Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22979 |
|---|---|
| ensemblid | ENSG00000084710.14 |
| hgncid | 29155 |
| symbol | EFR3B |
| name | EFR3 homolog B |
| refseq_nuc | NM_014971.2 |
| refseq_prot | NP_055786.1 |
| ensembl_nuc | ENST00000403714.8 |
| ensembl_prot | ENSP00000384081.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 25042076 |
| end | 25159135 |
| strand | + |
| ver | v1.2 |
| region | chr2:25042076-25159135 |
| region5000 | chr2:25037076-25164135 |
| regionname0 | EFR3B_chr2_25042076_25159135 |
| regionname5000 | EFR3B_chr2_25037076_25164135 |
| 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 | 1/1 | 817 | 302 | 86 | 56 | 114 | 10 | 34 | 82 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0002 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0003 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0004 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0005 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| 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 | 2454 | 171 | 50 | 26 | 70 | 3 | 22 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0002 | 0/0 | 2454 | 83 | 26 | 20 | 30 | 4 | 3 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0003 | 1/1 | 2454 | 33 | 3 | 10 | 7 | 3 | 8 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0004 | 0/0 | 2454 | 4 | 0 | 0 | 4 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0005 | 0/0 | 2454 | 4 | 4 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0006 | 0/0 | 2454 | 2 | 0 | 0 | 2 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0007 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0008 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0009 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0010 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0011 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0012 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0013 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0014 | 0/0 | 2454 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| c0015 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| 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 | 0/0 | 5034 | 79 | 29 | 18 | 20 | 5 | 7 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0002 | 0/0 | 5033 | 44 | 2 | 10 | 26 | 0 | 6 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0003 | 0/0 | 5033 | 30 | 0 | 3 | 23 | 0 | 4 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0004 | 0/0 | 5035 | 16 | 10 | 0 | 6 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0005 | 0/0 | 5033 | 16 | 13 | 2 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0006 | 0/0 | 5033 | 15 | 0 | 4 | 2 | 2 | 7 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0007 | 0/0 | 5034 | 11 | 0 | 3 | 5 | 0 | 3 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0008 | 0/0 | 5034 | 10 | 0 | 0 | 10 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0009 | 1/1 | 5033 | 9 | 0 | 5 | 0 | 1 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0010 | 0/0 | 5034 | 7 | 1 | 1 | 5 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0011 | 0/0 | 5033 | 7 | 2 | 1 | 3 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0012 | 0/0 | 5032 | 5 | 0 | 0 | 5 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0013 | 0/0 | 5033 | 5 | 0 | 0 | 5 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0014 | 0/0 | 5033 | 4 | 4 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0015 | 0/0 | 5034 | 4 | 2 | 0 | 0 | 0 | 2 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0016 | 0/0 | 5034 | 3 | 3 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0017 | 0/0 | 5035 | 3 | 3 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0018 | 0/0 | 5034 | 2 | 2 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0019 | 0/0 | 5033 | 2 | 2 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0020 | 0/0 | 5034 | 2 | 0 | 0 | 2 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0021 | 0/0 | 5034 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0022 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0023 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0024 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0025 | 0/0 | 5034 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0026 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0027 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0028 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0029 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0030 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0031 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0032 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0033 | 0/0 | 5034 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0034 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0035 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0036 | 0/0 | 5034 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0037 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0038 | 0/0 | 5035 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0039 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0040 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0041 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0042 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0043 | 0/0 | 5034 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0044 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0045 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0046 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0047 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0048 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0049 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0050 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0051 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| t0052 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| 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 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| 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 | 2454 | 171 | 50 | 26 | 70 | 3 | 22 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002 | 0/0 | 2454 | 83 | 26 | 20 | 30 | 4 | 3 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0003 | 1/1 | 2454 | 33 | 3 | 10 | 7 | 3 | 8 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0004 | 0/0 | 2454 | 4 | 0 | 0 | 4 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0005 | 0/0 | 2454 | 4 | 4 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0006 | 0/0 | 2454 | 2 | 0 | 0 | 2 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0008 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0009 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0010 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0014 | 0/0 | 2454 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0015 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0002c0012 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0003c0011 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0004c0007 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0005c0013 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7487 | 26 | 17 | 3 | 0 | 1 | 5 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0002 | 0/0 | 7486 | 38 | 2 | 10 | 21 | 0 | 5 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0003 | 0/0 | 7486 | 29 | 0 | 3 | 22 | 0 | 4 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0004 | 0/0 | 7488 | 3 | 2 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0005 | 0/0 | 7486 | 14 | 11 | 2 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0007 | 0/0 | 7487 | 11 | 0 | 3 | 5 | 0 | 3 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0008 | 0/0 | 7487 | 9 | 0 | 0 | 9 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0011 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0012 | 0/0 | 7485 | 5 | 0 | 0 | 5 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0013 | 0/0 | 7486 | 5 | 0 | 0 | 5 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0015 | 0/0 | 7487 | 4 | 2 | 0 | 0 | 0 | 2 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0016 | 0/0 | 7487 | 3 | 3 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0017 | 0/0 | 7488 | 3 | 3 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0019 | 0/0 | 7486 | 2 | 2 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0021 | 0/0 | 7487 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0022 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0023 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0024 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0026 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0028 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0029 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0030 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0039 | 0/0 | 7485 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0040 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0041 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0042 | 0/0 | 7486 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0043 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0046 | 0/0 | 7486 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0047 | 0/0 | 7486 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0048 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0049 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0001t0051 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0001 | 0/0 | 7487 | 51 | 12 | 15 | 18 | 4 | 2 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0002 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0004 | 0/0 | 7488 | 13 | 8 | 0 | 5 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0005 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0011 | 0/0 | 7486 | 5 | 1 | 0 | 3 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0020 | 0/0 | 7487 | 2 | 0 | 0 | 2 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0025 | 0/0 | 7487 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0031 | 0/0 | 7486 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0032 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0033 | 0/0 | 7487 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0034 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0035 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0036 | 0/0 | 7487 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0037 | 0/0 | 7488 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0038 | 0/0 | 7488 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0002t0052 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0003t0006 | 0/0 | 7486 | 15 | 0 | 4 | 2 | 2 | 7 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0003t0009 | 1/1 | 7486 | 9 | 0 | 5 | 0 | 1 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0003t0010 | 0/0 | 7487 | 7 | 1 | 1 | 5 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0003t0018 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0003t0027 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0004t0002 | 0/0 | 7486 | 4 | 0 | 0 | 4 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0005t0014 | 0/0 | 7486 | 4 | 4 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0006t0001 | 0/0 | 7487 | 2 | 0 | 0 | 2 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0008t0018 | 0/0 | 7487 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0009t0011 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0010t0005 | 0/0 | 7486 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0014t0002 | 0/0 | 7486 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0001c0015t0008 | 0/0 | 7487 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0002c0012t0050 | 0/0 | 7488 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0003c0011t0045 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0004c0007t0003 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| a0005c0013t0044 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | copy fasta | chr2 | 25037076 | 25164135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0012g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0013g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0013g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0013g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0013g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0015g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0015g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0015g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0015g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0017g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0017g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0017g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0019g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0021g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0022g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0023g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0024g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0026g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0028g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0029g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0030g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0039g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0040g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0041g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0042g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0043g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0046g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0047g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0048g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0049g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0001t0051g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0011g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0020g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0020g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0025g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0031g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0032g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0033g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0034g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0035g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0036g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0037g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0038g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0002t0052g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0009g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0010g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0010g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0018g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0003t0027g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0004t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0004t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0005t0014g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0005t0014g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0005t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0005t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0006t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0008t0018g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0009t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0010t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0014t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0001c0015t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0002c0012t0050g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0003c0011t0045g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0004c0007t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| a0005c0013t0044g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0046 | g0303 | EUR | GBR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0202 | EUR | GBR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00140 | hp1 | a0001 | c0003 | t0006 | g0117 | EUR | GBR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00280 | hp1 | a0001 | c0003 | t0009 | g0290 | EUR | FIN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0055 | EUR | FIN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00323 | hp1 | a0001 | c0001 | t0021 | g0139 | EUR | FIN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0286 | EUR | FIN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00423 | hp2 | a0001 | c0002 | t0011 | g0277 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00438 | hp1 | a0001 | c0001 | t0012 | g0089 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00438 | hp2 | a0001 | c0003 | t0006 | g0119 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00544 | hp1 | a0004 | c0007 | t0003 | g0070 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00558 | hp1 | a0005 | c0013 | t0044 | g0297 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0009 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00639 | hp1 | a0001 | c0001 | t0028 | g0197 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00639 | hp2 | a0001 | c0003 | t0006 | g0285 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00733 | hp2 | a0001 | c0001 | t0022 | g0178 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00735 | hp1 | a0001 | c0003 | t0009 | g0225 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00738 | hp1 | a0001 | c0002 | t0033 | g0045 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00738 | hp2 | a0001 | c0003 | t0006 | g0274 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00741 | hp1 | a0001 | c0003 | t0010 | g0105 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01070 | hp1 | a0001 | c0003 | t0009 | g0227 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01071 | hp1 | a0001 | c0003 | t0009 | g0226 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0138 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01106 | hp1 | a0001 | c0003 | t0006 | g0145 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0234 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01109 | hp1 | a0001 | c0003 | t0009 | g0292 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0157 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01192 | hp2 | a0001 | c0003 | t0006 | g0146 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01243 | hp1 | a0001 | c0001 | t0051 | g0125 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01255 | hp2 | a0001 | c0003 | t0009 | g0275 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01346 | hp2 | a0001 | c0002 | t0038 | g0133 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01358 | hp2 | a0001 | c0002 | t0031 | g0295 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01361 | hp1 | a0001 | c0001 | t0040 | g0103 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0221 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0284 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01884 | hp1 | a0001 | c0010 | t0005 | g0163 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0181 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0252 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG01952 | hp2 | a0001 | c0002 | t0025 | g0049 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02004 | hp2 | a0001 | c0002 | t0036 | g0033 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02040 | hp1 | a0001 | c0003 | t0006 | g0270 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0298 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0205 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02074 | hp1 | a0001 | c0001 | t0013 | g0034 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0243 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02080 | hp1 | a0001 | c0002 | t0037 | g0239 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0048 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02132 | hp2 | a0001 | c0001 | t0012 | g0242 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0113 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02135 | hp2 | a0001 | c0002 | t0004 | g0273 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0176 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0257 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CDX | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | CDX | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02257 | hp1 | a0001 | c0003 | t0010 | g0137 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02280 | hp2 | a0001 | c0005 | t0014 | g0214 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PEL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02451 | hp1 | a0001 | c0005 | t0014 | g0212 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02451 | hp2 | a0001 | c0001 | t0049 | g0059 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0152 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02602 | hp1 | a0001 | c0003 | t0006 | g0262 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0193 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02615 | hp2 | a0001 | c0001 | t0016 | g0153 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0150 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02630 | hp1 | a0001 | c0001 | t0024 | g0217 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0065 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02698 | hp1 | a0001 | c0001 | t0015 | g0200 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02717 | hp2 | a0001 | c0001 | t0026 | g0210 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02735 | hp2 | a0001 | c0003 | t0009 | g0283 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02738 | hp1 | a0001 | c0001 | t0015 | g0203 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0305 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02809 | hp1 | a0001 | c0001 | t0029 | g0171 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02818 | hp1 | a0001 | c0008 | t0018 | g0062 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02818 | hp2 | a0001 | c0002 | t0011 | g0169 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0063 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02965 | hp2 | a0001 | c0001 | t0016 | g0182 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02970 | hp2 | a0001 | c0003 | t0027 | g0184 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02976 | hp1 | a0001 | c0001 | t0039 | g0216 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0124 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03041 | hp2 | a0001 | c0003 | t0018 | g0159 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03098 | hp1 | a0001 | c0005 | t0014 | g0046 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0066 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03225 | hp1 | a0001 | c0001 | t0030 | g0126 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0168 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03490 | hp2 | a0001 | c0003 | t0006 | g0230 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03491 | hp1 | a0001 | c0003 | t0006 | g0148 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03491 | hp2 | a0001 | c0003 | t0006 | g0082 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03492 | hp1 | a0001 | c0003 | t0006 | g0149 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03516 | hp2 | a0001 | c0009 | t0011 | g0211 | AFR | ESN | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03540 | hp2 | a0001 | c0001 | t0019 | g0123 | AFR | GWD | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0158 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0201 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03654 | hp2 | a0001 | c0001 | t0047 | g0068 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03688 | hp1 | a0001 | c0002 | t0011 | g0279 | SAS | STU | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | BEB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0240 | SAS | BEB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | BEB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03834 | hp2 | a0001 | c0001 | t0042 | g0075 | SAS | BEB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03942 | hp1 | a0001 | c0003 | t0006 | g0147 | SAS | BEB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0232 | SAS | BEB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | STU | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG04204 | hp2 | a0001 | c0014 | t0002 | g0248 | SAS | STU | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18522 | hp1 | a0001 | c0005 | t0014 | g0213 | AFR | YRI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | YRI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18747 | hp1 | a0001 | c0015 | t0008 | g0078 | EAS | CHB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CHB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | YRI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18940 | hp1 | a0001 | c0001 | t0013 | g0011 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18940 | hp2 | a0002 | c0012 | t0050 | g0281 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18942 | hp2 | a0001 | c0001 | t0012 | g0084 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18954 | hp2 | a0001 | c0002 | t0011 | g0042 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18960 | hp1 | a0003 | c0011 | t0045 | g0272 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18963 | hp1 | a0001 | c0003 | t0010 | g0087 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18965 | hp2 | a0001 | c0001 | t0013 | g0022 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0291 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18968 | hp2 | a0001 | c0003 | t0010 | g0083 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18974 | hp2 | a0001 | c0004 | t0002 | g0056 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18975 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0228 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18977 | hp2 | a0001 | c0003 | t0010 | g0115 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18978 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18982 | hp1 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18983 | hp2 | a0001 | c0001 | t0013 | g0024 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18990 | hp2 | a0001 | c0001 | t0008 | g0098 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18991 | hp1 | a0001 | c0002 | t0011 | g0253 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18993 | hp2 | a0001 | c0001 | t0012 | g0093 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18999 | hp1 | a0001 | c0001 | t0043 | g0097 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA18999 | hp2 | a0001 | c0002 | t0020 | g0004 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19002 | hp1 | a0001 | c0006 | t0001 | g0044 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19004 | hp2 | a0001 | c0003 | t0010 | g0090 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19005 | hp2 | a0001 | c0002 | t0020 | g0003 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19011 | hp1 | a0001 | c0006 | t0001 | g0057 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19011 | hp2 | a0001 | c0001 | t0012 | g0071 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19012 | hp1 | a0001 | c0001 | t0008 | g0107 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19030 | hp1 | a0001 | c0002 | t0035 | g0208 | AFR | LWK | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19030 | hp2 | a0001 | c0001 | t0023 | g0204 | AFR | LWK | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19043 | hp1 | a0001 | c0002 | t0052 | g0180 | AFR | LWK | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19054 | hp1 | a0001 | c0004 | t0002 | g0014 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19056 | hp1 | a0001 | c0003 | t0010 | g0081 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19058 | hp2 | a0001 | c0001 | t0013 | g0037 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19066 | hp1 | a0001 | c0001 | t0008 | g0114 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19070 | hp1 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19088 | hp2 | a0001 | c0001 | t0041 | g0096 | EAS | JPT | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | YRI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | YRI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ASW | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ASW | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0222 | EUR | TSI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20752 | hp2 | a0001 | c0003 | t0006 | g0144 | EUR | TSI | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20905 | hp2 | a0001 | c0003 | t0006 | g0256 | SAS | GIH | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG03471 | hp2 | a0001 | c0002 | t0032 | g0167 | AFR | MSL | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG06807 | hp1 | a0001 | c0002 | t0005 | g0198 | AFR | USA | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | USA | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20300 | hp1 | a0001 | c0001 | t0048 | g0218 | AFR | USA | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA20300 | hp2 | a0001 | c0002 | t0034 | g0251 | AFR | USA | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0064 | AFR | LWK | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0170 | AFR | LWK | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0009 | g0263 | REF | REF | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0009 | g0122 | REF | REF | EFR3B_chr2_25037076_25164135 | EFR3B | chr2 | 25037076 | 25164135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:25132992
|
G | A | 1 | a0004 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.1237G>A | p.Ala413Thr | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 11/23 | 1474/7486 | 1237/2454 | 413/817 | chr2 | 25132992 | ||
| chr2:25132993
|
C | T | 1 | a0005 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1238C>T | p.Ala413Val | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 11/23 | 1475/7486 | 1238/2454 | 413/817 | chr2 | 25132993 | ||
| chr2:25135527
|
C | T | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.1372C>T | p.Arg458Cys | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 13/23 | 1609/7486 | 1372/2454 | 458/817 | chr2 | 25135527 | ||
| chr2:25143798
|
A | T | 1 | a0003 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.1986A>T | p.Glu662Asp | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/23 | 2223/7486 | 1986/2454 | 662/817 | chr2 | 25143798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:25091398
|
C | T | 1 | a0001c0015 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.81C>T | p.Pro27Pro | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/23 | 318/7486 | 81/2454 | 27/817 | chr2 | 25091398 | ||
| chr2:25093023
|
C | T | 1 | a0001c0014 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.105C>T | p.Asn35Asn | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/23 | 342/7486 | 105/2454 | 35/817 | chr2 | 25093023 | ||
| chr2:25093110
|
C | T | 1 | a0001c0014 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.192C>T | p.Asp64Asp | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/23 | 429/7486 | 192/2454 | 64/817 | chr2 | 25093110 | ||
| chr2:25133012
|
G | C | 1 | a0001c0004 | 4 | NA18974.hp2 NA18975.hp2 NA18982.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1257G>C | p.Thr419Thr | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 11/23 | 1494/7486 | 1257/2454 | 419/817 | chr2 | 25133012 | ||
| chr2:25136553
|
G | A | 5 | a0001c0002a0001c0006a0001c0008others(2): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
synonymous_variant | LOW | c.1515G>A | p.Leu505Leu | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/23 | 1752/7486 | 1515/2454 | 505/817 | chr2 | 25136553 | ||
| chr2:25137445
|
C | T | 1 | a0001c0006 | 2 | NA19002.hp1 NA19011.hp1 |
synonymous_variant | LOW | c.1665C>T | p.Ile555Ile | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/23 | 1902/7486 | 1665/2454 | 555/817 | chr2 | 25137445 | ||
| chr2:25137451
|
G | T | 1 | a0001c0005 | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.1671G>T | p.Leu557Leu | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/23 | 1908/7486 | 1671/2454 | 557/817 | chr2 | 25137451 | ||
| chr2:25139169
|
C | T | 1 | a0001c0009 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1833C>T | p.Ala611Ala | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/23 | 2070/7486 | 1833/2454 | 611/817 | chr2 | 25139169 | ||
| chr2:25143792
|
C | T | 1 | a0003c0011 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.1980C>T | p.Ile660Ile | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/23 | 2217/7486 | 1980/2454 | 660/817 | chr2 | 25143792 | ||
| chr2:25149705
|
C | T | 1 | a0001c0010 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.2154C>T | p.Ala718Ala | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/23 | 2391/7486 | 2154/2454 | 718/817 | chr2 | 25149705 | ||
| chr2:25154307
|
T | C | 13 | a0001c0001a0001c0002a0001c0004others(10): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
synonymous_variant | LOW | c.2421T>C | p.Tyr807Tyr | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2658/7486 | 2421/2454 | 807/817 | chr2 | 25154307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:25042079
|
A | C | 1 | a0001c0002t0020 | 2 | NA18999.hp2 NA19005.hp2 |
5_prime_UTR_variant | MODIFIER | c.-234A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/23 | 234 | chr2 | 25042079 | |||||
| chr2:25042104
|
G | T | 1 | a0001c0002t0052 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-209G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/23 | chr2 | 25042104 | ||||||
| chr2:25042139
|
G | T | 2 | a0001c0001t0019a0001c0001t0051 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
5_prime_UTR_variant | MODIFIER | c.-174G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/23 | 174 | chr2 | 25042139 | |||||
| chr2:25042312
|
G | A | 1 | a0001c0001t0021 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/23 | 1 | chr2 | 25042312 | |||||
| chr2:25154396
|
C | T | 1 | a0002c0012t0050 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 56 | chr2 | 25154396 | |||||
| chr2:25154460
|
C | T | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(26): Show | 144 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*120C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 120 | chr2 | 25154460 | |||||
| chr2:25154461
|
G | A | 2 | a0001c0001t0022a0001c0001t0023 | 2 | HG00733.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*121G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 121 | chr2 | 25154461 | |||||
| chr2:25154718
|
T | C | 1 | a0001c0005t0014 | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 378 | chr2 | 25154718 | |||||
| chr2:25154787
|
C | G | 1 | a0001c0001t0049 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*447C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 447 | chr2 | 25154787 | |||||
| chr2:25154936
|
G | A | 2 | a0001c0001t0024a0001c0001t0051 | 2 | HG01243.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*596G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 596 | chr2 | 25154936 | |||||
| chr2:25155043
|
C | G | 2 | a0001c0001t0024a0001c0001t0051 | 2 | HG01243.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*703C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 703 | chr2 | 25155043 | |||||
| chr2:25155213
|
G | A | 1 | a0001c0002t0025 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*873G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 873 | chr2 | 25155213 | |||||
| chr2:25155459
|
T | C | 2 | a0001c0001t0026a0001c0005t0014 | 5 | HG02280.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1119T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1119 | chr2 | 25155459 | |||||
| chr2:25155503
|
G | A | 5 | a0001c0003t0006a0001c0003t0010a0001c0003t0018others(2): Show | 25 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1163G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1163 | chr2 | 25155503 | |||||
| chr2:25155553
|
C | T | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(19): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1213C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1213 | chr2 | 25155553 | |||||
| chr2:25155564
|
A | T | 1 | a0001c0001t0048 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1224A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1224 | chr2 | 25155564 | |||||
| chr2:25155607
|
C | T | 1 | a0001c0001t0047 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1267 | chr2 | 25155607 | |||||
| chr2:25155627
|
T | A | 1 | a0001c0001t0030 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1287T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1287 | chr2 | 25155627 | |||||
| chr2:25155857
|
A | AT | 3 | a0001c0001t0016a0001c0001t0017a0001c0003t0027 | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1530dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1531 | INFO_REALIGN_3_PRIME | chr2 | 25155857 | ||||
| chr2:25155921
|
G | A | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(17): Show | 81 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1581G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1581 | chr2 | 25155921 | |||||
| chr2:25155934
|
TC | T | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(17): Show | 81 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1597delC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1597 | INFO_REALIGN_3_PRIME | chr2 | 25155934 | ||||
| chr2:25155966
|
C | T | 1 | a0001c0001t0046 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1626C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1626 | chr2 | 25155966 | |||||
| chr2:25156071
|
C | A | 2 | a0001c0001t0024a0001c0001t0051 | 2 | HG01243.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1731C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1731 | chr2 | 25156071 | |||||
| chr2:25156073
|
T | C | 26 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(23): Show | 90 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1733T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1733 | chr2 | 25156073 | |||||
| chr2:25156133
|
C | T | 1 | a0001c0002t0038 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1793C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1793 | chr2 | 25156133 | |||||
| chr2:25156150
|
C | T | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(19): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1810C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1810 | chr2 | 25156150 | |||||
| chr2:25156290
|
G | GT | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(25): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1975dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1976 | INFO_REALIGN_3_PRIME | chr2 | 25156290 | ||||
| chr2:25156290
|
G | GTT | 13 | a0001c0001t0004a0001c0001t0008a0001c0001t0015others(10): Show | 40 | HG00621.hp2 HG01346.hp2 HG01891.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1974_*1975dupTT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 1976 | INFO_REALIGN_3_PRIME | chr2 | 25156290 | ||||
| chr2:25156539
|
C | T | 1 | a0001c0002t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2199C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2199 | chr2 | 25156539 | |||||
| chr2:25156802
|
A | C | 2 | a0001c0003t0006a0001c0003t0010 | 22 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2462A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2462 | chr2 | 25156802 | |||||
| chr2:25156820
|
T | C | 2 | a0001c0001t0024a0001c0001t0051 | 2 | HG01243.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2480T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2480 | chr2 | 25156820 | |||||
| chr2:25156891
|
G | A | 1 | a0001c0002t0038 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2551G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2551 | chr2 | 25156891 | |||||
| chr2:25157039
|
T | C | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*2699T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2699 | chr2 | 25157039 | |||||
| chr2:25157170
|
C | T | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2830C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2830 | chr2 | 25157170 | |||||
| chr2:25157266
|
G | A | 1 | a0001c0002t0033 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2926G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2926 | chr2 | 25157266 | |||||
| chr2:25157318
|
C | T | 1 | a0001c0002t0036 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2978C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 2978 | chr2 | 25157318 | |||||
| chr2:25157378
|
A | G | 1 | a0003c0011t0045 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3038A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3038 | chr2 | 25157378 | |||||
| chr2:25157704
|
G | A | 44 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(41): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3364G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3364 | chr2 | 25157704 | |||||
| chr2:25157736
|
G | A | 1 | a0001c0001t0051 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3396G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3396 | chr2 | 25157736 | |||||
| chr2:25157822
|
G | A | 1 | a0001c0001t0040 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3482G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3482 | chr2 | 25157822 | |||||
| chr2:25157907
|
C | G | 1 | a0001c0001t0042 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3567C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3567 | chr2 | 25157907 | |||||
| chr2:25157985
|
C | T | 2 | a0001c0001t0041a0001c0001t0043 | 2 | NA18999.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3645C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3645 | chr2 | 25157985 | |||||
| chr2:25158168
|
G | A | 1 | a0001c0001t0013 | 5 | HG02074.hp1 NA18940.hp1 NA18965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3828G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3828 | chr2 | 25158168 | |||||
| chr2:25158174
|
A | G | 1 | a0001c0002t0031 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3834A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3834 | chr2 | 25158174 | |||||
| chr2:25158197
|
G | T | 1 | a0001c0001t0040 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3857G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3857 | chr2 | 25158197 | |||||
| chr2:25158279
|
G | A | 22 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(19): Show | 86 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3939G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 3939 | chr2 | 25158279 | |||||
| chr2:25158387
|
A | G | 1 | a0005c0013t0044 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4047A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 4047 | chr2 | 25158387 | |||||
| chr2:25158435
|
T | C | 1 | a0001c0002t0037 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4095T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 4095 | chr2 | 25158435 | |||||
| chr2:25158601
|
G | C | 11 | a0001c0001t0002a0001c0001t0007a0001c0001t0013others(8): Show | 65 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*4261G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 4261 | chr2 | 25158601 | |||||
| chr2:25158642
|
G | A | 2 | a0001c0001t0024a0001c0001t0051 | 2 | HG01243.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4302G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 4302 | chr2 | 25158642 | |||||
| chr2:25158771
|
G | A | 1 | a0001c0002t0034 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4431G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 4431 | chr2 | 25158771 | |||||
| chr2:25158983
|
G | A | 1 | a0001c0001t0024 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4643G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 4643 | chr2 | 25158983 | |||||
| chr2:25159100
|
G | A | 1 | a0001c0002t0035 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4760G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 23/23 | 4760 | chr2 | 25159100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:25042391
|
G | A | 1 | a0001c0001t0002g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.7+72G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25042391 | ||||||
| chr2:25042457
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.7+138C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25042457 | ||||||
| chr2:25042766
|
C | T | 3 | a0001c0001t0002g0304a0001c0001t0007g0305a0001c0001t0046g0303 | 3 | HG00099.hp1 HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.7+447C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25042766 | ||||||
| chr2:25042980
|
G | T | 1 | a0001c0001t0002g0302 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7+661G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25042980 | ||||||
| chr2:25043073
|
A | G | 4 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+754A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25043073 | ||||||
| chr2:25043129
|
G | C | 7 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(4): Show | 7 | HG01261.hp2 NA18952.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+810G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25043129 | ||||||
| chr2:25043172
|
C | T | 1 | a0005c0013t0044g0297 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.7+853C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25043172 | ||||||
| chr2:25043780
|
T | TC | 63 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(60): Show | 63 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.7+1466dupC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25043780 | |||||
| chr2:25043984
|
G | C | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+1665G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25043984 | ||||||
| chr2:25044459
|
C | T | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.7+2140C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25044459 | ||||||
| chr2:25044621
|
G | A | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7+2302G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25044621 | ||||||
| chr2:25044720
|
T | C | 1 | a0001c0002t0004g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7+2401T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25044720 | ||||||
| chr2:25044736
|
C | T | 1 | a0001c0001t0003g0296 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.7+2417C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25044736 | ||||||
| chr2:25044798
|
T | C | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7+2479T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25044798 | ||||||
| chr2:25045253
|
C | T | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+2934C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25045253 | ||||||
| chr2:25045395
|
A | C | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+3076A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25045395 | ||||||
| chr2:25045553
|
G | A | 1 | a0001c0001t0030g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7+3234G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25045553 | ||||||
| chr2:25045576
|
G | A | 1 | a0001c0001t0002g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.7+3257G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25045576 | ||||||
| chr2:25045783
|
C | CA | 27 | a0001c0001t0001g0127a0001c0001t0002g0017a0001c0001t0002g0018others(24): Show | 27 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(24): Show |
intron_variant | MODIFIER | c.7+3478dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25045783 | |||||
| chr2:25045848
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.7+3529G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25045848 | ||||||
| chr2:25046124
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7+3805G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046124 | ||||||
| chr2:25046128
|
G | A | 1 | a0001c0001t0004g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7+3809G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046128 | ||||||
| chr2:25046188
|
C | G | 1 | a0001c0002t0031g0295 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.7+3869C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046188 | ||||||
| chr2:25046325
|
C | T | 91 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.7+4006C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046325 | ||||||
| chr2:25046492
|
C | G | 1 | a0001c0001t0008g0121 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7+4173C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046492 | ||||||
| chr2:25046506
|
C | CTT | 62 | a0001c0001t0001g0219a0001c0001t0002g0017a0001c0001t0002g0018others(59): Show | 62 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.7+4202_7+4203dupTT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0003g0069a0001c0001t0047g0068 | 2 | HG00597.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.7+4194_7+4203dupTT others(8): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(5): Show |
1 | a0004c0007t0003g0070 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7+4192_7+4203dupTT others(10): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0012g0071 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.7+4191_7+4203dupTT others(11): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.7+4188_7+4203dupTT others(14): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(10): Show |
5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0008g0121others(2): Show | 5 | HG00621.hp2 HG03834.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(15): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0003g0076a0001c0001t0003g0077 | 2 | HG02523.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(16): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0015t0008g0078 | 3 | HG00423.hp1 NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(17): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(13): Show |
9 | a0001c0001t0003g0085a0001c0001t0003g0086a0001c0001t0003g0088others(6): Show | 9 | HG00438.hp1 HG02165.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(18): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(14): Show |
4 | a0001c0001t0002g0091a0001c0001t0003g0092a0001c0001t0012g0093others(1): Show | 4 | HG02132.hp1 NA18993.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(19): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0008g0094 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.7+4203_7+4204insTT others(20): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(16): Show |
4 | a0001c0001t0003g0095a0001c0001t0008g0098a0001c0001t0041g0096others(1): Show | 4 | NA18990.hp2 NA18999.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(21): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0003g0099 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.7+4203_7+4204insTT others(22): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(18): Show |
3 | a0001c0001t0003g0100a0001c0001t0003g0101a0001c0001t0003g0102 | 3 | HG02735.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(23): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0003g0104a0001c0001t0040g0103 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(25): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(24): Show |
2 | a0001c0001t0003g0106a0001c0003t0010g0105 | 2 | HG00741.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(29): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(25): Show |
5 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0110others(2): Show | 5 | HG00609.hp1 HG02015.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(30): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(26): Show |
2 | a0001c0001t0008g0112a0001c0001t0008g0113 | 2 | HG02135.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(31): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0008g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.7+4203_7+4204insTT others(32): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(30): Show |
2 | a0001c0001t0003g0116a0001c0003t0010g0115 | 2 | HG00558.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(35): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(31): Show |
2 | a0001c0001t0003g0118a0001c0003t0006g0117 | 2 | HG00140.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.7+4203_7+4204insTT others(36): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(33): Show |
1 | a0001c0003t0006g0119 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.7+4203_7+4204insTT others(38): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
C | CTTTTTTT others(36): Show |
1 | a0001c0001t0002g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.7+4203_7+4204insTT others(41): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046506
|
CT | C | 134 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(131): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.7+4203delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25046506 | |||||
| chr2:25046664
|
C | T | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+4345C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046664 | ||||||
| chr2:25046717
|
A | C | 2 | a0001c0001t0002g0287a0001c0001t0002g0288 | 2 | HG02300.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.7+4398A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046717 | ||||||
| chr2:25046937
|
C | A | 1 | a0001c0002t0001g0220 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.7+4618C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046937 | ||||||
| chr2:25046977
|
C | T | 14 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0106others(11): Show | 14 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+4658C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046977 | ||||||
| chr2:25046992
|
C | G | 6 | a0001c0001t0001g0172a0001c0001t0029g0171a0001c0002t0004g0168others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4673C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25046992 | ||||||
| chr2:25047137
|
G | A | 1 | a0004c0007t0003g0070 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7+4818G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047137 | ||||||
| chr2:25047215
|
A | G | 1 | a0001c0002t0001g0286 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.7+4896A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047215 | ||||||
| chr2:25047335
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+5016C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047335 | ||||||
| chr2:25047470
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7+5151C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047470 | ||||||
| chr2:25047564
|
T | C | 91 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.7+5245T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047564 | ||||||
| chr2:25047644
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7+5325G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047644 | ||||||
| chr2:25047879
|
G | A | 1 | a0001c0001t0007g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.7+5560G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047879 | ||||||
| chr2:25047886
|
C | T | 6 | a0001c0001t0001g0172a0001c0001t0029g0171a0001c0002t0004g0168others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+5567C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25047886 | ||||||
| chr2:25048012
|
G | T | 1 | a0001c0001t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7+5693G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25048012 | ||||||
| chr2:25048200
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7+5881G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25048200 | ||||||
| chr2:25048210
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.7+5891C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25048210 | ||||||
| chr2:25048258
|
C | G | 3 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008 | 3 | NA18952.hp1 NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.7+5939C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25048258 | ||||||
| chr2:25048302
|
C | T | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7+5983C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25048302 | ||||||
| chr2:25048631
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+6312C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25048631 | ||||||
| chr2:25048681
|
A | G | 1 | a0001c0001t0030g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7+6362A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25048681 | ||||||
| chr2:25049671
|
T | C | 55 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.7+7352T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25049671 | ||||||
| chr2:25049730
|
C | T | 1 | a0001c0003t0006g0285 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7+7411C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25049730 | ||||||
| chr2:25049731
|
G | C | 1 | a0001c0002t0036g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7+7412G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25049731 | ||||||
| chr2:25049840
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7+7521C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25049840 | ||||||
| chr2:25049933
|
T | A | 48 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(45): Show | 48 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.7+7614T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25049933 | ||||||
| chr2:25049933
|
T | C | 3 | a0001c0002t0001g0222a0001c0002t0001g0286a0001c0002t0001g0289 | 3 | HG00323.hp2 HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.7+7614T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25049933 | ||||||
| chr2:25049940
|
C | T | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+7621C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25049940 | ||||||
| chr2:25049952
|
T | TA | 56 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.7+7654dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25049952 | |||||
| chr2:25049952
|
TA | T | 22 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0164others(19): Show | 22 | HG01257.hp1 HG01358.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+7654delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25049952 | |||||
| chr2:25050027
|
G | A | 4 | a0001c0001t0003g0095a0001c0001t0008g0094a0001c0001t0041g0096others(1): Show | 4 | NA18999.hp1 NA19002.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+7708G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050027 | ||||||
| chr2:25050337
|
C | T | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7+8018C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050337 | ||||||
| chr2:25050555
|
A | G | 6 | a0001c0001t0017g0065a0001c0002t0001g0061a0001c0002t0004g0063others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+8236A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050555 | ||||||
| chr2:25050637
|
A | G | 1 | a0001c0001t0008g0098 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.7+8318A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050637 | ||||||
| chr2:25050732
|
T | A | 1 | a0001c0001t0013g0037 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.7+8413T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050732 | ||||||
| chr2:25050755
|
C | G | 2 | a0001c0001t0003g0088a0001c0001t0003g0092 | 2 | NA18975.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.7+8436C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050755 | ||||||
| chr2:25050768
|
G | C | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+8449G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050768 | ||||||
| chr2:25050772
|
A | G | 1 | a0001c0001t0051g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7+8453A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050772 | ||||||
| chr2:25050861
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+8542G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050861 | ||||||
| chr2:25050872
|
G | A | 62 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0120others(59): Show | 62 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.7+8553G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25050872 | ||||||
| chr2:25051059
|
G | T | 1 | a0001c0001t0051g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7+8740G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051059 | ||||||
| chr2:25051294
|
A | G | 1 | a0001c0002t0001g0029 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.7+8975A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051294 | ||||||
| chr2:25051390
|
C | T | 2 | a0001c0001t0019g0123a0001c0001t0019g0124 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7+9071C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051390 | ||||||
| chr2:25051623
|
T | TTG | 9 | a0001c0001t0007g0305a0001c0002t0001g0005a0001c0002t0001g0175others(6): Show | 9 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+9318_7+9319dupGT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25051623 | |||||
| chr2:25051635
|
G | T | 1 | a0001c0003t0010g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7+9316G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051635 | ||||||
| chr2:25051637
|
G | GT | 36 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.7+9334dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25051637 | |||||
| chr2:25051637
|
G | GTT | 7 | a0001c0001t0002g0067a0001c0001t0005g0209a0001c0001t0017g0065others(4): Show | 7 | HG02647.hp1 HG02895.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+9333_7+9334dupTT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25051637 | |||||
| chr2:25051637
|
G | T | 53 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.7+9318G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051637 | ||||||
| chr2:25051638
|
T | TG | 83 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+9319_7+9320insG | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051638 | ||||||
| chr2:25051639
|
T | G | 6 | a0001c0001t0002g0229a0001c0001t0008g0228a0001c0003t0006g0230others(3): Show | 6 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+9320T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051639 | ||||||
| chr2:25051697
|
G | T | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+9378G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051697 | ||||||
| chr2:25051757
|
T | C | 1 | a0001c0001t0013g0037 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.7+9438T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051757 | ||||||
| chr2:25051758
|
C | T | 1 | a0001c0001t0013g0037 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.7+9439C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051758 | ||||||
| chr2:25051854
|
G | A | 2 | a0001c0001t0049g0059a0001c0002t0001g0058 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.7+9535G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051854 | ||||||
| chr2:25051891
|
C | A | 2 | a0001c0001t0002g0039a0001c0001t0007g0038 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.7+9572C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25051891 | ||||||
| chr2:25052077
|
T | C | 1 | a0001c0002t0035g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7+9758T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052077 | ||||||
| chr2:25052137
|
A | G | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+9818A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052137 | ||||||
| chr2:25052157
|
T | C | 7 | a0001c0001t0002g0120a0001c0003t0006g0082a0001c0003t0006g0117others(4): Show | 7 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+9838T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052157 | ||||||
| chr2:25052496
|
CT | C | 127 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(124): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.7+10200delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25052496 | |||||
| chr2:25052496
|
CTT | C | 50 | a0001c0001t0001g0130a0001c0001t0002g0091a0001c0001t0002g0120others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.7+10199_7+10200del others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25052496 | |||||
| chr2:25052496
|
CTTT | C | 12 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0076others(9): Show | 12 | HG00423.hp1 HG00621.hp2 HG03654.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+10198_7+10200del others(3): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25052496 | |||||
| chr2:25052525
|
G | A | 1 | a0001c0001t0007g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7+10206G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052525 | ||||||
| chr2:25052539
|
T | G | 1 | a0001c0001t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7+10220T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052539 | ||||||
| chr2:25052542
|
C | T | 1 | a0001c0001t0012g0071 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.7+10223C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052542 | ||||||
| chr2:25052563
|
G | A | 55 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.7+10244G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052563 | ||||||
| chr2:25052646
|
G | GT | 55 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.7+10328dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25052646 | |||||
| chr2:25052749
|
C | T | 55 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.7+10430C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25052749 | ||||||
| chr2:25053197
|
G | A | 1 | a0001c0003t0018g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7+10878G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053197 | ||||||
| chr2:25053318
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0005g0157 | 2 | HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.7+10999C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053318 | ||||||
| chr2:25053415
|
G | A | 42 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.7+11096G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053415 | ||||||
| chr2:25053475
|
A | G | 56 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(53): Show | 56 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.7+11156A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053475 | ||||||
| chr2:25053680
|
G | A | 2 | a0001c0002t0001g0233a0001c0003t0009g0290 | 2 | HG00280.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.7+11361G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053680 | ||||||
| chr2:25053686
|
C | T | 38 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(35): Show | 38 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.7+11367C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053686 | ||||||
| chr2:25053822
|
G | A | 8 | a0001c0001t0002g0067a0001c0001t0007g0234a0001c0001t0017g0065others(5): Show | 8 | HG01106.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+11503G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053822 | ||||||
| chr2:25053828
|
A | G | 1 | a0001c0002t0011g0279 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.7+11509A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25053828 | ||||||
| chr2:25054101
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.7+11782G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25054101 | ||||||
| chr2:25054238
|
G | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+11919G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25054238 | ||||||
| chr2:25054323
|
T | C | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+12004T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25054323 | ||||||
| chr2:25054590
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.7+12271G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25054590 | ||||||
| chr2:25054625
|
T | C | 1 | a0001c0002t0032g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+12306T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25054625 | ||||||
| chr2:25054891
|
T | C | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.7+12572T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25054891 | ||||||
| chr2:25055140
|
A | G | 1 | a0001c0002t0005g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+12821A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055140 | ||||||
| chr2:25055494
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7+13175C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055494 | ||||||
| chr2:25055527
|
G | A | 5 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0156others(2): Show | 5 | HG01074.hp2 HG01109.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+13208G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055527 | ||||||
| chr2:25055678
|
C | G | 1 | a0001c0001t0007g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7+13359C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055678 | ||||||
| chr2:25055779
|
CA | C | 241 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.7+13462delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25055779 | |||||
| chr2:25055854
|
G | A | 62 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0120others(59): Show | 62 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.7+13535G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055854 | ||||||
| chr2:25055960
|
G | C | 64 | a0001c0001t0001g0172a0001c0001t0001g0219a0001c0001t0002g0017others(61): Show | 64 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.7+13641G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055960 | ||||||
| chr2:25055970
|
G | C | 1 | a0001c0002t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7+13651G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055970 | ||||||
| chr2:25055987
|
G | A | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+13668G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25055987 | ||||||
| chr2:25056045
|
C | T | 1 | a0001c0002t0001g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7+13726C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25056045 | ||||||
| chr2:25056222
|
A | AT | 6 | a0001c0001t0024g0217a0001c0001t0026g0210a0001c0005t0014g0212others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+13909dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25056222 | |||||
| chr2:25056384
|
T | G | 1 | a0001c0002t0005g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+14065T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25056384 | ||||||
| chr2:25056436
|
C | CT | 193 | a0001c0001t0001g0155a0001c0001t0001g0186a0001c0001t0001g0187others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.7+14131dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25056436 | |||||
| chr2:25056436
|
C | CTT | 15 | a0001c0001t0001g0172a0001c0001t0002g0067a0001c0001t0017g0065others(12): Show | 15 | HG01496.hp2 HG02559.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.7+14130_7+14131dup others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25056436 | |||||
| chr2:25056503
|
G | C | 42 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.7+14184G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25056503 | ||||||
| chr2:25056607
|
C | T | 5 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0036others(2): Show | 5 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+14288C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25056607 | ||||||
| chr2:25056873
|
A | T | 1 | a0001c0001t0005g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7+14554A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25056873 | ||||||
| chr2:25056970
|
G | A | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+14651G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25056970 | ||||||
| chr2:25057190
|
T | C | 1 | a0001c0001t0012g0071 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.7+14871T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057190 | ||||||
| chr2:25057291
|
A | C | 1 | a0001c0002t0001g0053 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.7+14972A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057291 | ||||||
| chr2:25057412
|
C | CA | 80 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0017others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.7+15104dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25057412 | |||||
| chr2:25057424
|
C | A | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0076 | 3 | NA18986.hp1 NA19060.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.7+15105C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057424 | ||||||
| chr2:25057450
|
C | T | 2 | a0001c0001t0004g0154a0001c0001t0030g0126 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.7+15131C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057450 | ||||||
| chr2:25057520
|
G | A | 1 | a0001c0002t0037g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.7+15201G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057520 | ||||||
| chr2:25057686
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7+15367G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057686 | ||||||
| chr2:25057780
|
C | T | 3 | a0001c0001t0005g0209a0001c0001t0016g0182a0001c0001t0017g0181 | 3 | HG01891.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.7+15461C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057780 | ||||||
| chr2:25057783
|
C | CA | 230 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.7+15479dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25057783 | |||||
| chr2:25057783
|
C | CAA | 14 | a0001c0001t0002g0040a0001c0001t0005g0185a0001c0001t0007g0240others(11): Show | 14 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+15478_7+15479dup others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25057783 | |||||
| chr2:25057863
|
A | G | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+15544A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25057863 | ||||||
| chr2:25058017
|
C | CA | 9 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+15704dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058017 | |||||
| chr2:25058217
|
A | T | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+15898A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058217 | ||||||
| chr2:25058314
|
G | A | 1 | a0001c0001t0002g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.7+15995G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058314 | ||||||
| chr2:25058619
|
C | T | 2 | a0001c0001t0019g0123a0001c0001t0019g0124 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7+16300C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058619 | ||||||
| chr2:25058760
|
CCG | C | 3 | a0001c0001t0001g0160a0001c0002t0001g0173a0001c0003t0018g0159 | 3 | HG01891.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.7+16445_7+16446del others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058760 | |||||
| chr2:25058762
|
G | GC | 20 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(17): Show | 20 | HG00140.hp2 HG01074.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.7+16444dupC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058762 | |||||
| chr2:25058762
|
G | GCC | 4 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0004g0129others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+16444_7+16445ins others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058762 | |||||
| chr2:25058763
|
CG | C | 3 | a0001c0001t0005g0161a0001c0001t0005g0165a0001c0001t0011g0138 | 3 | HG01071.hp2 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.7+16445delG | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058763 | ||||||
| chr2:25058764
|
G | C | 33 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(30): Show | 33 | HG00140.hp2 HG00323.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.7+16445G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058764 | ||||||
| chr2:25058764
|
G | GC | 18 | a0001c0001t0002g0026a0001c0001t0002g0039a0001c0001t0002g0051others(15): Show | 18 | HG00621.hp1 HG00735.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.7+16456dupC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058764 | |||||
| chr2:25058772
|
C | T | 90 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.7+16453C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058772 | ||||||
| chr2:25058775
|
C | CA | 10 | a0001c0001t0001g0186a0001c0001t0019g0123a0001c0001t0019g0124others(7): Show | 10 | HG02280.hp1 HG02300.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+16467dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058775 | |||||
| chr2:25058775
|
CA | C | 19 | a0001c0001t0002g0067a0001c0001t0003g0072a0001c0001t0003g0073others(16): Show | 19 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.7+16467delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058775 | |||||
| chr2:25058775
|
CAA | C | 33 | a0001c0001t0003g0069a0001c0001t0003g0077a0001c0001t0003g0079others(30): Show | 33 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.7+16466_7+16467del others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25058775 | |||||
| chr2:25058776
|
A | C | 7 | a0001c0001t0002g0091a0001c0001t0016g0150a0001c0001t0016g0153others(4): Show | 7 | HG02004.hp2 HG02132.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+16457A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058776 | ||||||
| chr2:25058777
|
A | C | 13 | a0001c0001t0003g0072a0001c0001t0003g0074a0001c0001t0003g0076others(10): Show | 13 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+16458A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25058777 | ||||||
| chr2:25059078
|
C | T | 48 | a0001c0001t0002g0091a0001c0001t0003g0069a0001c0001t0003g0072others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.7+16759C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059078 | ||||||
| chr2:25059079
|
A | G | 55 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.7+16760A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059079 | ||||||
| chr2:25059114
|
A | AT | 25 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0002g0294others(22): Show | 25 | HG00423.hp2 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.7+16811dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059114 | |||||
| chr2:25059114
|
A | ATT | 49 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.7+16810_7+16811dup others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059114 | |||||
| chr2:25059114
|
AT | A | 13 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0004g0129others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+16811delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059114 | |||||
| chr2:25059145
|
G | C | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.7+16826G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059145 | ||||||
| chr2:25059198
|
C | T | 1 | a0001c0003t0006g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7+16879C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059198 | ||||||
| chr2:25059290
|
G | A | 2 | a0001c0001t0012g0242a0001c0002t0001g0241 | 2 | HG02132.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.7+16971G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059290 | ||||||
| chr2:25059340
|
T | A | 1 | a0001c0002t0011g0042 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.7+17021T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059340 | ||||||
| chr2:25059484
|
C | G | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+17165C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059484 | ||||||
| chr2:25059487
|
G | A | 7 | a0001c0001t0001g0172a0001c0001t0029g0171a0001c0002t0004g0168others(4): Show | 7 | HG01496.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+17168G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059487 | ||||||
| chr2:25059533
|
C | T | 7 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0004g0129others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+17214C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059533 | ||||||
| chr2:25059572
|
C | CG | 35 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0261others(32): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.7+17267dupG | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059572 | |||||
| chr2:25059572
|
C | CGG | 55 | a0001c0001t0001g0187a0001c0001t0002g0235a0001c0001t0002g0249others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+17266_7+17267dup others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059572 | |||||
| chr2:25059572
|
CGG | C | 42 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.7+17266_7+17267del others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059572 | |||||
| chr2:25059572
|
CGGGGG | C | 51 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0072others(48): Show | 51 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.7+17263_7+17267del others(5): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059572 | |||||
| chr2:25059578
|
G | GC | 4 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0001g0183others(1): Show | 4 | HG00733.hp2 HG02280.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+17259_7+17260ins others(1): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059578 | ||||||
| chr2:25059578
|
G | T | 62 | a0001c0001t0001g0172a0001c0001t0001g0219a0001c0001t0002g0017others(59): Show | 62 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.7+17259G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059578 | ||||||
| chr2:25059580
|
G | T | 1 | a0001c0001t0002g0224 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7+17261G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059580 | ||||||
| chr2:25059581
|
G | T | 45 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.7+17262G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059581 | ||||||
| chr2:25059596
|
G | A | 1 | a0001c0002t0001g0284 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7+17277G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059596 | ||||||
| chr2:25059699
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7+17380C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059699 | ||||||
| chr2:25059732
|
G | A | 55 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.7+17413G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059732 | ||||||
| chr2:25059776
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7+17457G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059776 | ||||||
| chr2:25059830
|
G | A | 1 | a0001c0002t0020g0003 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.7+17511G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059830 | ||||||
| chr2:25059863
|
A | G | 56 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(53): Show | 56 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.7+17544A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059863 | ||||||
| chr2:25059875
|
C | CA | 21 | a0001c0001t0001g0136a0001c0001t0001g0219a0001c0001t0002g0023others(18): Show | 21 | HG00673.hp2 HG00741.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.7+17582dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059875 | |||||
| chr2:25059875
|
CA | C | 77 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0134others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.7+17582delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059875 | |||||
| chr2:25059875
|
CAAA | C | 10 | a0001c0001t0002g0091a0001c0001t0003g0073a0001c0001t0003g0111others(7): Show | 10 | HG01243.hp2 HG01361.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+17580_7+17582del others(3): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059875 | |||||
| chr2:25059875
|
CAAAA | C | 44 | a0001c0001t0002g0120a0001c0001t0003g0069a0001c0001t0003g0072others(41): Show | 44 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.7+17579_7+17582del others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25059875 | |||||
| chr2:25059994
|
C | T | 48 | a0001c0001t0002g0091a0001c0001t0003g0069a0001c0001t0003g0072others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.7+17675C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25059994 | ||||||
| chr2:25060190
|
C | T | 1 | a0001c0002t0004g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7+17871C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060190 | ||||||
| chr2:25060212
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7+17893C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060212 | ||||||
| chr2:25060326
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0120others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.7+18007A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060326 | ||||||
| chr2:25060338
|
G | T | 2 | a0001c0001t0002g0304a0001c0001t0007g0305 | 2 | HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.7+18019G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060338 | ||||||
| chr2:25060608
|
A | AG | 8 | a0001c0001t0002g0026a0001c0001t0005g0185a0001c0001t0007g0012others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+18294dupG | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25060608 | |||||
| chr2:25060792
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7+18473G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060792 | ||||||
| chr2:25060878
|
C | T | 63 | a0001c0001t0001g0172a0001c0001t0001g0219a0001c0001t0002g0017others(60): Show | 63 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.7+18559C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060878 | ||||||
| chr2:25060899
|
C | A | 1 | a0001c0002t0001g0284 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7+18580C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060899 | ||||||
| chr2:25060936
|
A | AAAC | 304 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.7+18632_7+18634dup others(3): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25060936 | |||||
| chr2:25060958
|
C | T | 4 | a0001c0001t0026g0210a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+18639C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25060958 | ||||||
| chr2:25061077
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+18758A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061077 | ||||||
| chr2:25061127
|
A | AT | 7 | a0001c0001t0002g0023a0001c0001t0007g0240a0001c0001t0051g0125others(4): Show | 7 | HG01243.hp1 HG02135.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+18824dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25061127 | |||||
| chr2:25061127
|
AT | A | 28 | a0001c0001t0001g0135a0001c0001t0001g0186a0001c0001t0001g0187others(25): Show | 28 | HG00099.hp2 HG00639.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.7+18824delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25061127 | |||||
| chr2:25061138
|
T | G | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.7+18819T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061138 | ||||||
| chr2:25061165
|
C | T | 1 | a0002c0012t0050g0281 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7+18846C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061165 | ||||||
| chr2:25061278
|
T | A | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7+18959T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061278 | ||||||
| chr2:25061339
|
C | T | 1 | a0001c0003t0006g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7+19020C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061339 | ||||||
| chr2:25061392
|
C | T | 1 | a0001c0003t0006g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7+19073C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061392 | ||||||
| chr2:25061402
|
C | T | 1 | a0001c0001t0008g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.7+19083C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061402 | ||||||
| chr2:25061445
|
C | T | 1 | a0001c0001t0008g0121 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7+19126C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061445 | ||||||
| chr2:25061667
|
T | C | 4 | a0001c0001t0002g0026a0001c0001t0002g0039a0001c0001t0002g0043others(1): Show | 4 | HG00621.hp1 HG00673.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+19348T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061667 | ||||||
| chr2:25061816
|
C | A | 1 | a0001c0001t0008g0010 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.7+19497C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061816 | ||||||
| chr2:25061836
|
A | G | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+19517A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25061836 | ||||||
| chr2:25062494
|
A | G | 3 | a0001c0003t0010g0083a0001c0003t0010g0087a0001c0003t0010g0090 | 3 | NA18963.hp1 NA18968.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.7+20175A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25062494 | ||||||
| chr2:25062539
|
C | T | 1 | a0001c0003t0006g0119 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.7+20220C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25062539 | ||||||
| chr2:25062744
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7+20425G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25062744 | ||||||
| chr2:25062801
|
C | T | 55 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(52): Show | 55 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.7+20482C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25062801 | ||||||
| chr2:25062872
|
A | C | 1 | a0001c0001t0003g0296 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.7+20553A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25062872 | ||||||
| chr2:25062918
|
A | ATTTTTCT | 62 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0120others(59): Show | 62 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.7+20604_7+20610dup others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25062918 | |||||
| chr2:25063048
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+20729C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25063048 | ||||||
| chr2:25063110
|
T | C | 1 | a0001c0003t0006g0256 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.7+20791T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25063110 | ||||||
| chr2:25063283
|
T | C | 2 | a0001c0001t0003g0099a0001c0001t0003g0102 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.7+20964T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25063283 | ||||||
| chr2:25063308
|
C | T | 1 | a0001c0002t0004g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7+20989C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25063308 | ||||||
| chr2:25063566
|
C | T | 91 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.7+21247C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25063566 | ||||||
| chr2:25063750
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7+21431G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25063750 | ||||||
| chr2:25063926
|
G | C | 1 | a0001c0002t0037g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.7+21607G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25063926 | ||||||
| chr2:25064308
|
C | T | 1 | a0001c0001t0012g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7+21989C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25064308 | ||||||
| chr2:25064317
|
C | T | 1 | a0003c0011t0045g0272 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.7+21998C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25064317 | ||||||
| chr2:25064565
|
C | G | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | NA18948.hp2 NA18959.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+22246C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25064565 | ||||||
| chr2:25064574
|
A | G | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+22255A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25064574 | ||||||
| chr2:25064575
|
T | C | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7+22256T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25064575 | ||||||
| chr2:25064642
|
C | T | 8 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0001t0048g0218others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+22323C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25064642 | ||||||
| chr2:25064841
|
T | C | 5 | a0001c0001t0005g0194a0001c0001t0005g0196a0001c0001t0005g0207others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+22522T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25064841 | ||||||
| chr2:25065079
|
C | CG | 49 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(46): Show | 49 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.7+22768dupG | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25065079 | |||||
| chr2:25065088
|
C | T | 1 | a0001c0001t0028g0197 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7+22769C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065088 | ||||||
| chr2:25065277
|
C | G | 42 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.7+22958C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065277 | ||||||
| chr2:25065293
|
T | G | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.7+22974T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065293 | ||||||
| chr2:25065318
|
C | A | 14 | a0001c0001t0001g0261a0001c0002t0001g0233a0001c0003t0006g0230others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.7+22999C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065318 | ||||||
| chr2:25065346
|
A | AT | 10 | a0001c0001t0002g0288a0001c0001t0005g0194a0001c0001t0007g0305others(7): Show | 10 | HG01255.hp2 HG02080.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+23051dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25065346 | |||||
| chr2:25065346
|
AT | A | 51 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(48): Show | 51 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.7+23051delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25065346 | |||||
| chr2:25065346
|
ATT | A | 108 | a0001c0001t0001g0219a0001c0001t0002g0017a0001c0001t0002g0018others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.7+23050_7+23051del others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25065346 | |||||
| chr2:25065513
|
C | T | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7+23194C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065513 | ||||||
| chr2:25065582
|
A | G | 62 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0120others(59): Show | 62 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.7+23263A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065582 | ||||||
| chr2:25065721
|
G | C | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.7+23402G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065721 | ||||||
| chr2:25065806
|
G | A | 91 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.7+23487G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065806 | ||||||
| chr2:25065811
|
C | G | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7+23492C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065811 | ||||||
| chr2:25065818
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7+23499C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065818 | ||||||
| chr2:25065864
|
C | G | 6 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0076others(3): Show | 6 | HG00423.hp1 HG03834.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+23545C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25065864 | ||||||
| chr2:25066101
|
A | G | 1 | a0001c0001t0007g0025 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.7+23782A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066101 | ||||||
| chr2:25066283
|
G | T | 1 | a0001c0001t0012g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7+23964G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066283 | ||||||
| chr2:25066300
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0043 | 2 | HG00673.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.7+23981T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066300 | ||||||
| chr2:25066406
|
A | G | 5 | a0001c0001t0005g0194a0001c0001t0005g0196a0001c0001t0005g0207others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+24087A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066406 | ||||||
| chr2:25066416
|
CT | C | 9 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+24100delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25066416 | |||||
| chr2:25066578
|
G | T | 1 | a0001c0002t0001g0260 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7+24259G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066578 | ||||||
| chr2:25066603
|
C | T | 1 | a0001c0002t0011g0277 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7+24284C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066603 | ||||||
| chr2:25066627
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.7+24308C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066627 | ||||||
| chr2:25066794
|
A | G | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+24475A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066794 | ||||||
| chr2:25066853
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.8-24472C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066853 | ||||||
| chr2:25066907
|
A | G | 2 | a0001c0002t0001g0233a0001c0003t0009g0290 | 2 | HG00280.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.8-24418A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066907 | ||||||
| chr2:25066932
|
G | A | 1 | a0001c0001t0008g0010 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.8-24393G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25066932 | ||||||
| chr2:25067191
|
T | A | 1 | a0001c0002t0004g0291 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.8-24134T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067191 | ||||||
| chr2:25067426
|
G | GT | 12 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0001g0175others(9): Show | 12 | HG00733.hp2 HG01255.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-23886dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25067426 | |||||
| chr2:25067426
|
G | T | 67 | a0001c0001t0001g0172a0001c0001t0001g0219a0001c0001t0002g0017others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.8-23899G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067426 | ||||||
| chr2:25067426
|
GT | G | 61 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0120others(58): Show | 61 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.8-23886delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25067426 | |||||
| chr2:25067428
|
T | G | 1 | a0001c0001t0002g0051 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.8-23897T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067428 | ||||||
| chr2:25067432
|
T | G | 12 | a0001c0001t0002g0028a0001c0001t0002g0051a0001c0001t0007g0025others(9): Show | 12 | HG00738.hp1 HG01952.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.8-23893T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067432 | ||||||
| chr2:25067433
|
T | G | 1 | a0001c0001t0051g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.8-23892T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067433 | ||||||
| chr2:25067436
|
T | G | 41 | a0001c0001t0001g0219a0001c0001t0002g0017a0001c0001t0002g0018others(38): Show | 41 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.8-23889T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067436 | ||||||
| chr2:25067440
|
G | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0177a0001c0002t0004g0176 | 3 | HG02145.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.8-23885G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067440 | ||||||
| chr2:25067447
|
G | T | 1 | a0001c0002t0001g0233 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.8-23878G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067447 | ||||||
| chr2:25067504
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.8-23821G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067504 | ||||||
| chr2:25067549
|
C | G | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.8-23776C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067549 | ||||||
| chr2:25067933
|
G | C | 2 | a0001c0001t0019g0123a0001c0001t0019g0124 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8-23392G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25067933 | ||||||
| chr2:25068037
|
C | T | 2 | a0001c0001t0002g0271a0003c0011t0045g0272 | 2 | HG00609.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.8-23288C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25068037 | ||||||
| chr2:25068166
|
G | A | 1 | a0001c0001t0007g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.8-23159G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25068166 | ||||||
| chr2:25068493
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-22832C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25068493 | ||||||
| chr2:25068633
|
G | GT | 59 | a0001c0001t0001g0219a0001c0001t0002g0017a0001c0001t0002g0018others(56): Show | 59 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.8-22678dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25068633 | |||||
| chr2:25068633
|
G | GTT | 9 | a0001c0001t0001g0172a0001c0001t0029g0171a0001c0002t0001g0032others(6): Show | 9 | HG00735.hp2 HG01496.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-22679_8-22678dup others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25068633 | |||||
| chr2:25068633
|
GT | G | 59 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0120others(56): Show | 59 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.8-22678delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25068633 | |||||
| chr2:25068639
|
T | G | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8-22686T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25068639 | ||||||
| chr2:25068670
|
C | T | 91 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.8-22655C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25068670 | ||||||
| chr2:25068698
|
C | T | 6 | a0001c0001t0017g0065a0001c0002t0001g0061a0001c0002t0004g0063others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-22627C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25068698 | ||||||
| chr2:25068786
|
C | A | 1 | a0001c0002t0005g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8-22539C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25068786 | ||||||
| chr2:25068930
|
C | CT | 6 | a0001c0001t0001g0219a0001c0001t0002g0023a0001c0001t0002g0294others(3): Show | 6 | HG02080.hp1 HG02486.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-22376dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25068930 | |||||
| chr2:25069292
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.8-22033G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25069292 | ||||||
| chr2:25069348
|
C | G | 1 | a0001c0002t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.8-21977C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25069348 | ||||||
| chr2:25069350
|
C | A | 3 | a0001c0002t0001g0222a0001c0002t0001g0286a0001c0002t0001g0289 | 3 | HG00323.hp2 HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.8-21975C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25069350 | ||||||
| chr2:25069448
|
C | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-21877C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25069448 | ||||||
| chr2:25069502
|
A | G | 26 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.8-21823A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25069502 | ||||||
| chr2:25069845
|
C | A | 1 | a0001c0001t0003g0296 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.8-21480C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25069845 | ||||||
| chr2:25069932
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-21393C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25069932 | ||||||
| chr2:25070115
|
G | T | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-21210G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070115 | ||||||
| chr2:25070196
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0004g0154a0001c0001t0030g0126 | 3 | HG03225.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.8-21129C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070196 | ||||||
| chr2:25070543
|
G | A | 1 | a0005c0013t0044g0297 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.8-20782G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070543 | ||||||
| chr2:25070552
|
C | T | 7 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0005g0161others(4): Show | 7 | HG01358.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-20773C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070552 | ||||||
| chr2:25070573
|
G | A | 54 | a0001c0001t0002g0091a0001c0001t0002g0120a0001c0001t0003g0069others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.8-20752G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070573 | ||||||
| chr2:25070637
|
T | C | 6 | a0001c0001t0017g0065a0001c0002t0001g0061a0001c0002t0004g0063others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-20688T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070637 | ||||||
| chr2:25070641
|
C | T | 1 | a0001c0010t0005g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-20684C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070641 | ||||||
| chr2:25070726
|
A | G | 1 | a0001c0001t0042g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.8-20599A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070726 | ||||||
| chr2:25070888
|
C | T | 2 | a0001c0001t0003g0095a0001c0001t0008g0094 | 2 | NA19002.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.8-20437C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070888 | ||||||
| chr2:25070988
|
T | C | 1 | a0001c0001t0042g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.8-20337T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070988 | ||||||
| chr2:25070991
|
C | T | 2 | a0001c0001t0046g0303a0001c0003t0006g0270 | 2 | HG00099.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.8-20334C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25070991 | ||||||
| chr2:25071030
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.8-20295G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071030 | ||||||
| chr2:25071175
|
T | C | 6 | a0001c0001t0017g0065a0001c0002t0001g0061a0001c0002t0004g0063others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-20150T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071175 | ||||||
| chr2:25071249
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.8-20076C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071249 | ||||||
| chr2:25071259
|
C | CT | 15 | a0001c0001t0001g0130a0001c0001t0002g0294a0001c0001t0003g0072others(12): Show | 15 | HG00735.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-20049dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25071259 | |||||
| chr2:25071291
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8-20034C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071291 | ||||||
| chr2:25071446
|
A | C | 1 | a0004c0007t0003g0070 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.8-19879A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071446 | ||||||
| chr2:25071475
|
G | A | 40 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(37): Show | 40 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.8-19850G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071475 | ||||||
| chr2:25071515
|
T | G | 1 | a0001c0001t0005g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.8-19810T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071515 | ||||||
| chr2:25071549
|
G | C | 63 | a0001c0001t0001g0172a0001c0001t0001g0219a0001c0001t0002g0017others(60): Show | 63 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.8-19776G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071549 | ||||||
| chr2:25071818
|
G | C | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8-19507G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25071818 | ||||||
| chr2:25072273
|
A | AT | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.8-19049dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25072273 | |||||
| chr2:25072415
|
G | C | 1 | a0001c0001t0007g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8-18910G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25072415 | ||||||
| chr2:25072493
|
G | A | 1 | a0001c0003t0006g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8-18832G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25072493 | ||||||
| chr2:25072624
|
G | A | 9 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-18701G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25072624 | ||||||
| chr2:25072754
|
C | T | 1 | a0001c0003t0009g0292 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.8-18571C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25072754 | ||||||
| chr2:25072861
|
G | A | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.8-18464G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25072861 | ||||||
| chr2:25073199
|
C | T | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-18126C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25073199 | ||||||
| chr2:25073360
|
C | CT | 92 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0223others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.8-17949dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25073360 | |||||
| chr2:25073362
|
T | C | 7 | a0001c0001t0002g0067a0001c0001t0017g0065a0001c0002t0001g0061others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-17963T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25073362 | ||||||
| chr2:25073640
|
G | A | 1 | a0001c0001t0008g0098 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.8-17685G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25073640 | ||||||
| chr2:25073856
|
T | A | 1 | a0001c0002t0036g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.8-17469T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25073856 | ||||||
| chr2:25074068
|
G | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-17257G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074068 | ||||||
| chr2:25074157
|
T | C | 5 | a0001c0002t0001g0061a0001c0002t0004g0063a0001c0002t0004g0064others(2): Show | 5 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-17168T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074157 | ||||||
| chr2:25074357
|
G | A | 1 | a0001c0001t0007g0025 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.8-16968G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074357 | ||||||
| chr2:25074395
|
G | A | 1 | a0001c0001t0005g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.8-16930G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074395 | ||||||
| chr2:25074458
|
A | G | 2 | a0001c0001t0004g0154a0001c0001t0030g0126 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.8-16867A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074458 | ||||||
| chr2:25074488
|
C | A | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.8-16837C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074488 | ||||||
| chr2:25074676
|
G | A | 4 | a0001c0001t0005g0174a0001c0001t0005g0185a0001c0001t0005g0195others(1): Show | 4 | HG01169.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-16649G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074676 | ||||||
| chr2:25074939
|
C | G | 1 | a0001c0002t0001g0220 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.8-16386C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074939 | ||||||
| chr2:25074975
|
A | C | 1 | a0001c0001t0005g0195 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.8-16350A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25074975 | ||||||
| chr2:25075004
|
C | A | 1 | a0001c0002t0001g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.8-16321C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25075004 | ||||||
| chr2:25075028
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.8-16297G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25075028 | ||||||
| chr2:25075096
|
T | A | 5 | a0001c0003t0006g0144a0001c0003t0006g0145a0001c0003t0006g0147others(2): Show | 5 | HG01106.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-16229T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25075096 | ||||||
| chr2:25075179
|
T | C | 3 | a0001c0002t0002g0041a0001c0002t0004g0009a0001c0002t0011g0042 | 3 | HG00621.hp2 NA18954.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.8-16146T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25075179 | ||||||
| chr2:25075664
|
T | A | 1 | a0001c0001t0002g0306 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.8-15661T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25075664 | ||||||
| chr2:25075847
|
C | T | 1 | a0001c0003t0018g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8-15478C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25075847 | ||||||
| chr2:25076494
|
C | T | 2 | a0001c0001t0003g0077a0001c0001t0003g0085 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.8-14831C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25076494 | ||||||
| chr2:25076966
|
A | C | 2 | a0001c0001t0002g0259a0001c0001t0002g0282 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.8-14359A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25076966 | ||||||
| chr2:25077108
|
A | T | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8-14217A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25077108 | ||||||
| chr2:25077228
|
TTAAA | T | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.8-14091_8-14088del others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25077228 | |||||
| chr2:25077326
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0048g0218 | 2 | HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.8-13999C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25077326 | ||||||
| chr2:25077362
|
A | C | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.8-13963A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25077362 | ||||||
| chr2:25078688
|
A | G | 1 | a0001c0002t0025g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.8-12637A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25078688 | ||||||
| chr2:25078886
|
A | T | 87 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0021others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.8-12439A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25078886 | ||||||
| chr2:25079311
|
G | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0007others(1): Show | 4 | HG01261.hp2 NA18952.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-12014G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079311 | ||||||
| chr2:25079332
|
T | C | 2 | a0001c0001t0002g0120a0001c0003t0006g0117 | 2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.8-11993T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079332 | ||||||
| chr2:25079368
|
A | G | 45 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.8-11957A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079368 | ||||||
| chr2:25079424
|
A | C | 1 | a0001c0001t0023g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8-11901A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079424 | ||||||
| chr2:25079579
|
T | A | 1 | a0001c0001t0047g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.8-11746T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079579 | ||||||
| chr2:25079794
|
A | G | 1 | a0001c0005t0014g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8-11531A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079794 | ||||||
| chr2:25079821
|
A | AAAG | 140 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.8-11501_8-11499dup others(3): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25079821 | |||||
| chr2:25079977
|
G | A | 73 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.8-11348G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079977 | ||||||
| chr2:25079981
|
T | C | 50 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.8-11344T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25079981 | ||||||
| chr2:25080037
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.8-11288G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080037 | ||||||
| chr2:25080058
|
C | T | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-11267C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080058 | ||||||
| chr2:25080238
|
A | G | 1 | a0001c0001t0007g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8-11087A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080238 | ||||||
| chr2:25080251
|
T | TC | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.8-11073dupC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080251 | |||||
| chr2:25080283
|
C | CT | 72 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(69): Show | 72 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.8-11014dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTT | 20 | a0001c0001t0001g0219a0001c0001t0003g0074a0001c0001t0004g0269others(17): Show | 20 | HG01433.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.8-11015_8-11014dup others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTT | 7 | a0001c0001t0003g0076a0001c0001t0003g0095a0001c0001t0008g0094others(4): Show | 7 | HG00621.hp2 HG03834.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-11016_8-11014dup others(3): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTT | 24 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(21): Show | 24 | HG00597.hp2 HG01192.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.8-11017_8-11014dup others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTT | 11 | a0001c0001t0001g0140a0001c0001t0003g0079a0001c0001t0003g0080others(8): Show | 11 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-11018_8-11014dup others(5): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0022g0178a0001c0001t0049g0059 | 2 | HG00733.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.8-11023_8-11014dup others(10): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0023g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8-11024_8-11014dup others(11): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(7): Show |
10 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.8-11027_8-11014dup others(14): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(8): Show |
15 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0005g0165others(12): Show | 15 | HG01169.hp1 HG01884.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-11028_8-11014dup others(15): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(9): Show |
9 | a0001c0001t0005g0185a0001c0001t0005g0192a0001c0001t0005g0194others(6): Show | 9 | HG01358.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-11029_8-11014dup others(16): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(10): Show |
4 | a0001c0001t0002g0120a0001c0001t0005g0161a0001c0003t0006g0082others(1): Show | 4 | HG01099.hp2 HG03209.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-11030_8-11014dup others(17): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0001g0136a0001c0003t0006g0119a0001c0003t0010g0105 | 3 | HG00438.hp2 HG00741.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.8-11031_8-11014dup others(18): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(12): Show |
10 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0156others(7): Show | 10 | HG00140.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-11032_8-11014dup others(19): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(13): Show |
9 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0001t0001g0142others(6): Show | 9 | HG01106.hp1 HG01192.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-11033_8-11014dup others(20): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(14): Show |
4 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0003t0010g0087others(1): Show | 4 | HG02572.hp1 HG02602.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-11034_8-11014dup others(21): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0004g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8-11035_8-11014dup others(22): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(16): Show |
4 | a0001c0001t0001g0155a0001c0001t0015g0158a0001c0003t0006g0147others(1): Show | 4 | HG03491.hp1 HG03579.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-11036_8-11014dup others(23): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(17): Show |
1 | a0001c0003t0006g0149 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.8-11037_8-11014dup others(24): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0028g0197 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8-11038_8-11014dup others(25): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0005g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8-11039_8-11014dup others(26): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0151 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-11014_8-11013ins others(30): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
CT | C | 7 | a0001c0001t0001g0261a0001c0001t0003g0296a0001c0001t0008g0228others(4): Show | 7 | HG00558.hp1 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-11014delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0014t0002g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-11024_8-11014del others(11): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0052g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.8-11026_8-11014del others(13): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080283
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0131a0001c0001t0021g0139 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.8-11027_8-11014del others(14): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25080283 | |||||
| chr2:25080334
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0002g0067 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.8-10991G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080334 | ||||||
| chr2:25080443
|
C | T | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8-10882C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080443 | ||||||
| chr2:25080469
|
A | G | 3 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008 | 3 | NA18952.hp1 NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.8-10856A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080469 | ||||||
| chr2:25080483
|
C | T | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.8-10842C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080483 | ||||||
| chr2:25080530
|
G | A | 47 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.8-10795G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080530 | ||||||
| chr2:25080540
|
C | T | 45 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.8-10785C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080540 | ||||||
| chr2:25080903
|
G | A | 90 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.8-10422G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25080903 | ||||||
| chr2:25081179
|
C | T | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.8-10146C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25081179 | ||||||
| chr2:25081376
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.8-9949T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25081376 | ||||||
| chr2:25081418
|
C | T | 69 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-9907C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25081418 | ||||||
| chr2:25081705
|
A | G | 138 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.8-9620A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25081705 | ||||||
| chr2:25081718
|
C | T | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.8-9607C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25081718 | ||||||
| chr2:25081729
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.8-9596G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25081729 | ||||||
| chr2:25082037
|
C | T | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.8-9288C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082037 | ||||||
| chr2:25082174
|
C | T | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.8-9151C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082174 | ||||||
| chr2:25082187
|
T | C | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.8-9138T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082187 | ||||||
| chr2:25082267
|
C | T | 87 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0021others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.8-9058C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082267 | ||||||
| chr2:25082306
|
G | C | 2 | a0001c0003t0010g0083a0001c0003t0010g0090 | 2 | NA18968.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.8-9019G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082306 | ||||||
| chr2:25082485
|
CAACTGTT others(10): Show |
C | 1 | a0001c0002t0001g0005 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.8-8835_8-8819delGT others(15): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25082485 | |||||
| chr2:25082635
|
G | A | 137 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(134): Show | 137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.8-8690G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082635 | ||||||
| chr2:25082685
|
C | T | 1 | a0001c0001t0028g0197 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.8-8640C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082685 | ||||||
| chr2:25082708
|
C | T | 48 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.8-8617C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082708 | ||||||
| chr2:25082739
|
G | A | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.8-8586G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082739 | ||||||
| chr2:25082887
|
C | T | 87 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0021others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.8-8438C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25082887 | ||||||
| chr2:25083199
|
A | G | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-8126A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083199 | ||||||
| chr2:25083446
|
T | C | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-7879T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083446 | ||||||
| chr2:25083479
|
T | A | 1 | a0001c0002t0001g0238 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.8-7846T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083479 | ||||||
| chr2:25083544
|
G | A | 1 | a0001c0001t0015g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.8-7781G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083544 | ||||||
| chr2:25083648
|
C | T | 4 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0049g0059others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-7677C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083648 | ||||||
| chr2:25083675
|
C | T | 45 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.8-7650C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083675 | ||||||
| chr2:25083727
|
C | G | 1 | a0002c0012t0050g0281 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-7598C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083727 | ||||||
| chr2:25083900
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.8-7425G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083900 | ||||||
| chr2:25083901
|
A | C | 1 | a0001c0001t0003g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.8-7424A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083901 | ||||||
| chr2:25083902
|
C | A | 1 | a0001c0001t0003g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.8-7423C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083902 | ||||||
| chr2:25083996
|
C | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-7329C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25083996 | ||||||
| chr2:25084136
|
C | T | 89 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.8-7189C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084136 | ||||||
| chr2:25084141
|
A | G | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.8-7184A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084141 | ||||||
| chr2:25084188
|
C | T | 1 | a0001c0002t0001g0206 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8-7137C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084188 | ||||||
| chr2:25084211
|
T | A | 74 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8-7114T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084211 | ||||||
| chr2:25084221
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0004g0154a0001c0001t0030g0126 | 3 | HG03225.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.8-7104A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084221 | ||||||
| chr2:25084224
|
T | A | 2 | a0001c0002t0001g0254a0001c0002t0001g0284 | 2 | HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.8-7101T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084224 | ||||||
| chr2:25084232
|
A | T | 1 | a0001c0001t0005g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8-7093A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084232 | ||||||
| chr2:25084319
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8-7006C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084319 | ||||||
| chr2:25084326
|
T | C | 1 | a0001c0001t0003g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.8-6999T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084326 | ||||||
| chr2:25084327
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.8-6998C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084327 | ||||||
| chr2:25084338
|
G | A | 11 | a0001c0001t0002g0120a0001c0003t0006g0082a0001c0003t0006g0117others(8): Show | 11 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-6987G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084338 | ||||||
| chr2:25084351
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.8-6974C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084351 | ||||||
| chr2:25084354
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.8-6971C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084354 | ||||||
| chr2:25084431
|
G | T | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.8-6894G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084431 | ||||||
| chr2:25084459
|
G | A | 1 | a0001c0001t0007g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.8-6866G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084459 | ||||||
| chr2:25084534
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.8-6791C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084534 | ||||||
| chr2:25084613
|
C | T | 39 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(36): Show | 39 | HG00639.hp1 HG01169.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.8-6712C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25084613 | ||||||
| chr2:25085138
|
C | T | 1 | a0001c0001t0016g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.8-6187C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085138 | ||||||
| chr2:25085303
|
A | C | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8-6022A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085303 | ||||||
| chr2:25085367
|
C | T | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8-5958C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085367 | ||||||
| chr2:25085465
|
T | G | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | NA18942.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.8-5860T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085465 | ||||||
| chr2:25085487
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.8-5838C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085487 | ||||||
| chr2:25085640
|
T | G | 1 | a0001c0001t0002g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.8-5685T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085640 | ||||||
| chr2:25085692
|
T | C | 1 | a0001c0003t0018g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8-5633T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085692 | ||||||
| chr2:25085707
|
T | C | 140 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.8-5618T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25085707 | ||||||
| chr2:25086887
|
C | G | 90 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.8-4438C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25086887 | ||||||
| chr2:25086931
|
A | T | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-4394A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25086931 | ||||||
| chr2:25086932
|
A | T | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-4393A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25086932 | ||||||
| chr2:25086985
|
C | T | 47 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.8-4340C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25086985 | ||||||
| chr2:25087104
|
G | A | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-4221G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087104 | ||||||
| chr2:25087159
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.8-4166G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087159 | ||||||
| chr2:25087165
|
A | T | 6 | a0001c0001t0002g0040a0001c0001t0002g0224a0001c0001t0002g0259others(3): Show | 6 | HG00099.hp1 HG01070.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-4160A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087165 | ||||||
| chr2:25087286
|
G | T | 90 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.8-4039G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087286 | ||||||
| chr2:25087320
|
A | G | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-4005A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087320 | ||||||
| chr2:25087361
|
G | GTA | 12 | a0001c0001t0002g0120a0001c0002t0011g0042a0001c0003t0006g0082others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-3947_8-3946dupTA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25087361 | |||||
| chr2:25087361
|
GTA | G | 180 | a0001c0001t0001g0132a0001c0001t0001g0186a0001c0001t0001g0187others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.8-3947_8-3946delTA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25087361 | |||||
| chr2:25087378
|
T | C | 89 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0021others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.8-3947T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087378 | ||||||
| chr2:25087462
|
G | A | 43 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-3863G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087462 | ||||||
| chr2:25087464
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-3861C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087464 | ||||||
| chr2:25087482
|
A | AT | 85 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(82): Show | 85 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.8-3828dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25087482 | |||||
| chr2:25087500
|
G | T | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-3825G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087500 | ||||||
| chr2:25087511
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0004g0129others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3814G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087511 | ||||||
| chr2:25087613
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-3712C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087613 | ||||||
| chr2:25087762
|
C | T | 2 | a0001c0001t0004g0154a0001c0001t0030g0126 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.8-3563C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087762 | ||||||
| chr2:25087811
|
A | G | 1 | a0001c0001t0002g0278 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.8-3514A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087811 | ||||||
| chr2:25087853
|
TAAG | T | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.8-3468_8-3466delAA others(1): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25087853 | |||||
| chr2:25087991
|
A | T | 182 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.8-3334A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25087991 | ||||||
| chr2:25088129
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.8-3196G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25088129 | ||||||
| chr2:25088668
|
A | C | 184 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(181): Show | 184 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.8-2657A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25088668 | ||||||
| chr2:25088744
|
A | G | 43 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(40): Show | 43 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.8-2581A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25088744 | ||||||
| chr2:25088979
|
G | A | 2 | a0001c0001t0019g0123a0001c0001t0019g0124 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8-2346G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25088979 | ||||||
| chr2:25088984
|
C | G | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-2341C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25088984 | ||||||
| chr2:25088992
|
C | T | 7 | a0001c0003t0006g0144a0001c0003t0006g0145a0001c0003t0006g0146others(4): Show | 7 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-2333C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25088992 | ||||||
| chr2:25089138
|
G | A | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.8-2187G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089138 | ||||||
| chr2:25089402
|
A | G | 92 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(89): Show | 92 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.8-1923A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089402 | ||||||
| chr2:25089452
|
T | A | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-1873T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089452 | ||||||
| chr2:25089453
|
C | A | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-1872C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089453 | ||||||
| chr2:25089455
|
T | C | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-1870T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089455 | ||||||
| chr2:25089483
|
T | G | 43 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(40): Show | 43 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.8-1842T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089483 | ||||||
| chr2:25089578
|
C | T | 1 | a0001c0003t0006g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8-1747C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089578 | ||||||
| chr2:25089579
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.8-1746G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089579 | ||||||
| chr2:25089836
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0004g0154a0001c0001t0030g0126 | 3 | HG03225.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.8-1489G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25089836 | ||||||
| chr2:25090025
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.8-1300C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090025 | ||||||
| chr2:25090132
|
C | G | 236 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(233): Show | 236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.8-1193C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090132 | ||||||
| chr2:25090133
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.8-1192G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090133 | ||||||
| chr2:25090152
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.8-1173T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090152 | ||||||
| chr2:25090284
|
G | T | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-1041G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090284 | ||||||
| chr2:25090502
|
G | C | 1 | a0001c0001t0003g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.8-823G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090502 | ||||||
| chr2:25090510
|
T | A | 1 | a0001c0001t0003g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.8-815T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090510 | ||||||
| chr2:25090676
|
G | A | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.8-649G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090676 | ||||||
| chr2:25090703
|
C | T | 1 | a0001c0001t0003g0111 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.8-622C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090703 | ||||||
| chr2:25090777
|
G | A | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8-548G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090777 | ||||||
| chr2:25090783
|
G | A | 2 | a0001c0001t0002g0264a0001c0001t0002g0302 | 2 | HG01255.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.8-542G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090783 | ||||||
| chr2:25090823
|
A | G | 1 | a0001c0002t0035g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.8-502A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090823 | ||||||
| chr2:25090922
|
T | G | 3 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0036 | 3 | HG00735.hp2 HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.8-403T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25090922 | ||||||
| chr2:25091062
|
C | A | 11 | a0001c0001t0002g0120a0001c0003t0006g0082a0001c0003t0006g0117others(8): Show | 11 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-263C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25091062 | ||||||
| chr2:25091119
|
T | TG | 43 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(40): Show | 43 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.8-204dupG | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 25091119 | |||||
| chr2:25091187
|
G | A | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0002t0011g0253 | 3 | NA18942.hp1 NA18991.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.8-138G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25091187 | ||||||
| chr2:25091317
|
T | C | 183 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(180): Show | 183 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(180): Show |
splice_region_variant&intron_variant | LOW | c.8-8T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 1/22 | chr2 | 25091317 | ||||||
| chr2:25091442
|
C | G | 1 | a0001c0001t0002g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.84+41C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25091442 | ||||||
| chr2:25091626
|
G | A | 2 | a0001c0001t0016g0182a0001c0001t0017g0181 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.84+225G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25091626 | ||||||
| chr2:25091630
|
C | A | 5 | a0001c0002t0001g0061a0001c0002t0004g0063a0001c0002t0004g0064others(2): Show | 5 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+229C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25091630 | ||||||
| chr2:25091877
|
C | T | 25 | a0001c0001t0002g0021a0001c0001t0002g0249a0001c0001t0002g0250others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.84+476C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25091877 | ||||||
| chr2:25091889
|
T | C | 92 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(89): Show | 92 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.84+488T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25091889 | ||||||
| chr2:25091909
|
C | T | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.84+508C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25091909 | ||||||
| chr2:25091975
|
G | A | 5 | a0001c0002t0001g0061a0001c0002t0004g0063a0001c0002t0004g0064others(2): Show | 5 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+574G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25091975 | ||||||
| chr2:25092045
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0004g0154a0001c0001t0022g0178others(2): Show | 5 | HG00733.hp2 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+644C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092045 | ||||||
| chr2:25092092
|
C | T | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.84+691C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092092 | ||||||
| chr2:25092364
|
G | A | 6 | a0001c0002t0001g0031a0001c0002t0001g0053a0001c0002t0001g0233others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-639G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092364 | ||||||
| chr2:25092365
|
G | C | 1 | a0001c0004t0002g0056 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.85-638G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092365 | ||||||
| chr2:25092403
|
TAC | T | 49 | a0001c0001t0002g0278a0001c0001t0003g0069a0001c0001t0003g0072others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.85-581_85-580delAC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 25092403 | |||||
| chr2:25092421
|
C | CTT | 46 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0040others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.85-582_85-581insTT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092421 | ||||||
| chr2:25092422
|
A | T | 43 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(40): Show | 43 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.85-581A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092422 | ||||||
| chr2:25092423
|
C | T | 43 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(40): Show | 43 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.85-580C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092423 | ||||||
| chr2:25092424
|
T | A | 90 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.85-579T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092424 | ||||||
| chr2:25092425
|
T | C | 90 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.85-578T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092425 | ||||||
| chr2:25092425
|
T | TAC | 3 | a0001c0002t0001g0246a0001c0002t0004g0048a0001c0010t0005g0163 | 3 | HG01884.hp1 HG02080.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.85-561_85-560dupAC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 25092425 | |||||
| chr2:25092443
|
C | CACAT | 39 | a0001c0001t0001g0261a0001c0001t0002g0021a0001c0001t0002g0026others(36): Show | 39 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.85-560_85-559insAC others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092443 | ||||||
| chr2:25092443
|
C | CAT | 96 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(93): Show | 96 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.85-560_85-559insAT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092443 | ||||||
| chr2:25092443
|
C | T | 49 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0040others(46): Show | 49 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.85-560C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092443 | ||||||
| chr2:25092572
|
G | A | 6 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0036others(3): Show | 6 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-431G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092572 | ||||||
| chr2:25092642
|
G | A | 89 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.85-361G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092642 | ||||||
| chr2:25092690
|
A | G | 1 | a0001c0001t0016g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.85-313A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092690 | ||||||
| chr2:25092923
|
C | T | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85-80C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092923 | ||||||
| chr2:25092958
|
A | AGCCATAG others(4): Show |
3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85-36_85-35insAGGC others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 25092958 | |||||
| chr2:25092968
|
T | A | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85-35T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 2/22 | chr2 | 25092968 | ||||||
| chr2:25093176
|
T | C | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.212+46T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093176 | ||||||
| chr2:25093270
|
G | A | 1 | a0001c0003t0006g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.212+140G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093270 | ||||||
| chr2:25093467
|
A | C | 182 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.212+337A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093467 | ||||||
| chr2:25093715
|
C | A | 89 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.212+585C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093715 | ||||||
| chr2:25093748
|
A | G | 7 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0134others(4): Show | 7 | HG01074.hp2 HG01109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.212+618A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093748 | ||||||
| chr2:25093799
|
G | A | 1 | a0005c0013t0044g0297 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.212+669G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093799 | ||||||
| chr2:25093820
|
G | A | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.212+690G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093820 | ||||||
| chr2:25093868
|
G | A | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.212+738G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25093868 | ||||||
| chr2:25094013
|
A | G | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.212+883A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094013 | ||||||
| chr2:25094052
|
T | C | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.212+922T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094052 | ||||||
| chr2:25094146
|
G | A | 1 | a0005c0013t0044g0297 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.212+1016G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094146 | ||||||
| chr2:25094282
|
C | CA | 167 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0164others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.212+1171dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25094282 | |||||
| chr2:25094282
|
C | CAA | 16 | a0001c0001t0004g0154a0001c0001t0004g0269a0001c0001t0030g0126others(13): Show | 16 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.212+1170_212+1171d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25094282 | |||||
| chr2:25094282
|
C | CAAA | 27 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(24): Show | 27 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.212+1169_212+1171d others(5): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25094282 | |||||
| chr2:25094282
|
C | CAAAA | 42 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.212+1168_212+1171d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25094282 | |||||
| chr2:25094282
|
C | CAAAAA | 11 | a0001c0001t0001g0188a0001c0001t0003g0074a0001c0001t0003g0111others(8): Show | 11 | HG01243.hp2 HG02135.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.212+1167_212+1171d others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25094282 | |||||
| chr2:25094282
|
C | CAAAAAA | 31 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(28): Show | 31 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.212+1166_212+1171d others(8): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25094282 | |||||
| chr2:25094282
|
C | CAAAAAAA | 7 | a0001c0001t0001g0186a0001c0001t0005g0195a0001c0001t0005g0201others(4): Show | 7 | HG01884.hp1 HG02738.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.212+1165_212+1171d others(9): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25094282 | |||||
| chr2:25094332
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0162 | 3 | HG02895.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.212+1202G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094332 | ||||||
| chr2:25094504
|
A | T | 91 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(88): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.212+1374A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094504 | ||||||
| chr2:25094507
|
A | G | 4 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0004g0129others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+1377A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094507 | ||||||
| chr2:25094784
|
C | T | 180 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.212+1654C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094784 | ||||||
| chr2:25094797
|
A | T | 1 | a0001c0002t0001g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.212+1667A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094797 | ||||||
| chr2:25094800
|
A | T | 39 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(36): Show | 39 | HG00639.hp1 HG01169.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.212+1670A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094800 | ||||||
| chr2:25094936
|
A | G | 1 | a0001c0002t0052g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.212+1806A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094936 | ||||||
| chr2:25094972
|
G | A | 1 | a0001c0002t0001g0241 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.212+1842G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25094972 | ||||||
| chr2:25095005
|
G | T | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.212+1875G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25095005 | ||||||
| chr2:25095133
|
G | A | 1 | a0001c0003t0018g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.212+2003G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25095133 | ||||||
| chr2:25095144
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.212+2014T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25095144 | ||||||
| chr2:25095190
|
A | G | 182 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.212+2060A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25095190 | ||||||
| chr2:25095467
|
G | A | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.212+2337G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25095467 | ||||||
| chr2:25095653
|
G | A | 138 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.212+2523G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25095653 | ||||||
| chr2:25095803
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.212+2673C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25095803 | ||||||
| chr2:25096021
|
G | C | 1 | a0001c0002t0001g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.212+2891G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096021 | ||||||
| chr2:25096023
|
C | CT | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.212+2903dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25096023 | |||||
| chr2:25096030
|
T | C | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212+2900T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096030 | ||||||
| chr2:25096165
|
G | A | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.212+3035G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096165 | ||||||
| chr2:25096303
|
C | T | 1 | a0001c0001t0016g0150 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.212+3173C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096303 | ||||||
| chr2:25096321
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.212+3191A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096321 | ||||||
| chr2:25096405
|
G | C | 3 | a0001c0002t0001g0222a0001c0002t0001g0286a0001c0002t0001g0289 | 3 | HG00323.hp2 HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.212+3275G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096405 | ||||||
| chr2:25096472
|
A | G | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.212+3342A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096472 | ||||||
| chr2:25096601
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.212+3471C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096601 | ||||||
| chr2:25096602
|
G | A | 89 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.212+3472G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096602 | ||||||
| chr2:25096699
|
A | G | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.212+3569A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096699 | ||||||
| chr2:25096710
|
T | G | 1 | a0001c0001t0008g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.212+3580T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096710 | ||||||
| chr2:25096772
|
G | A | 6 | a0001c0001t0001g0261a0001c0003t0006g0230a0001c0003t0006g0262others(3): Show | 6 | HG00639.hp2 HG00738.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.212+3642G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096772 | ||||||
| chr2:25096911
|
C | T | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.212+3781C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25096911 | ||||||
| chr2:25097010
|
A | G | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.212+3880A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097010 | ||||||
| chr2:25097131
|
T | A | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212+4001T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097131 | ||||||
| chr2:25097168
|
C | T | 3 | a0001c0002t0001g0053a0001c0002t0001g0233a0001c0002t0025g0049 | 3 | HG01257.hp2 HG01258.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.212+4038C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097168 | ||||||
| chr2:25097225
|
G | A | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.212+4095G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097225 | ||||||
| chr2:25097270
|
C | G | 1 | a0001c0003t0010g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.212+4140C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097270 | ||||||
| chr2:25097278
|
T | C | 3 | a0001c0003t0006g0147a0001c0003t0006g0148a0001c0003t0006g0149 | 3 | HG03491.hp1 HG03492.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.212+4148T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097278 | ||||||
| chr2:25097308
|
C | A | 2 | a0001c0001t0004g0154a0001c0001t0030g0126 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.212+4178C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097308 | ||||||
| chr2:25097390
|
G | T | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.212+4260G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097390 | ||||||
| chr2:25097781
|
A | G | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.212+4651A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097781 | ||||||
| chr2:25097794
|
G | A | 1 | a0001c0003t0006g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.212+4664G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097794 | ||||||
| chr2:25097844
|
C | T | 3 | a0001c0001t0003g0069a0001c0001t0003g0108a0001c0001t0003g0110 | 3 | HG00597.hp2 HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.212+4714C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25097844 | ||||||
| chr2:25098068
|
G | A | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.212+4938G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25098068 | ||||||
| chr2:25098096
|
G | A | 1 | a0001c0002t0005g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.212+4966G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25098096 | ||||||
| chr2:25098201
|
G | A | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212+5071G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25098201 | ||||||
| chr2:25098553
|
C | T | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.213-5084C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25098553 | ||||||
| chr2:25098610
|
A | G | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.213-5027A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25098610 | ||||||
| chr2:25098831
|
A | AT | 86 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.213-4780dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25098831 | |||||
| chr2:25098831
|
A | ATT | 11 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0162others(8): Show | 11 | HG00733.hp2 HG01884.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.213-4781_213-4780d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25098831 | |||||
| chr2:25098831
|
A | T | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213-4806A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25098831 | ||||||
| chr2:25098831
|
AT | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0051a0001c0001t0002g0264others(7): Show | 10 | HG01255.hp1 HG01346.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.213-4780delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25098831 | |||||
| chr2:25098831
|
ATTTTTTT others(4): Show |
A | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.213-4790_213-4780d others(13): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25098831 | |||||
| chr2:25098863
|
G | A | 6 | a0001c0001t0001g0261a0001c0003t0006g0230a0001c0003t0006g0262others(3): Show | 6 | HG00639.hp2 HG00738.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-4774G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25098863 | ||||||
| chr2:25098899
|
A | AT | 140 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.213-4732dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25098899 | |||||
| chr2:25099230
|
A | C | 1 | a0001c0003t0006g0256 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.213-4407A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25099230 | ||||||
| chr2:25099391
|
G | T | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.213-4246G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25099391 | ||||||
| chr2:25099523
|
G | A | 1 | a0001c0002t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.213-4114G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25099523 | ||||||
| chr2:25099777
|
G | T | 1 | a0001c0002t0005g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.213-3860G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25099777 | ||||||
| chr2:25099844
|
T | C | 40 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(37): Show | 40 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.213-3793T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25099844 | ||||||
| chr2:25099870
|
TA | T | 129 | a0001c0001t0001g0142a0001c0001t0001g0162a0001c0001t0001g0172others(126): Show | 129 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.213-3750delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25099870 | |||||
| chr2:25099898
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213-3739A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25099898 | ||||||
| chr2:25099957
|
A | G | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.213-3680A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25099957 | ||||||
| chr2:25100214
|
A | T | 78 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(75): Show | 78 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.213-3423A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100214 | ||||||
| chr2:25100215
|
T | A | 6 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-3422T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100215 | ||||||
| chr2:25100223
|
T | A | 2 | a0001c0005t0014g0212a0001c0005t0014g0214 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.213-3414T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100223 | ||||||
| chr2:25100402
|
C | A | 1 | a0001c0003t0009g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.213-3235C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100402 | ||||||
| chr2:25100535
|
C | T | 1 | a0002c0012t0050g0281 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.213-3102C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100535 | ||||||
| chr2:25100594
|
A | T | 4 | a0001c0001t0005g0174a0001c0001t0005g0185a0001c0001t0005g0195others(1): Show | 4 | HG01169.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-3043A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100594 | ||||||
| chr2:25100739
|
G | A | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.213-2898G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100739 | ||||||
| chr2:25100788
|
G | A | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.213-2849G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100788 | ||||||
| chr2:25100822
|
C | T | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213-2815C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100822 | ||||||
| chr2:25100838
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.213-2799G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100838 | ||||||
| chr2:25100878
|
G | A | 48 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.213-2759G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25100878 | ||||||
| chr2:25101354
|
G | A | 1 | a0001c0008t0018g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.213-2283G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25101354 | ||||||
| chr2:25101359
|
T | C | 91 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(88): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.213-2278T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25101359 | ||||||
| chr2:25101431
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.213-2206C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25101431 | ||||||
| chr2:25101616
|
G | A | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213-2021G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25101616 | ||||||
| chr2:25101695
|
C | T | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.213-1942C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25101695 | ||||||
| chr2:25101839
|
AAAG | A | 76 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(73): Show | 76 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.213-1796_213-1794d others(5): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25101839 | |||||
| chr2:25102160
|
A | C | 1 | a0001c0001t0015g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213-1477A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25102160 | ||||||
| chr2:25102407
|
G | T | 1 | a0001c0002t0001g0002 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.213-1230G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25102407 | ||||||
| chr2:25102469
|
G | A | 5 | a0001c0002t0001g0061a0001c0002t0004g0063a0001c0002t0004g0064others(2): Show | 5 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.213-1168G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25102469 | ||||||
| chr2:25102575
|
C | T | 76 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(73): Show | 76 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.213-1062C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25102575 | ||||||
| chr2:25102621
|
G | GC | 11 | a0001c0001t0005g0174a0001c0001t0005g0185a0001c0001t0005g0192others(8): Show | 11 | HG01169.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.213-1010dupC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 25102621 | |||||
| chr2:25102626
|
C | G | 1 | a0001c0001t0003g0166 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.213-1011C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25102626 | ||||||
| chr2:25102934
|
A | G | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.213-703A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25102934 | ||||||
| chr2:25103343
|
T | C | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.213-294T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25103343 | ||||||
| chr2:25103378
|
G | A | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213-259G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25103378 | ||||||
| chr2:25103435
|
C | G | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0076 | 3 | NA18986.hp1 NA19060.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.213-202C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25103435 | ||||||
| chr2:25103449
|
T | A | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.213-188T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25103449 | ||||||
| chr2:25103501
|
C | T | 3 | a0001c0001t0003g0069a0001c0001t0003g0108a0001c0001t0003g0110 | 3 | HG00597.hp2 HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.213-136C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 3/22 | chr2 | 25103501 | ||||||
| chr2:25103825
|
G | A | 2 | a0001c0001t0002g0259a0001c0001t0002g0282 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.363+38G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25103825 | ||||||
| chr2:25103861
|
G | T | 1 | a0001c0002t0004g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.363+74G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25103861 | ||||||
| chr2:25103892
|
G | C | 1 | a0001c0002t0004g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.363+105G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25103892 | ||||||
| chr2:25104038
|
T | C | 1 | a0001c0001t0046g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.363+251T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104038 | ||||||
| chr2:25104061
|
G | T | 1 | a0001c0002t0033g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.363+274G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104061 | ||||||
| chr2:25104134
|
G | C | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.363+347G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104134 | ||||||
| chr2:25104182
|
T | G | 1 | a0001c0001t0005g0195 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.363+395T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104182 | ||||||
| chr2:25104213
|
A | G | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.363+426A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104213 | ||||||
| chr2:25104612
|
A | G | 1 | a0001c0002t0001g0280 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.363+825A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104612 | ||||||
| chr2:25104718
|
C | T | 1 | a0001c0001t0015g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+931C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104718 | ||||||
| chr2:25104776
|
T | C | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.363+989T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104776 | ||||||
| chr2:25104794
|
T | A | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.363+1007T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104794 | ||||||
| chr2:25104902
|
A | C | 39 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(36): Show | 39 | HG00639.hp1 HG01169.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.363+1115A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104902 | ||||||
| chr2:25104981
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.363+1194A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25104981 | ||||||
| chr2:25105340
|
G | A | 57 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.363+1553G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25105340 | ||||||
| chr2:25105431
|
G | A | 1 | a0001c0002t0037g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.363+1644G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25105431 | ||||||
| chr2:25105443
|
G | A | 50 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.363+1656G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25105443 | ||||||
| chr2:25105834
|
C | T | 168 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.363+2047C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25105834 | ||||||
| chr2:25106147
|
C | T | 77 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(74): Show | 77 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.363+2360C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106147 | ||||||
| chr2:25106211
|
T | C | 1 | a0001c0001t0008g0107 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.363+2424T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106211 | ||||||
| chr2:25106253
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.363+2466C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106253 | ||||||
| chr2:25106403
|
C | T | 77 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(74): Show | 77 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.363+2616C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106403 | ||||||
| chr2:25106404
|
T | C | 2 | a0001c0001t0001g0136a0001c0003t0006g0082 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.363+2617T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106404 | ||||||
| chr2:25106456
|
A | AT | 71 | a0001c0001t0001g0143a0001c0001t0001g0172a0001c0001t0001g0261others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.363+2688dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25106456 | |||||
| chr2:25106456
|
AT | A | 117 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0134others(114): Show | 117 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.363+2688delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25106456 | |||||
| chr2:25106560
|
T | A | 1 | a0002c0012t0050g0281 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.363+2773T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106560 | ||||||
| chr2:25106671
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0049g0059 | 2 | HG00140.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.363+2884G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106671 | ||||||
| chr2:25106863
|
T | C | 70 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0026others(67): Show | 70 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.363+3076T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25106863 | ||||||
| chr2:25107029
|
T | C | 70 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0026others(67): Show | 70 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.363+3242T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25107029 | ||||||
| chr2:25107056
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0043 | 2 | HG00673.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.363+3269C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25107056 | ||||||
| chr2:25107180
|
T | C | 2 | a0001c0001t0049g0059a0001c0002t0001g0247 | 2 | HG01361.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.363+3393T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25107180 | ||||||
| chr2:25107233
|
A | T | 305 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.363+3446A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25107233 | ||||||
| chr2:25107809
|
C | CT | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.363+4036dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25107809 | |||||
| chr2:25107809
|
CT | C | 79 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.363+4036delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25107809 | |||||
| chr2:25107868
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.363+4081G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25107868 | ||||||
| chr2:25107918
|
G | A | 1 | a0001c0001t0005g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.363+4131G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25107918 | ||||||
| chr2:25108248
|
C | T | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0051g0125 | 3 | HG01243.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.363+4461C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25108248 | ||||||
| chr2:25108265
|
T | G | 1 | a0001c0001t0023g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363+4478T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25108265 | ||||||
| chr2:25108303
|
A | G | 182 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.363+4516A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25108303 | ||||||
| chr2:25108658
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0162 | 3 | HG02895.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+4871G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25108658 | ||||||
| chr2:25108728
|
G | A | 49 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.363+4941G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25108728 | ||||||
| chr2:25108803
|
A | G | 1 | a0001c0003t0006g0262 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.363+5016A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25108803 | ||||||
| chr2:25108807
|
T | TGGCCAAC others(13): Show |
7 | a0001c0003t0006g0144a0001c0003t0006g0145a0001c0003t0006g0146others(4): Show | 7 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+5021_363+5040d others(22): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25108807 | |||||
| chr2:25108830
|
C | T | 1 | a0001c0001t0047g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.363+5043C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25108830 | ||||||
| chr2:25109172
|
C | CA | 42 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(39): Show | 42 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.363+5396dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25109172 | |||||
| chr2:25109172
|
CA | C | 77 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(74): Show | 77 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.363+5396delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25109172 | |||||
| chr2:25109175
|
A | C | 1 | a0001c0001t0012g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.363+5388A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25109175 | ||||||
| chr2:25109516
|
G | A | 8 | a0001c0002t0001g0175a0001c0002t0001g0177a0001c0002t0001g0179others(5): Show | 8 | HG01934.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+5729G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25109516 | ||||||
| chr2:25109584
|
C | T | 1 | a0001c0001t0007g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.363+5797C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25109584 | ||||||
| chr2:25109642
|
C | T | 1 | a0001c0009t0011g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.363+5855C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25109642 | ||||||
| chr2:25109827
|
C | T | 89 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.363+6040C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25109827 | ||||||
| chr2:25109997
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.363+6210G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25109997 | ||||||
| chr2:25109997
|
G | C | 6 | a0001c0001t0003g0079a0001c0002t0001g0298a0001c0002t0001g0299others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+6210G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25109997 | ||||||
| chr2:25110048
|
C | G | 1 | a0001c0003t0006g0256 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.363+6261C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110048 | ||||||
| chr2:25110236
|
A | C | 71 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.363+6449A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110236 | ||||||
| chr2:25110336
|
C | G | 45 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(42): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.363+6549C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110336 | ||||||
| chr2:25110597
|
C | T | 1 | a0001c0002t0004g0243 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.363+6810C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110597 | ||||||
| chr2:25110632
|
A | G | 3 | a0001c0001t0003g0077a0001c0001t0003g0085a0001c0001t0008g0098 | 3 | HG02165.hp1 HG02523.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.363+6845A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110632 | ||||||
| chr2:25110709
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0162 | 3 | HG02895.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+6922G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110709 | ||||||
| chr2:25110781
|
AAT | A | 3 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008 | 3 | NA18952.hp1 NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.363+6997_363+6998d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25110781 | |||||
| chr2:25110839
|
T | C | 1 | a0001c0001t0007g0038 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.363+7052T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110839 | ||||||
| chr2:25110866
|
T | C | 91 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.363+7079T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110866 | ||||||
| chr2:25110960
|
G | A | 1 | a0001c0002t0037g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.363+7173G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25110960 | ||||||
| chr2:25111010
|
T | A | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+7223T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111010 | ||||||
| chr2:25111240
|
T | C | 11 | a0001c0001t0005g0174a0001c0001t0005g0185a0001c0001t0005g0192others(8): Show | 11 | HG01169.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+7453T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111240 | ||||||
| chr2:25111324
|
G | A | 44 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(41): Show | 44 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.363+7537G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111324 | ||||||
| chr2:25111380
|
C | CGTGCCCA others(328): Show |
2 | a0001c0001t0003g0100a0001c0001t0003g0265 | 2 | HG01192.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.363+7606_363+7607i others(337): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25111380 | |||||
| chr2:25111380
|
C | CGTGCCCA others(329): Show |
3 | a0001c0001t0003g0104a0001c0001t0003g0118a0001c0001t0040g0103 | 3 | HG01243.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.363+7606_363+7607i others(338): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25111380 | |||||
| chr2:25111404
|
C | T | 1 | a0001c0003t0006g0256 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.363+7617C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111404 | ||||||
| chr2:25111413
|
C | A | 69 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.363+7626C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111413 | ||||||
| chr2:25111471
|
C | T | 91 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.363+7684C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111471 | ||||||
| chr2:25111574
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0162 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.363+7787C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111574 | ||||||
| chr2:25111937
|
C | G | 1 | a0001c0002t0004g0273 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.363+8150C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25111937 | ||||||
| chr2:25112187
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.363+8400C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112187 | ||||||
| chr2:25112220
|
G | A | 90 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.363+8433G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112220 | ||||||
| chr2:25112264
|
G | C | 2 | a0001c0001t0016g0182a0001c0001t0017g0181 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.363+8477G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112264 | ||||||
| chr2:25112623
|
T | C | 92 | a0001c0001t0001g0127a0001c0001t0001g0186a0001c0001t0001g0187others(89): Show | 92 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.363+8836T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112623 | ||||||
| chr2:25112643
|
G | A | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.363+8856G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112643 | ||||||
| chr2:25112706
|
G | C | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.363+8919G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112706 | ||||||
| chr2:25112967
|
A | G | 1 | a0001c0001t0015g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.364-8706A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112967 | ||||||
| chr2:25112983
|
GC | G | 59 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.364-8689delC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25112983 | ||||||
| chr2:25113118
|
A | C | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.364-8555A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113118 | ||||||
| chr2:25113253
|
A | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0134others(4): Show | 7 | HG01074.hp2 HG01109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-8420A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113253 | ||||||
| chr2:25113408
|
G | A | 77 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(74): Show | 77 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.364-8265G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113408 | ||||||
| chr2:25113414
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.364-8259G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113414 | ||||||
| chr2:25113486
|
G | T | 1 | a0001c0001t0003g0111 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.364-8187G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113486 | ||||||
| chr2:25113564
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.364-8109A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113564 | ||||||
| chr2:25113592
|
T | A | 8 | a0001c0001t0001g0172a0001c0001t0029g0171a0001c0002t0004g0168others(5): Show | 8 | HG01496.hp2 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-8081T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113592 | ||||||
| chr2:25113599
|
T | C | 91 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(88): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.364-8074T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113599 | ||||||
| chr2:25113667
|
CAAAAA | C | 77 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(74): Show | 77 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.364-7995_364-7991d others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25113667 | |||||
| chr2:25113679
|
A | G | 91 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(88): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.364-7994A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113679 | ||||||
| chr2:25113698
|
A | G | 1 | a0001c0001t0002g0271 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.364-7975A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25113698 | ||||||
| chr2:25114126
|
T | C | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.364-7547T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25114126 | ||||||
| chr2:25114286
|
C | T | 16 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0136others(13): Show | 16 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-7387C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25114286 | ||||||
| chr2:25114287
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.364-7386G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25114287 | ||||||
| chr2:25114327
|
G | A | 1 | a0001c0002t0036g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.364-7346G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25114327 | ||||||
| chr2:25114399
|
G | T | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.364-7274G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25114399 | ||||||
| chr2:25114477
|
G | A | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.364-7196G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25114477 | ||||||
| chr2:25115184
|
G | A | 126 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(123): Show | 126 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.364-6489G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25115184 | ||||||
| chr2:25115316
|
A | G | 3 | a0001c0001t0016g0150a0001c0001t0016g0153a0001c0001t0017g0152 | 3 | HG02572.hp2 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364-6357A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25115316 | ||||||
| chr2:25115601
|
A | G | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.364-6072A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25115601 | ||||||
| chr2:25116087
|
G | A | 1 | a0001c0001t0012g0071 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.364-5586G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116087 | ||||||
| chr2:25116220
|
A | G | 1 | a0001c0002t0001g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.364-5453A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116220 | ||||||
| chr2:25116221
|
T | C | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-5452T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116221 | ||||||
| chr2:25116452
|
C | T | 1 | a0001c0002t0002g0041 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.364-5221C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116452 | ||||||
| chr2:25116488
|
G | A | 1 | a0001c0002t0004g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.364-5185G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116488 | ||||||
| chr2:25116536
|
AT | A | 78 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(75): Show | 78 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.364-5135delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25116536 | |||||
| chr2:25116633
|
T | A | 1 | a0001c0001t0013g0022 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.364-5040T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116633 | ||||||
| chr2:25116646
|
G | T | 1 | a0001c0001t0007g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.364-5027G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116646 | ||||||
| chr2:25116745
|
T | C | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.364-4928T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116745 | ||||||
| chr2:25116770
|
G | A | 3 | a0001c0001t0003g0079a0001c0015t0008g0078a0003c0011t0045g0272 | 3 | NA18747.hp1 NA18960.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.364-4903G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116770 | ||||||
| chr2:25116789
|
G | A | 77 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(74): Show | 77 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.364-4884G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116789 | ||||||
| chr2:25116864
|
G | A | 5 | a0001c0001t0003g0100a0001c0001t0003g0104a0001c0001t0003g0118others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-4809G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116864 | ||||||
| chr2:25116881
|
G | A | 1 | a0001c0009t0011g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.364-4792G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25116881 | ||||||
| chr2:25117138
|
C | T | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.364-4535C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25117138 | ||||||
| chr2:25117330
|
C | T | 2 | a0001c0001t0002g0120a0001c0003t0006g0117 | 2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.364-4343C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25117330 | ||||||
| chr2:25117516
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.364-4157G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25117516 | ||||||
| chr2:25117679
|
T | C | 1 | a0001c0004t0002g0056 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.364-3994T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25117679 | ||||||
| chr2:25117707
|
C | T | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-3966C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25117707 | ||||||
| chr2:25117741
|
A | G | 141 | a0001c0001t0001g0219a0001c0001t0001g0261a0001c0001t0002g0001others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.364-3932A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25117741 | ||||||
| chr2:25117902
|
A | G | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-3771A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25117902 | ||||||
| chr2:25118018
|
C | T | 2 | a0001c0001t0003g0265a0001c0002t0036g0033 | 2 | HG01192.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.364-3655C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25118018 | ||||||
| chr2:25118041
|
G | A | 1 | a0001c0002t0001g0260 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.364-3632G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25118041 | ||||||
| chr2:25118104
|
C | T | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.364-3569C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25118104 | ||||||
| chr2:25118132
|
G | A | 127 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(124): Show | 127 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.364-3541G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25118132 | ||||||
| chr2:25118167
|
G | T | 1 | a0001c0003t0006g0256 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.364-3506G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25118167 | ||||||
| chr2:25118726
|
C | CA | 21 | a0001c0001t0001g0136a0001c0001t0002g0028a0001c0001t0002g0051others(18): Show | 21 | HG00735.hp2 HG01952.hp1 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-2915dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
C | CAA | 12 | a0001c0001t0001g0172a0001c0002t0001g0177a0001c0002t0001g0202others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-2916_364-2915d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
C | CAAA | 30 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0156others(27): Show | 30 | HG01070.hp1 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.364-2917_364-2915d others(5): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
C | CAAAA | 27 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0140others(24): Show | 27 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.364-2918_364-2915d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
C | CAAAAA | 7 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0151others(4): Show | 7 | HG00438.hp2 HG00741.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-2919_364-2915d others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
CA | C | 64 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(61): Show | 64 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.364-2915delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
CAAAA | C | 13 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.364-2918_364-2915d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
CAAAAA | C | 34 | a0001c0001t0002g0294a0001c0001t0003g0074a0001c0001t0003g0076others(31): Show | 34 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.364-2919_364-2915d others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.364-2925_364-2915d others(13): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0005g0174a0001c0001t0005g0209 | 2 | HG01169.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.364-2927_364-2915d others(15): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0002t0052g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.364-2930_364-2915d others(18): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118726
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0002t0001g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.364-2931_364-2915d others(19): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25118726 | |||||
| chr2:25118868
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-2805G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25118868 | ||||||
| chr2:25118969
|
A | G | 56 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0040others(53): Show | 56 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.364-2704A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25118969 | ||||||
| chr2:25119008
|
A | C | 1 | a0001c0003t0006g0274 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.364-2665A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119008 | ||||||
| chr2:25119022
|
T | C | 4 | a0001c0001t0003g0095a0001c0001t0008g0094a0001c0001t0041g0096others(1): Show | 4 | NA18999.hp1 NA19002.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-2651T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119022 | ||||||
| chr2:25119056
|
T | C | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-2617T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119056 | ||||||
| chr2:25119160
|
G | A | 1 | a0001c0001t0012g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.364-2513G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119160 | ||||||
| chr2:25119392
|
T | C | 1 | a0001c0001t0003g0265 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.364-2281T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119392 | ||||||
| chr2:25119441
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.364-2232G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119441 | ||||||
| chr2:25119560
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.364-2113G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119560 | ||||||
| chr2:25119593
|
C | T | 2 | a0001c0001t0022g0178a0001c0001t0023g0204 | 2 | HG00733.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.364-2080C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119593 | ||||||
| chr2:25119893
|
G | A | 3 | a0001c0001t0013g0011a0001c0001t0013g0024a0001c0001t0051g0125 | 3 | HG01243.hp1 NA18940.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.364-1780G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119893 | ||||||
| chr2:25119926
|
C | G | 2 | a0001c0002t0001g0047a0001c0002t0004g0048 | 2 | HG01081.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.364-1747C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119926 | ||||||
| chr2:25119951
|
G | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0043 | 2 | HG00673.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.364-1722G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25119951 | ||||||
| chr2:25120045
|
A | G | 102 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(99): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.364-1628A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120045 | ||||||
| chr2:25120191
|
C | CA | 80 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(77): Show | 80 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.364-1472dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25120191 | |||||
| chr2:25120256
|
C | T | 84 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(81): Show | 84 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.364-1417C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120256 | ||||||
| chr2:25120310
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.364-1363C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120310 | ||||||
| chr2:25120350
|
C | CA | 88 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(85): Show | 88 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.364-1314dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25120350 | |||||
| chr2:25120381
|
C | G | 1 | a0001c0003t0009g0263 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.364-1292C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120381 | ||||||
| chr2:25120505
|
A | G | 134 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(131): Show | 134 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.364-1168A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120505 | ||||||
| chr2:25120599
|
G | A | 134 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(131): Show | 134 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.364-1074G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120599 | ||||||
| chr2:25120600
|
C | T | 134 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(131): Show | 134 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.364-1073C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120600 | ||||||
| chr2:25120610
|
C | T | 39 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(36): Show | 39 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-1063C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120610 | ||||||
| chr2:25120645
|
A | AAACAAC | 39 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(36): Show | 39 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-1014_364-1009d others(8): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25120645 | |||||
| chr2:25120645
|
A | G | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.364-1028A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120645 | ||||||
| chr2:25120645
|
AAAC | A | 48 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(45): Show | 48 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.364-1011_364-1009d others(5): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 25120645 | |||||
| chr2:25120665
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.364-1008G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120665 | ||||||
| chr2:25120730
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.364-943G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120730 | ||||||
| chr2:25120824
|
T | G | 39 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(36): Show | 39 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-849T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120824 | ||||||
| chr2:25120828
|
G | A | 1 | a0001c0001t0030g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-845G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120828 | ||||||
| chr2:25120928
|
G | T | 100 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(97): Show | 100 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.364-745G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120928 | ||||||
| chr2:25120951
|
G | A | 100 | a0001c0001t0001g0172a0001c0001t0002g0017a0001c0001t0002g0018others(97): Show | 100 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.364-722G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120951 | ||||||
| chr2:25120954
|
C | T | 137 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(134): Show | 137 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.364-719C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25120954 | ||||||
| chr2:25121153
|
C | T | 45 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.364-520C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121153 | ||||||
| chr2:25121191
|
T | C | 2 | a0001c0001t0002g0268a0001c0001t0002g0293 | 2 | NA19060.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.364-482T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121191 | ||||||
| chr2:25121195
|
C | G | 35 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(32): Show | 35 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.364-478C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121195 | ||||||
| chr2:25121264
|
T | C | 1 | a0001c0001t0002g0278 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.364-409T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121264 | ||||||
| chr2:25121286
|
G | A | 11 | a0001c0001t0005g0174a0001c0001t0005g0185a0001c0001t0005g0192others(8): Show | 11 | HG01169.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-387G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121286 | ||||||
| chr2:25121407
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.364-266C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121407 | ||||||
| chr2:25121478
|
A | G | 1 | a0001c0001t0030g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-195A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121478 | ||||||
| chr2:25121595
|
G | A | 47 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(44): Show | 47 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.364-78G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 4/22 | chr2 | 25121595 | ||||||
| chr2:25121827
|
G | C | 1 | a0001c0002t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.485+33G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25121827 | ||||||
| chr2:25121844
|
C | T | 1 | a0001c0002t0033g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485+50C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25121844 | ||||||
| chr2:25121865
|
T | G | 1 | a0001c0002t0004g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.485+71T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25121865 | ||||||
| chr2:25121964
|
G | GT | 7 | a0001c0001t0002g0023a0001c0001t0003g0110a0001c0001t0005g0174others(4): Show | 7 | HG00609.hp1 HG01169.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+184dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25121964 | |||||
| chr2:25121998
|
A | G | 1 | a0001c0002t0011g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.485+204A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25121998 | ||||||
| chr2:25122121
|
C | T | 1 | a0001c0001t0047g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.485+327C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25122121 | ||||||
| chr2:25122228
|
G | A | 281 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.485+434G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25122228 | ||||||
| chr2:25122446
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.485+652C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25122446 | ||||||
| chr2:25122545
|
C | T | 6 | a0001c0002t0001g0061a0001c0002t0001g0177a0001c0002t0001g0206others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+751C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25122545 | ||||||
| chr2:25122547
|
C | T | 1 | a0001c0001t0007g0234 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.485+753C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25122547 | ||||||
| chr2:25122816
|
C | A | 10 | a0001c0003t0006g0082a0001c0003t0006g0117a0001c0003t0006g0119others(7): Show | 10 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+1022C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25122816 | ||||||
| chr2:25122864
|
C | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.485+1070C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25122864 | ||||||
| chr2:25123020
|
G | C | 2 | a0001c0001t0024g0217a0001c0001t0026g0210 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.485+1226G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123020 | ||||||
| chr2:25123201
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.485+1407A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123201 | ||||||
| chr2:25123359
|
C | CA | 58 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0162others(55): Show | 58 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.485+1579dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25123359 | |||||
| chr2:25123375
|
A | G | 1 | a0001c0002t0002g0041 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.485+1581A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123375 | ||||||
| chr2:25123569
|
A | G | 7 | a0001c0001t0002g0091a0001c0001t0002g0264a0001c0001t0002g0278others(4): Show | 7 | HG02004.hp1 HG02132.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+1775A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123569 | ||||||
| chr2:25123699
|
C | T | 48 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(45): Show | 48 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.485+1905C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123699 | ||||||
| chr2:25123711
|
G | C | 1 | a0001c0003t0006g0145 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.485+1917G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123711 | ||||||
| chr2:25123729
|
G | A | 10 | a0001c0003t0006g0082a0001c0003t0006g0117a0001c0003t0006g0119others(7): Show | 10 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+1935G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123729 | ||||||
| chr2:25123818
|
A | T | 48 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(45): Show | 48 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.485+2024A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123818 | ||||||
| chr2:25123979
|
A | G | 47 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.485+2185A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25123979 | ||||||
| chr2:25124100
|
A | T | 6 | a0001c0002t0001g0061a0001c0002t0001g0177a0001c0002t0001g0206others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+2306A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124100 | ||||||
| chr2:25124177
|
T | C | 101 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(98): Show | 101 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.485+2383T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124177 | ||||||
| chr2:25124243
|
C | T | 1 | a0001c0002t0001g0175 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+2449C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124243 | ||||||
| chr2:25124277
|
A | AGT | 21 | a0001c0001t0007g0025a0001c0001t0013g0034a0001c0002t0001g0002others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+2537_485+2538d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
A | AGTGT | 16 | a0001c0001t0002g0023a0001c0002t0001g0032a0001c0002t0001g0047others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+2535_485+2538d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGT | A | 22 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0002g0020others(19): Show | 22 | HG00099.hp2 HG01074.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.485+2537_485+2538d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGT | A | 14 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0007g0232others(11): Show | 14 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.485+2535_485+2538d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGT | A | 14 | a0001c0001t0001g0172a0001c0001t0002g0040a0001c0001t0002g0120others(11): Show | 14 | HG01070.hp2 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.485+2533_485+2538d others(8): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(1): Show |
A | 12 | a0001c0001t0002g0001a0001c0001t0002g0051a0001c0001t0002g0224others(9): Show | 12 | HG00733.hp2 HG01934.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+2531_485+2538d others(10): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(3): Show |
A | 71 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.485+2529_485+2538d others(12): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(5): Show |
A | 4 | a0001c0001t0001g0219a0001c0001t0002g0067a0001c0001t0048g0218others(1): Show | 4 | HG01884.hp1 HG02486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2527_485+2538d others(14): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(7): Show |
A | 10 | a0001c0001t0007g0038a0001c0001t0007g0234a0001c0001t0015g0200others(7): Show | 10 | HG00639.hp1 HG01106.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+2525_485+2538d others(16): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(9): Show |
A | 24 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(21): Show | 24 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.485+2523_485+2538d others(18): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(11): Show |
A | 4 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0049g0059others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2521_485+2538d others(20): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(13): Show |
A | 1 | a0001c0001t0001g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.485+2519_485+2538d others(22): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(15): Show |
A | 2 | a0001c0001t0024g0217a0001c0001t0026g0210 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.485+2517_485+2538d others(24): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124277
|
AGTGTGTG others(17): Show |
A | 51 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.485+2515_485+2538d others(26): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124277 | |||||
| chr2:25124312
|
G | C | 35 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.485+2518G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124312 | ||||||
| chr2:25124331
|
T | A | 5 | a0001c0003t0010g0081a0001c0003t0010g0083a0001c0003t0010g0087others(2): Show | 5 | NA18963.hp1 NA18968.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+2537T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124331 | ||||||
| chr2:25124522
|
T | C | 101 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(98): Show | 101 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.485+2728T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124522 | ||||||
| chr2:25124549
|
G | A | 1 | a0001c0002t0001g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.485+2755G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124549 | ||||||
| chr2:25124600
|
C | T | 48 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(45): Show | 48 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.485+2806C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124600 | ||||||
| chr2:25124738
|
C | CA | 6 | a0001c0001t0001g0186a0001c0001t0005g0165a0001c0001t0005g0185others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+2969dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124738 | |||||
| chr2:25124738
|
CA | C | 228 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.485+2969delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124738 | |||||
| chr2:25124738
|
CAA | C | 8 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0008g0228others(5): Show | 8 | HG02451.hp1 HG02735.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+2968_485+2969d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25124738 | |||||
| chr2:25124799
|
A | G | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3005A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25124799 | ||||||
| chr2:25125039
|
C | T | 48 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0021others(45): Show | 48 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.486-3144C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125039 | ||||||
| chr2:25125334
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.486-2849G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125334 | ||||||
| chr2:25125506
|
G | A | 1 | a0001c0002t0004g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.486-2677G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125506 | ||||||
| chr2:25125598
|
C | T | 1 | a0001c0001t0008g0228 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.486-2585C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125598 | ||||||
| chr2:25125623
|
A | G | 137 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(134): Show | 137 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.486-2560A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125623 | ||||||
| chr2:25125671
|
A | G | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-2512A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125671 | ||||||
| chr2:25125675
|
A | G | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-2508A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125675 | ||||||
| chr2:25125677
|
G | A | 13 | a0001c0001t0001g0261a0001c0003t0006g0144a0001c0003t0006g0145others(10): Show | 13 | HG00639.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.486-2506G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125677 | ||||||
| chr2:25125684
|
C | T | 1 | a0001c0003t0009g0263 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.486-2499C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125684 | ||||||
| chr2:25125686
|
C | T | 6 | a0001c0002t0001g0061a0001c0002t0001g0177a0001c0002t0001g0206others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-2497C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125686 | ||||||
| chr2:25125715
|
A | G | 105 | a0001c0001t0001g0130a0001c0001t0001g0172a0001c0001t0002g0017others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.486-2468A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125715 | ||||||
| chr2:25125723
|
A | C | 1 | a0001c0003t0009g0275 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.486-2460A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125723 | ||||||
| chr2:25125731
|
A | G | 1 | a0001c0003t0009g0275 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.486-2452A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125731 | ||||||
| chr2:25125739
|
C | G | 145 | a0001c0001t0001g0131a0001c0001t0001g0160a0001c0001t0001g0164others(142): Show | 145 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.486-2444C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125739 | ||||||
| chr2:25125742
|
A | C | 1 | a0001c0001t0022g0178 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.486-2441A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125742 | ||||||
| chr2:25125749
|
C | T | 17 | a0001c0003t0006g0119a0001c0003t0006g0144a0001c0003t0006g0146others(14): Show | 17 | HG00438.hp2 HG00738.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.486-2434C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125749 | ||||||
| chr2:25125751
|
A | G | 18 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0134others(15): Show | 18 | HG01071.hp2 HG01074.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-2432A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125751 | ||||||
| chr2:25125759
|
T | C | 1 | a0001c0001t0012g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.486-2424T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125759 | ||||||
| chr2:25125775
|
T | C | 12 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0164others(9): Show | 12 | HG01884.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-2408T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125775 | ||||||
| chr2:25125864
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.486-2319C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125864 | ||||||
| chr2:25125877
|
G | A | 19 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(16): Show | 19 | HG00140.hp2 HG01071.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.486-2306G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125877 | ||||||
| chr2:25125903
|
G | A | 46 | a0001c0001t0003g0069a0001c0001t0003g0073a0001c0001t0003g0074others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.486-2280G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25125903 | ||||||
| chr2:25125933
|
C | CA | 6 | a0001c0001t0007g0013a0001c0001t0008g0113a0001c0001t0015g0203others(3): Show | 6 | HG02135.hp1 HG02145.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-2241dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25125933 | |||||
| chr2:25126190
|
C | T | 141 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(138): Show | 141 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.486-1993C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126190 | ||||||
| chr2:25126367
|
T | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-1816T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126367 | ||||||
| chr2:25126368
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.486-1815T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126368 | ||||||
| chr2:25126374
|
T | C | 3 | a0001c0001t0003g0069a0001c0001t0003g0108a0001c0001t0003g0110 | 3 | HG00597.hp2 HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.486-1809T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126374 | ||||||
| chr2:25126386
|
G | C | 1 | a0001c0002t0001g0244 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.486-1797G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126386 | ||||||
| chr2:25126755
|
A | C | 47 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.486-1428A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126755 | ||||||
| chr2:25126853
|
T | C | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.486-1330T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126853 | ||||||
| chr2:25126875
|
A | T | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.486-1308A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126875 | ||||||
| chr2:25126908
|
G | A | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.486-1275G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25126908 | ||||||
| chr2:25127093
|
A | G | 141 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(138): Show | 141 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.486-1090A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25127093 | ||||||
| chr2:25127147
|
G | A | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.486-1036G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25127147 | ||||||
| chr2:25127148
|
C | T | 46 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0026others(43): Show | 46 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.486-1035C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25127148 | ||||||
| chr2:25127191
|
C | CA | 16 | a0001c0001t0001g0127a0001c0001t0002g0026a0001c0001t0002g0249others(13): Show | 16 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.486-967dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25127191 | |||||
| chr2:25127191
|
CA | C | 124 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0134others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.486-967delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 25127191 | |||||
| chr2:25127303
|
G | A | 36 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-880G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25127303 | ||||||
| chr2:25127427
|
C | G | 88 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(85): Show | 88 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.486-756C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25127427 | ||||||
| chr2:25127452
|
G | T | 53 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0026others(50): Show | 53 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.486-731G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25127452 | ||||||
| chr2:25127453
|
A | G | 2 | a0001c0001t0002g0304a0001c0001t0007g0240 | 2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.486-730A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25127453 | ||||||
| chr2:25128122
|
C | T | 1 | a0001c0002t0001g0280 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.486-61C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 5/22 | chr2 | 25128122 | ||||||
| chr2:25128376
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.635+44C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25128376 | ||||||
| chr2:25128824
|
G | C | 52 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.635+492G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25128824 | ||||||
| chr2:25128872
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.635+540A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25128872 | ||||||
| chr2:25128896
|
C | T | 36 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.635+564C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25128896 | ||||||
| chr2:25128960
|
C | CA | 12 | a0001c0001t0001g0261a0001c0003t0006g0117a0001c0003t0006g0119others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.635+669dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
C | CAA | 8 | a0001c0003t0006g0144a0001c0003t0006g0145a0001c0003t0006g0147others(5): Show | 8 | HG01106.hp1 HG02257.hp1 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.635+668_635+669dup others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CA | C | 7 | a0001c0001t0002g0039a0001c0001t0002g0224a0001c0001t0002g0235others(4): Show | 7 | HG00621.hp1 HG01106.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.635+669delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAA | C | 25 | a0001c0001t0002g0001a0001c0001t0002g0051a0001c0001t0002g0091others(22): Show | 25 | HG00099.hp1 HG01109.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.635+668_635+669del others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAA | C | 26 | a0001c0001t0001g0136a0001c0001t0001g0160a0001c0001t0001g0164others(23): Show | 26 | HG00280.hp1 HG00673.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.635+667_635+669del others(3): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAA | C | 20 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0219others(17): Show | 20 | HG00280.hp2 HG00558.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.635+666_635+669del others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAA | C | 31 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(28): Show | 31 | HG00140.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.635+665_635+669del others(5): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAA | C | 31 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0001g0162others(28): Show | 31 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.635+664_635+669del others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAAA | C | 41 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0001g0156others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.635+663_635+669del others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAAA others(1): Show |
C | 45 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(42): Show | 45 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.635+662_635+669del others(8): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAAA others(2): Show |
C | 21 | a0001c0001t0003g0072a0001c0001t0003g0079a0001c0001t0003g0080others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.635+661_635+669del others(9): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAAA others(3): Show |
C | 25 | a0001c0001t0003g0073a0001c0001t0003g0076a0001c0001t0003g0077others(22): Show | 25 | HG01169.hp1 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.635+660_635+669del others(10): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0003g0074a0001c0001t0003g0296a0001c0001t0012g0071others(1): Show | 4 | HG02970.hp2 NA18982.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+659_635+669del others(11): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0130a0001c0002t0001g0047 | 2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.635+654_635+669del others(16): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25128960
|
CAAAAAAA others(11): Show |
C | 1 | a0003c0011t0045g0272 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.635+652_635+669del others(18): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25128960 | |||||
| chr2:25129142
|
G | C | 1 | a0001c0001t0004g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.635+810G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129142 | ||||||
| chr2:25129222
|
G | A | 53 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0026others(50): Show | 53 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.636-753G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129222 | ||||||
| chr2:25129318
|
A | ACGGGGG | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.636-627_636-622dup others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25129318 | |||||
| chr2:25129318
|
ACGGGGGC others(5): Show |
A | 11 | a0001c0001t0002g0026a0001c0001t0002g0039a0001c0001t0002g0043others(8): Show | 11 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.636-633_636-622del others(12): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25129318 | |||||
| chr2:25129331
|
C | T | 43 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0040others(40): Show | 43 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.636-644C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129331 | ||||||
| chr2:25129343
|
CGGGGGCG others(11): Show |
C | 3 | a0001c0001t0048g0218a0001c0001t0051g0125a0001c0003t0027g0184 | 3 | HG01243.hp1 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.636-627_636-610del others(18): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25129343 | |||||
| chr2:25129349
|
CGGGGCGT others(5): Show |
C | 1 | a0001c0010t0005g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.636-609_636-598del others(12): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25129349 | |||||
| chr2:25129351
|
G | T | 2 | a0001c0001t0019g0123a0001c0001t0019g0124 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.636-624G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129351 | ||||||
| chr2:25129354
|
C | G | 35 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(32): Show | 35 | HG00639.hp1 HG01169.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.636-621C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129354 | ||||||
| chr2:25129355
|
G | C | 33 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(30): Show | 33 | HG00639.hp1 HG01169.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.636-620G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129355 | ||||||
| chr2:25129356
|
T | G | 33 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(30): Show | 33 | HG00639.hp1 HG01169.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.636-619T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129356 | ||||||
| chr2:25129361
|
T | C | 33 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(30): Show | 33 | HG00639.hp1 HG01169.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.636-614T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129361 | ||||||
| chr2:25129455
|
GTCC | G | 55 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0026others(52): Show | 55 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.636-516_636-514del others(3): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 25129455 | |||||
| chr2:25129583
|
T | A | 1 | a0001c0001t0002g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.636-392T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129583 | ||||||
| chr2:25129617
|
A | G | 1 | a0001c0002t0011g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.636-358A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129617 | ||||||
| chr2:25129640
|
G | C | 1 | a0001c0001t0002g0302 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.636-335G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129640 | ||||||
| chr2:25129648
|
A | G | 4 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.636-327A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129648 | ||||||
| chr2:25129652
|
G | A | 1 | a0002c0012t0050g0281 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.636-323G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129652 | ||||||
| chr2:25129837
|
C | G | 1 | a0001c0001t0007g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.636-138C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129837 | ||||||
| chr2:25129939
|
A | G | 6 | a0001c0002t0001g0061a0001c0002t0001g0177a0001c0002t0001g0206others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-36A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 6/22 | chr2 | 25129939 | ||||||
| chr2:25130138
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0187others(1): Show | 4 | HG01884.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+29C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 7/22 | chr2 | 25130138 | ||||||
| chr2:25130348
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.771-204A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 7/22 | chr2 | 25130348 | ||||||
| chr2:25130410
|
C | T | 7 | a0001c0002t0001g0031a0001c0002t0001g0053a0001c0002t0001g0233others(4): Show | 7 | HG00621.hp2 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.771-142C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 7/22 | chr2 | 25130410 | ||||||
| chr2:25130535
|
C | T | 1 | a0005c0013t0044g0297 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.771-17C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 7/22 | chr2 | 25130535 | ||||||
| chr2:25130650
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.849+20C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 8/22 | chr2 | 25130650 | ||||||
| chr2:25130655
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.849+25C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 8/22 | chr2 | 25130655 | ||||||
| chr2:25130656
|
G | A | 2 | a0001c0001t0002g0259a0001c0001t0002g0282 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.849+26G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 8/22 | chr2 | 25130656 | ||||||
| chr2:25130957
|
C | G | 1 | a0001c0002t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.849+327C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 8/22 | chr2 | 25130957 | ||||||
| chr2:25131094
|
G | C | 1 | a0001c0010t0005g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-274G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 8/22 | chr2 | 25131094 | ||||||
| chr2:25131183
|
G | C | 1 | a0001c0001t0003g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.850-185G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 8/22 | chr2 | 25131183 | ||||||
| chr2:25131222
|
G | C | 69 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(66): Show | 69 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.850-146G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 8/22 | chr2 | 25131222 | ||||||
| chr2:25131599
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985+96C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 9/22 | chr2 | 25131599 | ||||||
| chr2:25131639
|
C | CAGAGGAA others(14): Show |
1 | a0001c0001t0013g0037 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.986-110_986-90dupA others(20): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 25131639 | |||||
| chr2:25131687
|
G | A | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-63G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 9/22 | chr2 | 25131687 | ||||||
| chr2:25131932
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0029g0171 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1147+21G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 10/22 | chr2 | 25131932 | ||||||
| chr2:25132060
|
C | T | 81 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1147+149C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 10/22 | chr2 | 25132060 | ||||||
| chr2:25132366
|
G | C | 1 | a0001c0001t0005g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1147+455G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 10/22 | chr2 | 25132366 | ||||||
| chr2:25132388
|
C | A | 66 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(63): Show | 66 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1147+477C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 10/22 | chr2 | 25132388 | ||||||
| chr2:25132803
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1148-100C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 10/22 | chr2 | 25132803 | ||||||
| chr2:25133543
|
A | C | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1311+109A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25133543 | ||||||
| chr2:25133805
|
G | A | 1 | a0001c0001t0007g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1311+371G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25133805 | ||||||
| chr2:25133942
|
A | G | 58 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1311+508A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25133942 | ||||||
| chr2:25134177
|
AT | A | 283 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1311+762delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr2 | 25134177 | |||||
| chr2:25134178
|
T | A | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1311+744T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134178 | ||||||
| chr2:25134179
|
T | A | 182 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(179): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1311+745T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134179 | ||||||
| chr2:25134180
|
T | A | 4 | a0001c0002t0001g0175a0001c0002t0001g0179a0001c0002t0001g0183others(1): Show | 4 | HG01934.hp1 HG02280.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+746T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134180 | ||||||
| chr2:25134182
|
T | A | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1311+748T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134182 | ||||||
| chr2:25134185
|
T | A | 1 | a0001c0001t0049g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1311+751T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134185 | ||||||
| chr2:25134186
|
T | A | 182 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(179): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1311+752T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134186 | ||||||
| chr2:25134201
|
T | C | 288 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1311+767T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134201 | ||||||
| chr2:25134202
|
G | A | 2 | a0001c0001t0003g0296a0001c0001t0008g0010 | 2 | NA18982.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1311+768G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134202 | ||||||
| chr2:25134354
|
G | A | 6 | a0001c0002t0001g0061a0001c0002t0001g0177a0001c0002t0001g0206others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+920G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134354 | ||||||
| chr2:25134354
|
G | C | 1 | a0001c0001t0012g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1311+920G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134354 | ||||||
| chr2:25134368
|
C | T | 102 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(99): Show | 102 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1311+934C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134368 | ||||||
| chr2:25134513
|
C | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(26): Show | 29 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1312-954C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134513 | ||||||
| chr2:25134618
|
G | C | 102 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(99): Show | 102 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1312-849G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134618 | ||||||
| chr2:25134628
|
C | T | 2 | a0001c0001t0004g0154a0001c0001t0030g0126 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1312-839C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134628 | ||||||
| chr2:25134823
|
C | T | 1 | a0001c0002t0036g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1312-644C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25134823 | ||||||
| chr2:25135096
|
A | G | 1 | a0001c0002t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1312-371A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25135096 | ||||||
| chr2:25135099
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0004g0129 | 3 | HG02630.hp2 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1312-368C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25135099 | ||||||
| chr2:25135216
|
G | A | 3 | a0001c0002t0001g0222a0001c0002t0001g0286a0001c0002t0001g0289 | 3 | HG00323.hp2 HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1312-251G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 12/22 | chr2 | 25135216 | ||||||
| chr2:25135914
|
G | T | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0266 | 3 | HG00673.hp1 NA18942.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1484+275G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 13/22 | chr2 | 25135914 | ||||||
| chr2:25135997
|
A | G | 1 | a0001c0002t0011g0042 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1484+358A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 13/22 | chr2 | 25135997 | ||||||
| chr2:25136328
|
A | G | 1 | a0001c0003t0027g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1485-195A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 13/22 | chr2 | 25136328 | ||||||
| chr2:25136385
|
C | T | 142 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 142 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1485-138C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 13/22 | chr2 | 25136385 | ||||||
| chr2:25136466
|
G | T | 2 | a0001c0001t0001g0172a0001c0001t0029g0171 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1485-57G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 13/22 | chr2 | 25136466 | ||||||
| chr2:25136634
|
G | A | 1 | a0001c0001t0016g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1560+36G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25136634 | ||||||
| chr2:25136676
|
C | G | 46 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1560+78C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25136676 | ||||||
| chr2:25136788
|
C | T | 1 | a0001c0003t0009g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1560+190C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25136788 | ||||||
| chr2:25136813
|
G | A | 2 | a0001c0001t0003g0099a0001c0001t0003g0102 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1560+215G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25136813 | ||||||
| chr2:25136865
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1560+267G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25136865 | ||||||
| chr2:25137198
|
C | T | 3 | a0001c0001t0003g0099a0001c0001t0003g0101a0001c0001t0003g0102 | 3 | HG03490.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1561-143C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25137198 | ||||||
| chr2:25137223
|
G | A | 46 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1561-118G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25137223 | ||||||
| chr2:25137317
|
C | T | 23 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(20): Show | 23 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1561-24C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25137317 | ||||||
| chr2:25137327
|
G | A | 35 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(32): Show | 35 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1561-14G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 14/22 | chr2 | 25137327 | ||||||
| chr2:25137729
|
G | A | 1 | a0001c0002t0005g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1722+227G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25137729 | ||||||
| chr2:25137749
|
C | T | 2 | a0001c0001t0003g0085a0001c0002t0001g0280 | 2 | HG02165.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1722+247C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25137749 | ||||||
| chr2:25137750
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1722+248G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25137750 | ||||||
| chr2:25137894
|
G | A | 35 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(32): Show | 35 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1722+392G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25137894 | ||||||
| chr2:25137914
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1722+412G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25137914 | ||||||
| chr2:25138029
|
G | A | 7 | a0001c0002t0001g0047a0001c0002t0001g0061a0001c0002t0001g0177others(4): Show | 7 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1722+527G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25138029 | ||||||
| chr2:25138120
|
A | C | 1 | a0001c0002t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1722+618A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25138120 | ||||||
| chr2:25138121
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1722+619G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25138121 | ||||||
| chr2:25138127
|
T | G | 1 | a0001c0002t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1722+625T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25138127 | ||||||
| chr2:25138330
|
T | C | 1 | a0001c0002t0001g0220 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1723-729T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25138330 | ||||||
| chr2:25138437
|
C | T | 1 | a0001c0002t0004g0168 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1723-622C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 15/22 | chr2 | 25138437 | ||||||
| chr2:25139325
|
G | A | 103 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(100): Show | 103 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1854+135G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25139325 | ||||||
| chr2:25139495
|
G | GCCTCAGA others(37): Show |
28 | a0001c0001t0002g0001a0001c0001t0002g0021a0001c0001t0002g0026others(25): Show | 28 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1854+369_1854+412d others(46): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr2 | 25139495 | |||||
| chr2:25139495
|
GCCTCAGA others(37): Show |
G | 1 | a0001c0010t0005g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1854+369_1854+412d others(46): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr2 | 25139495 | |||||
| chr2:25139604
|
A | C | 1 | a0001c0001t0013g0037 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1854+414A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25139604 | ||||||
| chr2:25139618
|
G | A | 1 | a0001c0003t0009g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1854+428G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25139618 | ||||||
| chr2:25139646
|
T | C | 265 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1854+456T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25139646 | ||||||
| chr2:25139715
|
G | A | 21 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1854+525G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25139715 | ||||||
| chr2:25139767
|
T | A | 1 | a0001c0002t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1854+577T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25139767 | ||||||
| chr2:25139815
|
G | A | 53 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(50): Show | 53 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1854+625G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25139815 | ||||||
| chr2:25140079
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0004g0154a0001c0001t0030g0126 | 3 | HG03225.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1854+889G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25140079 | ||||||
| chr2:25140137
|
C | A | 52 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1854+947C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25140137 | ||||||
| chr2:25140182
|
G | A | 47 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1854+992G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25140182 | ||||||
| chr2:25140297
|
ACT | A | 87 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1855-1066_1855-106 others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr2 | 25140297 | |||||
| chr2:25140509
|
C | T | 1 | a0001c0003t0006g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1855-857C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25140509 | ||||||
| chr2:25140597
|
G | T | 288 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1855-769G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | chr2 | 25140597 | ||||||
| chr2:25141040
|
C | CA | 74 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1855-306dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr2 | 25141040 | |||||
| chr2:25141040
|
C | CAA | 8 | a0001c0001t0002g0051a0001c0001t0002g0268a0001c0001t0002g0294others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1855-307_1855-306d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr2 | 25141040 | |||||
| chr2:25141040
|
CA | C | 23 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(20): Show | 23 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1855-306delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr2 | 25141040 | |||||
| chr2:25141690
|
C | A | 1 | a0001c0001t0002g0271 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1922+257C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25141690 | ||||||
| chr2:25141886
|
T | C | 1 | a0001c0002t0004g0291 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1922+453T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25141886 | ||||||
| chr2:25142013
|
G | A | 33 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0164others(30): Show | 33 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1922+580G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142013 | ||||||
| chr2:25142028
|
G | A | 2 | a0001c0001t0002g0259a0001c0001t0002g0282 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1922+595G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142028 | ||||||
| chr2:25142045
|
G | A | 104 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1922+612G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142045 | ||||||
| chr2:25142085
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0043 | 2 | HG00673.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1922+652G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142085 | ||||||
| chr2:25142142
|
T | C | 1 | a0001c0003t0006g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1922+709T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142142 | ||||||
| chr2:25142428
|
A | G | 1 | a0001c0001t0008g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1922+995A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142428 | ||||||
| chr2:25142447
|
T | TA | 51 | a0001c0001t0002g0223a0001c0001t0003g0069a0001c0001t0003g0072others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1922+1032dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 25142447 | |||||
| chr2:25142472
|
C | T | 3 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0005g0198 | 3 | HG00733.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1922+1039C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142472 | ||||||
| chr2:25142601
|
A | T | 1 | a0001c0002t0001g0220 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1923-1134A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142601 | ||||||
| chr2:25142610
|
T | A | 1 | a0001c0002t0001g0220 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1923-1125T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142610 | ||||||
| chr2:25142682
|
C | T | 1 | a0001c0003t0006g0230 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1923-1053C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142682 | ||||||
| chr2:25142773
|
TAATA | T | 141 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1923-943_1923-940d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 25142773 | |||||
| chr2:25142944
|
T | TA | 19 | a0001c0001t0001g0172a0001c0001t0001g0219a0001c0001t0003g0069others(16): Show | 19 | HG00597.hp2 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1923-770dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 25142944 | |||||
| chr2:25142983
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1923-752C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25142983 | ||||||
| chr2:25143013
|
C | G | 3 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0005g0198 | 3 | HG00733.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1923-722C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143013 | ||||||
| chr2:25143185
|
C | T | 2 | a0001c0003t0010g0081a0001c0003t0010g0115 | 2 | NA18977.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1923-550C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143185 | ||||||
| chr2:25143199
|
G | A | 3 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0005g0198 | 3 | HG00733.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1923-536G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143199 | ||||||
| chr2:25143211
|
G | A | 137 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1923-524G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143211 | ||||||
| chr2:25143243
|
G | A | 1 | a0001c0001t0015g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1923-492G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143243 | ||||||
| chr2:25143247
|
T | C | 1 | a0001c0002t0036g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1923-488T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143247 | ||||||
| chr2:25143261
|
A | T | 104 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(101): Show | 104 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.1923-474A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143261 | ||||||
| chr2:25143286
|
T | C | 1 | a0001c0001t0017g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1923-449T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143286 | ||||||
| chr2:25143380
|
C | T | 32 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1923-355C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143380 | ||||||
| chr2:25143488
|
G | A | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1923-247G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143488 | ||||||
| chr2:25143511
|
T | A | 104 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(101): Show | 104 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.1923-224T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 17/22 | chr2 | 25143511 | ||||||
| chr2:25144340
|
C | G | 1 | a0001c0003t0009g0275 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2050+478C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | chr2 | 25144340 | ||||||
| chr2:25144372
|
A | G | 297 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2050+510A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | chr2 | 25144372 | ||||||
| chr2:25144425
|
TC | T | 23 | a0001c0001t0001g0261a0001c0003t0006g0082a0001c0003t0006g0117others(20): Show | 23 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2051-532delC | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr2 | 25144425 | |||||
| chr2:25144435
|
T | G | 3 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0005g0198 | 3 | HG00733.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2051-525T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | chr2 | 25144435 | ||||||
| chr2:25144469
|
G | A | 1 | a0001c0001t0023g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2051-491G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | chr2 | 25144469 | ||||||
| chr2:25144561
|
C | A | 1 | a0001c0001t0003g0111 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2051-399C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | chr2 | 25144561 | ||||||
| chr2:25144562
|
A | C | 1 | a0001c0001t0003g0111 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2051-398A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | chr2 | 25144562 | ||||||
| chr2:25144724
|
C | T | 23 | a0001c0001t0001g0261a0001c0003t0006g0082a0001c0003t0006g0117others(20): Show | 23 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2051-236C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 18/22 | chr2 | 25144724 | ||||||
| chr2:25145136
|
G | A | 160 | a0001c0001t0001g0172a0001c0001t0001g0186a0001c0001t0001g0188others(157): Show | 160 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.2142+85G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25145136 | ||||||
| chr2:25145161
|
T | C | 162 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(159): Show | 162 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.2142+110T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25145161 | ||||||
| chr2:25145205
|
C | T | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2142+154C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25145205 | ||||||
| chr2:25145497
|
C | G | 1 | a0001c0001t0002g0028 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2142+446C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25145497 | ||||||
| chr2:25145568
|
C | T | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2142+517C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25145568 | ||||||
| chr2:25145630
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2142+579T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25145630 | ||||||
| chr2:25146081
|
TG | T | 30 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2142+1031delG | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146081 | ||||||
| chr2:25146082
|
G | GT | 18 | a0001c0001t0001g0261a0001c0001t0003g0111a0001c0001t0008g0010others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2142+1051dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25146082 | |||||
| chr2:25146082
|
G | T | 1 | a0001c0002t0001g0298 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2142+1031G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146082 | ||||||
| chr2:25146082
|
GT | G | 16 | a0001c0001t0001g0141a0001c0001t0002g0199a0001c0001t0002g0235others(13): Show | 16 | HG00621.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2142+1051delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25146082 | |||||
| chr2:25146082
|
GTT | G | 102 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(99): Show | 102 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.2142+1050_2142+105 others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25146082 | |||||
| chr2:25146093
|
T | G | 7 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01109.hp2 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2142+1042T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146093 | ||||||
| chr2:25146102
|
T | A | 1 | a0001c0014t0002g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2142+1051T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146102 | ||||||
| chr2:25146126
|
A | C | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2142+1075A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146126 | ||||||
| chr2:25146130
|
G | C | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2142+1079G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146130 | ||||||
| chr2:25146131
|
T | G | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2142+1080T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146131 | ||||||
| chr2:25146133
|
C | T | 102 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(99): Show | 102 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.2142+1082C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146133 | ||||||
| chr2:25146137
|
G | T | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2142+1086G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146137 | ||||||
| chr2:25146139
|
A | T | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2142+1088A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146139 | ||||||
| chr2:25146140
|
C | T | 1 | a0001c0001t0007g0252 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2142+1089C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146140 | ||||||
| chr2:25146171
|
C | T | 108 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(105): Show | 108 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.2142+1120C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146171 | ||||||
| chr2:25146354
|
T | C | 52 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.2142+1303T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146354 | ||||||
| chr2:25146467
|
C | T | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142+1416C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146467 | ||||||
| chr2:25146500
|
T | G | 23 | a0001c0001t0001g0261a0001c0003t0006g0082a0001c0003t0006g0117others(20): Show | 23 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2142+1449T>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146500 | ||||||
| chr2:25146717
|
A | T | 32 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.2142+1666A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146717 | ||||||
| chr2:25146810
|
G | C | 1 | a0001c0002t0011g0279 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2142+1759G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146810 | ||||||
| chr2:25146840
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2142+1789G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25146840 | ||||||
| chr2:25147015
|
G | A | 1 | a0001c0002t0004g0257 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2142+1964G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25147015 | ||||||
| chr2:25147147
|
C | T | 23 | a0001c0001t0001g0261a0001c0003t0006g0082a0001c0003t0006g0117others(20): Show | 23 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2142+2096C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25147147 | ||||||
| chr2:25147443
|
T | C | 4 | a0001c0005t0014g0046a0001c0005t0014g0212a0001c0005t0014g0213others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2143-2251T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25147443 | ||||||
| chr2:25147558
|
A | G | 1 | a0001c0001t0017g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2143-2136A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25147558 | ||||||
| chr2:25147747
|
G | A | 1 | a0001c0003t0010g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2143-1947G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25147747 | ||||||
| chr2:25147958
|
G | A | 1 | a0001c0001t0002g0306 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2143-1736G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25147958 | ||||||
| chr2:25148013
|
G | A | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-1681G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148013 | ||||||
| chr2:25148025
|
C | CA | 76 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2143-1647dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148025 | |||||
| chr2:25148025
|
C | CAA | 8 | a0001c0001t0003g0099a0001c0001t0003g0101a0001c0001t0003g0102others(5): Show | 8 | HG00609.hp1 HG02738.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2143-1648_2143-164 others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148025 | |||||
| chr2:25148025
|
CA | C | 121 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.2143-1647delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148025 | |||||
| chr2:25148025
|
CAA | C | 12 | a0001c0001t0001g0160a0001c0002t0001g0053a0001c0002t0001g0055others(9): Show | 12 | HG00280.hp2 HG01257.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.2143-1648_2143-164 others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148025 | |||||
| chr2:25148246
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2143-1448G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148246 | ||||||
| chr2:25148246
|
G | T | 1 | a0001c0001t0008g0228 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2143-1448G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148246 | ||||||
| chr2:25148261
|
T | A | 1 | a0001c0008t0018g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2143-1433T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148261 | ||||||
| chr2:25148261
|
TA | T | 6 | a0001c0001t0008g0010a0001c0001t0013g0037a0001c0001t0022g0178others(3): Show | 6 | HG00099.hp2 HG00733.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.2143-1419delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148261 | |||||
| chr2:25148262
|
A | T | 7 | a0001c0001t0003g0231a0001c0001t0008g0228a0001c0002t0001g0183others(4): Show | 7 | HG02004.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2143-1432A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148262 | ||||||
| chr2:25148463
|
C | T | 107 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(104): Show | 107 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.2143-1231C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148463 | ||||||
| chr2:25148497
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2143-1197C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148497 | ||||||
| chr2:25148501
|
C | T | 1 | a0001c0001t0012g0071 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2143-1193C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148501 | ||||||
| chr2:25148544
|
C | T | 1 | a0001c0002t0001g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2143-1150C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148544 | ||||||
| chr2:25148601
|
C | T | 1 | a0001c0002t0001g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2143-1093C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148601 | ||||||
| chr2:25148608
|
G | A | 35 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(32): Show | 35 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2143-1086G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148608 | ||||||
| chr2:25148689
|
A | G | 193 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2143-1005A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148689 | ||||||
| chr2:25148817
|
G | A | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-877G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148817 | ||||||
| chr2:25148870
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2143-824T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25148870 | ||||||
| chr2:25148921
|
C | CA | 16 | a0001c0001t0002g0018a0001c0001t0002g0051a0001c0001t0002g0223others(13): Show | 16 | HG01261.hp1 HG01934.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.2143-747dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148921 | |||||
| chr2:25148921
|
CAAAAA | C | 133 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.2143-751_2143-747d others(7): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148921 | |||||
| chr2:25148921
|
CAAAAAA | C | 47 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.2143-752_2143-747d others(8): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 25148921 | |||||
| chr2:25149117
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2143-577G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25149117 | ||||||
| chr2:25149121
|
C | T | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2143-573C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25149121 | ||||||
| chr2:25149155
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0134others(3): Show | 6 | HG01074.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2143-539C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25149155 | ||||||
| chr2:25149360
|
C | A | 112 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(109): Show | 112 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.2143-334C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25149360 | ||||||
| chr2:25149508
|
G | A | 5 | a0001c0002t0001g0029a0001c0002t0001g0236a0001c0002t0001g0241others(2): Show | 5 | HG02040.hp2 HG02080.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.2143-186G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25149508 | ||||||
| chr2:25149549
|
G | T | 1 | a0001c0001t0028g0197 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2143-145G>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25149549 | ||||||
| chr2:25149678
|
G | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0293 | 2 | NA19060.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2143-16G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 19/22 | chr2 | 25149678 | ||||||
| chr2:25149835
|
C | T | 1 | a0001c0005t0014g0213 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2191+93C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25149835 | ||||||
| chr2:25149880
|
T | C | 2 | a0001c0001t0002g0259a0001c0001t0002g0282 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2191+138T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25149880 | ||||||
| chr2:25149978
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2191+236G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25149978 | ||||||
| chr2:25150160
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2191+418G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150160 | ||||||
| chr2:25150162
|
C | T | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2191+420C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150162 | ||||||
| chr2:25150300
|
C | CA | 11 | a0001c0001t0001g0136a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG00741.hp1 HG02602.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.2191+577dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 25150300 | |||||
| chr2:25150300
|
CA | C | 82 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.2191+577delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 25150300 | |||||
| chr2:25150324
|
A | G | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2191+582A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150324 | ||||||
| chr2:25150429
|
G | A | 185 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2191+687G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150429 | ||||||
| chr2:25150487
|
C | G | 3 | a0001c0001t0005g0192a0001c0001t0005g0215a0001c0001t0015g0205 | 3 | HG02055.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2191+745C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150487 | ||||||
| chr2:25150496
|
T | C | 5 | a0001c0003t0006g0144a0001c0003t0006g0145a0001c0003t0006g0147others(2): Show | 5 | HG01106.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191+754T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150496 | ||||||
| chr2:25150561
|
A | AGG | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2191+819_2191+820i others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150561 | ||||||
| chr2:25150562
|
T | A | 3 | a0001c0005t0014g0212a0001c0005t0014g0213a0001c0005t0014g0214 | 3 | HG02280.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2191+820T>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150562 | ||||||
| chr2:25150611
|
C | CT | 6 | a0001c0001t0003g0111a0001c0001t0005g0194a0001c0001t0015g0203others(3): Show | 6 | HG01361.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2191+884dupT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 25150611 | |||||
| chr2:25150611
|
CT | C | 101 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.2191+884delT | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 25150611 | |||||
| chr2:25150830
|
C | T | 11 | a0001c0001t0005g0174a0001c0001t0005g0185a0001c0001t0005g0192others(8): Show | 11 | HG01169.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2192-1084C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25150830 | ||||||
| chr2:25151057
|
T | TA | 14 | a0001c0001t0001g0143a0001c0001t0001g0160a0001c0001t0001g0164others(11): Show | 14 | HG00280.hp2 HG00438.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2192-840dupA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 25151057 | |||||
| chr2:25151057
|
TA | T | 7 | a0001c0001t0001g0136a0001c0001t0002g0278a0001c0001t0002g0282others(4): Show | 7 | HG00733.hp2 HG01257.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.2192-840delA | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 25151057 | |||||
| chr2:25151057
|
TAA | T | 47 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.2192-841_2192-840d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 25151057 | |||||
| chr2:25151072
|
A | C | 2 | a0001c0001t0003g0099a0001c0001t0003g0102 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2192-842A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151072 | ||||||
| chr2:25151099
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0164others(5): Show | 8 | HG01884.hp2 HG02818.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2192-815G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151099 | ||||||
| chr2:25151194
|
C | A | 1 | a0001c0003t0010g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2192-720C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151194 | ||||||
| chr2:25151195
|
A | C | 1 | a0001c0003t0010g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2192-719A>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151195 | ||||||
| chr2:25151196
|
C | A | 1 | a0001c0003t0010g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2192-718C>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151196 | ||||||
| chr2:25151210
|
T | C | 1 | a0001c0001t0007g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2192-704T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151210 | ||||||
| chr2:25151493
|
A | G | 87 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0164others(84): Show | 87 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2192-421A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151493 | ||||||
| chr2:25151543
|
A | T | 3 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0005g0198 | 3 | HG00733.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2192-371A>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151543 | ||||||
| chr2:25151881
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2192-33G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 20/22 | chr2 | 25151881 | ||||||
| chr2:25152043
|
G | A | 17 | a0001c0001t0005g0157a0001c0001t0005g0161a0001c0001t0005g0194others(14): Show | 17 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2298+23G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152043 | ||||||
| chr2:25152131
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2298+111C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152131 | ||||||
| chr2:25152236
|
T | C | 226 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(223): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2298+216T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152236 | ||||||
| chr2:25152243
|
C | T | 5 | a0001c0001t0002g0040a0001c0001t0002g0120a0001c0001t0002g0224others(2): Show | 5 | HG01070.hp2 HG01099.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+223C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152243 | ||||||
| chr2:25152369
|
C | T | 31 | a0001c0001t0003g0069a0001c0001t0003g0077a0001c0001t0003g0079others(28): Show | 31 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2298+349C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152369 | ||||||
| chr2:25152388
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2298+368G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152388 | ||||||
| chr2:25152565
|
A | G | 4 | a0001c0001t0022g0178a0001c0001t0023g0204a0001c0002t0031g0295others(1): Show | 4 | HG00733.hp2 HG01358.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+545A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152565 | ||||||
| chr2:25152614
|
A | G | 1 | a0001c0001t0003g0111 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2298+594A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152614 | ||||||
| chr2:25152667
|
T | C | 6 | a0001c0001t0024g0217a0001c0001t0026g0210a0001c0005t0014g0046others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2298+647T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152667 | ||||||
| chr2:25152758
|
T | C | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2298+738T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152758 | ||||||
| chr2:25152813
|
A | AGT | 38 | a0001c0001t0002g0120a0001c0001t0002g0224a0001c0001t0002g0259others(35): Show | 38 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2298+822_2298+823d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152813 | |||||
| chr2:25152813
|
A | AGTGT | 20 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0079others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.2298+820_2298+823d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152813 | |||||
| chr2:25152813
|
A | AGTGTGT | 3 | a0001c0001t0002g0028a0001c0001t0003g0111a0001c0015t0008g0078 | 3 | NA18747.hp1 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.2298+818_2298+823d others(8): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152813 | |||||
| chr2:25152813
|
AGT | A | 4 | a0001c0001t0002g0067a0001c0001t0016g0182a0001c0001t0047g0068others(1): Show | 4 | HG01109.hp1 HG02965.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+822_2298+823d others(4): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152813 | |||||
| chr2:25152813
|
AGTGT | A | 3 | a0001c0001t0019g0123a0001c0001t0019g0124a0001c0001t0026g0210 | 3 | HG02717.hp2 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2298+820_2298+823d others(6): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152813 | |||||
| chr2:25152813
|
AGTGTGTG others(1): Show |
A | 34 | a0001c0001t0004g0269a0001c0002t0001g0002a0001c0002t0001g0005others(31): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2298+816_2298+823d others(10): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152813 | |||||
| chr2:25152813
|
AGTGTGTG others(3): Show |
A | 94 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.2298+814_2298+823d others(12): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152813 | |||||
| chr2:25152834
|
GTGTGTGT others(3): Show |
G | 19 | a0001c0003t0006g0117a0001c0003t0006g0144a0001c0003t0006g0145others(16): Show | 19 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.2298+816_2298+825d others(12): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25152834 | |||||
| chr2:25152842
|
G | A | 1 | a0001c0001t0048g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2298+822G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152842 | ||||||
| chr2:25152844
|
A | G | 4 | a0001c0001t0003g0095a0001c0001t0003g0166a0001c0001t0008g0094others(1): Show | 4 | HG02015.hp1 NA18942.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+824A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25152844 | ||||||
| chr2:25153036
|
C | G | 154 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(151): Show | 154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.2299-676C>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153036 | ||||||
| chr2:25153041
|
G | C | 1 | a0001c0002t0011g0279 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2299-671G>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153041 | ||||||
| chr2:25153156
|
C | T | 117 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2299-556C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153156 | ||||||
| chr2:25153237
|
C | T | 6 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2299-475C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153237 | ||||||
| chr2:25153291
|
T | C | 1 | a0001c0001t0024g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2299-421T>C | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153291 | ||||||
| chr2:25153330
|
G | A | 1 | a0001c0003t0006g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2299-382G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153330 | ||||||
| chr2:25153505
|
A | G | 1 | a0001c0001t0026g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2299-207A>G | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153505 | ||||||
| chr2:25153510
|
G | A | 1 | a0001c0003t0006g0274 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2299-202G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153510 | ||||||
| chr2:25153538
|
G | A | 49 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2299-174G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | chr2 | 25153538 | ||||||
| chr2:25153695
|
CGT | C | 49 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0073others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2299-12_2299-11del others(2): Show |
EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 25153695 | |||||
| chr2:25153812
|
G | A | 19 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2348+51G>A | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 22/22 | chr2 | 25153812 | ||||||
| chr2:25153987
|
C | T | 1 | a0001c0001t0021g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2348+226C>T | EFR3B | ENSG00000084710.14 | transcript | ENST00000403714.8 | protein_coding | 22/22 | chr2 | 25153987 |