0002t0001g0279a0002c0002t0001g0294others(2): Show | 5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+2888G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364409 | ||||||
| chr17:47364438
|
G | A | 53 | a0002c0002t0001g0002a0002c0002t0001g0056a0002c0002t0001g0259others(50): Show | 55 | HG00099.hp2 HG00673.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.805+2917G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364438 | ||||||
| chr17:47364459
|
C | T | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+2938C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364459 | ||||||
| chr17:47364478
|
A | C | 1 | a0004c0003t0001g0021 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.805+2957A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364478 | ||||||
| chr17:47364513
|
A | G | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+2992A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364513 | ||||||
| chr17:47364591
|
G | A | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.805+3070G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364591 | ||||||
| chr17:47364598
|
A | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.805+3077A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364598 | ||||||
| chr17:47364683
|
G | A | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.805+3162G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364683 | ||||||
| chr17:47364997
|
C | T | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.805+3476C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47364997 | ||||||
| chr17:47365087
|
T | C | 2 | a0003c0008t0004g0011a0003c0008t0004g0012 | 2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.805+3566T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365087 | ||||||
| chr17:47365097
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.805+3576C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365097 | ||||||
| chr17:47365237
|
C | T | 1 | a0003c0008t0004g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.805+3716C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365237 | ||||||
| chr17:47365238
|
G | A | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+3717G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365238 | ||||||
| chr17:47365356
|
G | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.805+3835G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365356 | ||||||
| chr17:47365458
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.805+3937T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365458 | ||||||
| chr17:47365474
|
G | A | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.805+3953G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365474 | ||||||
| chr17:47365525
|
C | T | 1 | a0005c0005t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.805+4004C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47365525 | ||||||
| chr17:47365831
|
CAA | C | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.805+4312_805+4313d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47365831 | |||||
| chr17:47366032
|
A | G | 1 | a0002c0002t0001g0330 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.806-4405A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366032 | ||||||
| chr17:47366128
|
A | G | 139 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.806-4309A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366128 | ||||||
| chr17:47366137
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.806-4300A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366137 | ||||||
| chr17:47366298
|
C | G | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.806-4139C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366298 | ||||||
| chr17:47366314
|
G | GT | 62 | a0001c0001t0001g0175a0001c0006t0001g0094a0001c0006t0001g0095others(59): Show | 63 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.806-4109dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47366314 | |||||
| chr17:47366314
|
GT | G | 10 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG02615.hp1 HG02717.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-4109delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr17 | 47366314 | |||||
| chr17:47366372
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.806-4065G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366372 | ||||||
| chr17:47366462
|
G | A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.806-3975G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366462 | ||||||
| chr17:47366674
|
G | A | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.806-3763G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366674 | ||||||
| chr17:47366707
|
A | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.806-3730A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366707 | ||||||
| chr17:47366723
|
C | T | 1 | a0004c0003t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.806-3714C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366723 | ||||||
| chr17:47366800
|
T | C | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.806-3637T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366800 | ||||||
| chr17:47366923
|
T | G | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.806-3514T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47366923 | ||||||
| chr17:47367245
|
C | T | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.806-3192C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367245 | ||||||
| chr17:47367502
|
G | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.806-2935G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367502 | ||||||
| chr17:47367531
|
G | A | 2 | a0001c0001t0005g0255a0001c0001t0005g0257 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.806-2906G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367531 | ||||||
| chr17:47367656
|
G | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.806-2781G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367656 | ||||||
| chr17:47367811
|
G | A | 50 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.806-2626G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367811 | ||||||
| chr17:47367835
|
G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.806-2602G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367835 | ||||||
| chr17:47367863
|
C | T | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.806-2574C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47367863 | ||||||
| chr17:47368074
|
T | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.806-2363T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368074 | ||||||
| chr17:47368435
|
C | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0108 | 3 | HG01169.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.806-2002C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368435 | ||||||
| chr17:47368453
|
T | A | 9 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0198others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.806-1984T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368453 | ||||||
| chr17:47368517
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.806-1920A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368517 | ||||||
| chr17:47368792
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.806-1645A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368792 | ||||||
| chr17:47368886
|
G | T | 6 | a0007c0009t0001g0221a0007c0009t0002g0218a0007c0009t0002g0234others(3): Show | 6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.806-1551G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47368886 | ||||||
| chr17:47369113
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.806-1324C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369113 | ||||||
| chr17:47369137
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.806-1300A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369137 | ||||||
| chr17:47369163
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.806-1274C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369163 | ||||||
| chr17:47369163
|
C | T | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-1274C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369163 | ||||||
| chr17:47369288
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.806-1149T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369288 | ||||||
| chr17:47369358
|
G | A | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-1079G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369358 | ||||||
| chr17:47369392
|
A | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.806-1045A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369392 | ||||||
| chr17:47369579
|
C | T | 1 | a0002c0002t0001g0332 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.806-858C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369579 | ||||||
| chr17:47369694
|
T | A | 3 | a0002c0002t0003g0331a0002c0002t0003g0335a0002c0002t0003g0338 | 3 | HG01069.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.806-743T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47369694 | ||||||
| chr17:47370238
|
A | G | 2 | a0001c0001t0001g0135a0003c0008t0001g0141 | 2 | NA18960.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.806-199A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370238 | ||||||
| chr17:47370268
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.806-169C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370268 | ||||||
| chr17:47370368
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0156 | 2 | HG01433.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.806-69A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370368 | ||||||
| chr17:47370436
|
G | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
splice_acceptor_variant&intron_variant | HIGH | c.806-1G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 10/24 | chr17 | 47370436 | ||||||
| chr17:47370715
|
G | GT | 14 | a0003c0004t0002g0239a0006c0007t0001g0059a0006c0007t0001g0060others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.877+213dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47370715 | |||||
| chr17:47370722
|
G | T | 55 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(52): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.877+214G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370722 | ||||||
| chr17:47370738
|
GT | G | 176 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.877+250delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47370738 | |||||
| chr17:47370738
|
GTT | G | 50 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.877+249_877+250del others(2): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47370738 | |||||
| chr17:47370742
|
T | G | 6 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0126others(3): Show | 6 | HG02965.hp2 HG03540.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+234T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370742 | ||||||
| chr17:47370743
|
T | G | 134 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 134 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.877+235T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370743 | ||||||
| chr17:47370746
|
T | G | 2 | a0001c0001t0005g0255a0001c0001t0005g0257 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.877+238T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370746 | ||||||
| chr17:47370747
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0005g0256 | 2 | HG02738.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.877+239T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370747 | ||||||
| chr17:47370748
|
T | G | 1 | a0004c0003t0001g0032 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.877+240T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370748 | ||||||
| chr17:47370749
|
T | G | 1 | a0001c0006t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.877+241T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370749 | ||||||
| chr17:47370908
|
G | A | 1 | a0002c0002t0003g0055 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.877+400G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47370908 | ||||||
| chr17:47371032
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.877+524G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371032 | ||||||
| chr17:47371062
|
G | GT | 23 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0108others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.877+575dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47371062 | |||||
| chr17:47371062
|
G | T | 9 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0198others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.877+554G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371062 | ||||||
| chr17:47371062
|
GT | G | 101 | a0001c0001t0001g0174a0001c0001t0001g0180a0001c0015t0001g0106others(98): Show | 103 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.877+575delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47371062 | |||||
| chr17:47371064
|
T | TG | 35 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(32): Show | 38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.877+556_877+557ins others(1): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371064 | ||||||
| chr17:47371070
|
T | C | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.877+562T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371070 | ||||||
| chr17:47371249
|
G | T | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.877+741G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371249 | ||||||
| chr17:47371407
|
A | C | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+899A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371407 | ||||||
| chr17:47371654
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0177 | 3 | HG00673.hp2 HG02523.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.877+1146C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371654 | ||||||
| chr17:47371806
|
G | T | 1 | a0002c0002t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.877+1298G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371806 | ||||||
| chr17:47371915
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.877+1407C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371915 | ||||||
| chr17:47371915
|
CTG | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.877+1411_877+1412d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47371915 | |||||
| chr17:47371967
|
T | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.877+1459T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47371967 | ||||||
| chr17:47372124
|
A | G | 37 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(34): Show | 40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.877+1616A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47372124 | ||||||
| chr17:47372746
|
A | AAT | 6 | a0002c0010t0001g0265a0002c0010t0001g0267a0002c0010t0001g0268others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.878-1720_878-1719d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47372746 | |||||
| chr17:47372761
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.878-1711C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47372761 | ||||||
| chr17:47372921
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.878-1551A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47372921 | ||||||
| chr17:47373017
|
CT | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.878-1452delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr17 | 47373017 | |||||
| chr17:47373041
|
T | C | 1 | a0002c0002t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.878-1431T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373041 | ||||||
| chr17:47373054
|
A | G | 1 | a0002c0002t0001g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.878-1418A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373054 | ||||||
| chr17:47373273
|
T | C | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.878-1199T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373273 | ||||||
| chr17:47373819
|
C | T | 1 | a0002c0002t0001g0292 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.878-653C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373819 | ||||||
| chr17:47373837
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.878-635G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373837 | ||||||
| chr17:47373845
|
G | A | 50 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.878-627G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47373845 | ||||||
| chr17:47374084
|
T | A | 1 | a0002c0002t0001g0322 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.878-388T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47374084 | ||||||
| chr17:47374139
|
A | G | 1 | a0006c0007t0001g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.878-333A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47374139 | ||||||
| chr17:47374156
|
A | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.878-316A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 11/24 | chr17 | 47374156 | ||||||
| chr17:47375304
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1372+338T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375304 | ||||||
| chr17:47375327
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1372+361G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375327 | ||||||
| chr17:47375483
|
CG | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1372+522delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr17 | 47375483 | |||||
| chr17:47375493
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1372+527A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375493 | ||||||
| chr17:47375565
|
C | T | 2 | a0002c0002t0001g0296a0002c0002t0001g0300 | 2 | NA19010.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1372+599C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375565 | ||||||
| chr17:47375767
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1372+801C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375767 | ||||||
| chr17:47375830
|
G | C | 1 | a0002c0002t0001g0297 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1372+864G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375830 | ||||||
| chr17:47375915
|
A | G | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1372+949A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375915 | ||||||
| chr17:47375992
|
T | C | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1372+1026T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47375992 | ||||||
| chr17:47376216
|
G | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1372+1250G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376216 | ||||||
| chr17:47376339
|
T | TG | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1372+1375dupG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr17 | 47376339 | |||||
| chr17:47376550
|
TG | T | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-1215delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376550 | ||||||
| chr17:47376551
|
G | C | 1 | a0002c0002t0001g0310 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1373-1215G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376551 | ||||||
| chr17:47376579
|
A | G | 1 | a0002c0002t0003g0335 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1373-1187A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376579 | ||||||
| chr17:47376584
|
T | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1373-1182T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376584 | ||||||
| chr17:47376885
|
T | C | 3 | a0003c0004t0002g0220a0003c0004t0002g0225a0003c0004t0002g0226 | 3 | NA18945.hp1 NA18984.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1373-881T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47376885 | ||||||
| chr17:47377186
|
A | AAC | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1373-565_1373-564d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr17 | 47377186 | |||||
| chr17:47377204
|
C | T | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1373-562C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377204 | ||||||
| chr17:47377213
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1373-553A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377213 | ||||||
| chr17:47377349
|
A | G | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-417A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377349 | ||||||
| chr17:47377361
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18944.hp1 NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1373-405C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377361 | ||||||
| chr17:47377438
|
A | T | 6 | a0007c0009t0001g0221a0007c0009t0002g0218a0007c0009t0002g0234others(3): Show | 6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-328A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377438 | ||||||
| chr17:47377517
|
G | A | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1373-249G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377517 | ||||||
| chr17:47377566
|
G | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1373-200G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 12/24 | chr17 | 47377566 | ||||||
| chr17:47378089
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1510+186A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378089 | ||||||
| chr17:47378107
|
G | A | 239 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(236): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1510+204G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378107 | ||||||
| chr17:47378203
|
G | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1510+300G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378203 | ||||||
| chr17:47378216
|
C | T | 335 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1510+313C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378216 | ||||||
| chr17:47378237
|
G | T | 2 | a0005c0005t0001g0202a0005c0005t0001g0209 | 2 | HG03834.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1510+334G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378237 | ||||||
| chr17:47378257
|
A | C | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1510+354A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378257 | ||||||
| chr17:47378303
|
G | A | 3 | a0002c0002t0003g0055a0002c0002t0003g0057a0002c0002t0003g0058 | 3 | HG01255.hp1 HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1510+400G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378303 | ||||||
| chr17:47378304
|
G | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1510+401G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378304 | ||||||
| chr17:47378322
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1510+419A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378322 | ||||||
| chr17:47378342
|
A | G | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510+439A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378342 | ||||||
| chr17:47378727
|
A | G | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1511-455A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378727 | ||||||
| chr17:47378734
|
A | G | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1511-448A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378734 | ||||||
| chr17:47378831
|
A | C | 1 | a0002c0002t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1511-351A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378831 | ||||||
| chr17:47378967
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1511-215G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378967 | ||||||
| chr17:47378984
|
T | G | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1511-198T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378984 | ||||||
| chr17:47378996
|
T | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1511-186T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47378996 | ||||||
| chr17:47379094
|
A | C | 50 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(47): Show | 53 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1511-88A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 13/24 | chr17 | 47379094 | ||||||
| chr17:47379279
|
G | T | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582+26G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379279 | ||||||
| chr17:47379365
|
ACT | A | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+115_1582+116d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47379365 | |||||
| chr17:47379476
|
A | T | 1 | a0002c0002t0001g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1582+223A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379476 | ||||||
| chr17:47379545
|
T | C | 37 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(34): Show | 40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1582+292T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379545 | ||||||
| chr17:47379562
|
TG | T | 129 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1582+310delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379562 | ||||||
| chr17:47379563
|
G | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0107a0001c0001t0001g0123others(5): Show | 8 | HG00735.hp1 HG01175.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1582+310G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379563 | ||||||
| chr17:47379639
|
G | A | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1582+386G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379639 | ||||||
| chr17:47379691
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1582+438T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379691 | ||||||
| chr17:47379726
|
A | C | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1582+473A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379726 | ||||||
| chr17:47379736
|
G | T | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1582+483G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379736 | ||||||
| chr17:47379770
|
A | AT | 123 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.1582+523dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47379770 | |||||
| chr17:47379922
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1582+669T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47379922 | ||||||
| chr17:47380000
|
G | T | 2 | a0003c0008t0004g0162a0003c0008t0004g0258 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1582+747G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380000 | ||||||
| chr17:47380037
|
C | T | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1582+784C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380037 | ||||||
| chr17:47380100
|
C | CT | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+850dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380100 | |||||
| chr17:47380349
|
C | T | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1582+1096C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380349 | ||||||
| chr17:47380366
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1582+1113T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380366 | ||||||
| chr17:47380441
|
T | C | 1 | a0002c0002t0001g0310 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1582+1188T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380441 | ||||||
| chr17:47380544
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1582+1291T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380544 | ||||||
| chr17:47380693
|
C | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1582+1440C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380693 | ||||||
| chr17:47380715
|
A | G | 1 | a0005c0005t0002g0238 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1582+1462A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380715 | ||||||
| chr17:47380769
|
A | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+1516A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380769 | ||||||
| chr17:47380876
|
T | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1582+1623T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47380876 | ||||||
| chr17:47380880
|
C | CT | 28 | a0001c0001t0001g0051a0001c0001t0001g0156a0001c0001t0005g0257others(25): Show | 28 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.1582+1647dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380880 | |||||
| chr17:47380880
|
C | CTT | 49 | a0001c0006t0001g0100a0003c0004t0001g0140a0003c0004t0002g0109others(46): Show | 50 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1582+1646_1582+164 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380880 | |||||
| chr17:47380880
|
C | CTTTT | 34 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(31): Show | 37 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1582+1644_1582+164 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47380880 | |||||
| chr17:47381098
|
G | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+1845G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47381098 | ||||||
| chr17:47381180
|
T | C | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+1927T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47381180 | ||||||
| chr17:47381202
|
G | GT | 35 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(32): Show | 38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1582+1958dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47381202 | |||||
| chr17:47381892
|
G | GA | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+2642dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47381892 | |||||
| chr17:47381909
|
T | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1582+2656T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47381909 | ||||||
| chr17:47382052
|
T | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1582+2799T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382052 | ||||||
| chr17:47382211
|
C | T | 3 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053 | 3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1582+2958C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382211 | ||||||
| chr17:47382240
|
C | A | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1582+2987C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382240 | ||||||
| chr17:47382330
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1582+3077T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382330 | ||||||
| chr17:47382372
|
G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1582+3119G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382372 | ||||||
| chr17:47382647
|
G | A | 5 | a0002c0002t0001g0259a0002c0002t0001g0279a0002c0002t0001g0294others(2): Show | 5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1582+3394G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382647 | ||||||
| chr17:47382786
|
T | C | 2 | a0006c0007t0001g0059a0006c0007t0001g0062 | 2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1582+3533T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382786 | ||||||
| chr17:47382813
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+3560G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382813 | ||||||
| chr17:47382823
|
C | T | 239 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(236): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1582+3570C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382823 | ||||||
| chr17:47382847
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1582+3594C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47382847 | ||||||
| chr17:47383242
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1582+3989A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383242 | ||||||
| chr17:47383463
|
G | A | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4210G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383463 | ||||||
| chr17:47383497
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1582+4244T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383497 | ||||||
| chr17:47383526
|
T | C | 1 | a0002c0002t0001g0306 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1582+4273T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383526 | ||||||
| chr17:47383716
|
T | C | 1 | a0003c0004t0002g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1582+4463T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383716 | ||||||
| chr17:47383805
|
T | C | 1 | a0005c0005t0001g0007 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1582+4552T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47383805 | ||||||
| chr17:47384011
|
C | T | 1 | a0001c0015t0001g0192 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1582+4758C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384011 | ||||||
| chr17:47384017
|
A | G | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1582+4764A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384017 | ||||||
| chr17:47384020
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1582+4767C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384020 | ||||||
| chr17:47384083
|
G | A | 1 | a0002c0002t0001g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1582+4830G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384083 | ||||||
| chr17:47384095
|
C | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0158 | 2 | HG01123.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1582+4842C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384095 | ||||||
| chr17:47384120
|
TCA | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+4870_1582+487 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384120 | |||||
| chr17:47384143
|
CA | C | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4891delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384143 | ||||||
| chr17:47384144
|
A | G | 51 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(48): Show | 54 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1582+4891A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384144 | ||||||
| chr17:47384145
|
G | GT | 38 | a0001c0001t0001g0138a0001c0001t0001g0275a0004c0003t0001g0001others(35): Show | 41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4904dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384145 | |||||
| chr17:47384145
|
GT | G | 15 | a0001c0001t0005g0255a0001c0001t0005g0257a0001c0006t0001g0093others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1582+4904delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384145 | |||||
| chr17:47384146
|
T | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582+4893T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384146 | ||||||
| chr17:47384154
|
T | G | 1 | a0006c0007t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1582+4901T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384154 | ||||||
| chr17:47384157
|
T | G | 1 | a0007c0009t0002g0248 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1582+4904T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384157 | ||||||
| chr17:47384158
|
G | GT | 7 | a0001c0001t0001g0123a0002c0002t0001g0302a0002c0002t0001g0303others(4): Show | 7 | HG00438.hp1 HG03927.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582+4918dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384158 | |||||
| chr17:47384158
|
G | T | 16 | a0001c0001t0001g0052a0001c0001t0001g0138a0006c0007t0001g0059others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1582+4905G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384158 | ||||||
| chr17:47384159
|
T | G | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG02135.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1582+4906T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384159 | ||||||
| chr17:47384165
|
T | C | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+4912T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384165 | ||||||
| chr17:47384223
|
G | A | 1 | a0003c0004t0002g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1582+4970G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384223 | ||||||
| chr17:47384340
|
C | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1582+5087C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384340 | ||||||
| chr17:47384426
|
G | GT | 6 | a0001c0001t0001g0084a0001c0001t0001g0119a0001c0001t0001g0138others(3): Show | 6 | HG00735.hp1 HG01099.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582+5185dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384426 | |||||
| chr17:47384449
|
G | GTATTAAG others(13): Show |
1 | a0006c0007t0001g0064 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1582+5214_1582+523 others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384449 | |||||
| chr17:47384488
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+5235C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384488 | ||||||
| chr17:47384558
|
G | A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1582+5305G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384558 | ||||||
| chr17:47384629
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1582+5376G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384629 | ||||||
| chr17:47384667
|
C | A | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1582+5414C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47384667 | ||||||
| chr17:47384789
|
GAGA | G | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1582+5539_1582+554 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47384789 | |||||
| chr17:47385006
|
T | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1582+5753T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385006 | ||||||
| chr17:47385022
|
C | T | 4 | a0005c0005t0001g0110a0005c0005t0001g0116a0005c0005t0001g0203others(1): Show | 4 | NA18981.hp2 NA19000.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+5769C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385022 | ||||||
| chr17:47385095
|
G | A | 1 | a0005c0005t0003g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1582+5842G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385095 | ||||||
| chr17:47385203
|
G | A | 3 | a0002c0002t0001g0307a0002c0002t0001g0314a0002c0002t0009g0313 | 3 | NA18961.hp1 NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1582+5950G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385203 | ||||||
| chr17:47385507
|
T | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-5930T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385507 | ||||||
| chr17:47385522
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1583-5915G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385522 | ||||||
| chr17:47385636
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-5801C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385636 | ||||||
| chr17:47385760
|
G | T | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1583-5677G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385760 | ||||||
| chr17:47385801
|
G | C | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1583-5636G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385801 | ||||||
| chr17:47385852
|
T | C | 1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1583-5585T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385852 | ||||||
| chr17:47385875
|
A | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1583-5562A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385875 | ||||||
| chr17:47385891
|
T | C | 1 | a0002c0002t0001g0320 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1583-5546T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47385891 | ||||||
| chr17:47386285
|
G | A | 1 | a0002c0002t0001g0311 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1583-5152G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386285 | ||||||
| chr17:47386473
|
T | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-4964T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386473 | ||||||
| chr17:47386476
|
C | T | 30 | a0001c0001t0001g0070a0001c0001t0001g0090a0001c0001t0001g0091others(27): Show | 30 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1583-4961C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386476 | ||||||
| chr17:47386642
|
A | C | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1583-4795A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386642 | ||||||
| chr17:47386653
|
G | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-4784G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386653 | ||||||
| chr17:47386770
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1583-4667G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386770 | ||||||
| chr17:47386891
|
C | T | 1 | a0002c0002t0001g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1583-4546C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47386891 | ||||||
| chr17:47387021
|
C | T | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-4416C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387021 | ||||||
| chr17:47387161
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-4276G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387161 | ||||||
| chr17:47387309
|
A | C | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1583-4128A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387309 | ||||||
| chr17:47387311
|
T | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-4126T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387311 | ||||||
| chr17:47387405
|
T | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-4032T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387405 | ||||||
| chr17:47387577
|
A | G | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1583-3860A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387577 | ||||||
| chr17:47387601
|
A | G | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1583-3836A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387601 | ||||||
| chr17:47387636
|
C | CTT | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3801_1583-380 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387636 | ||||||
| chr17:47387639
|
T | TAA | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3798_1583-379 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387639 | ||||||
| chr17:47387641
|
C | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3796C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387641 | ||||||
| chr17:47387643
|
G | GGAT | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3794_1583-379 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387643 | ||||||
| chr17:47387645
|
C | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3792C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387645 | ||||||
| chr17:47387649
|
T | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-3788T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387649 | ||||||
| chr17:47387661
|
A | T | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1583-3776A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387661 | ||||||
| chr17:47387922
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1583-3515T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47387922 | ||||||
| chr17:47388369
|
A | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-3068A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388369 | ||||||
| chr17:47388468
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-2969T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388468 | ||||||
| chr17:47388543
|
T | C | 7 | a0003c0008t0001g0006a0003c0008t0004g0005a0003c0008t0004g0011others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1583-2894T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388543 | ||||||
| chr17:47388577
|
C | T | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-2860C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388577 | ||||||
| chr17:47388719
|
T | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1583-2718T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47388719 | ||||||
| chr17:47388915
|
AT | A | 52 | a0003c0008t0001g0006a0004c0003t0001g0001a0004c0003t0001g0003others(49): Show | 55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1583-2511delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47388915 | |||||
| chr17:47388915
|
ATTTT | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-2514_1583-251 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47388915 | |||||
| chr17:47389099
|
CA | C | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1583-2337delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389099 | ||||||
| chr17:47389248
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1583-2189G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389248 | ||||||
| chr17:47389405
|
C | T | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1583-2032C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389405 | ||||||
| chr17:47389508
|
G | A | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-1929G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389508 | ||||||
| chr17:47389578
|
C | CT | 50 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0111others(47): Show | 51 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1583-1841dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47389578 | |||||
| chr17:47389578
|
C | CTT | 8 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(5): Show | 8 | HG00408.hp1 HG02135.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1583-1842_1583-184 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47389578 | |||||
| chr17:47389596
|
T | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1583-1841T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389596 | ||||||
| chr17:47389598
|
C | T | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1583-1839C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389598 | ||||||
| chr17:47389822
|
A | G | 1 | a0005c0005t0001g0210 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1583-1615A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389822 | ||||||
| chr17:47389940
|
CTGTA | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-1492_1583-148 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47389940 | |||||
| chr17:47389945
|
T | A | 2 | a0003c0008t0001g0006a0003c0008t0004g0005 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1583-1492T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47389945 | ||||||
| chr17:47390044
|
A | G | 1 | a0002c0002t0001g0056 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1583-1393A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390044 | ||||||
| chr17:47390116
|
T | C | 335 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1583-1321T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390116 | ||||||
| chr17:47390237
|
T | C | 1 | a0002c0002t0001g0320 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1583-1200T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390237 | ||||||
| chr17:47390238
|
TGA | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1583-1193_1583-119 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390238 | |||||
| chr17:47390305
|
C | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-1132C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390305 | ||||||
| chr17:47390325
|
T | TAC | 10 | a0001c0001t0001g0120a0001c0001t0001g0169a0001c0001t0001g0170others(7): Show | 10 | HG00438.hp1 HG02165.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1583-1093_1583-109 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | |||||
| chr17:47390325
|
T | TACACAC | 12 | a0003c0004t0002g0220a0006c0007t0001g0059a0006c0007t0001g0060others(9): Show | 12 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1583-1097_1583-109 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | |||||
| chr17:47390325
|
T | TACACACA others(3): Show |
34 | a0003c0004t0002g0217a0003c0004t0002g0219a0003c0004t0002g0222others(31): Show | 35 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1583-1101_1583-109 others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | |||||
| chr17:47390325
|
T | TACACACA others(5): Show |
1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583-1103_1583-109 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | |||||
| chr17:47390325
|
T | TACACACA others(7): Show |
40 | a0003c0004t0002g0109a0003c0004t0002g0247a0003c0008t0003g0276others(37): Show | 43 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1583-1105_1583-109 others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390325 | |||||
| chr17:47390349
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1583-1088C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390349 | ||||||
| chr17:47390910
|
G | GTCTTATC others(6): Show |
1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583-524_1583-523i others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390910 | |||||
| chr17:47390914
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583-523G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390914 | ||||||
| chr17:47390914
|
G | GTCTA | 47 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0070others(44): Show | 47 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1583-511_1583-508d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTATCT others(1): Show |
71 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(68): Show | 71 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1583-515_1583-508d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTATCT others(5): Show |
26 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0077others(23): Show | 26 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1583-519_1583-508d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTATCT others(13): Show |
1 | a0001c0001t0001g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1583-508_1583-507i others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTTA | 5 | a0003c0004t0002g0219a0003c0004t0002g0233a0003c0004t0002g0239others(2): Show | 5 | HG02083.hp1 HG03688.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTTATC others(2): Show |
29 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0220others(26): Show | 30 | HG00558.hp1 HG01346.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(11): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTTATC others(6): Show |
8 | a0003c0004t0002g0217a0003c0004t0002g0227a0003c0004t0002g0231others(5): Show | 8 | HG00438.hp2 HG00544.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTTATC others(10): Show |
3 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054 | 3 | HG02647.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1583-520_1583-519i others(19): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTTATC others(14): Show |
4 | a0006c0007t0001g0060a0006c0007t0001g0063a0006c0007t0001g0064others(1): Show | 4 | HG02135.hp2 NA18997.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(23): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390914
|
G | GTCTTATC others(18): Show |
6 | a0006c0007t0001g0059a0006c0007t0001g0062a0006c0007t0001g0339others(3): Show | 6 | HG00408.hp1 HG00423.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-520_1583-519i others(27): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390914 | |||||
| chr17:47390916
|
C | CT | 35 | a0003c0004t0002g0247a0004c0003t0001g0001a0004c0003t0001g0003others(32): Show | 38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1583-520dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr17 | 47390916 | |||||
| chr17:47390930
|
G | A | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1583-507G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47390930 | ||||||
| chr17:47391005
|
T | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1583-432T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391005 | ||||||
| chr17:47391026
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-411A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391026 | ||||||
| chr17:47391054
|
C | T | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1583-383C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391054 | ||||||
| chr17:47391216
|
A | C | 1 | a0003c0004t0002g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1583-221A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391216 | ||||||
| chr17:47391328
|
G | A | 2 | a0003c0008t0004g0162a0003c0008t0004g0258 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1583-109G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 14/24 | chr17 | 47391328 | ||||||
| chr17:47391591
|
T | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1726+11T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391591 | ||||||
| chr17:47391641
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1726+61A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391641 | ||||||
| chr17:47391665
|
AT | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1726+92delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47391665 | |||||
| chr17:47391765
|
C | T | 1 | a0001c0006t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1726+185C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391765 | ||||||
| chr17:47391787
|
TA | T | 8 | a0001c0001t0001g0076a0002c0002t0001g0263a0002c0010t0001g0265others(5): Show | 8 | HG00323.hp1 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1726+216delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47391787 | |||||
| chr17:47391788
|
A | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726+208A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391788 | ||||||
| chr17:47391821
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726+241A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391821 | ||||||
| chr17:47391840
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1726+260T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391840 | ||||||
| chr17:47391857
|
G | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726+277G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391857 | ||||||
| chr17:47391925
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1726+345A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47391925 | ||||||
| chr17:47392238
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1726+658G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392238 | ||||||
| chr17:47392353
|
C | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1726+773C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392353 | ||||||
| chr17:47392487
|
C | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1726+907C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392487 | ||||||
| chr17:47392879
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1727-1146A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392879 | ||||||
| chr17:47392916
|
T | G | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1727-1109T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392916 | ||||||
| chr17:47392975
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-1050C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392975 | ||||||
| chr17:47392992
|
T | C | 49 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(46): Show | 52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1727-1033T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392992 | ||||||
| chr17:47392997
|
G | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-1028G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47392997 | ||||||
| chr17:47393072
|
G | A | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1727-953G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393072 | ||||||
| chr17:47393074
|
G | A | 2 | a0003c0004t0002g0219a0003c0004t0002g0239 | 2 | NA18747.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1727-951G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393074 | ||||||
| chr17:47393091
|
A | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1727-934A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393091 | ||||||
| chr17:47393101
|
T | TA | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-914dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393101 | |||||
| chr17:47393177
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-848C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393177 | ||||||
| chr17:47393334
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-691A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393334 | ||||||
| chr17:47393357
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0180 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1727-668A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393357 | ||||||
| chr17:47393409
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1727-616G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393409 | ||||||
| chr17:47393412
|
G | A | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1727-613G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393412 | ||||||
| chr17:47393547
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-478A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393547 | ||||||
| chr17:47393560
|
A | C | 2 | a0002c0002t0001g0289a0002c0002t0001g0295 | 2 | NA18987.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1727-465A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393560 | ||||||
| chr17:47393717
|
A | AAAAT | 44 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0262others(41): Show | 44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1727-272_1727-269d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | |||||
| chr17:47393717
|
A | AAAATAAA others(1): Show |
22 | a0002c0010t0001g0267a0002c0010t0001g0268a0002c0010t0001g0269others(19): Show | 22 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.1727-276_1727-269d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | |||||
| chr17:47393717
|
A | AAAATAAA others(5): Show |
1 | a0002c0010t0001g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1727-280_1727-269d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | |||||
| chr17:47393717
|
AAAAT | A | 144 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1727-272_1727-269d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | |||||
| chr17:47393717
|
AAAATAAA others(1): Show |
A | 5 | a0001c0001t0001g0018a0001c0001t0001g0087a0001c0001t0001g0137others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1727-276_1727-269d others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | |||||
| chr17:47393717
|
AAAATAAA others(5): Show |
A | 27 | a0001c0001t0001g0070a0001c0001t0001g0090a0001c0001t0001g0091others(24): Show | 27 | HG00280.hp1 HG01071.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1727-280_1727-269d others(14): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393717 | |||||
| chr17:47393753
|
T | A | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1727-272T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393753 | ||||||
| chr17:47393753
|
TAAAA | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1727-270_1727-267d others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393753 | |||||
| chr17:47393757
|
A | T | 3 | a0002c0002t0008g0323a0004c0003t0001g0033a0005c0005t0001g0116 | 3 | HG01358.hp1 HG03669.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1727-268A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393757 | ||||||
| chr17:47393766
|
AAAT | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0134 | 3 | HG02132.hp2 NA19064.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1727-256_1727-254d others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr17 | 47393766 | |||||
| chr17:47393862
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1727-163A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 15/24 | chr17 | 47393862 | ||||||
| chr17:47394339
|
C | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1801+240C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47394339 | ||||||
| chr17:47394618
|
G | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1801+519G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47394618 | ||||||
| chr17:47394861
|
CAG | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1801+765_1801+766d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr17 | 47394861 | |||||
| chr17:47394877
|
A | G | 1 | a0005c0005t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1801+778A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47394877 | ||||||
| chr17:47395030
|
C | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1802-804C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395030 | ||||||
| chr17:47395036
|
C | T | 2 | a0002c0002t0001g0298a0002c0002t0001g0302 | 2 | NA18991.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1802-798C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395036 | ||||||
| chr17:47395037
|
G | A | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1802-797G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395037 | ||||||
| chr17:47395357
|
T | G | 1 | a0002c0002t0008g0323 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1802-477T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395357 | ||||||
| chr17:47395435
|
G | A | 1 | a0002c0002t0001g0292 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1802-399G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395435 | ||||||
| chr17:47395741
|
A | G | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1802-93A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395741 | ||||||
| chr17:47395804
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1802-30C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 16/24 | chr17 | 47395804 | ||||||
| chr17:47396047
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945+70A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396047 | ||||||
| chr17:47396258
|
A | G | 5 | a0002c0002t0001g0259a0002c0002t0001g0279a0002c0002t0001g0294others(2): Show | 5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+281A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396258 | ||||||
| chr17:47396293
|
G | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+316G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396293 | ||||||
| chr17:47396664
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+687C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396664 | ||||||
| chr17:47396748
|
T | C | 3 | a0004c0003t0001g0028a0004c0003t0001g0031a0004c0003t0001g0040 | 3 | NA18956.hp1 NA18963.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1945+771T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396748 | ||||||
| chr17:47396817
|
G | A | 1 | a0003c0004t0002g0217 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1945+840G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396817 | ||||||
| chr17:47396856
|
T | C | 1 | a0004c0003t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1945+879T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47396856 | ||||||
| chr17:47397008
|
GTCCCTC | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+1042_1945+104 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397008 | |||||
| chr17:47397019
|
T | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1945+1042T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397019 | ||||||
| chr17:47397027
|
T | TCCC | 17 | a0003c0004t0002g0109a0003c0004t0002g0219a0003c0004t0002g0225others(14): Show | 17 | HG00544.hp1 HG01515.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.1945+1053_1945+105 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397027 | |||||
| chr17:47397027
|
T | TCCCC | 16 | a0003c0004t0002g0214a0003c0004t0002g0217a0003c0004t0002g0220others(13): Show | 17 | HG00438.hp2 HG01346.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1945+1052_1945+105 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397027 | |||||
| chr17:47397033
|
T | C | 1 | a0003c0004t0002g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1945+1056T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397033 | ||||||
| chr17:47397033
|
T | TC | 5 | a0001c0001t0001g0014a0001c0001t0001g0122a0002c0002t0001g0318others(2): Show | 5 | HG01496.hp1 HG02055.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+1061dupC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397033 | |||||
| chr17:47397060
|
G | C | 1 | a0004c0003t0001g0027 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1945+1083G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397060 | ||||||
| chr17:47397157
|
G | A | 140 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1945+1180G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397157 | ||||||
| chr17:47397169
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1945+1192G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397169 | ||||||
| chr17:47397201
|
AC | A | 40 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1945+1225delC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397201 | ||||||
| chr17:47397202
|
C | G | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1945+1225C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397202 | ||||||
| chr17:47397242
|
A | G | 2 | a0003c0004t0002g0222a0003c0004t0002g0229 | 2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1945+1265A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397242 | ||||||
| chr17:47397353
|
G | A | 1 | a0003c0004t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1945+1376G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397353 | ||||||
| chr17:47397410
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1945+1433T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397410 | ||||||
| chr17:47397424
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945+1447C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397424 | ||||||
| chr17:47397466
|
GC | G | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1945+1491delC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397466 | |||||
| chr17:47397489
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1512G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397489 | ||||||
| chr17:47397540
|
C | T | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+1563C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397540 | ||||||
| chr17:47397542
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0132 | 2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1945+1565G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397542 | ||||||
| chr17:47397552
|
CATCTAGG others(33): Show |
C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1595_1945+163 others(44): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397552 | |||||
| chr17:47397555
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1945+1578C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397555 | ||||||
| chr17:47397592
|
T | C | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1945+1615T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397592 | ||||||
| chr17:47397621
|
G | A | 1 | a0004c0003t0001g0029 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1945+1644G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397621 | ||||||
| chr17:47397626
|
C | G | 2 | a0003c0008t0001g0006a0003c0008t0004g0005 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1945+1649C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397626 | ||||||
| chr17:47397631
|
C | A | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.1945+1654C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397631 | ||||||
| chr17:47397664
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1687G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397664 | ||||||
| chr17:47397669
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1945+1692G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397669 | ||||||
| chr17:47397709
|
A | T | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1945+1732A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397709 | ||||||
| chr17:47397763
|
A | ACCCTCCG others(32): Show |
3 | a0003c0004t0002g0222a0003c0004t0002g0229a0003c0004t0002g0232 | 3 | NA18942.hp1 NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1945+1796_1945+183 others(43): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397763 | |||||
| chr17:47397790
|
A | C | 1 | a0005c0005t0001g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1945+1813A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397790 | ||||||
| chr17:47397905
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+1928A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397905 | ||||||
| chr17:47397937
|
A | AGGCCAGC others(42): Show |
1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+1967_1945+196 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397937 | |||||
| chr17:47397945
|
C | CGCCCCGT others(43): Show |
1 | a0004c0003t0001g0032 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1945+1995_1945+199 others(54): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397945 | |||||
| chr17:47397945
|
C | CGCCCCGT others(42): Show |
81 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(78): Show | 85 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1945+2016_1945+201 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397945 | |||||
| chr17:47397945
|
C | T | 2 | a0004c0003t0006g0260a0016c0020t0001g0346 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1945+1968C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397945 | ||||||
| chr17:47397946
|
G | GCCCCGTC others(42): Show |
4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+2016_1945+201 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397946 | |||||
| chr17:47397951
|
G | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+1974G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47397951 | ||||||
| chr17:47397965
|
T | TGGGGGGG others(43): Show |
3 | a0003c0004t0001g0140a0003c0004t0002g0233a0004c0003t0001g0067 | 3 | HG02965.hp1 NA18985.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1945+2016_1945+201 others(54): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47397965 | |||||
| chr17:47398000
|
G | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+2023G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398000 | ||||||
| chr17:47398013
|
G | A | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1945+2036G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398013 | ||||||
| chr17:47398020
|
G | A | 2 | a0003c0008t0004g0162a0003c0008t0004g0258 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1945+2043G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398020 | ||||||
| chr17:47398020
|
G | C | 41 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1945+2043G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398020 | ||||||
| chr17:47398030
|
TGCCCGGC others(42): Show |
T | 14 | a0002c0002t0001g0010a0002c0002t0001g0262a0002c0002t0001g0263others(11): Show | 14 | HG02615.hp1 HG02717.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.1945+2068_1945+211 others(53): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398030 | |||||
| chr17:47398035
|
G | A | 37 | a0002c0002t0001g0292a0004c0003t0001g0001a0004c0003t0001g0003others(34): Show | 40 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1945+2058G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398035 | ||||||
| chr17:47398043
|
G | A | 13 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1945+2066G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398043 | ||||||
| chr17:47398045
|
T | C | 2 | a0006c0007t0001g0059a0006c0007t0001g0062 | 2 | HG00408.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1945+2068T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398045 | ||||||
| chr17:47398051
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1945+2074C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398051 | ||||||
| chr17:47398065
|
G | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+2088G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398065 | ||||||
| chr17:47398079
|
CGCCCGGC others(119): Show |
C | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1945+2152_1945+227 others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398079 | |||||
| chr17:47398097
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1945+2120G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398097 | ||||||
| chr17:47398101
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1945+2124G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398101 | ||||||
| chr17:47398127
|
C | G | 5 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053others(2): Show | 5 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+2150C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398127 | ||||||
| chr17:47398128
|
C | CG | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1945+2151_1945+215 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398128 | ||||||
| chr17:47398130
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1945+2153C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398130 | ||||||
| chr17:47398130
|
CT | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0157a0001c0001t0001g0166 | 3 | HG02135.hp1 HG02257.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1945+2154delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398130 | ||||||
| chr17:47398173
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2196A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398173 | ||||||
| chr17:47398173
|
AGCCGCCC others(120): Show |
A | 2 | a0002c0002t0001g0056a0002c0002t0001g0309 | 2 | HG00673.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1945+2238_1945+236 others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398173 | |||||
| chr17:47398226
|
C | T | 14 | a0001c0001t0001g0019a0006c0007t0001g0059a0006c0007t0001g0060others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1945+2249C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398226 | ||||||
| chr17:47398258
|
C | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+2281C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398258 | ||||||
| chr17:47398259
|
G | A | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+2282G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398259 | ||||||
| chr17:47398267
|
A | G | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2290A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398267 | ||||||
| chr17:47398273
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2296C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398273 | ||||||
| chr17:47398276
|
G | A | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1945+2299G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398276 | ||||||
| chr17:47398303
|
C | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1945+2326C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398303 | ||||||
| chr17:47398401
|
C | T | 1 | a0003c0008t0004g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1945+2424C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398401 | ||||||
| chr17:47398421
|
G | C | 1 | a0007c0009t0002g0234 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1945+2444G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398421 | ||||||
| chr17:47398432
|
G | A | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1945+2455G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398432 | ||||||
| chr17:47398466
|
T | G | 1 | a0005c0005t0007g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1945+2489T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398466 | ||||||
| chr17:47398469
|
G | C | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.1945+2492G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398469 | ||||||
| chr17:47398474
|
G | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1945+2497G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398474 | ||||||
| chr17:47398480
|
G | A | 1 | a0003c0004t0002g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1945+2503G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398480 | ||||||
| chr17:47398577
|
T | A | 1 | a0004c0003t0001g0029 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1945+2600T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398577 | ||||||
| chr17:47398783
|
G | C | 238 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1945+2806G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398783 | ||||||
| chr17:47398824
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+2847C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398824 | ||||||
| chr17:47398850
|
AAAAT | A | 40 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(37): Show | 43 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1945+2893_1945+289 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47398850 | |||||
| chr17:47398906
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+2929A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398906 | ||||||
| chr17:47398930
|
C | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1945+2953C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398930 | ||||||
| chr17:47398934
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1945+2957C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398934 | ||||||
| chr17:47398984
|
C | T | 1 | a0004c0003t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1945+3007C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398984 | ||||||
| chr17:47398993
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1945+3016G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47398993 | ||||||
| chr17:47399020
|
T | A | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1945+3043T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399020 | ||||||
| chr17:47399075
|
A | G | 1 | a0004c0003t0001g0045 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1946-3057A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399075 | ||||||
| chr17:47399277
|
T | C | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1946-2855T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399277 | ||||||
| chr17:47399293
|
CAT | C | 3 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345 | 3 | HG03654.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1946-2838_1946-283 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399293 | ||||||
| chr17:47399367
|
A | G | 1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1946-2765A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399367 | ||||||
| chr17:47399670
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1946-2462C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399670 | ||||||
| chr17:47399680
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1946-2452C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399680 | ||||||
| chr17:47399714
|
G | GTGGTA | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1946-2416_1946-241 others(9): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47399714 | |||||
| chr17:47399732
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1946-2400T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399732 | ||||||
| chr17:47399793
|
G | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1946-2339G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399793 | ||||||
| chr17:47399806
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1946-2326G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399806 | ||||||
| chr17:47399853
|
T | C | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1946-2279T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399853 | ||||||
| chr17:47399859
|
C | T | 91 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1946-2273C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399859 | ||||||
| chr17:47399922
|
C | CA | 3 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0151 | 3 | NA18993.hp1 NA19009.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1946-2205dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47399922 | |||||
| chr17:47399929
|
G | A | 3 | a0004c0003t0001g0028a0004c0003t0001g0031a0004c0003t0001g0040 | 3 | NA18956.hp1 NA18963.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1946-2203G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399929 | ||||||
| chr17:47399977
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1946-2155C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47399977 | ||||||
| chr17:47400003
|
A | G | 1 | a0005c0005t0001g0203 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1946-2129A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400003 | ||||||
| chr17:47400207
|
C | T | 237 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(234): Show | 241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1946-1925C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400207 | ||||||
| chr17:47400260
|
A | G | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1946-1872A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400260 | ||||||
| chr17:47400302
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1946-1830G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400302 | ||||||
| chr17:47400455
|
C | T | 1 | a0004c0003t0001g0032 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1946-1677C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400455 | ||||||
| chr17:47400598
|
CTTGCCTC others(1): Show |
C | 4 | a0001c0001t0001g0137a0001c0001t0001g0155a0008c0011t0001g0054others(1): Show | 4 | HG01891.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1946-1533_1946-152 others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400598 | ||||||
| chr17:47400814
|
G | T | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1946-1318G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400814 | ||||||
| chr17:47400815
|
C | T | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1946-1317C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47400815 | ||||||
| chr17:47401092
|
G | A | 1 | a0004c0003t0001g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1946-1040G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401092 | ||||||
| chr17:47401116
|
A | AT | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1946-1016_1946-101 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401116 | ||||||
| chr17:47401217
|
A | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1946-915A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401217 | ||||||
| chr17:47401372
|
C | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1946-760C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401372 | ||||||
| chr17:47401477
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1946-655A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401477 | ||||||
| chr17:47401590
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1946-542A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401590 | ||||||
| chr17:47401597
|
A | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1946-535A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401597 | ||||||
| chr17:47401640
|
C | CT | 119 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(116): Show | 119 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1946-470dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47401640 | |||||
| chr17:47401640
|
C | CTT | 6 | a0001c0001t0001g0014a0001c0001t0001g0081a0001c0001t0001g0084others(3): Show | 6 | HG02027.hp1 HG02055.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1946-471_1946-470d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47401640 | |||||
| chr17:47401640
|
CT | C | 57 | a0002c0002t0001g0286a0002c0002t0001g0321a0002c0002t0003g0336others(54): Show | 60 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1946-470delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr17 | 47401640 | |||||
| chr17:47401643
|
T | C | 1 | a0001c0006t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1946-489T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401643 | ||||||
| chr17:47401669
|
G | A | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1946-463G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401669 | ||||||
| chr17:47401733
|
C | A | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1946-399C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401733 | ||||||
| chr17:47401930
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1946-202C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47401930 | ||||||
| chr17:47402080
|
A | C | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.1946-52A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 17/24 | chr17 | 47402080 | ||||||
| chr17:47402321
|
T | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017+118T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402321 | ||||||
| chr17:47402330
|
G | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2017+127G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402330 | ||||||
| chr17:47402340
|
C | G | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2017+137C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402340 | ||||||
| chr17:47402367
|
A | C | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2017+164A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402367 | ||||||
| chr17:47402473
|
G | A | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2017+270G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402473 | ||||||
| chr17:47402551
|
C | A | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2017+348C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402551 | ||||||
| chr17:47402801
|
T | A | 11 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2017+598T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402801 | ||||||
| chr17:47402963
|
G | C | 1 | a0008c0011t0001g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2017+760G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47402963 | ||||||
| chr17:47403162
|
T | C | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-716T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403162 | ||||||
| chr17:47403245
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2018-633G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403245 | ||||||
| chr17:47403392
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2018-486A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403392 | ||||||
| chr17:47403527
|
G | A | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2018-351G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403527 | ||||||
| chr17:47403691
|
C | T | 96 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(93): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2018-187C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403691 | ||||||
| chr17:47403825
|
G | A | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2018-53G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403825 | ||||||
| chr17:47403835
|
A | G | 1 | a0003c0016t0002g0223 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2018-43A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 18/24 | chr17 | 47403835 | ||||||
| chr17:47404048
|
GT | G | 7 | a0003c0004t0002g0222a0003c0004t0002g0229a0003c0004t0002g0232others(4): Show | 7 | NA18942.hp1 NA18946.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2161+37delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr17 | 47404048 | |||||
| chr17:47404199
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2161+178T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | chr17 | 47404199 | ||||||
| chr17:47404265
|
T | G | 1 | a0006c0007t0010g0061 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2161+244T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | chr17 | 47404265 | ||||||
| chr17:47404497
|
T | C | 3 | a0001c0013t0001g0117a0001c0013t0001g0196a0001c0013t0001g0197 | 3 | HG01070.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2162-65T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 19/24 | chr17 | 47404497 | ||||||
| chr17:47405180
|
G | A | 1 | a0004c0003t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2233+547G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405180 | ||||||
| chr17:47405446
|
T | A | 89 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(86): Show | 93 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2233+813T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405446 | ||||||
| chr17:47405491
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2233+858A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405491 | ||||||
| chr17:47405525
|
T | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2233+892T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405525 | ||||||
| chr17:47405549
|
T | C | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2233+916T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405549 | ||||||
| chr17:47405709
|
G | T | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2233+1076G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405709 | ||||||
| chr17:47405807
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2233+1174T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405807 | ||||||
| chr17:47405863
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2233+1230A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47405863 | ||||||
| chr17:47405913
|
AT | A | 44 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(41): Show | 44 | HG00673.hp2 HG01070.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2233+1288delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr17 | 47405913 | |||||
| chr17:47406074
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2233+1441T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406074 | ||||||
| chr17:47406129
|
T | C | 1 | a0002c0002t0003g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2233+1496T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406129 | ||||||
| chr17:47406136
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2233+1503G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406136 | ||||||
| chr17:47406256
|
T | C | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2233+1623T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406256 | ||||||
| chr17:47406503
|
G | A | 1 | a0002c0002t0003g0335 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2233+1870G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406503 | ||||||
| chr17:47406582
|
A | G | 1 | a0002c0002t0001g0325 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2233+1949A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406582 | ||||||
| chr17:47406633
|
T | G | 3 | a0003c0004t0002g0236a0003c0004t0002g0250a0013c0017t0001g0205 | 3 | HG02056.hp2 NA18943.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2233+2000T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406633 | ||||||
| chr17:47406683
|
G | A | 3 | a0006c0007t0001g0339a0006c0007t0001g0340a0006c0007t0001g0341 | 3 | HG00423.hp2 NA18965.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2233+2050G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406683 | ||||||
| chr17:47406745
|
G | A | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2233+2112G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47406745 | ||||||
| chr17:47407064
|
TA | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2233+2435delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr17 | 47407064 | |||||
| chr17:47407121
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2233+2488T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407121 | ||||||
| chr17:47407174
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2234-2473G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407174 | ||||||
| chr17:47407214
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2234-2433T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407214 | ||||||
| chr17:47407573
|
T | C | 1 | a0012c0026t0001g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2234-2074T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407573 | ||||||
| chr17:47407680
|
A | G | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2234-1967A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407680 | ||||||
| chr17:47407744
|
TTTTGTTT others(4): Show |
T | 1 | a0001c0001t0001g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2234-1888_2234-187 others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr17 | 47407744 | |||||
| chr17:47407819
|
T | C | 1 | a0002c0002t0001g0292 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2234-1828T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407819 | ||||||
| chr17:47407821
|
A | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2234-1826A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47407821 | ||||||
| chr17:47408373
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2234-1274G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408373 | ||||||
| chr17:47408410
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG01169.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2234-1237G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408410 | ||||||
| chr17:47408504
|
T | C | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2234-1143T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408504 | ||||||
| chr17:47408616
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.2234-1031C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408616 | ||||||
| chr17:47408631
|
G | A | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2234-1016G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408631 | ||||||
| chr17:47408637
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2234-1010A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408637 | ||||||
| chr17:47408654
|
G | A | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2234-993G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408654 | ||||||
| chr17:47408975
|
T | G | 1 | a0004c0003t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2234-672T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47408975 | ||||||
| chr17:47409111
|
A | G | 6 | a0007c0009t0001g0221a0007c0009t0002g0218a0007c0009t0002g0234others(3): Show | 6 | HG00558.hp1 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2234-536A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409111 | ||||||
| chr17:47409234
|
A | G | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2234-413A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409234 | ||||||
| chr17:47409285
|
T | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2234-362T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409285 | ||||||
| chr17:47409303
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2234-344C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409303 | ||||||
| chr17:47409396
|
G | A | 1 | a0002c0010t0001g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2234-251G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409396 | ||||||
| chr17:47409450
|
CCAAGTA | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2234-196_2234-191d others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409450 | ||||||
| chr17:47409483
|
A | G | 1 | a0005c0005t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2234-164A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 20/24 | chr17 | 47409483 | ||||||
| chr17:47409765
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2278+74A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47409765 | ||||||
| chr17:47410069
|
G | A | 96 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(93): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2278+378G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410069 | ||||||
| chr17:47410118
|
T | TA | 91 | a0001c0001t0005g0255a0002c0002t0001g0294a0003c0004t0001g0140others(88): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2278+439dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr17 | 47410118 | |||||
| chr17:47410254
|
G | A | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2278+563G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410254 | ||||||
| chr17:47410705
|
A | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0150 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2278+1014A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410705 | ||||||
| chr17:47410800
|
G | A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2278+1109G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410800 | ||||||
| chr17:47410843
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2278+1152C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47410843 | ||||||
| chr17:47411037
|
A | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2278+1346A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411037 | ||||||
| chr17:47411041
|
T | C | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2278+1350T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411041 | ||||||
| chr17:47411240
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0176 | 2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2279-1533C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411240 | ||||||
| chr17:47411369
|
C | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2279-1404C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411369 | ||||||
| chr17:47411510
|
G | T | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2279-1263G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411510 | ||||||
| chr17:47411515
|
A | G | 49 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(46): Show | 52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.2279-1258A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411515 | ||||||
| chr17:47411556
|
T | G | 1 | a0003c0004t0002g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2279-1217T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411556 | ||||||
| chr17:47411940
|
A | T | 5 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053others(2): Show | 5 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2279-833A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47411940 | ||||||
| chr17:47412279
|
T | G | 1 | a0003c0004t0002g0217 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2279-494T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412279 | ||||||
| chr17:47412392
|
T | C | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2279-381T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412392 | ||||||
| chr17:47412413
|
C | G | 3 | a0001c0013t0001g0117a0001c0013t0001g0196a0001c0013t0001g0197 | 3 | HG01070.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2279-360C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412413 | ||||||
| chr17:47412593
|
G | T | 2 | a0005c0005t0001g0110a0005c0005t0001g0116 | 2 | NA19000.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2279-180G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 21/24 | chr17 | 47412593 | ||||||
| chr17:47413010
|
G | A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2422+94G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413010 | ||||||
| chr17:47413153
|
A | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2422+237A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413153 | ||||||
| chr17:47413245
|
AT | A | 233 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2422+339delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47413245 | |||||
| chr17:47413310
|
A | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2422+394A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413310 | ||||||
| chr17:47413642
|
T | C | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2422+726T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47413642 | ||||||
| chr17:47413731
|
A | AT | 53 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(50): Show | 56 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.2422+825dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47413731 | |||||
| chr17:47414239
|
A | ATG | 236 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(233): Show | 240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.2423-598_2423-597d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47414239 | |||||
| chr17:47414253
|
A | G | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2423-595A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414253 | ||||||
| chr17:47414426
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2423-422C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414426 | ||||||
| chr17:47414512
|
C | CA | 8 | a0001c0001t0001g0070a0001c0001t0001g0090a0003c0008t0004g0005others(5): Show | 8 | HG01106.hp1 HG02809.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.2423-319dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47414512 | |||||
| chr17:47414512
|
CA | C | 93 | a0001c0001t0001g0088a0001c0001t0001g0123a0001c0001t0001g0148others(90): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2423-319delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr17 | 47414512 | |||||
| chr17:47414570
|
C | T | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2423-278C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414570 | ||||||
| chr17:47414613
|
C | T | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2423-235C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414613 | ||||||
| chr17:47414692
|
A | C | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2423-156A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 22/24 | chr17 | 47414692 | ||||||
| chr17:47414935
|
T | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2494+16T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47414935 | ||||||
| chr17:47414965
|
T | C | 2 | a0002c0002t0001g0334a0015c0018t0001g0337 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2494+46T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47414965 | ||||||
| chr17:47414975
|
A | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+56A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47414975 | ||||||
| chr17:47415137
|
A | C | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2494+218A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415137 | ||||||
| chr17:47415138
|
C | A | 1 | a0003c0004t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2494+219C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415138 | ||||||
| chr17:47415158
|
A | G | 1 | a0004c0003t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2494+239A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415158 | ||||||
| chr17:47415276
|
T | C | 1 | a0003c0004t0002g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2494+357T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415276 | ||||||
| chr17:47415314
|
C | G | 1 | a0003c0004t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2494+395C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415314 | ||||||
| chr17:47415368
|
C | A | 1 | a0002c0002t0001g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2494+449C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415368 | ||||||
| chr17:47415634
|
CAT | C | 3 | a0006c0007t0001g0339a0006c0007t0001g0340a0006c0007t0001g0341 | 3 | HG00423.hp2 NA18965.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2494+716_2494+717d others(4): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415634 | ||||||
| chr17:47415890
|
G | A | 2 | a0008c0011t0001g0054a0008c0011t0001g0273 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2494+971G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415890 | ||||||
| chr17:47415965
|
A | AT | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2494+1046_2494+104 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415965 | ||||||
| chr17:47415966
|
C | T | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2494+1047C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415966 | ||||||
| chr17:47415984
|
A | G | 1 | a0002c0002t0001g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2494+1065A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415984 | ||||||
| chr17:47415997
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2494+1078C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47415997 | ||||||
| chr17:47416065
|
T | C | 1 | a0002c0002t0003g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2494+1146T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416065 | ||||||
| chr17:47416328
|
G | C | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+1409G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416328 | ||||||
| chr17:47416460
|
T | C | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2494+1541T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416460 | ||||||
| chr17:47416485
|
C | T | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+1566C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416485 | ||||||
| chr17:47416648
|
G | A | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2494+1729G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416648 | ||||||
| chr17:47416751
|
C | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+1832C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47416751 | ||||||
| chr17:47417224
|
G | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+2305G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417224 | ||||||
| chr17:47417279
|
G | A | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2494+2360G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417279 | ||||||
| chr17:47417473
|
C | A | 1 | a0002c0010t0001g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2494+2554C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417473 | ||||||
| chr17:47417498
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2494+2579C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417498 | ||||||
| chr17:47417543
|
C | T | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+2624C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417543 | ||||||
| chr17:47417904
|
G | A | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2494+2985G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47417904 | ||||||
| chr17:47418238
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2494+3319C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418238 | ||||||
| chr17:47418319
|
A | G | 5 | a0002c0002t0001g0259a0002c0002t0001g0279a0002c0002t0001g0294others(2): Show | 5 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494+3400A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418319 | ||||||
| chr17:47418340
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+3421T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418340 | ||||||
| chr17:47418374
|
C | CG | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+3455_2494+345 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418374 | ||||||
| chr17:47418401
|
A | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+3482A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418401 | ||||||
| chr17:47418511
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2494+3592A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47418511 | ||||||
| chr17:47419014
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2494+4095G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419014 | ||||||
| chr17:47419250
|
A | G | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+4331A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419250 | ||||||
| chr17:47419302
|
T | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+4383T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419302 | ||||||
| chr17:47419330
|
A | G | 3 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053 | 3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2494+4411A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419330 | ||||||
| chr17:47419508
|
T | A | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+4589T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419508 | ||||||
| chr17:47419726
|
G | A | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+4807G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419726 | ||||||
| chr17:47419767
|
C | T | 1 | a0004c0003t0006g0260 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2494+4848C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419767 | ||||||
| chr17:47419829
|
T | C | 1 | a0001c0001t0005g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2494+4910T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419829 | ||||||
| chr17:47419867
|
A | T | 2 | a0002c0002t0001g0089a0003c0004t0001g0140 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2494+4948A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419867 | ||||||
| chr17:47419913
|
C | CCCCTCT | 134 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 134 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.2494+5018_2494+502 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47419913 | |||||
| chr17:47419913
|
CCCCTCT | C | 5 | a0001c0001t0001g0124a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 5 | NA18962.hp2 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+5018_2494+502 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47419913 | |||||
| chr17:47419961
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2494+5042C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419961 | ||||||
| chr17:47419969
|
C | G | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+5050C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419969 | ||||||
| chr17:47419978
|
C | A | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+5059C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419978 | ||||||
| chr17:47419993
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+5074G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47419993 | ||||||
| chr17:47420000
|
G | A | 30 | a0001c0001t0001g0070a0001c0001t0001g0090a0001c0001t0001g0091others(27): Show | 30 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2494+5081G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420000 | ||||||
| chr17:47420010
|
C | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5091C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420010 | ||||||
| chr17:47420052
|
A | T | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2494+5133A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420052 | ||||||
| chr17:47420073
|
A | G | 235 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.2494+5154A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420073 | ||||||
| chr17:47420182
|
T | C | 235 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.2494+5263T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420182 | ||||||
| chr17:47420209
|
A | G | 49 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(46): Show | 52 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.2494+5290A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420209 | ||||||
| chr17:47420215
|
C | G | 1 | a0002c0002t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2494+5296C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420215 | ||||||
| chr17:47420240
|
C | T | 1 | a0006c0007t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2494+5321C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420240 | ||||||
| chr17:47420340
|
C | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5421C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420340 | ||||||
| chr17:47420341
|
G | A | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2494+5422G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420341 | ||||||
| chr17:47420555
|
C | T | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+5636C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420555 | ||||||
| chr17:47420635
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2494+5716C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420635 | ||||||
| chr17:47420639
|
A | G | 2 | a0002c0002t0001g0262a0002c0002t0001g0266 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2494+5720A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420639 | ||||||
| chr17:47420662
|
G | A | 1 | a0002c0002t0001g0334 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2494+5743G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420662 | ||||||
| chr17:47420671
|
C | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5752C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420671 | ||||||
| chr17:47420681
|
G | A | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+5762G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420681 | ||||||
| chr17:47420698
|
A | C | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2494+5779A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420698 | ||||||
| chr17:47420698
|
ACCCTCCG others(33): Show |
A | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2494+5797_2494+583 others(44): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47420698 | |||||
| chr17:47420704
|
C | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5785C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420704 | ||||||
| chr17:47420708
|
C | T | 1 | a0005c0005t0001g0206 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2494+5789C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420708 | ||||||
| chr17:47420721
|
A | G | 232 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(229): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2494+5802A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420721 | ||||||
| chr17:47420740
|
C | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+5821C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420740 | ||||||
| chr17:47420749
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+5830G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420749 | ||||||
| chr17:47420793
|
G | A | 5 | a0002c0002t0001g0281a0002c0002t0001g0282a0002c0002t0001g0334others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+5874G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420793 | ||||||
| chr17:47420825
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0156 | 2 | HG01433.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2494+5906C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420825 | ||||||
| chr17:47420829
|
C | A | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+5910C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420829 | ||||||
| chr17:47420860
|
G | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.2494+5941G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420860 | ||||||
| chr17:47420868
|
G | T | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2494+5949G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420868 | ||||||
| chr17:47420878
|
C | T | 17 | a0001c0006t0003g0096a0001c0006t0003g0101a0002c0002t0001g0325others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2494+5959C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420878 | ||||||
| chr17:47420879
|
G | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2494+5960G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420879 | ||||||
| chr17:47420891
|
G | A | 4 | a0008c0011t0001g0049a0008c0011t0001g0050a0008c0011t0001g0054others(1): Show | 4 | HG02647.hp2 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+5972G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420891 | ||||||
| chr17:47420913
|
C | A | 6 | a0003c0008t0004g0005a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494+5994C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420913 | ||||||
| chr17:47420927
|
C | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+6008C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420927 | ||||||
| chr17:47420967
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2494+6048C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420967 | ||||||
| chr17:47420994
|
G | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6075G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47420994 | ||||||
| chr17:47421006
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6087G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421006 | ||||||
| chr17:47421009
|
C | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494+6090C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421009 | ||||||
| chr17:47421010
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6091G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421010 | ||||||
| chr17:47421020
|
T | TG | 123 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.2494+6108dupG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421020 | |||||
| chr17:47421042
|
G | C | 3 | a0002c0002t0001g0307a0002c0002t0001g0314a0002c0002t0009g0313 | 3 | NA18961.hp1 NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2494+6123G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421042 | ||||||
| chr17:47421083
|
G | A | 1 | a0002c0002t0001g0316 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2494+6164G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421083 | ||||||
| chr17:47421086
|
C | T | 1 | a0001c0001t0005g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2494+6167C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421086 | ||||||
| chr17:47421119
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2494+6200C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421119 | ||||||
| chr17:47421132
|
G | A | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2494+6213G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421132 | ||||||
| chr17:47421234
|
C | G | 1 | a0008c0011t0001g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2494+6315C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421234 | ||||||
| chr17:47421255
|
T | G | 11 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2494+6336T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421255 | ||||||
| chr17:47421358
|
CAT | C | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+6440_2494+644 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421358 | ||||||
| chr17:47421364
|
T | C | 90 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(87): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494+6445T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421364 | ||||||
| chr17:47421562
|
T | C | 6 | a0003c0008t0004g0005a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494+6643T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421562 | ||||||
| chr17:47421571
|
G | T | 131 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(128): Show | 131 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2494+6652G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421571 | ||||||
| chr17:47421582
|
G | C | 96 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(93): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2494+6663G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421582 | ||||||
| chr17:47421600
|
C | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2494+6681C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421600 | ||||||
| chr17:47421600
|
C | T | 1 | a0003c0008t0003g0276 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2494+6681C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421600 | ||||||
| chr17:47421624
|
T | TAAA | 184 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 185 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.2494+6711_2494+671 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421624 | |||||
| chr17:47421629
|
A | AAAAAAAT | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+6713_2494+671 others(11): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421629 | |||||
| chr17:47421633
|
G | A | 35 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(32): Show | 38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2494+6714G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421633 | ||||||
| chr17:47421633
|
G | T | 41 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(38): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2494+6714G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421633 | ||||||
| chr17:47421637
|
G | T | 36 | a0003c0004t0001g0140a0004c0003t0001g0001a0004c0003t0001g0003others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+6718G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421637 | ||||||
| chr17:47421640
|
AG | A | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+6722delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421640 | ||||||
| chr17:47421641
|
G | GAA | 161 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.2494+6733_2494+673 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421641 | |||||
| chr17:47421641
|
G | GAAAGAA | 35 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(32): Show | 38 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2494+6725_2494+672 others(10): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47421641 | |||||
| chr17:47421653
|
AG | A | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2494+6735delG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421653 | ||||||
| chr17:47421654
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2494+6735G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421654 | ||||||
| chr17:47421869
|
A | T | 1 | a0002c0002t0001g0295 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2494+6950A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421869 | ||||||
| chr17:47421945
|
T | C | 1 | a0001c0022t0001g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2494+7026T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47421945 | ||||||
| chr17:47422030
|
A | G | 2 | a0002c0002t0001g0262a0002c0002t0001g0266 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2494+7111A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422030 | ||||||
| chr17:47422038
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2494+7119T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422038 | ||||||
| chr17:47422055
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2494+7136A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422055 | ||||||
| chr17:47422091
|
G | T | 5 | a0002c0002t0001g0281a0002c0002t0001g0282a0002c0002t0001g0334others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+7172G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422091 | ||||||
| chr17:47422138
|
TATTA | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2494+7225_2494+722 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47422138 | |||||
| chr17:47422145
|
TAAC | T | 13 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2494+7229_2494+723 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47422145 | |||||
| chr17:47422165
|
C | A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2494+7246C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422165 | ||||||
| chr17:47422723
|
C | A | 1 | a0002c0010t0001g0267 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2495-7095C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422723 | ||||||
| chr17:47422742
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-7076A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422742 | ||||||
| chr17:47422917
|
C | T | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2495-6901C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47422917 | ||||||
| chr17:47423249
|
G | T | 6 | a0003c0008t0004g0005a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-6569G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423249 | ||||||
| chr17:47423261
|
T | A | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2495-6557T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423261 | ||||||
| chr17:47423312
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2495-6506G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423312 | ||||||
| chr17:47423400
|
A | T | 1 | a0005c0005t0007g0213 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2495-6418A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423400 | ||||||
| chr17:47423411
|
G | T | 1 | a0006c0007t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2495-6407G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423411 | ||||||
| chr17:47423481
|
C | A | 1 | a0017c0021t0006g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2495-6337C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423481 | ||||||
| chr17:47423495
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-6323C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423495 | ||||||
| chr17:47423533
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2495-6285C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47423533 | ||||||
| chr17:47423607
|
CCGCGCGC others(47): Show |
C | 1 | a0005c0005t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2495-6204_2495-615 others(58): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47423607 | |||||
| chr17:47423802
|
C | CACCCTCC others(8): Show |
3 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053 | 3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2495-6005_2495-599 others(19): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47423802 | |||||
| chr17:47424210
|
C | T | 1 | a0002c0002t0001g0333 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2495-5608C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424210 | ||||||
| chr17:47424443
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2495-5375A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424443 | ||||||
| chr17:47424502
|
A | T | 2 | a0002c0002t0001g0316a0002c0002t0001g0317 | 2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.2495-5316A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424502 | ||||||
| chr17:47424601
|
T | A | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2495-5217T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424601 | ||||||
| chr17:47424659
|
CA | C | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2495-5158delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424659 | ||||||
| chr17:47424730
|
G | C | 235 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.2495-5088G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424730 | ||||||
| chr17:47424799
|
A | G | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2495-5019A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424799 | ||||||
| chr17:47424874
|
C | CT | 59 | a0001c0013t0001g0117a0001c0013t0001g0196a0001c0013t0001g0197others(56): Show | 62 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.2495-4918dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTT | 8 | a0001c0001t0001g0169a0002c0002t0001g0301a0002c0002t0001g0310others(5): Show | 8 | HG01106.hp2 HG02015.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.2495-4919_2495-491 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0090a0001c0001t0001g0201a0001c0006t0002g0099others(1): Show | 4 | HG01175.hp1 HG02683.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-4928_2495-491 others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0070a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG00280.hp1 HG01517.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2495-4929_2495-491 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(6): Show |
14 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0189others(11): Show | 14 | HG01192.hp1 HG01256.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2495-4930_2495-491 others(17): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(7): Show |
32 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0113others(29): Show | 32 | HG01070.hp2 HG01074.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.2495-4931_2495-491 others(18): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(8): Show |
24 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0114others(21): Show | 24 | HG00423.hp2 HG01081.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.2495-4932_2495-491 others(19): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(9): Show |
19 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0082others(16): Show | 19 | HG00408.hp1 HG01106.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.2495-4933_2495-491 others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(10): Show |
13 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0111others(10): Show | 13 | HG00673.hp2 HG01243.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.2495-4934_2495-491 others(21): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(11): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0104others(5): Show | 8 | HG00323.hp1 HG00408.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-4935_2495-491 others(22): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(12): Show |
11 | a0001c0001t0001g0088a0001c0001t0001g0108a0001c0001t0001g0128others(8): Show | 11 | HG02109.hp2 HG02602.hp2 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.2495-4936_2495-491 others(23): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(13): Show |
10 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0080others(7): Show | 10 | HG00741.hp1 HG01074.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2495-4937_2495-491 others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(14): Show |
8 | a0001c0001t0001g0087a0001c0001t0001g0150a0001c0006t0001g0098others(5): Show | 8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-4938_2495-491 others(25): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(15): Show |
9 | a0001c0001t0001g0051a0001c0006t0001g0097a0001c0006t0001g0100others(6): Show | 9 | HG00438.hp1 HG00735.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-4939_2495-491 others(26): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(16): Show |
8 | a0001c0001t0001g0137a0001c0001t0001g0155a0001c0006t0001g0093others(5): Show | 8 | HG01168.hp1 HG01169.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-4940_2495-491 others(27): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(17): Show |
2 | a0002c0002t0001g0089a0002c0002t0003g0284 | 2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2495-4941_2495-491 others(28): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(18): Show |
4 | a0001c0001t0001g0159a0001c0006t0002g0092a0001c0006t0003g0096others(1): Show | 4 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-4942_2495-491 others(29): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(19): Show |
2 | a0005c0005t0001g0071a0005c0005t0003g0327 | 2 | HG00423.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2495-4943_2495-491 others(30): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
C | CTTTTTTT others(22): Show |
3 | a0001c0006t0003g0101a0003c0008t0004g0162a0003c0008t0004g0258 | 3 | HG02818.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2495-4918_2495-491 others(33): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
CT | C | 7 | a0002c0002t0003g0057a0003c0004t0002g0109a0003c0004t0002g0239others(4): Show | 7 | HG01255.hp1 HG03471.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-4918delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
CTT | C | 39 | a0001c0006t0001g0095a0002c0002t0003g0055a0002c0002t0003g0058others(36): Show | 40 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2495-4919_2495-491 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424874
|
CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-4928_2495-491 others(15): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424874 | |||||
| chr17:47424896
|
T | TTTTTTTT others(13): Show |
1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2495-4918_2495-491 others(24): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47424896 | |||||
| chr17:47424964
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0108 | 3 | HG01169.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2495-4854G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424964 | ||||||
| chr17:47424976
|
G | C | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2495-4842G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424976 | ||||||
| chr17:47424977
|
G | A | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-4841G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47424977 | ||||||
| chr17:47425007
|
C | T | 11 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2495-4811C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425007 | ||||||
| chr17:47425099
|
G | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-4719G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425099 | ||||||
| chr17:47425125
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-4693G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425125 | ||||||
| chr17:47425171
|
C | A | 9 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0198others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-4647C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425171 | ||||||
| chr17:47425210
|
A | C | 1 | a0005c0005t0001g0209 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2495-4608A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425210 | ||||||
| chr17:47425442
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18982.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2495-4376T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425442 | ||||||
| chr17:47425473
|
T | G | 1 | a0002c0002t0001g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2495-4345T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425473 | ||||||
| chr17:47425650
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2495-4168G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425650 | ||||||
| chr17:47425662
|
T | C | 1 | a0012c0026t0001g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2495-4156T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425662 | ||||||
| chr17:47425755
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0189 | 2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2495-4063T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425755 | ||||||
| chr17:47425859
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2495-3959A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425859 | ||||||
| chr17:47425887
|
G | C | 1 | a0002c0002t0003g0331 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2495-3931G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425887 | ||||||
| chr17:47425891
|
C | T | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2495-3927C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425891 | ||||||
| chr17:47425980
|
A | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-3838A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47425980 | ||||||
| chr17:47426173
|
T | C | 41 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(38): Show | 44 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2495-3645T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426173 | ||||||
| chr17:47426252
|
T | C | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-3566T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426252 | ||||||
| chr17:47426387
|
T | C | 3 | a0001c0015t0001g0106a0001c0015t0001g0192a0001c0024t0001g0191 | 3 | NA18981.hp1 NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2495-3431T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426387 | ||||||
| chr17:47426555
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-3263T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426555 | ||||||
| chr17:47426658
|
T | A | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2495-3160T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426658 | ||||||
| chr17:47426907
|
T | C | 1 | a0002c0002t0003g0315 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2495-2911T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47426907 | ||||||
| chr17:47427005
|
T | G | 1 | a0003c0004t0002g0233 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2495-2813T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427005 | ||||||
| chr17:47427201
|
A | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-2617A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427201 | ||||||
| chr17:47427320
|
A | G | 1 | a0004c0003t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2495-2498A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427320 | ||||||
| chr17:47427504
|
C | T | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2495-2314C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427504 | ||||||
| chr17:47427786
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2495-2032C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427786 | ||||||
| chr17:47427816
|
T | C | 1 | a0003c0008t0004g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2495-2002T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427816 | ||||||
| chr17:47427828
|
T | C | 7 | a0002c0002t0001g0010a0002c0002t0001g0262a0002c0002t0001g0266others(4): Show | 7 | HG02895.hp2 HG02922.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2495-1990T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427828 | ||||||
| chr17:47427913
|
T | A | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2495-1905T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427913 | ||||||
| chr17:47427988
|
C | A | 1 | a0003c0008t0001g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2495-1830C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47427988 | ||||||
| chr17:47428086
|
T | C | 1 | a0005c0005t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2495-1732T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428086 | ||||||
| chr17:47428127
|
CTA | C | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-1689_2495-168 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47428127 | |||||
| chr17:47428323
|
T | TC | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2495-1494dupC | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47428323 | |||||
| chr17:47428488
|
A | G | 2 | a0002c0002t0001g0298a0002c0002t0001g0302 | 2 | NA18991.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2495-1330A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428488 | ||||||
| chr17:47428490
|
G | A | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-1328G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428490 | ||||||
| chr17:47428545
|
A | G | 1 | a0002c0002t0001g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2495-1273A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428545 | ||||||
| chr17:47428835
|
T | C | 1 | a0005c0005t0001g0071 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2495-983T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47428835 | ||||||
| chr17:47429238
|
T | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2495-580T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429238 | ||||||
| chr17:47429247
|
C | A | 1 | a0004c0003t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2495-571C>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429247 | ||||||
| chr17:47429316
|
T | G | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2495-502T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429316 | ||||||
| chr17:47429464
|
T | C | 6 | a0003c0008t0004g0005a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-354T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429464 | ||||||
| chr17:47429546
|
A | AG | 40 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(37): Show | 43 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2495-269dupG | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr17 | 47429546 | |||||
| chr17:47429564
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-254C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 23/24 | chr17 | 47429564 | ||||||
| chr17:47430002
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2638+41C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430002 | ||||||
| chr17:47430091
|
G | A | 1 | a0002c0002t0001g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2638+130G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430091 | ||||||
| chr17:47430131
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2638+170G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430131 | ||||||
| chr17:47430185
|
A | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2638+224A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430185 | ||||||
| chr17:47430220
|
T | G | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2638+259T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430220 | ||||||
| chr17:47430850
|
T | C | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2638+889T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430850 | ||||||
| chr17:47430928
|
A | C | 6 | a0003c0008t0004g0005a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2638+967A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430928 | ||||||
| chr17:47430948
|
G | A | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+987G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47430948 | ||||||
| chr17:47431325
|
C | G | 1 | a0002c0002t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2638+1364C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431325 | ||||||
| chr17:47431524
|
T | C | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+1563T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431524 | ||||||
| chr17:47431605
|
T | C | 1 | a0005c0005t0002g0238 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2638+1644T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431605 | ||||||
| chr17:47431676
|
T | C | 5 | a0004c0003t0001g0003a0004c0003t0001g0020a0004c0003t0001g0021others(2): Show | 6 | HG00738.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.2638+1715T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431676 | ||||||
| chr17:47431744
|
T | G | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2638+1783T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47431744 | ||||||
| chr17:47432088
|
T | G | 1 | a0008c0011t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2638+2127T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432088 | ||||||
| chr17:47432130
|
G | A | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.2638+2169G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432130 | ||||||
| chr17:47432130
|
G | C | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2638+2169G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432130 | ||||||
| chr17:47432181
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2638+2220C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432181 | ||||||
| chr17:47432328
|
G | C | 9 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0198others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2638+2367G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432328 | ||||||
| chr17:47432399
|
A | AAAAT | 80 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(77): Show |
intron_variant | MODIFIER | c.2638+2479_2638+248 others(8): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | |||||
| chr17:47432399
|
A | AAAATAAA others(1): Show |
86 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0076others(83): Show | 86 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.2638+2475_2638+248 others(12): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | |||||
| chr17:47432399
|
A | AAAATAAA others(5): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0180a0001c0001t0001g0182 | 3 | HG01884.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2638+2471_2638+248 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | |||||
| chr17:47432399
|
AAAATAAA others(5): Show |
A | 38 | a0001c0001t0005g0255a0003c0004t0001g0140a0004c0003t0001g0001others(35): Show | 41 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2638+2471_2638+248 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | |||||
| chr17:47432399
|
AAAATAAA others(9): Show |
A | 44 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(41): Show | 45 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2638+2467_2638+248 others(20): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47432399 | |||||
| chr17:47432845
|
G | A | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+2884G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47432845 | ||||||
| chr17:47433224
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2638+3263C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433224 | ||||||
| chr17:47433240
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2638+3279A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433240 | ||||||
| chr17:47433354
|
G | A | 1 | a0003c0004t0002g0231 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2638+3393G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433354 | ||||||
| chr17:47433426
|
C | CAAG | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+3471_2638+347 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47433426 | |||||
| chr17:47433452
|
A | G | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2638+3491A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433452 | ||||||
| chr17:47433605
|
G | A | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2638+3644G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433605 | ||||||
| chr17:47433631
|
T | C | 2 | a0003c0004t0002g0224a0003c0004t0002g0251 | 2 | NA18964.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2638+3670T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433631 | ||||||
| chr17:47433713
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2638+3752T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433713 | ||||||
| chr17:47433873
|
T | G | 1 | a0001c0001t0005g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2638+3912T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47433873 | ||||||
| chr17:47433981
|
T | TTG | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2638+4022_2638+402 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47433981 | |||||
| chr17:47434022
|
C | T | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2638+4061C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434022 | ||||||
| chr17:47434093
|
A | G | 1 | a0002c0002t0001g0292 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2638+4132A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434093 | ||||||
| chr17:47434182
|
T | C | 34 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(31): Show | 37 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.2638+4221T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434182 | ||||||
| chr17:47434314
|
C | CA | 13 | a0001c0001t0001g0111a0001c0006t0001g0093a0001c0006t0001g0094others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.2638+4363dupA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47434314 | |||||
| chr17:47434314
|
CA | C | 82 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(79): Show | 86 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.2638+4363delA | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47434314 | |||||
| chr17:47434321
|
A | T | 6 | a0001c0001t0001g0185a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG00280.hp1 HG01106.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2638+4360A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434321 | ||||||
| chr17:47434322
|
A | T | 1 | a0001c0001t0001g0151 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2638+4361A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434322 | ||||||
| chr17:47434325
|
T | A | 63 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(60): Show | 63 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.2638+4364T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434325 | ||||||
| chr17:47434328
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2638+4367A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434328 | ||||||
| chr17:47434759
|
C | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2638+4798C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434759 | ||||||
| chr17:47434774
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2638+4813A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434774 | ||||||
| chr17:47434807
|
C | T | 6 | a0003c0008t0004g0005a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2638+4846C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47434807 | ||||||
| chr17:47435046
|
A | C | 1 | a0003c0004t0002g0226 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2638+5085A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435046 | ||||||
| chr17:47435117
|
A | G | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.2638+5156A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435117 | ||||||
| chr17:47435376
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0107 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2639-5055C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435376 | ||||||
| chr17:47435380
|
A | G | 1 | a0006c0007t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2639-5051A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435380 | ||||||
| chr17:47435555
|
T | C | 3 | a0003c0008t0004g0011a0003c0008t0004g0012a0003c0008t0004g0053 | 3 | HG01106.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2639-4876T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435555 | ||||||
| chr17:47435593
|
T | C | 2 | a0003c0004t0002g0245a0003c0004t0002g0249 | 2 | NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2639-4838T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435593 | ||||||
| chr17:47435683
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2639-4748A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435683 | ||||||
| chr17:47435723
|
C | CAT | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2639-4707_2639-470 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47435723 | |||||
| chr17:47435726
|
C | T | 39 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(36): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2639-4705C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435726 | ||||||
| chr17:47435875
|
G | A | 2 | a0005c0005t0003g0118a0011c0027t0001g0121 | 2 | HG01123.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2639-4556G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435875 | ||||||
| chr17:47435910
|
C | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG01169.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2639-4521C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435910 | ||||||
| chr17:47435913
|
C | T | 3 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2639-4518C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435913 | ||||||
| chr17:47435926
|
A | G | 138 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2639-4505A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435926 | ||||||
| chr17:47435943
|
C | T | 1 | a0004c0003t0001g0028 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2639-4488C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435943 | ||||||
| chr17:47435967
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2639-4464C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47435967 | ||||||
| chr17:47436031
|
T | C | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2639-4400T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436031 | ||||||
| chr17:47436226
|
G | A | 1 | a0015c0018t0001g0337 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2639-4205G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436226 | ||||||
| chr17:47436565
|
T | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2639-3866T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436565 | ||||||
| chr17:47436830
|
G | C | 36 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(33): Show | 39 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2639-3601G>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436830 | ||||||
| chr17:47436839
|
G | A | 1 | a0003c0008t0004g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2639-3592G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47436839 | ||||||
| chr17:47437053
|
T | A | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2639-3378T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437053 | ||||||
| chr17:47437397
|
C | G | 11 | a0001c0006t0001g0093a0001c0006t0001g0094a0001c0006t0001g0095others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2639-3034C>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437397 | ||||||
| chr17:47437536
|
G | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-2895G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437536 | ||||||
| chr17:47437537
|
C | T | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-2894C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437537 | ||||||
| chr17:47437801
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2639-2630A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47437801 | ||||||
| chr17:47438008
|
T | A | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2639-2423T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438008 | ||||||
| chr17:47438089
|
G | A | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2639-2342G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438089 | ||||||
| chr17:47438158
|
T | C | 1 | a0003c0004t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2639-2273T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438158 | ||||||
| chr17:47438312
|
T | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2639-2119T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438312 | ||||||
| chr17:47438325
|
G | A | 2 | a0008c0011t0001g0049a0008c0011t0001g0050 | 2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2639-2106G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438325 | ||||||
| chr17:47438417
|
T | G | 34 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(31): Show | 37 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.2639-2014T>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438417 | ||||||
| chr17:47438453
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2639-1978A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438453 | ||||||
| chr17:47438498
|
C | CT | 137 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2639-1919dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47438498 | |||||
| chr17:47438498
|
CT | C | 76 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(73): Show | 80 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2639-1919delT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47438498 | |||||
| chr17:47438720
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2639-1711G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438720 | ||||||
| chr17:47438744
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0138a0003c0008t0001g0141 | 3 | NA18956.hp2 NA18960.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2639-1687T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438744 | ||||||
| chr17:47438768
|
T | C | 6 | a0003c0008t0004g0005a0003c0008t0004g0011a0003c0008t0004g0012others(3): Show | 6 | HG01106.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2639-1663T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438768 | ||||||
| chr17:47438830
|
G | A | 1 | a0002c0002t0003g0324 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2639-1601G>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47438830 | ||||||
| chr17:47439171
|
G | GT | 114 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 114 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.2639-1236dupT | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | |||||
| chr17:47439171
|
G | GTT | 41 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0088others(38): Show | 41 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-1237_2639-123 others(6): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | |||||
| chr17:47439171
|
G | GTTT | 6 | a0001c0001t0001g0052a0001c0001t0001g0081a0001c0001t0001g0111others(3): Show | 6 | HG01175.hp1 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2639-1238_2639-123 others(7): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | |||||
| chr17:47439171
|
GTTTTTTT others(5): Show |
G | 41 | a0004c0003t0001g0001a0004c0003t0001g0003a0004c0003t0001g0020others(38): Show | 44 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2639-1247_2639-123 others(16): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr17 | 47439171 | |||||
| chr17:47439177
|
T | TG | 37 | a0003c0004t0002g0109a0003c0004t0002g0214a0003c0004t0002g0217others(34): Show | 38 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2639-1254_2639-125 others(5): Show |
EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439177 | ||||||
| chr17:47439198
|
A | T | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2639-1233A>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439198 | ||||||
| chr17:47439199
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2639-1232C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439199 | ||||||
| chr17:47439301
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.2639-1130C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439301 | ||||||
| chr17:47439514
|
C | T | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2639-917C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439514 | ||||||
| chr17:47439654
|
C | T | 9 | a0006c0007t0001g0059a0006c0007t0001g0060a0006c0007t0001g0062others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2639-777C>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439654 | ||||||
| chr17:47439935
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2639-496T>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47439935 | ||||||
| chr17:47440073
|
A | G | 1 | a0016c0020t0001g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2639-358A>G | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440073 | ||||||
| chr17:47440337
|
A | C | 40 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(37): Show | 41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2639-94A>C | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440337 | ||||||
| chr17:47440405
|
T | A | 81 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(78): Show | 85 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2639-26T>A | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440405 | ||||||
| chr17:47440408
|
G | T | 87 | a0003c0004t0001g0140a0003c0004t0002g0109a0003c0004t0002g0214others(84): Show | 91 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2639-23G>T | EFCAB13 | ENSG00000178852.16 | transcript | ENST00000331493.7 | protein_coding | 24/24 | chr17 | 47440408 |