| geneid | 2494 |
|---|---|
| ensemblid | ENSG00000116833.14 |
| hgncid | 7984 |
| symbol | NR5A2 |
| name | nuclear receptor subfamily 5 group A member 2 |
| refseq_nuc | NM_205860.3 |
| refseq_prot | NP_995582.1 |
| ensembl_nuc | ENST00000367362.8 |
| ensembl_prot | ENSP00000356331.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 200027710 |
| end | 200177415 |
| strand | + |
| ver | v1.2 |
| region | chr1:200027710-200177415 |
| region5000 | chr1:200022710-200182415 |
| regionname0 | NR5A2_chr1_200027710_200177415 |
| regionname5000 | NR5A2_chr1_200022710_200182415 |
| 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 | 541 | 274 | 81 | 57 | 84 | 10 | 40 | 58 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0002 | 0/0 | 541 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0003 | 0/0 | 541 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0004 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0005 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0006 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| 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 | 1/0 | 1626 | 130 | 22 | 33 | 41 | 6 | 27 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0002 | 0/1 | 1626 | 73 | 11 | 11 | 38 | 3 | 9 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0003 | 0/0 | 1626 | 35 | 20 | 10 | 1 | 1 | 3 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0004 | 0/0 | 1626 | 24 | 17 | 2 | 4 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0005 | 0/0 | 1626 | 9 | 8 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0006 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0007 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0008 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0009 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0010 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0011 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0012 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| c0013 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3344 | 86 | 6 | 12 | 53 | 3 | 10 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0002 | 0/0 | 3343 | 51 | 13 | 23 | 1 | 4 | 10 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0003 | 0/0 | 3343 | 28 | 0 | 6 | 16 | 0 | 6 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0004 | 0/0 | 3344 | 23 | 22 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0005 | 0/0 | 3343 | 21 | 4 | 8 | 2 | 3 | 4 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0006 | 0/0 | 3343 | 17 | 16 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0007 | 0/0 | 3344 | 8 | 6 | 1 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0008 | 0/0 | 3342 | 8 | 0 | 2 | 5 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0009 | 0/0 | 3343 | 6 | 6 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0010 | 0/0 | 3340 | 5 | 1 | 1 | 0 | 0 | 3 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0011 | 0/0 | 3343 | 5 | 0 | 0 | 5 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0012 | 0/0 | 3343 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0013 | 0/0 | 3343 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0014 | 0/0 | 3344 | 2 | 0 | 2 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0015 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0016 | 0/0 | 3343 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0017 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0018 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0019 | 0/0 | 3344 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0020 | 0/0 | 3344 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0021 | 0/0 | 3344 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0022 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0023 | 0/0 | 3342 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0024 | 0/0 | 3343 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0025 | 0/0 | 3343 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0026 | 0/0 | 3343 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0027 | 0/0 | 3343 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0028 | 0/0 | 3344 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0029 | 0/0 | 3344 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0030 | 0/0 | 3344 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0031 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| t0032 | 0/0 | 3343 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| 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 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| 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 | 1/0 | 1626 | 130 | 22 | 33 | 41 | 6 | 27 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0002 | 0/1 | 1626 | 73 | 11 | 11 | 38 | 3 | 9 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003 | 0/0 | 1626 | 35 | 20 | 10 | 1 | 1 | 3 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0004 | 0/0 | 1626 | 24 | 17 | 2 | 4 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0005 | 0/0 | 1626 | 9 | 8 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0007 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0002c0008 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0002c0009 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0003c0006 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0003c0010 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0004c0013 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0005c0012 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0006c0011 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4969 | 12 | 0 | 0 | 11 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0002 | 0/0 | 4968 | 33 | 7 | 16 | 0 | 3 | 7 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0003 | 0/0 | 4968 | 28 | 0 | 6 | 16 | 0 | 6 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0005 | 0/0 | 4968 | 19 | 3 | 7 | 2 | 3 | 4 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0006 | 0/0 | 4968 | 7 | 7 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0007 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0008 | 0/0 | 4967 | 8 | 0 | 2 | 5 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0009 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0010 | 0/0 | 4965 | 5 | 1 | 1 | 0 | 0 | 3 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0011 | 0/0 | 4968 | 5 | 0 | 0 | 5 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0012 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0014 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0015 | 0/0 | 4967 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0018 | 0/0 | 4967 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0019 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0023 | 0/0 | 4967 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0024 | 0/0 | 4968 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0025 | 0/0 | 4968 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0026 | 0/0 | 4968 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0027 | 0/0 | 4968 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0001t0028 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0002t0001 | 0/1 | 4969 | 63 | 3 | 10 | 37 | 3 | 9 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0002t0004 | 0/0 | 4969 | 5 | 5 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0002t0005 | 0/0 | 4968 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0002t0007 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0002t0021 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0002t0029 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0001 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0002 | 0/0 | 4968 | 16 | 4 | 7 | 1 | 1 | 3 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0005 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0006 | 0/0 | 4968 | 4 | 3 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0009 | 0/0 | 4968 | 5 | 5 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0013 | 0/0 | 4968 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0014 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0016 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0017 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0022 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0003t0031 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0004t0001 | 0/0 | 4969 | 6 | 0 | 1 | 4 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0004t0004 | 0/0 | 4969 | 13 | 12 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0004t0006 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0004t0007 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0004t0020 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0005t0001 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0005t0004 | 0/0 | 4969 | 5 | 5 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0005t0006 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0005t0007 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0007t0006 | 0/0 | 4968 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0001c0007t0015 | 0/0 | 4967 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0002c0008t0002 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0002c0008t0012 | 0/0 | 4968 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0002c0009t0006 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0002c0009t0007 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0003c0006t0002 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0003c0006t0006 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0003c0006t0016 | 0/0 | 4968 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0003c0010t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0004c0013t0032 | 0/0 | 4968 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0005c0012t0001 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| a0006c0011t0030 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | copy fasta | chr1 | 200022710 | 200182415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0008g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0010g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0011g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0011g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0014g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0019g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0023g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0024g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0025g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0026g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0027g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0001t0028g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0021g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0002t0029g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0013g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0014g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0003t0031g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0004t0020g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0005t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0007t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0007t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0001c0007t0015g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0002c0008t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0002c0008t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0002c0008t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0002c0009t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0002c0009t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0003c0006t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0003c0006t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0003c0006t0016g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0003c0010t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0004c0013t0032g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0005c0012t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| a0006c0011t0030g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0185 | EUR | FIN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0243 | EUR | FIN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00408 | hp2 | a0001 | c0001 | t0011 | g0124 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0155 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00639 | hp2 | a0004 | c0013 | t0032 | g0149 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00642 | hp2 | a0001 | c0003 | t0002 | g0170 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0152 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0167 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0274 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01074 | hp2 | a0001 | c0003 | t0006 | g0061 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0097 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01106 | hp2 | a0001 | c0001 | t0014 | g0264 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0141 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01109 | hp2 | a0001 | c0004 | t0004 | g0057 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0115 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0273 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0056 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0203 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01256 | hp2 | a0001 | c0003 | t0002 | g0154 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0107 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0108 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0275 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0195 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01361 | hp2 | a0001 | c0003 | t0014 | g0272 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0169 | EUR | IBS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0132 | EUR | IBS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0177 | EUR | IBS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0019 | EUR | IBS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0168 | EUR | IBS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0020 | EUR | IBS | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01884 | hp1 | a0001 | c0007 | t0006 | g0062 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01884 | hp2 | a0002 | c0009 | t0006 | g0086 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0231 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0027 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02015 | hp1 | a0001 | c0001 | t0011 | g0100 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02027 | hp2 | a0001 | c0001 | t0011 | g0253 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02040 | hp1 | a0001 | c0001 | t0007 | g0176 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02055 | hp1 | a0003 | c0006 | t0002 | g0004 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02055 | hp2 | a0001 | c0003 | t0006 | g0014 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02080 | hp2 | a0001 | c0001 | t0026 | g0255 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | KHV | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02145 | hp2 | a0001 | c0004 | t0007 | g0016 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02148 | hp2 | a0001 | c0005 | t0007 | g0281 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | CDX | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | CDX | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02257 | hp2 | a0001 | c0003 | t0005 | g0055 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0284 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02258 | hp2 | a0001 | c0003 | t0009 | g0257 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02280 | hp1 | a0001 | c0003 | t0009 | g0223 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0286 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02451 | hp1 | a0001 | c0005 | t0006 | g0060 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02451 | hp2 | a0001 | c0003 | t0016 | g0153 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02615 | hp1 | a0001 | c0004 | t0004 | g0038 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0279 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02622 | hp1 | a0001 | c0004 | t0004 | g0015 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02622 | hp2 | a0001 | c0004 | t0007 | g0049 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02630 | hp1 | a0001 | c0003 | t0009 | g0064 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02647 | hp1 | a0001 | c0002 | t0007 | g0026 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0090 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0158 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0181 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02717 | hp2 | a0001 | c0004 | t0004 | g0058 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02723 | hp1 | a0001 | c0004 | t0004 | g0066 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02723 | hp2 | a0001 | c0005 | t0004 | g0083 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02809 | hp2 | a0001 | c0004 | t0004 | g0037 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02886 | hp2 | a0001 | c0004 | t0004 | g0088 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02895 | hp1 | a0001 | c0007 | t0015 | g0278 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02896 | hp1 | a0001 | c0004 | t0004 | g0008 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02896 | hp2 | a0001 | c0004 | t0004 | g0067 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02897 | hp1 | a0001 | c0004 | t0004 | g0010 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02922 | hp1 | a0001 | c0003 | t0031 | g0039 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02965 | hp1 | a0001 | c0005 | t0004 | g0021 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02965 | hp2 | a0003 | c0010 | t0001 | g0002 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02970 | hp1 | a0001 | c0003 | t0009 | g0013 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02970 | hp2 | a0001 | c0003 | t0013 | g0048 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02976 | hp1 | a0001 | c0005 | t0004 | g0277 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02976 | hp2 | a0001 | c0005 | t0004 | g0023 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03098 | hp1 | a0001 | c0004 | t0006 | g0045 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03098 | hp2 | a0001 | c0002 | t0021 | g0046 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03130 | hp1 | a0001 | c0003 | t0009 | g0224 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0091 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03139 | hp1 | a0002 | c0008 | t0002 | g0087 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0282 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03209 | hp1 | a0001 | c0007 | t0006 | g0283 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0180 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03225 | hp1 | a0001 | c0003 | t0006 | g0036 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03225 | hp2 | a0001 | c0003 | t0022 | g0007 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03239 | hp1 | a0001 | c0001 | t0019 | g0209 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03453 | hp1 | a0001 | c0004 | t0004 | g0285 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0059 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0182 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03490 | hp2 | a0001 | c0001 | t0023 | g0225 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0268 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0116 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03492 | hp2 | a0001 | c0001 | t0010 | g0140 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03516 | hp1 | a0001 | c0003 | t0013 | g0051 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03516 | hp2 | a0001 | c0003 | t0006 | g0035 | AFR | ESN | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0179 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03540 | hp2 | a0002 | c0008 | t0012 | g0085 | AFR | GWD | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0144 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0103 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0156 | SAS | BEB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | BEB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03927 | hp1 | a0001 | c0001 | t0027 | g0245 | SAS | BEB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03927 | hp2 | a0001 | c0001 | t0028 | g0099 | SAS | BEB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04115 | hp1 | a0001 | c0001 | t0024 | g0029 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04115 | hp2 | a0001 | c0001 | t0025 | g0074 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0172 | SAS | BEB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0266 | SAS | BEB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0256 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0157 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0267 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | STU | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18522 | hp1 | a0001 | c0004 | t0007 | g0050 | AFR | YRI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18522 | hp2 | a0001 | c0005 | t0004 | g0022 | AFR | YRI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | CHB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | CHB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | CHB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | YRI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18906 | hp2 | a0001 | c0002 | t0007 | g0093 | AFR | YRI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18942 | hp2 | a0001 | c0004 | t0001 | g0053 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0126 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18953 | hp1 | a0006 | c0011 | t0030 | g0218 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0123 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0138 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18977 | hp1 | a0001 | c0001 | t0011 | g0078 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19001 | hp2 | a0005 | c0012 | t0001 | g0194 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19005 | hp2 | a0001 | c0004 | t0001 | g0054 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19012 | hp1 | a0001 | c0001 | t0008 | g0128 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0065 | AFR | LWK | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19030 | hp2 | a0003 | c0006 | t0006 | g0003 | AFR | LWK | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19043 | hp1 | a0002 | c0008 | t0012 | g0084 | AFR | LWK | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0178 | AFR | LWK | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0052 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19088 | hp2 | a0001 | c0002 | t0029 | g0142 | EAS | JPT | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19240 | hp1 | a0001 | c0003 | t0013 | g0269 | AFR | YRI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0043 | AFR | YRI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0098 | EUR | TSI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0127 | EUR | TSI | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0186 | SAS | GIH | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | GIH | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02109 | hp1 | a0001 | c0004 | t0020 | g0063 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0041 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG02559 | hp2 | a0001 | c0004 | t0004 | g0044 | AFR | ACB | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03471 | hp1 | a0002 | c0009 | t0007 | g0089 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG03471 | hp2 | a0001 | c0004 | t0004 | g0276 | AFR | MSL | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG06807 | hp1 | a0003 | c0006 | t0016 | g0001 | AFR | USA | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | USA | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | USA | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA20300 | hp2 | a0001 | c0003 | t0017 | g0042 | AFR | USA | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0092 | AFR | LWK | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0102 | AFR | LWK | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0134 | REF | REF | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0131 | REF | REF | NR5A2_chr1_200022710_200182415 | NR5A2 | chr1 | 200022710 | 200182415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:200027875
|
T | A | 1 | a0003 | 4 | HG02055.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.28T>A | p.Leu10Ile | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/8 | 166/4969 | 28/1626 | 10/541 | chr1 | 200027875 | ||
| chr1:200048706
|
G | C | 1 | a0002 | 5 | HG01884.hp2 HG03139.hp1 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.998G>C | p.Arg333Pro | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/8 | 1136/4969 | 998/1626 | 333/541 | chr1 | 200048706 | ||
| chr1:200111319
|
C | A | 1 | a0006 | 1 | NA18953.hp1 | missense_variant&splice_region_variant | MODERATE | c.1228C>A | p.Gln410Lys | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/8 | 1366/4969 | 1228/1626 | 410/541 | chr1 | 200111319 | ||
| chr1:200111320
|
A | C | 1 | a0006 | 1 | NA18953.hp1 | missense_variant&splice_region_variant | MODERATE | c.1229A>C | p.Gln410Pro | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/8 | 1367/4969 | 1229/1626 | 410/541 | chr1 | 200111320 | ||
| chr1:200174053
|
C | T | 1 | a0004 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1469C>T | p.Pro490Leu | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1607/4969 | 1469/1626 | 490/541 | chr1 | 200174053 | ||
| chr1:200174154
|
G | T | 1 | a0005 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.1570G>T | p.Gly524Trp | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1708/4969 | 1570/1626 | 524/541 | chr1 | 200174154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:200045454
|
G | A | 2 | a0001c0005a0001c0007 | 12 | HG01884.hp1 HG02148.hp2 HG02258.hp1 others(9): Show |
synonymous_variant | LOW | c.333G>A | p.Lys111Lys | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/8 | 471/4969 | 333/1626 | 111/541 | chr1 | 200045454 | ||
| chr1:200048458
|
C | G | 4 | a0001c0003a0001c0004a0001c0005others(1): Show | 71 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(68): Show |
synonymous_variant | LOW | c.750C>G | p.Pro250Pro | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/8 | 888/4969 | 750/1626 | 250/541 | chr1 | 200048458 | ||
| chr1:200174153
|
C | T | 5 | a0001c0002a0001c0004a0001c0005others(2): Show | 109 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(106): Show |
synonymous_variant | LOW | c.1569C>T | p.Asn523Asn | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1707/4969 | 1569/1626 | 523/541 | chr1 | 200174153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:200174285
|
A | C | 1 | a0004c0013t0032 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 75 | chr1 | 200174285 | |||||
| chr1:200174314
|
T | C | 30 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(27): Show | 116 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 104 | chr1 | 200174314 | |||||
| chr1:200174479
|
G | A | 1 | a0001c0003t0017 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 269 | chr1 | 200174479 | |||||
| chr1:200174532
|
G | A | 1 | a0001c0001t0026 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 322 | chr1 | 200174532 | |||||
| chr1:200174715
|
C | T | 1 | a0001c0003t0031 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 505 | chr1 | 200174715 | |||||
| chr1:200174716
|
C | G | 35 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(32): Show | 154 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*506C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 506 | chr1 | 200174716 | |||||
| chr1:200174961
|
T | G | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(37): Show | 160 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*751T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 751 | chr1 | 200174961 | |||||
| chr1:200175397
|
A | G | 2 | a0001c0003t0016a0003c0006t0016 | 2 | HG02451.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1187A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1187 | chr1 | 200175397 | |||||
| chr1:200175720
|
G | A | 4 | a0001c0002t0004a0001c0004t0004a0001c0004t0020others(1): Show | 24 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1510G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1510 | chr1 | 200175720 | |||||
| chr1:200175755
|
C | T | 1 | a0001c0001t0025 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1545C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1545 | chr1 | 200175755 | |||||
| chr1:200175763
|
A | G | 1 | a0001c0001t0028 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1553A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1553 | chr1 | 200175763 | |||||
| chr1:200175929
|
T | C | 1 | a0001c0003t0013 | 3 | HG02970.hp2 HG03516.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1719T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1719 | chr1 | 200175929 | |||||
| chr1:200176194
|
A | G | 1 | a0001c0002t0029 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1984A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 1984 | chr1 | 200176194 | |||||
| chr1:200176241
|
T | C | 1 | a0001c0002t0021 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2031T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2031 | chr1 | 200176241 | |||||
| chr1:200176378
|
G | A | 7 | a0001c0001t0005a0001c0001t0009a0001c0002t0005others(4): Show | 29 | HG00609.hp1 HG00639.hp1 HG01081.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2168G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2168 | chr1 | 200176378 | |||||
| chr1:200176381
|
G | A | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(34): Show | 161 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*2171G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2171 | chr1 | 200176381 | |||||
| chr1:200176405
|
G | A | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(35): Show | 162 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*2195G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2195 | chr1 | 200176405 | |||||
| chr1:200176534
|
G | T | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(35): Show | 162 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*2324G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2324 | chr1 | 200176534 | |||||
| chr1:200176544
|
T | G | 1 | a0001c0004t0020 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2334T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2334 | chr1 | 200176544 | |||||
| chr1:200176617
|
G | A | 1 | a0001c0003t0022 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2407G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2407 | chr1 | 200176617 | |||||
| chr1:200176633
|
CAAA | C | 1 | a0001c0001t0010 | 5 | HG01255.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2428_*2430delAAA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2428 | INFO_REALIGN_3_PRIME | chr1 | 200176633 | ||||
| chr1:200176765
|
A | G | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(37): Show | 164 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2555A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2555 | chr1 | 200176765 | |||||
| chr1:200176778
|
G | A | 1 | a0001c0001t0023 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2568G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 2568 | chr1 | 200176778 | |||||
| chr1:200177275
|
T | C | 9 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(6): Show | 43 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3065T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 3065 | chr1 | 200177275 | |||||
| chr1:200177365
|
GA | G | 32 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(29): Show | 149 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*3157delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 3157 | INFO_REALIGN_3_PRIME | chr1 | 200177365 | ||||
| chr1:200177366
|
AAT | A | 5 | a0001c0001t0008a0001c0001t0015a0001c0001t0018others(2): Show | 12 | HG01358.hp2 HG01981.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3157_*3158delAT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 8/8 | 3157 | chr1 | 200177366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:200028120
|
T | C | 4 | a0003c0006t0002g0004a0003c0006t0006g0003a0003c0006t0016g0001others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+209T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028120 | ||||||
| chr1:200028128
|
T | A | 2 | a0001c0001t0003g0006a0001c0001t0008g0005 | 2 | HG02040.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.64+217T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028128 | ||||||
| chr1:200028217
|
A | C | 11 | a0001c0001t0002g0280a0001c0003t0002g0279a0001c0003t0002g0286others(8): Show | 11 | HG02148.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+306A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028217 | ||||||
| chr1:200028275
|
T | C | 41 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(38): Show | 41 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.64+364T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028275 | ||||||
| chr1:200028425
|
C | CA | 40 | a0001c0001t0001g0071a0001c0001t0002g0034a0001c0001t0002g0068others(37): Show | 40 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.64+532dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200028425 | |||||
| chr1:200028425
|
C | CAA | 19 | a0001c0001t0006g0059a0001c0002t0004g0065a0001c0003t0002g0056others(16): Show | 19 | HG01074.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.64+531_64+532dupAA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200028425 | |||||
| chr1:200028425
|
C | CAAA | 31 | a0001c0001t0003g0030a0001c0001t0005g0009a0001c0001t0005g0025others(28): Show | 31 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+530_64+532dupAA others(1): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200028425 | |||||
| chr1:200028425
|
C | CAAAA | 11 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0005g0019others(8): Show | 11 | HG01516.hp2 HG01517.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+529_64+532dupAA others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200028425 | |||||
| chr1:200028444
|
C | A | 4 | a0001c0001t0005g0009a0001c0003t0022g0007a0001c0004t0004g0008others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+533C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028444 | ||||||
| chr1:200028450
|
A | T | 40 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(37): Show | 40 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.64+539A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028450 | ||||||
| chr1:200028650
|
A | G | 95 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(92): Show | 95 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(92): Show |
intron_variant | MODIFIER | c.64+739A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028650 | ||||||
| chr1:200028722
|
T | TGC | 11 | a0001c0001t0002g0280a0001c0003t0002g0279a0001c0003t0002g0286others(8): Show | 11 | HG02148.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+811_64+812insGC | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028722 | ||||||
| chr1:200028724
|
TGGC | T | 11 | a0001c0001t0002g0280a0001c0003t0002g0279a0001c0003t0002g0286others(8): Show | 11 | HG02148.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+814_64+816delGG others(1): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028724 | ||||||
| chr1:200028760
|
C | T | 1 | a0001c0002t0001g0268 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.64+849C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028760 | ||||||
| chr1:200028868
|
T | C | 3 | a0001c0003t0031g0039a0001c0004t0004g0037a0001c0004t0004g0038 | 3 | HG02615.hp1 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64+957T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028868 | ||||||
| chr1:200028975
|
G | A | 4 | a0003c0006t0002g0004a0003c0006t0006g0003a0003c0006t0016g0001others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1064G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200028975 | ||||||
| chr1:200029064
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.64+1153G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029064 | ||||||
| chr1:200029153
|
G | T | 10 | a0001c0001t0003g0030a0001c0001t0005g0019a0001c0001t0005g0020others(7): Show | 10 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+1242G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029153 | ||||||
| chr1:200029167
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.64+1256G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029167 | ||||||
| chr1:200029176
|
G | A | 38 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(35): Show | 38 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.64+1265G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029176 | ||||||
| chr1:200029211
|
A | G | 1 | a0001c0002t0001g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64+1300A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029211 | ||||||
| chr1:200029363
|
C | G | 85 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(82): Show | 85 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.64+1452C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029363 | ||||||
| chr1:200029440
|
CTG | C | 38 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(35): Show | 38 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.64+1533_64+1534del others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200029440 | |||||
| chr1:200029462
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+1551C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029462 | ||||||
| chr1:200029612
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64+1701A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029612 | ||||||
| chr1:200029787
|
C | A | 38 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(35): Show | 38 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.64+1876C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029787 | ||||||
| chr1:200029993
|
G | A | 4 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0005g0097others(1): Show | 4 | HG00735.hp1 HG01081.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2082G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200029993 | ||||||
| chr1:200030667
|
A | G | 1 | a0001c0001t0005g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+2756A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200030667 | ||||||
| chr1:200030789
|
G | A | 41 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(38): Show | 41 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.64+2878G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200030789 | ||||||
| chr1:200030927
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+3016C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200030927 | ||||||
| chr1:200030980
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.64+3069C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200030980 | ||||||
| chr1:200030981
|
G | A | 34 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(31): Show | 34 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+3070G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200030981 | ||||||
| chr1:200030997
|
A | G | 108 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.64+3086A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200030997 | ||||||
| chr1:200031019
|
C | T | 34 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(31): Show | 34 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+3108C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200031019 | ||||||
| chr1:200031040
|
G | C | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+3129G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200031040 | ||||||
| chr1:200031201
|
CCAGAGTT others(2): Show |
C | 3 | a0001c0003t0013g0048a0001c0004t0007g0049a0001c0004t0007g0050 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+3298_64+3306del others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200031201 | |||||
| chr1:200031295
|
G | C | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64+3384G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200031295 | ||||||
| chr1:200031558
|
TTTTC | T | 9 | a0001c0001t0002g0280a0001c0003t0002g0279a0001c0004t0004g0276others(6): Show | 9 | HG02148.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+3651_64+3654del others(4): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200031558 | |||||
| chr1:200031562
|
C | A | 1 | a0001c0001t0028g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64+3651C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200031562 | ||||||
| chr1:200031571
|
C | CT | 40 | a0001c0001t0001g0163a0001c0001t0001g0261a0001c0001t0002g0069others(37): Show | 40 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.64+3684dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200031571 | |||||
| chr1:200031571
|
CT | C | 42 | a0001c0001t0003g0174a0001c0001t0005g0094a0001c0001t0005g0175others(39): Show | 42 | HG01074.hp1 HG01109.hp2 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.64+3684delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200031571 | |||||
| chr1:200031571
|
CTT | C | 29 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(26): Show | 29 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.64+3683_64+3684del others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200031571 | |||||
| chr1:200031571
|
CTTT | C | 9 | a0001c0001t0002g0280a0001c0003t0002g0279a0001c0004t0004g0008others(6): Show | 9 | HG02148.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+3682_64+3684del others(3): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200031571 | |||||
| chr1:200031571
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0006g0040a0001c0001t0015g0041 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.64+3674_64+3684del others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200031571 | |||||
| chr1:200031641
|
T | A | 34 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(31): Show | 34 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+3730T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200031641 | ||||||
| chr1:200031658
|
A | G | 10 | a0001c0001t0002g0034a0001c0001t0002g0280a0001c0003t0002g0279others(7): Show | 10 | HG01358.hp1 HG02148.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+3747A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200031658 | ||||||
| chr1:200032089
|
T | C | 1 | a0001c0004t0004g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64+4178T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032089 | ||||||
| chr1:200032277
|
G | A | 45 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(42): Show | 45 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.64+4366G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032277 | ||||||
| chr1:200032419
|
G | A | 107 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(104): Show | 107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.64+4508G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032419 | ||||||
| chr1:200032422
|
ATTTGGAG others(6): Show |
A | 2 | a0001c0001t0006g0270a0001c0001t0006g0271 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.64+4515_64+4527del others(13): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200032422 | |||||
| chr1:200032630
|
T | A | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64+4719T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032630 | ||||||
| chr1:200032663
|
A | G | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64+4752A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032663 | ||||||
| chr1:200032666
|
G | GAT | 11 | a0001c0001t0006g0040a0001c0001t0015g0041a0001c0002t0001g0070others(8): Show | 11 | HG01074.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+4770_64+4771dup others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200032666 | |||||
| chr1:200032688
|
G | A | 90 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(87): Show | 90 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(87): Show |
intron_variant | MODIFIER | c.64+4777G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032688 | ||||||
| chr1:200032774
|
G | GAGGTCAA others(14): Show |
1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+4864_64+4884dup others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200032774 | |||||
| chr1:200032939
|
T | G | 80 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(77): Show | 80 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.64+5028T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032939 | ||||||
| chr1:200032940
|
G | A | 80 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(77): Show | 80 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.64+5029G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032940 | ||||||
| chr1:200032998
|
C | A | 34 | a0001c0001t0005g0094a0001c0001t0006g0040a0001c0001t0006g0059others(31): Show | 34 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+5087C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200032998 | ||||||
| chr1:200033209
|
A | G | 90 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(87): Show | 90 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(87): Show |
intron_variant | MODIFIER | c.64+5298A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200033209 | ||||||
| chr1:200033216
|
G | T | 2 | a0001c0001t0005g0159a0001c0002t0001g0160 | 2 | HG00609.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.64+5305G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200033216 | ||||||
| chr1:200033341
|
TAAAC | T | 5 | a0001c0004t0004g0285a0003c0006t0002g0004a0003c0006t0006g0003others(2): Show | 5 | HG02055.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+5436_64+5439del others(4): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200033341 | |||||
| chr1:200033452
|
AT | A | 29 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0003g0030others(26): Show | 29 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.64+5542delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200033452 | ||||||
| chr1:200033614
|
T | A | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+5703T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200033614 | ||||||
| chr1:200033672
|
ATC | A | 5 | a0001c0004t0004g0285a0003c0006t0002g0004a0003c0006t0006g0003others(2): Show | 5 | HG02055.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+5768_64+5769del others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200033672 | |||||
| chr1:200033728
|
A | T | 217 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(214): Show | 217 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.64+5817A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200033728 | ||||||
| chr1:200033812
|
C | T | 1 | a0001c0004t0004g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.65-5846C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200033812 | ||||||
| chr1:200034072
|
G | A | 5 | a0001c0004t0004g0285a0003c0006t0002g0004a0003c0006t0006g0003others(2): Show | 5 | HG02055.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-5586G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034072 | ||||||
| chr1:200034103
|
T | C | 3 | a0001c0003t0013g0048a0001c0004t0007g0049a0001c0004t0007g0050 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-5555T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034103 | ||||||
| chr1:200034194
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.65-5464G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034194 | ||||||
| chr1:200034207
|
C | A | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.65-5451C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034207 | ||||||
| chr1:200034262
|
T | G | 17 | a0001c0001t0006g0059a0001c0003t0002g0056a0001c0003t0002g0274others(14): Show | 17 | HG01074.hp1 HG01109.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-5396T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034262 | ||||||
| chr1:200034387
|
C | T | 8 | a0001c0001t0006g0075a0001c0001t0009g0181a0001c0001t0012g0182others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-5271C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034387 | ||||||
| chr1:200034429
|
C | G | 4 | a0001c0001t0005g0009a0001c0003t0022g0007a0001c0004t0004g0008others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-5229C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034429 | ||||||
| chr1:200034543
|
G | A | 21 | a0001c0001t0006g0059a0001c0003t0002g0056a0001c0003t0002g0274others(18): Show | 21 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.65-5115G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034543 | ||||||
| chr1:200034588
|
GAGGTTGC others(21): Show |
G | 1 | a0001c0001t0002g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.65-5063_65-5036del others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034588 | |||||
| chr1:200034600
|
G | C | 5 | a0001c0004t0004g0285a0003c0006t0002g0004a0003c0006t0006g0003others(2): Show | 5 | HG02055.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-5058G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034600 | ||||||
| chr1:200034607
|
G | C | 6 | a0001c0001t0002g0110a0001c0001t0003g0105a0001c0001t0005g0106others(3): Show | 6 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-5051G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034607 | ||||||
| chr1:200034633
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG01496.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.65-5025A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034633 | ||||||
| chr1:200034677
|
C | T | 1 | a0004c0013t0032g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.65-4981C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034677 | ||||||
| chr1:200034742
|
G | A | 1 | a0001c0003t0002g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.65-4916G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034742 | ||||||
| chr1:200034783
|
C | CT | 27 | a0001c0001t0002g0110a0001c0001t0002g0173a0001c0001t0003g0143others(24): Show | 27 | HG00544.hp2 HG00735.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.65-4844dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
C | CTTTTTT | 6 | a0001c0001t0010g0092a0001c0002t0004g0091a0001c0002t0007g0093others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-4849_65-4844dup others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0011a0001c0001t0005g0094a0001c0004t0004g0015others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-4853_65-4844dup others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-4854_65-4844dup others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
C | CTTTTTTT others(5): Show |
2 | a0001c0003t0009g0013a0001c0003t0022g0007 | 2 | HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.65-4855_65-4844dup others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
C | CTTTTTTT others(6): Show |
3 | a0001c0003t0006g0036a0001c0004t0004g0008a0001c0004t0004g0010 | 3 | HG02896.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.65-4856_65-4844dup others(13): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
C | CTTTTTTT others(7): Show |
1 | a0001c0003t0006g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.65-4857_65-4844dup others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0006g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.65-4860_65-4844dup others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
CT | C | 11 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0003g0105others(8): Show | 11 | HG01099.hp2 HG01168.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-4844delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
CTTT | C | 10 | a0001c0001t0001g0229a0001c0001t0002g0081a0001c0001t0002g0262others(7): Show | 10 | HG00544.hp1 HG00738.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-4846_65-4844del others(3): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
CTTTT | C | 47 | a0001c0001t0001g0216a0001c0001t0001g0221a0001c0001t0001g0261others(44): Show | 47 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.65-4847_65-4844del others(4): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
CTTTTT | C | 44 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(41): Show | 44 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.65-4848_65-4844del others(5): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
CTTTTTT | C | 13 | a0001c0001t0002g0280a0001c0002t0001g0018a0001c0002t0001g0033others(10): Show | 13 | HG02148.hp2 HG02258.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-4849_65-4844del others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0006g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.65-4855_65-4844del others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034783
|
CTTTTTTT others(6): Show |
C | 25 | a0001c0001t0006g0059a0001c0003t0002g0056a0001c0003t0002g0274others(22): Show | 25 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.65-4856_65-4844del others(13): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200034783 | |||||
| chr1:200034814
|
T | A | 1 | a0001c0002t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.65-4844T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034814 | ||||||
| chr1:200034968
|
G | A | 1 | a0001c0005t0004g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.65-4690G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200034968 | ||||||
| chr1:200035012
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.65-4646G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035012 | ||||||
| chr1:200035077
|
C | G | 1 | a0001c0001t0003g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.65-4581C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035077 | ||||||
| chr1:200035088
|
G | A | 1 | a0001c0002t0004g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-4570G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035088 | ||||||
| chr1:200035111
|
C | G | 40 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(37): Show | 40 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.65-4547C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035111 | ||||||
| chr1:200035119
|
C | T | 1 | a0001c0001t0005g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.65-4539C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035119 | ||||||
| chr1:200035395
|
T | C | 91 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(88): Show | 91 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(88): Show |
intron_variant | MODIFIER | c.65-4263T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035395 | ||||||
| chr1:200035903
|
G | A | 1 | a0001c0003t0006g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.65-3755G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035903 | ||||||
| chr1:200035963
|
G | C | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.65-3695G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200035963 | ||||||
| chr1:200036015
|
A | G | 22 | a0001c0001t0005g0094a0001c0001t0006g0059a0001c0001t0010g0092others(19): Show | 22 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-3643A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036015 | ||||||
| chr1:200036035
|
G | A | 6 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0171others(3): Show | 6 | HG01070.hp1 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-3623G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036035 | ||||||
| chr1:200036065
|
C | G | 106 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(103): Show | 106 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.65-3593C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036065 | ||||||
| chr1:200036092
|
G | A | 1 | a0001c0004t0004g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65-3566G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036092 | ||||||
| chr1:200036117
|
G | A | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0005g0009others(15): Show | 18 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-3541G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036117 | ||||||
| chr1:200036125
|
C | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG01496.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.65-3533C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036125 | ||||||
| chr1:200036188
|
C | T | 25 | a0001c0001t0002g0280a0001c0001t0006g0270a0001c0001t0006g0271others(22): Show | 25 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.65-3470C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036188 | ||||||
| chr1:200036332
|
A | G | 14 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0024others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-3326A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036332 | ||||||
| chr1:200036483
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.65-3175A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036483 | ||||||
| chr1:200036491
|
G | T | 3 | a0001c0001t0010g0116a0001c0001t0010g0140a0001c0002t0001g0139 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.65-3167G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036491 | ||||||
| chr1:200036905
|
A | G | 12 | a0001c0001t0002g0034a0001c0001t0003g0030a0001c0001t0005g0019others(9): Show | 12 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-2753A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036905 | ||||||
| chr1:200036983
|
C | A | 93 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(90): Show | 93 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.65-2675C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200036983 | ||||||
| chr1:200037089
|
G | T | 108 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.65-2569G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037089 | ||||||
| chr1:200037169
|
G | A | 1 | a0001c0003t0002g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-2489G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037169 | ||||||
| chr1:200037372
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.65-2286A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037372 | ||||||
| chr1:200037412
|
G | A | 1 | a0001c0002t0001g0118 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.65-2246G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037412 | ||||||
| chr1:200037582
|
T | C | 11 | a0001c0001t0002g0280a0001c0003t0002g0279a0001c0004t0004g0008others(8): Show | 11 | HG02148.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-2076T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037582 | ||||||
| chr1:200037709
|
C | A | 1 | a0001c0003t0009g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.65-1949C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037709 | ||||||
| chr1:200037733
|
C | T | 108 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.65-1925C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037733 | ||||||
| chr1:200037865
|
C | A | 1 | a0001c0003t0002g0170 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.65-1793C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200037865 | ||||||
| chr1:200038149
|
GGT | G | 4 | a0003c0006t0002g0004a0003c0006t0006g0003a0003c0006t0016g0001others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-1508_65-1507del others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038149 | ||||||
| chr1:200038164
|
G | A | 1 | a0001c0001t0011g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.65-1494G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038164 | ||||||
| chr1:200038197
|
G | T | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.65-1461G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038197 | ||||||
| chr1:200038251
|
C | A | 41 | a0001c0001t0002g0280a0001c0001t0006g0040a0001c0001t0006g0059others(38): Show | 41 | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.65-1407C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038251 | ||||||
| chr1:200038271
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.65-1387A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038271 | ||||||
| chr1:200038304
|
A | G | 97 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(94): Show | 97 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.65-1354A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038304 | ||||||
| chr1:200038554
|
C | T | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.65-1104C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038554 | ||||||
| chr1:200038736
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.65-922G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038736 | ||||||
| chr1:200038802
|
G | T | 2 | a0001c0003t0013g0269a0001c0004t0004g0088 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.65-856G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200038802 | ||||||
| chr1:200038949
|
ACCCCTCA others(12): Show |
A | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.65-705_65-687delCT others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 200038949 | |||||
| chr1:200039083
|
A | G | 3 | a0001c0001t0001g0261a0001c0001t0003g0206a0001c0002t0001g0233 | 3 | NA18945.hp2 NA18960.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.65-575A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200039083 | ||||||
| chr1:200039127
|
C | A | 1 | a0002c0008t0012g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-531C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200039127 | ||||||
| chr1:200039143
|
A | G | 204 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(201): Show | 204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.65-515A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200039143 | ||||||
| chr1:200039209
|
G | A | 108 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.65-449G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200039209 | ||||||
| chr1:200039356
|
G | T | 1 | a0001c0001t0008g0231 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.65-302G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200039356 | ||||||
| chr1:200039375
|
C | T | 2 | a0001c0005t0006g0060a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.65-283C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200039375 | ||||||
| chr1:200039541
|
G | T | 3 | a0001c0005t0004g0021a0001c0005t0004g0022a0001c0005t0004g0023 | 3 | HG02965.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.65-117G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 1/7 | chr1 | 200039541 | ||||||
| chr1:200039805
|
C | T | 2 | a0001c0001t0002g0252a0001c0001t0003g0205 | 2 | HG03710.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.202+10C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200039805 | ||||||
| chr1:200039813
|
G | T | 13 | a0001c0001t0001g0137a0001c0001t0003g0030a0001c0001t0005g0019others(10): Show | 13 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+18G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200039813 | ||||||
| chr1:200040043
|
C | A | 3 | a0001c0001t0010g0092a0001c0002t0004g0091a0001c0002t0007g0093 | 3 | HG03130.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.202+248C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040043 | ||||||
| chr1:200040208
|
C | T | 28 | a0001c0001t0002g0280a0001c0001t0006g0040a0001c0001t0006g0059others(25): Show | 28 | HG02148.hp2 HG02258.hp1 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.202+413C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040208 | ||||||
| chr1:200040266
|
A | G | 4 | a0001c0004t0001g0047a0001c0004t0001g0052a0001c0004t0001g0053others(1): Show | 4 | NA18942.hp2 NA19005.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+471A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040266 | ||||||
| chr1:200040309
|
G | A | 1 | a0001c0002t0004g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202+514G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040309 | ||||||
| chr1:200040561
|
A | AGATC | 90 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(87): Show | 90 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(87): Show |
intron_variant | MODIFIER | c.202+766_202+767ins others(4): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040561 | ||||||
| chr1:200040877
|
C | A | 5 | a0001c0001t0005g0094a0001c0001t0010g0092a0001c0002t0004g0090others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+1082C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040877 | ||||||
| chr1:200040900
|
A | T | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.202+1105A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040900 | ||||||
| chr1:200040904
|
C | T | 4 | a0003c0006t0002g0004a0003c0006t0006g0003a0003c0006t0016g0001others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+1109C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040904 | ||||||
| chr1:200040913
|
TCCTGGGG others(6): Show |
T | 1 | a0001c0001t0005g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.202+1120_202+1132d others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 200040913 | |||||
| chr1:200040938
|
G | A | 2 | a0001c0005t0006g0060a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.202+1143G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200040938 | ||||||
| chr1:200041071
|
G | A | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0005g0009others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+1276G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041071 | ||||||
| chr1:200041218
|
A | G | 28 | a0001c0001t0002g0280a0001c0001t0006g0040a0001c0001t0006g0059others(25): Show | 28 | HG02148.hp2 HG02258.hp1 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.202+1423A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041218 | ||||||
| chr1:200041228
|
AGAGCG | A | 28 | a0001c0001t0002g0280a0001c0001t0006g0040a0001c0001t0006g0059others(25): Show | 28 | HG02148.hp2 HG02258.hp1 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.202+1437_202+1441d others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 200041228 | |||||
| chr1:200041364
|
T | C | 10 | a0001c0001t0005g0094a0001c0001t0010g0092a0001c0002t0004g0090others(7): Show | 10 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+1569T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041364 | ||||||
| chr1:200041505
|
G | A | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0005g0009others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+1710G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041505 | ||||||
| chr1:200041653
|
G | C | 1 | a0001c0003t0005g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.202+1858G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041653 | ||||||
| chr1:200041670
|
C | T | 1 | a0001c0003t0002g0157 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.202+1875C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041670 | ||||||
| chr1:200041694
|
C | A | 4 | a0001c0001t0006g0059a0001c0003t0013g0048a0001c0004t0007g0049others(1): Show | 4 | HG02622.hp2 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+1899C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041694 | ||||||
| chr1:200041696
|
C | T | 110 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.202+1901C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041696 | ||||||
| chr1:200041746
|
C | G | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.202+1951C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041746 | ||||||
| chr1:200041800
|
A | G | 91 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(88): Show | 91 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(88): Show |
intron_variant | MODIFIER | c.203-1974A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200041800 | ||||||
| chr1:200041908
|
GTTTAC | G | 13 | a0001c0001t0001g0137a0001c0001t0002g0173a0001c0001t0003g0030others(10): Show | 13 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.203-1862_203-1858d others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 200041908 | |||||
| chr1:200042217
|
G | A | 3 | a0001c0003t0013g0048a0001c0004t0007g0049a0001c0004t0007g0050 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.203-1557G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042217 | ||||||
| chr1:200042264
|
T | G | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.203-1510T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042264 | ||||||
| chr1:200042275
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.203-1499G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042275 | ||||||
| chr1:200042335
|
T | A | 1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-1439T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042335 | ||||||
| chr1:200042375
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.203-1399A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042375 | ||||||
| chr1:200042429
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.203-1345G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042429 | ||||||
| chr1:200042449
|
T | C | 1 | a0001c0004t0004g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.203-1325T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042449 | ||||||
| chr1:200042512
|
C | G | 1 | a0001c0003t0002g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.203-1262C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042512 | ||||||
| chr1:200042529
|
T | TC | 5 | a0001c0001t0002g0280a0003c0006t0002g0004a0003c0006t0006g0003others(2): Show | 5 | HG02055.hp1 HG02965.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.203-1240dupC | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 200042529 | |||||
| chr1:200042543
|
C | T | 2 | a0001c0002t0001g0183a0001c0002t0001g0244 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.203-1231C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042543 | ||||||
| chr1:200042690
|
C | T | 55 | a0001c0001t0002g0112a0001c0001t0006g0040a0001c0001t0006g0059others(52): Show | 55 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.203-1084C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042690 | ||||||
| chr1:200042946
|
TTTAATAG others(5): Show |
T | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.203-826_203-815del others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 200042946 | |||||
| chr1:200042960
|
C | A | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.203-814C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200042960 | ||||||
| chr1:200043427
|
T | C | 1 | a0001c0002t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.203-347T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200043427 | ||||||
| chr1:200043520
|
G | A | 2 | a0003c0006t0016g0001a0003c0010t0001g0002 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.203-254G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200043520 | ||||||
| chr1:200043593
|
T | C | 2 | a0001c0001t0006g0270a0001c0001t0006g0271 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.203-181T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200043593 | ||||||
| chr1:200043673
|
G | A | 1 | a0001c0001t0019g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.203-101G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 2/7 | chr1 | 200043673 | ||||||
| chr1:200043987
|
T | A | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0003t0006g0014others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+95T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200043987 | ||||||
| chr1:200043995
|
C | A | 27 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0003t0002g0056others(24): Show | 27 | HG01074.hp1 HG01109.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.321+103C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200043995 | ||||||
| chr1:200044122
|
A | C | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+230A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200044122 | ||||||
| chr1:200044167
|
T | C | 2 | a0001c0001t0003g0234a0001c0001t0011g0078 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.321+275T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200044167 | ||||||
| chr1:200044385
|
T | G | 52 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0216others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.321+493T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200044385 | ||||||
| chr1:200044713
|
G | C | 7 | a0001c0001t0002g0280a0001c0001t0006g0270a0001c0001t0006g0271others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-730G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200044713 | ||||||
| chr1:200044781
|
C | A | 25 | a0001c0003t0001g0027a0001c0003t0002g0043a0001c0003t0002g0102others(22): Show | 25 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.322-662C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200044781 | ||||||
| chr1:200044980
|
T | TA | 30 | a0001c0001t0001g0137a0001c0001t0002g0110a0001c0001t0002g0173others(27): Show | 30 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.322-448dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 200044980 | |||||
| chr1:200044980
|
TA | T | 14 | a0001c0001t0002g0034a0001c0001t0002g0151a0001c0001t0002g0169others(11): Show | 14 | HG01358.hp1 HG01496.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.322-448delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 200044980 | |||||
| chr1:200044995
|
AT | A | 14 | a0001c0003t0001g0027a0001c0003t0002g0102a0001c0003t0002g0152others(11): Show | 14 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.322-447delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200044995 | ||||||
| chr1:200044996
|
T | A | 2 | a0001c0003t0002g0154a0001c0004t0020g0063 | 2 | HG01256.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.322-447T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200044996 | ||||||
| chr1:200045050
|
A | C | 2 | a0001c0001t0002g0133a0001c0002t0001g0134 | 2 | HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.322-393A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200045050 | ||||||
| chr1:200045138
|
TA | T | 7 | a0001c0001t0002g0280a0001c0001t0006g0270a0001c0001t0006g0271others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-296delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 200045138 | |||||
| chr1:200045147
|
A | T | 2 | a0003c0006t0002g0004a0003c0006t0006g0003 | 2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.322-296A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200045147 | ||||||
| chr1:200045160
|
G | A | 7 | a0001c0001t0002g0280a0001c0001t0006g0270a0001c0001t0006g0271others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-283G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200045160 | ||||||
| chr1:200045222
|
C | T | 3 | a0001c0001t0005g0031a0001c0001t0005g0032a0001c0001t0005g0097 | 3 | HG00639.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.322-221C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200045222 | ||||||
| chr1:200045288
|
G | C | 13 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(10): Show | 13 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-155G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200045288 | ||||||
| chr1:200045432
|
C | T | 13 | a0001c0001t0001g0137a0001c0001t0002g0173a0001c0001t0003g0030others(10): Show | 13 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.322-11C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 3/7 | chr1 | 200045432 | ||||||
| chr1:200045628
|
G | A | 3 | a0001c0003t0013g0048a0001c0004t0007g0049a0001c0004t0007g0050 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.463+44G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200045628 | ||||||
| chr1:200045634
|
A | G | 106 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(103): Show | 106 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.463+50A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200045634 | ||||||
| chr1:200045638
|
G | T | 35 | a0001c0001t0001g0137a0001c0001t0002g0034a0001c0001t0002g0110others(32): Show | 35 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.463+54G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200045638 | ||||||
| chr1:200045662
|
A | G | 71 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0059others(68): Show | 71 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.463+78A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200045662 | ||||||
| chr1:200045731
|
G | A | 28 | a0001c0001t0001g0137a0001c0001t0002g0034a0001c0001t0002g0110others(25): Show | 28 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.463+147G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200045731 | ||||||
| chr1:200045968
|
T | C | 2 | a0001c0002t0001g0119a0001c0002t0001g0120 | 2 | NA18980.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.463+384T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200045968 | ||||||
| chr1:200046051
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.463+467A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046051 | ||||||
| chr1:200046100
|
T | C | 18 | a0001c0003t0001g0027a0001c0003t0002g0102a0001c0003t0002g0152others(15): Show | 18 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.463+516T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046100 | ||||||
| chr1:200046141
|
C | G | 1 | a0001c0003t0031g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.463+557C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046141 | ||||||
| chr1:200046189
|
C | T | 1 | a0001c0004t0004g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.463+605C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046189 | ||||||
| chr1:200046467
|
A | C | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.463+883A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046467 | ||||||
| chr1:200046468
|
G | A | 15 | a0001c0003t0002g0286a0001c0003t0006g0035a0001c0003t0006g0061others(12): Show | 15 | HG01074.hp2 HG01884.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.463+884G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046468 | ||||||
| chr1:200046470
|
G | C | 1 | a0001c0001t0002g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.463+886G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046470 | ||||||
| chr1:200046602
|
A | G | 13 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(10): Show | 13 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.463+1018A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200046602 | ||||||
| chr1:200047018
|
T | C | 106 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(103): Show | 106 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.464-1154T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047018 | ||||||
| chr1:200047107
|
C | G | 2 | a0001c0003t0002g0043a0001c0003t0017g0042 | 2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.464-1065C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047107 | ||||||
| chr1:200047109
|
A | G | 3 | a0001c0003t0013g0048a0001c0004t0007g0049a0001c0004t0007g0050 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.464-1063A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047109 | ||||||
| chr1:200047193
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.464-979G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047193 | ||||||
| chr1:200047240
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.464-932G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047240 | ||||||
| chr1:200047267
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.464-905A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047267 | ||||||
| chr1:200047299
|
T | C | 7 | a0001c0001t0002g0280a0001c0001t0006g0270a0001c0001t0006g0271others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-873T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047299 | ||||||
| chr1:200047332
|
C | A | 37 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(34): Show | 37 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.464-840C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047332 | ||||||
| chr1:200047431
|
A | G | 7 | a0001c0003t0002g0043a0001c0003t0013g0269a0001c0003t0017g0042others(4): Show | 7 | HG02615.hp1 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-741A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047431 | ||||||
| chr1:200047508
|
G | A | 1 | a0001c0003t0002g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.464-664G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047508 | ||||||
| chr1:200047584
|
C | CTTTTTTT | 31 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(28): Show | 31 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.464-586_464-580dup others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 200047584 | |||||
| chr1:200047584
|
C | CTTTTTTT others(1): Show |
66 | a0001c0003t0001g0027a0001c0003t0002g0043a0001c0003t0002g0056others(63): Show | 66 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.464-587_464-580dup others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 200047584 | |||||
| chr1:200047584
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0002g0280a0001c0001t0006g0270a0001c0001t0006g0271others(6): Show | 9 | HG01256.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-580_464-579ins others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 200047584 | |||||
| chr1:200047778
|
A | C | 1 | a0001c0003t0002g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.464-394A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047778 | ||||||
| chr1:200047874
|
C | T | 2 | a0001c0001t0002g0165a0001c0001t0003g0148 | 2 | HG00738.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.464-298C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 4/7 | chr1 | 200047874 | ||||||
| chr1:200049075
|
T | C | 1 | a0001c0003t0016g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+257T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200049075 | ||||||
| chr1:200049203
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1110+385T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200049203 | ||||||
| chr1:200049311
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+493G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200049311 | ||||||
| chr1:200049476
|
T | C | 11 | a0001c0001t0002g0280a0001c0001t0006g0270a0001c0001t0006g0271others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+658T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200049476 | ||||||
| chr1:200049723
|
G | A | 28 | a0001c0003t0002g0056a0001c0003t0002g0098a0001c0003t0002g0274others(25): Show | 28 | HG01074.hp1 HG01109.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.1110+905G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200049723 | ||||||
| chr1:200049975
|
C | A | 7 | a0001c0003t0002g0279a0001c0004t0004g0276a0002c0008t0002g0087others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+1157C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200049975 | ||||||
| chr1:200050045
|
G | A | 11 | a0001c0001t0001g0071a0001c0001t0003g0113a0001c0001t0003g0122others(8): Show | 11 | HG00408.hp2 HG00621.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1227G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050045 | ||||||
| chr1:200050060
|
G | C | 62 | a0001c0001t0005g0094a0001c0001t0006g0059a0001c0002t0004g0090others(59): Show | 62 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1110+1242G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050060 | ||||||
| chr1:200050167
|
C | T | 1 | a0001c0004t0001g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1110+1349C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050167 | ||||||
| chr1:200050229
|
T | C | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1110+1411T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050229 | ||||||
| chr1:200050429
|
A | T | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1110+1611A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050429 | ||||||
| chr1:200050446
|
G | A | 1 | a0001c0001t0005g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1110+1628G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050446 | ||||||
| chr1:200050545
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1110+1727C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050545 | ||||||
| chr1:200050546
|
G | A | 1 | a0002c0008t0002g0087 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1110+1728G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050546 | ||||||
| chr1:200050560
|
T | G | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1110+1742T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050560 | ||||||
| chr1:200050662
|
G | A | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1110+1844G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050662 | ||||||
| chr1:200050688
|
C | A | 1 | a0001c0001t0006g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1110+1870C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050688 | ||||||
| chr1:200050694
|
C | A | 2 | a0001c0001t0005g0031a0001c0001t0005g0032 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1110+1876C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050694 | ||||||
| chr1:200050823
|
C | T | 62 | a0001c0001t0005g0094a0001c0001t0006g0059a0001c0002t0004g0090others(59): Show | 62 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1110+2005C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050823 | ||||||
| chr1:200050879
|
C | T | 4 | a0001c0004t0001g0047a0001c0004t0001g0052a0001c0004t0001g0053others(1): Show | 4 | NA18942.hp2 NA19005.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+2061C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050879 | ||||||
| chr1:200050932
|
T | A | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1110+2114T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200050932 | ||||||
| chr1:200051054
|
G | A | 117 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(114): Show | 117 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(114): Show |
intron_variant | MODIFIER | c.1110+2236G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051054 | ||||||
| chr1:200051110
|
G | A | 1 | a0001c0001t0019g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1110+2292G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051110 | ||||||
| chr1:200051130
|
AAAC | A | 7 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+2316_1110+231 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200051130 | |||||
| chr1:200051133
|
C | T | 18 | a0001c0003t0001g0027a0001c0003t0002g0102a0001c0003t0002g0152others(15): Show | 18 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1110+2315C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051133 | ||||||
| chr1:200051239
|
T | C | 4 | a0001c0004t0001g0047a0001c0004t0001g0052a0001c0004t0001g0053others(1): Show | 4 | NA18942.hp2 NA19005.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+2421T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051239 | ||||||
| chr1:200051294
|
C | CATT | 102 | a0001c0001t0001g0137a0001c0001t0002g0034a0001c0001t0002g0173others(99): Show | 102 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.1110+2478_1110+247 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200051294 | |||||
| chr1:200051334
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+2516G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051334 | ||||||
| chr1:200051652
|
T | G | 2 | a0001c0001t0002g0133a0001c0002t0001g0134 | 2 | HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1110+2834T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051652 | ||||||
| chr1:200051675
|
CA | C | 7 | a0001c0003t0006g0014a0001c0003t0006g0036a0001c0003t0009g0013others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+2860delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200051675 | |||||
| chr1:200051764
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1110+2946C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051764 | ||||||
| chr1:200051806
|
G | C | 1 | a0001c0001t0006g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1110+2988G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051806 | ||||||
| chr1:200051888
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1110+3070A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051888 | ||||||
| chr1:200051915
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1110+3097C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200051915 | ||||||
| chr1:200052026
|
C | G | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1110+3208C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052026 | ||||||
| chr1:200052037
|
T | C | 1 | a0001c0003t0022g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+3219T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052037 | ||||||
| chr1:200052098
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1110+3280C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052098 | ||||||
| chr1:200052099
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1110+3281G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052099 | ||||||
| chr1:200052133
|
A | G | 63 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(60): Show | 63 | HG00558.hp1 HG00642.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1110+3315A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052133 | ||||||
| chr1:200052140
|
C | A | 5 | a0002c0008t0002g0087a0002c0008t0012g0084a0002c0008t0012g0085others(2): Show | 5 | HG01884.hp2 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+3322C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052140 | ||||||
| chr1:200052176
|
G | A | 3 | a0001c0001t0005g0094a0001c0002t0004g0090a0001c0002t0004g0091 | 3 | HG02630.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1110+3358G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052176 | ||||||
| chr1:200052338
|
T | C | 18 | a0001c0001t0003g0105a0001c0001t0010g0116a0001c0001t0010g0140others(15): Show | 18 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1110+3520T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052338 | ||||||
| chr1:200052446
|
G | GAAGTGCT others(447): Show |
1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1110+4042_1110+404 others(458): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200052446 | |||||
| chr1:200052460
|
A | G | 1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+3642A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052460 | ||||||
| chr1:200052648
|
C | CT | 36 | a0001c0001t0006g0024a0001c0001t0006g0270a0001c0001t0006g0271others(33): Show | 36 | HG01074.hp2 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1110+3841dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200052648 | |||||
| chr1:200052685
|
A | G | 1 | a0001c0002t0001g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1110+3867A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052685 | ||||||
| chr1:200052688
|
T | C | 2 | a0001c0002t0001g0222a0001c0003t0002g0286 | 2 | HG02280.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1110+3870T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052688 | ||||||
| chr1:200052693
|
G | A | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110+3875G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052693 | ||||||
| chr1:200052717
|
T | C | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110+3899T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052717 | ||||||
| chr1:200052753
|
T | C | 91 | a0001c0001t0001g0229a0001c0001t0002g0081a0001c0001t0002g0110others(88): Show | 91 | HG00544.hp1 HG01074.hp2 HG01109.hp2 others(88): Show |
intron_variant | MODIFIER | c.1110+3935T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052753 | ||||||
| chr1:200052766
|
T | C | 2 | a0001c0001t0002g0133a0001c0004t0007g0050 | 2 | HG01070.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1110+3948T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052766 | ||||||
| chr1:200052786
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1110+3968T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052786 | ||||||
| chr1:200052790
|
T | C | 3 | a0001c0001t0002g0133a0001c0001t0006g0024a0001c0001t0027g0245 | 3 | HG01070.hp2 HG02886.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1110+3972T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052790 | ||||||
| chr1:200052797
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1110+3979A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052797 | ||||||
| chr1:200052799
|
G | GC | 18 | a0001c0001t0002g0133a0001c0003t0002g0056a0001c0003t0009g0224others(15): Show | 18 | HG01070.hp2 HG01109.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1110+3983dupC | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200052799 | |||||
| chr1:200052821
|
T | C | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+4003T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052821 | ||||||
| chr1:200052830
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1110+4012C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052830 | ||||||
| chr1:200052831
|
G | A | 16 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0003g0105others(13): Show | 16 | HG00741.hp1 HG00741.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1110+4013G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052831 | ||||||
| chr1:200052833
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0003g0256a0001c0002t0001g0187 | 3 | HG04199.hp1 NA18906.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1110+4015T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052833 | ||||||
| chr1:200052851
|
A | G | 24 | a0001c0001t0002g0110a0001c0001t0002g0161a0001c0001t0002g0168others(21): Show | 24 | HG00639.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1110+4033A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052851 | ||||||
| chr1:200052861
|
T | C | 115 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(112): Show | 115 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1110+4043T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052861 | ||||||
| chr1:200052867
|
C | G | 110 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1110+4049C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052867 | ||||||
| chr1:200052884
|
C | T | 6 | a0001c0003t0006g0014a0001c0003t0006g0036a0001c0003t0009g0013others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+4066C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052884 | ||||||
| chr1:200052886
|
C | T | 2 | a0001c0001t0005g0094a0001c0002t0004g0090 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1110+4068C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052886 | ||||||
| chr1:200052905
|
T | G | 1 | a0001c0001t0003g0206 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1110+4087T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052905 | ||||||
| chr1:200052915
|
T | C | 11 | a0001c0001t0002g0252a0001c0001t0002g0262a0001c0002t0001g0028others(8): Show | 11 | HG00738.hp1 HG01109.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+4097T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052915 | ||||||
| chr1:200052920
|
A | G | 62 | a0001c0001t0001g0229a0001c0001t0002g0034a0001c0001t0002g0110others(59): Show | 62 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1110+4102A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052920 | ||||||
| chr1:200052929
|
C | T | 1 | a0001c0001t0027g0245 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1110+4111C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052929 | ||||||
| chr1:200052930
|
G | A | 1 | a0001c0001t0008g0195 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1110+4112G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052930 | ||||||
| chr1:200052932
|
A | G | 2 | a0001c0001t0003g0030a0001c0001t0006g0017 | 2 | HG02809.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1110+4114A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200052932 | ||||||
| chr1:200053053
|
T | G | 11 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+4235T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053053 | ||||||
| chr1:200053126
|
AAAG | A | 21 | a0001c0003t0002g0056a0001c0003t0006g0014a0001c0003t0006g0036others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110+4315_1110+431 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053126 | |||||
| chr1:200053148
|
A | G | 7 | a0001c0003t0006g0014a0001c0003t0006g0036a0001c0003t0009g0013others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+4330A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053148 | ||||||
| chr1:200053368
|
C | T | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1110+4550C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053368 | ||||||
| chr1:200053472
|
T | C | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+4654T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053472 | ||||||
| chr1:200053479
|
C | G | 1 | a0001c0001t0002g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1110+4661C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053479 | ||||||
| chr1:200053539
|
G | A | 88 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0104others(85): Show | 88 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1110+4721G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053539 | ||||||
| chr1:200053548
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1110+4730C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053548 | ||||||
| chr1:200053567
|
A | ACG | 37 | a0001c0001t0001g0202a0001c0001t0002g0034a0001c0001t0002g0151others(34): Show | 37 | HG00639.hp1 HG00735.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110+4751_1110+475 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053567 | |||||
| chr1:200053569
|
G | GCA | 35 | a0001c0001t0001g0137a0001c0001t0001g0229a0001c0001t0002g0112others(32): Show | 35 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1110+4788_1110+478 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCACA | 59 | a0001c0001t0001g0071a0001c0001t0001g0261a0001c0001t0002g0011others(56): Show | 59 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1110+4786_1110+478 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCACACA | 12 | a0001c0001t0001g0163a0001c0001t0001g0201a0001c0001t0008g0005others(9): Show | 12 | HG02155.hp1 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+4784_1110+478 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCACACAC others(1): Show |
7 | a0001c0001t0002g0207a0001c0001t0003g0247a0001c0001t0008g0138others(4): Show | 7 | HG00408.hp2 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+4782_1110+478 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0003g0006a0001c0001t0003g0256a0001c0002t0029g0142 | 3 | HG02040.hp2 HG04199.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1110+4780_1110+478 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0002g0251 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1110+4778_1110+478 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCGCA | 16 | a0001c0001t0001g0192a0001c0001t0001g0221a0001c0001t0002g0150others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1110+4752_1110+475 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCGCACA | 12 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0002t0001g0267others(9): Show | 12 | HG01515.hp1 HG01517.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+4752_1110+475 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCGCACAC others(1): Show |
10 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0171others(7): Show | 10 | HG01255.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+4752_1110+475 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCGCACAC others(3): Show |
12 | a0001c0001t0003g0105a0001c0001t0005g0097a0001c0001t0005g0214others(9): Show | 12 | HG00741.hp1 HG01081.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+4752_1110+475 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCGCACAC others(5): Show |
10 | a0001c0001t0001g0095a0001c0001t0008g0103a0001c0003t0002g0056others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+4752_1110+475 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCGCACAC others(7): Show |
2 | a0001c0003t0017g0042a0001c0004t0006g0045 | 2 | HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+4752_1110+475 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
G | GCGCGCAC others(5): Show |
1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1110+4752_1110+475 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
GCA | G | 11 | a0001c0001t0001g0216a0001c0001t0002g0104a0001c0001t0003g0206others(8): Show | 11 | HG00558.hp1 HG01074.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+4788_1110+478 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
GCACA | G | 3 | a0001c0001t0002g0117a0001c0002t0001g0033a0001c0004t0004g0067 | 3 | HG01081.hp1 HG02735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1110+4786_1110+478 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053569
|
GCACACAC others(1): Show |
G | 15 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(12): Show | 15 | HG01346.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+4782_1110+478 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200053569 | |||||
| chr1:200053571
|
A | G | 16 | a0001c0001t0005g0019a0001c0001t0006g0017a0001c0001t0006g0271others(13): Show | 16 | HG00558.hp2 HG01256.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1110+4753A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053571 | ||||||
| chr1:200053573
|
A | G | 5 | a0001c0001t0002g0104a0001c0001t0006g0270a0001c0003t0002g0274others(2): Show | 5 | HG01074.hp1 HG01192.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+4755A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053573 | ||||||
| chr1:200053575
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1110+4757A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053575 | ||||||
| chr1:200053577
|
A | G | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+4759A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053577 | ||||||
| chr1:200053607
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1110+4789_1110+479 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053607 | ||||||
| chr1:200053607
|
A | ACACACAC others(8): Show |
1 | a0001c0003t0002g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1110+4789_1110+479 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053607 | ||||||
| chr1:200053659
|
G | A | 5 | a0001c0001t0006g0270a0001c0001t0006g0271a0001c0003t0002g0286others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+4841G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053659 | ||||||
| chr1:200053668
|
A | G | 2 | a0001c0001t0002g0112a0001c0002t0001g0132 | 2 | HG01099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1110+4850A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053668 | ||||||
| chr1:200053958
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1110+5140C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053958 | ||||||
| chr1:200053987
|
A | G | 19 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0161others(16): Show | 19 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+5169A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200053987 | ||||||
| chr1:200054013
|
G | A | 9 | a0001c0002t0021g0046a0001c0003t0006g0014a0001c0003t0006g0036others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1110+5195G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054013 | ||||||
| chr1:200054025
|
C | T | 19 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0161others(16): Show | 19 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+5207C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054025 | ||||||
| chr1:200054138
|
A | G | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+5320A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054138 | ||||||
| chr1:200054210
|
A | C | 1 | a0001c0003t0006g0035 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1110+5392A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054210 | ||||||
| chr1:200054249
|
T | C | 21 | a0001c0002t0021g0046a0001c0003t0002g0056a0001c0003t0006g0014others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110+5431T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054249 | ||||||
| chr1:200054335
|
CAAG | C | 21 | a0001c0002t0021g0046a0001c0003t0002g0056a0001c0003t0006g0014others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110+5522_1110+552 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200054335 | |||||
| chr1:200054347
|
C | CT | 12 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+5538dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200054347 | |||||
| chr1:200054362
|
AT | A | 37 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0204others(34): Show | 37 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.1110+5554delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200054362 | |||||
| chr1:200054390
|
T | G | 5 | a0001c0001t0006g0270a0001c0001t0006g0271a0001c0003t0002g0286others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+5572T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054390 | ||||||
| chr1:200054535
|
T | C | 15 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(12): Show | 15 | HG01346.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+5717T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054535 | ||||||
| chr1:200054724
|
C | T | 15 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(12): Show | 15 | HG01346.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+5906C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054724 | ||||||
| chr1:200054775
|
T | A | 15 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0161others(12): Show | 15 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1110+5957T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054775 | ||||||
| chr1:200054784
|
T | C | 1 | a0001c0001t0005g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1110+5966T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054784 | ||||||
| chr1:200054830
|
C | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0145 | 2 | HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1110+6012C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200054830 | ||||||
| chr1:200055141
|
T | C | 124 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0011others(121): Show | 124 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1110+6323T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200055141 | ||||||
| chr1:200055172
|
G | A | 94 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0104others(91): Show | 94 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1110+6354G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200055172 | ||||||
| chr1:200055282
|
A | G | 94 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0104others(91): Show | 94 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1110+6464A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200055282 | ||||||
| chr1:200055321
|
G | A | 1 | a0001c0002t0001g0184 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1110+6503G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200055321 | ||||||
| chr1:200055327
|
C | T | 5 | a0001c0001t0006g0270a0001c0001t0006g0271a0001c0003t0002g0286others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+6509C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200055327 | ||||||
| chr1:200055367
|
G | A | 21 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(18): Show | 21 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1110+6549G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200055367 | ||||||
| chr1:200055570
|
G | A | 1 | a0001c0001t0011g0124 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1110+6752G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200055570 | ||||||
| chr1:200056038
|
A | G | 16 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0197others(13): Show | 16 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1110+7220A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056038 | ||||||
| chr1:200056137
|
A | G | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+7319A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056137 | ||||||
| chr1:200056279
|
G | C | 2 | a0003c0006t0016g0001a0003c0010t0001g0002 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1110+7461G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056279 | ||||||
| chr1:200056368
|
A | G | 14 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0105others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+7550A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056368 | ||||||
| chr1:200056386
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110+7568C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056386 | ||||||
| chr1:200056546
|
T | C | 1 | a0001c0003t0022g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+7728T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056546 | ||||||
| chr1:200056614
|
A | C | 1 | a0001c0002t0001g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1110+7796A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056614 | ||||||
| chr1:200056681
|
C | T | 2 | a0001c0003t0009g0223a0001c0003t0009g0257 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1110+7863C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056681 | ||||||
| chr1:200056758
|
T | C | 94 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0104others(91): Show | 94 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1110+7940T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056758 | ||||||
| chr1:200056940
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1110+8122G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200056940 | ||||||
| chr1:200057014
|
T | G | 5 | a0001c0001t0006g0270a0001c0001t0006g0271a0001c0003t0002g0286others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+8196T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057014 | ||||||
| chr1:200057095
|
A | G | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+8277A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057095 | ||||||
| chr1:200057260
|
C | T | 2 | a0002c0008t0002g0087a0002c0009t0007g0089 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1110+8442C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057260 | ||||||
| chr1:200057428
|
T | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0212 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1110+8610T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057428 | ||||||
| chr1:200057561
|
C | A | 2 | a0001c0001t0002g0168a0001c0001t0002g0169 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1110+8743C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057561 | ||||||
| chr1:200057593
|
C | T | 1 | a0001c0001t0005g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1110+8775C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057593 | ||||||
| chr1:200057768
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1110+8950A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057768 | ||||||
| chr1:200057781
|
G | A | 118 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0011others(115): Show | 118 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110+8963G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057781 | ||||||
| chr1:200057819
|
T | C | 21 | a0001c0002t0021g0046a0001c0003t0002g0056a0001c0003t0006g0014others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110+9001T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200057819 | ||||||
| chr1:200058093
|
C | T | 1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+9275C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058093 | ||||||
| chr1:200058187
|
G | A | 5 | a0001c0001t0002g0104a0001c0003t0002g0274a0001c0003t0006g0061others(2): Show | 5 | HG01074.hp1 HG01074.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+9369G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058187 | ||||||
| chr1:200058542
|
G | A | 14 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(11): Show | 14 | HG01346.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110+9724G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058542 | ||||||
| chr1:200058627
|
C | T | 1 | a0001c0001t0005g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1110+9809C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058627 | ||||||
| chr1:200058739
|
A | G | 1 | a0001c0001t0006g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1110+9921A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058739 | ||||||
| chr1:200058768
|
C | T | 1 | a0001c0002t0004g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1110+9950C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058768 | ||||||
| chr1:200058799
|
G | GT | 28 | a0001c0001t0006g0017a0001c0001t0006g0024a0001c0002t0021g0046others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1110+9992dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200058799 | |||||
| chr1:200058805
|
T | G | 1 | a0001c0001t0008g0231 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1110+9987T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058805 | ||||||
| chr1:200058838
|
G | C | 19 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(16): Show | 19 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+10020G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058838 | ||||||
| chr1:200058897
|
G | A | 19 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(16): Show | 19 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+10079G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058897 | ||||||
| chr1:200058907
|
C | T | 95 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0002g0104others(92): Show | 95 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1110+10089C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058907 | ||||||
| chr1:200058917
|
C | G | 2 | a0001c0001t0002g0161a0001c0001t0025g0074 | 2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1110+10099C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058917 | ||||||
| chr1:200058965
|
C | T | 23 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(20): Show | 23 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1110+10147C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058965 | ||||||
| chr1:200058968
|
G | A | 19 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(16): Show | 19 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+10150G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200058968 | ||||||
| chr1:200059050
|
C | T | 22 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(19): Show | 22 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1110+10232C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059050 | ||||||
| chr1:200059064
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1110+10246C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059064 | ||||||
| chr1:200059123
|
A | C | 19 | a0001c0001t0002g0110a0001c0001t0005g0009a0001c0001t0005g0025others(16): Show | 19 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+10305A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059123 | ||||||
| chr1:200059250
|
A | G | 33 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0204others(30): Show | 33 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1110+10432A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059250 | ||||||
| chr1:200059303
|
C | T | 35 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0204others(32): Show | 35 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1110+10485C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059303 | ||||||
| chr1:200059567
|
A | G | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1110+10749A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059567 | ||||||
| chr1:200059723
|
A | G | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110+10905A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059723 | ||||||
| chr1:200059768
|
A | G | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1110+10950A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200059768 | ||||||
| chr1:200060068
|
T | C | 1 | a0001c0002t0001g0208 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1110+11250T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060068 | ||||||
| chr1:200060147
|
A | G | 5 | a0001c0001t0002g0117a0001c0001t0005g0025a0001c0002t0001g0135others(2): Show | 5 | HG01081.hp1 HG02015.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+11329A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060147 | ||||||
| chr1:200060278
|
G | C | 1 | a0001c0002t0001g0118 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1110+11460G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060278 | ||||||
| chr1:200060407
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1110+11589C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060407 | ||||||
| chr1:200060504
|
T | C | 1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1110+11686T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060504 | ||||||
| chr1:200060533
|
G | T | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1110+11715G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060533 | ||||||
| chr1:200060535
|
A | T | 114 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(111): Show | 114 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1110+11717A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060535 | ||||||
| chr1:200060549
|
C | T | 1 | a0003c0006t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1110+11731C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060549 | ||||||
| chr1:200060825
|
T | C | 118 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(115): Show | 118 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110+12007T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060825 | ||||||
| chr1:200060885
|
C | T | 1 | a0001c0001t0008g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1110+12067C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060885 | ||||||
| chr1:200060939
|
T | TA | 122 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(119): Show | 122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1110+12144dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200060939 | |||||
| chr1:200060939
|
T | TAA | 13 | a0001c0001t0002g0110a0001c0001t0002g0161a0001c0001t0005g0031others(10): Show | 13 | HG00642.hp2 HG01099.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+12143_1110+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200060939 | |||||
| chr1:200060939
|
TA | T | 13 | a0001c0002t0001g0125a0001c0003t0002g0286a0001c0003t0009g0223others(10): Show | 13 | HG01109.hp2 HG02129.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+12144delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200060939 | |||||
| chr1:200060980
|
C | T | 5 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0004t0004g0066others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+12162C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200060980 | ||||||
| chr1:200061042
|
C | A | 13 | a0001c0003t0002g0286a0001c0003t0009g0223a0001c0003t0009g0224others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+12224C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061042 | ||||||
| chr1:200061116
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1110+12298G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061116 | ||||||
| chr1:200061120
|
C | CA | 13 | a0001c0001t0001g0163a0001c0001t0001g0202a0001c0001t0002g0068others(10): Show | 13 | HG00280.hp1 HG00735.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+12324dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200061120 | |||||
| chr1:200061120
|
CA | C | 23 | a0001c0001t0003g0105a0001c0001t0005g0097a0001c0001t0006g0059others(20): Show | 23 | HG00642.hp1 HG01081.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1110+12324delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200061120 | |||||
| chr1:200061120
|
CAA | C | 106 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(103): Show | 106 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1110+12323_1110+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200061120 | |||||
| chr1:200061154
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1110+12336G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061154 | ||||||
| chr1:200061275
|
C | CT | 89 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(86): Show | 89 | HG00639.hp1 HG00642.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.1110+12476dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200061275 | |||||
| chr1:200061275
|
C | CTT | 52 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(49): Show | 52 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1110+12475_1110+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200061275 | |||||
| chr1:200061275
|
C | CTTT | 8 | a0001c0001t0002g0110a0001c0001t0002g0161a0001c0001t0006g0075others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+12474_1110+12 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200061275 | |||||
| chr1:200061570
|
G | A | 1 | a0001c0002t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1110+12752G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061570 | ||||||
| chr1:200061911
|
T | G | 13 | a0001c0003t0002g0286a0001c0003t0009g0223a0001c0003t0009g0224others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+13093T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061911 | ||||||
| chr1:200061921
|
T | G | 13 | a0001c0003t0002g0286a0001c0003t0009g0223a0001c0003t0009g0224others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+13103T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061921 | ||||||
| chr1:200061979
|
C | T | 133 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(130): Show | 133 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1110+13161C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061979 | ||||||
| chr1:200061987
|
A | G | 2 | a0001c0001t0003g0220a0001c0002t0001g0077 | 2 | NA18973.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1110+13169A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200061987 | ||||||
| chr1:200062040
|
C | T | 2 | a0001c0001t0001g0221a0001c0002t0001g0215 | 2 | HG00408.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.1110+13222C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062040 | ||||||
| chr1:200062042
|
T | C | 13 | a0001c0003t0002g0286a0001c0003t0009g0223a0001c0003t0009g0224others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+13224T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062042 | ||||||
| chr1:200062128
|
C | T | 130 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1110+13310C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062128 | ||||||
| chr1:200062227
|
T | G | 2 | a0001c0001t0001g0163a0001c0003t0006g0061 | 2 | HG01074.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1110+13409T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062227 | ||||||
| chr1:200062227
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0024g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1110+13409_1110+13 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062227 | ||||||
| chr1:200062227
|
T | TGTGTGTG others(14): Show |
1 | a0001c0002t0001g0082 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1110+13409_1110+13 others(27): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062227 | ||||||
| chr1:200062227
|
T | TTG | 112 | a0001c0001t0001g0137a0001c0001t0001g0201a0001c0001t0001g0202others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1110+13439_1110+13 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTG | 16 | a0001c0001t0001g0071a0001c0001t0001g0261a0001c0001t0003g0206others(13): Show | 16 | HG01109.hp1 HG01168.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1110+13437_1110+13 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTG | 14 | a0001c0001t0002g0262a0001c0001t0010g0144a0001c0002t0001g0188others(11): Show | 14 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110+13435_1110+13 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(1): Show |
32 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0104others(29): Show | 32 | HG00741.hp1 HG01074.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1110+13433_1110+13 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(3): Show |
11 | a0001c0001t0002g0204a0001c0001t0006g0040a0001c0002t0001g0268others(8): Show | 11 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+13431_1110+13 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(5): Show |
3 | a0001c0002t0004g0090a0001c0003t0006g0036a0001c0003t0009g0013 | 3 | HG02647.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+13429_1110+13 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0002g0168a0001c0001t0002g0169 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1110+13427_1110+13 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(9): Show |
4 | a0001c0001t0005g0097a0001c0004t0004g0285a0001c0005t0004g0022others(1): Show | 4 | HG01081.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+13425_1110+13 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(11): Show |
12 | a0001c0001t0002g0280a0001c0001t0003g0171a0001c0001t0003g0234others(9): Show | 12 | HG01255.hp1 HG01256.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+13423_1110+13 others(24): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(13): Show |
15 | a0001c0001t0002g0110a0001c0001t0003g0105a0001c0001t0003g0235others(12): Show | 15 | HG01993.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+13421_1110+13 others(26): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(15): Show |
10 | a0001c0001t0002g0151a0001c0001t0005g0009a0001c0001t0005g0106others(7): Show | 10 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+13419_1110+13 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(17): Show |
7 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0003g0030others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+13417_1110+13 others(30): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
T | TTGTGTGT others(19): Show |
5 | a0001c0001t0002g0173a0001c0001t0005g0019a0001c0001t0005g0020others(2): Show | 5 | HG01099.hp1 HG01261.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+13415_1110+13 others(32): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062227
|
TTG | T | 10 | a0001c0003t0009g0223a0001c0003t0009g0257a0001c0003t0017g0042others(7): Show | 10 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+13439_1110+13 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062227 | |||||
| chr1:200062229
|
G | A | 1 | a0001c0003t0009g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1110+13411G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062229 | ||||||
| chr1:200062231
|
G | A | 10 | a0001c0003t0009g0223a0001c0003t0009g0257a0001c0003t0017g0042others(7): Show | 10 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+13413G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062231 | ||||||
| chr1:200062257
|
G | GTGTGTGT others(7): Show |
1 | a0001c0002t0001g0162 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1110+13440_1110+13 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062257 | |||||
| chr1:200062257
|
G | GTGTGTGT others(13): Show |
14 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(11): Show | 14 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+13440_1110+13 others(26): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062257 | |||||
| chr1:200062257
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0008g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1110+13440_1110+13 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062257 | |||||
| chr1:200062257
|
G | GTGTGTGT others(21): Show |
3 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054 | 3 | NA18942.hp2 NA19005.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1110+13440_1110+13 others(34): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062257 | |||||
| chr1:200062257
|
G | GTGTGTGT others(23): Show |
1 | a0001c0002t0001g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1110+13440_1110+13 others(36): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200062257 | |||||
| chr1:200062340
|
A | G | 7 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+13522A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062340 | ||||||
| chr1:200062405
|
C | T | 142 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(139): Show | 142 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1110+13587C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062405 | ||||||
| chr1:200062562
|
G | A | 20 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(17): Show | 20 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1110+13744G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062562 | ||||||
| chr1:200062588
|
G | A | 5 | a0001c0003t0006g0014a0001c0003t0006g0036a0001c0003t0009g0013others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+13770G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062588 | ||||||
| chr1:200062701
|
G | A | 2 | a0003c0006t0016g0001a0003c0010t0001g0002 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1110+13883G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062701 | ||||||
| chr1:200062745
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1110+13927A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062745 | ||||||
| chr1:200062885
|
A | G | 1 | a0001c0001t0005g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1110+14067A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062885 | ||||||
| chr1:200062952
|
C | A | 110 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(107): Show | 110 | HG00639.hp1 HG00642.hp1 HG01070.hp1 others(107): Show |
intron_variant | MODIFIER | c.1110+14134C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200062952 | ||||||
| chr1:200063028
|
GT | G | 10 | a0001c0001t0006g0059a0001c0002t0001g0188a0001c0002t0004g0091others(7): Show | 10 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1110+14223delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200063028 | |||||
| chr1:200063093
|
G | A | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1110+14275G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063093 | ||||||
| chr1:200063196
|
GT | G | 12 | a0001c0003t0002g0286a0001c0003t0009g0223a0001c0003t0009g0224others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+14387delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200063196 | |||||
| chr1:200063197
|
T | G | 1 | a0001c0002t0001g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1110+14379T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063197 | ||||||
| chr1:200063198
|
T | G | 10 | a0001c0001t0005g0025a0001c0001t0006g0059a0001c0002t0004g0091others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1110+14380T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063198 | ||||||
| chr1:200063208
|
T | C | 20 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0280others(17): Show | 20 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1110+14390T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063208 | ||||||
| chr1:200063282
|
G | A | 5 | a0001c0003t0006g0014a0001c0003t0006g0036a0001c0003t0009g0013others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+14464G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063282 | ||||||
| chr1:200063394
|
G | A | 117 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(114): Show | 117 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.1110+14576G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063394 | ||||||
| chr1:200063693
|
G | A | 130 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1110+14875G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063693 | ||||||
| chr1:200063751
|
C | T | 41 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(38): Show | 41 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1110+14933C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063751 | ||||||
| chr1:200063961
|
C | G | 16 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(13): Show | 16 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1110+15143C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200063961 | ||||||
| chr1:200064112
|
G | A | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1110+15294G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064112 | ||||||
| chr1:200064113
|
C | T | 1 | a0001c0001t0003g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1110+15295C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064113 | ||||||
| chr1:200064167
|
C | T | 3 | a0001c0003t0013g0269a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1110+15349C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064167 | ||||||
| chr1:200064168
|
G | A | 21 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110+15350G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064168 | ||||||
| chr1:200064174
|
C | T | 13 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(10): Show | 13 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+15356C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064174 | ||||||
| chr1:200064332
|
T | A | 132 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(129): Show | 132 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1110+15514T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064332 | ||||||
| chr1:200064395
|
G | T | 9 | a0001c0001t0005g0094a0001c0003t0006g0035a0001c0003t0016g0153others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1110+15577G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064395 | ||||||
| chr1:200064641
|
A | G | 103 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(100): Show | 103 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1110+15823A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064641 | ||||||
| chr1:200064848
|
T | C | 1 | a0001c0007t0015g0278 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1110+16030T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200064848 | ||||||
| chr1:200065385
|
C | A | 64 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1110+16567C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065385 | ||||||
| chr1:200065385
|
C | T | 2 | a0001c0002t0007g0026a0001c0003t0002g0056 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1110+16567C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065385 | ||||||
| chr1:200065422
|
C | T | 1 | a0001c0001t0011g0078 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1110+16604C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065422 | ||||||
| chr1:200065735
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1110+16917G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065735 | ||||||
| chr1:200065808
|
A | G | 12 | a0001c0001t0006g0059a0001c0001t0006g0075a0001c0001t0009g0181others(9): Show | 12 | HG02145.hp1 HG02717.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+16990A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065808 | ||||||
| chr1:200065841
|
A | G | 103 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(100): Show | 103 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1110+17023A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065841 | ||||||
| chr1:200065853
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1110+17035G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065853 | ||||||
| chr1:200065915
|
A | G | 18 | a0001c0001t0005g0094a0001c0001t0006g0270a0001c0001t0006g0271others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1110+17097A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065915 | ||||||
| chr1:200065941
|
T | G | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1110+17123T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200065941 | ||||||
| chr1:200066157
|
G | C | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+17339G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066157 | ||||||
| chr1:200066316
|
G | C | 101 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(98): Show | 101 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1110+17498G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066316 | ||||||
| chr1:200066377
|
GT | G | 14 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0105others(11): Show | 14 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110+17561delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066377 | |||||
| chr1:200066386
|
C | G | 14 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0105others(11): Show | 14 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110+17568C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066386 | ||||||
| chr1:200066588
|
C | CTTTTTT | 15 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0105others(12): Show | 15 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+17782_1110+17 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(1): Show |
36 | a0001c0001t0001g0221a0001c0001t0002g0110a0001c0001t0002g0161others(33): Show | 36 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1110+17780_1110+17 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(2): Show |
25 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0002g0104others(22): Show | 25 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1110+17779_1110+17 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(3): Show |
19 | a0001c0001t0005g0094a0001c0001t0006g0270a0001c0001t0006g0271others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1110+17778_1110+17 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(4): Show |
1 | a0001c0004t0004g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1110+17777_1110+17 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0010g0092a0001c0002t0001g0240a0001c0002t0007g0093 | 3 | HG01255.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+17775_1110+17 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(7): Show |
27 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(24): Show | 27 | HG00639.hp1 HG01070.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.1110+17774_1110+17 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0005g0031a0001c0001t0011g0078a0001c0001t0024g0029others(1): Show | 4 | HG01099.hp1 HG04115.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+17773_1110+17 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066588
|
C | CTTTTTTT others(10): Show |
1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1110+17771_1110+17 others(23): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200066588 | |||||
| chr1:200066639
|
G | T | 7 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(4): Show | 7 | HG01255.hp2 HG02155.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+17821G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066639 | ||||||
| chr1:200066650
|
C | T | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+17832C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066650 | ||||||
| chr1:200066800
|
G | C | 100 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1110+17982G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066800 | ||||||
| chr1:200066803
|
A | G | 100 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1110+17985A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066803 | ||||||
| chr1:200066814
|
C | G | 2 | a0001c0002t0007g0026a0001c0003t0002g0056 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1110+17996C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066814 | ||||||
| chr1:200066924
|
T | C | 58 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0168others(55): Show | 58 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.1110+18106T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066924 | ||||||
| chr1:200066993
|
C | T | 2 | a0001c0003t0002g0167a0001c0005t0007g0281 | 2 | HG01070.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1110+18175C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200066993 | ||||||
| chr1:200067011
|
C | T | 69 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1110+18193C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067011 | ||||||
| chr1:200067017
|
A | C | 1 | a0001c0002t0001g0260 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1110+18199A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067017 | ||||||
| chr1:200067195
|
G | T | 16 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(13): Show | 16 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1110+18377G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067195 | ||||||
| chr1:200067198
|
G | A | 16 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(13): Show | 16 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1110+18380G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067198 | ||||||
| chr1:200067239
|
C | T | 2 | a0001c0004t0007g0049a0001c0004t0007g0050 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1110+18421C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067239 | ||||||
| chr1:200067468
|
G | A | 95 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1110+18650G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067468 | ||||||
| chr1:200067569
|
G | A | 1 | a0001c0004t0004g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1110+18751G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067569 | ||||||
| chr1:200067662
|
A | G | 93 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1110+18844A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067662 | ||||||
| chr1:200067719
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110+18901C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067719 | ||||||
| chr1:200067879
|
A | G | 45 | a0001c0001t0001g0071a0001c0001t0001g0201a0001c0001t0001g0216others(42): Show | 45 | HG00544.hp2 HG00609.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.1110+19061A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067879 | ||||||
| chr1:200067912
|
G | C | 1 | a0001c0001t0003g0113 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1110+19094G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067912 | ||||||
| chr1:200067966
|
T | C | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1110+19148T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200067966 | ||||||
| chr1:200068094
|
C | A | 1 | a0001c0001t0011g0100 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1110+19276C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068094 | ||||||
| chr1:200068244
|
G | C | 16 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(13): Show | 16 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1110+19426G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068244 | ||||||
| chr1:200068312
|
T | C | 1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+19494T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068312 | ||||||
| chr1:200068412
|
C | T | 2 | a0001c0001t0006g0017a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1110+19594C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068412 | ||||||
| chr1:200068453
|
G | A | 133 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(130): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1110+19635G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068453 | ||||||
| chr1:200068599
|
C | T | 53 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(50): Show | 53 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1110+19781C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068599 | ||||||
| chr1:200068698
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1110+19880T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068698 | ||||||
| chr1:200068807
|
T | C | 6 | a0001c0003t0002g0043a0001c0003t0013g0048a0001c0003t0013g0051others(3): Show | 6 | HG02886.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+19989T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200068807 | ||||||
| chr1:200069069
|
G | A | 1 | a0001c0003t0002g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1110+20251G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069069 | ||||||
| chr1:200069208
|
A | AT | 12 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0105others(9): Show | 12 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+20391dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200069208 | |||||
| chr1:200069251
|
A | C | 1 | a0001c0002t0001g0132 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1110+20433A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069251 | ||||||
| chr1:200069261
|
C | CT | 133 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(130): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1110+20454dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200069261 | |||||
| chr1:200069387
|
A | G | 12 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0105others(9): Show | 12 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+20569A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069387 | ||||||
| chr1:200069406
|
A | G | 1 | a0001c0001t0008g0231 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1110+20588A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069406 | ||||||
| chr1:200069417
|
T | C | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+20599T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069417 | ||||||
| chr1:200069485
|
C | T | 54 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(51): Show | 54 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1110+20667C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069485 | ||||||
| chr1:200069508
|
C | T | 2 | a0001c0001t0006g0017a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1110+20690C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069508 | ||||||
| chr1:200069533
|
C | T | 1 | a0001c0001t0006g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1110+20715C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069533 | ||||||
| chr1:200069798
|
A | G | 27 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.1110+20980A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069798 | ||||||
| chr1:200069852
|
A | G | 4 | a0001c0002t0001g0200a0001c0004t0001g0052a0001c0004t0001g0053others(1): Show | 4 | HG02129.hp1 NA18942.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+21034A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069852 | ||||||
| chr1:200069879
|
C | CAT | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+21061_1110+21 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200069879 | ||||||
| chr1:200070135
|
T | C | 133 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(130): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1110+21317T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070135 | ||||||
| chr1:200070423
|
A | C | 133 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(130): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1110+21605A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070423 | ||||||
| chr1:200070496
|
G | C | 2 | a0001c0001t0005g0146a0001c0001t0005g0159 | 2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1110+21678G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070496 | ||||||
| chr1:200070621
|
G | C | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+21803G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070621 | ||||||
| chr1:200070628
|
T | C | 173 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(170): Show | 173 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.1110+21810T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070628 | ||||||
| chr1:200070635
|
G | A | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0024others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+21817G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070635 | ||||||
| chr1:200070656
|
G | C | 2 | a0001c0001t0003g0210a0001c0001t0003g0263 | 2 | NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1110+21838G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070656 | ||||||
| chr1:200070679
|
C | CA | 12 | a0001c0001t0002g0114a0001c0001t0002g0262a0001c0001t0003g0198others(9): Show | 12 | HG00738.hp1 HG01109.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+21876dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200070679 | |||||
| chr1:200070679
|
C | CAA | 123 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(120): Show | 123 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1110+21875_1110+21 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200070679 | |||||
| chr1:200070679
|
C | CAAA | 6 | a0001c0001t0019g0209a0001c0001t0026g0255a0001c0002t0001g0130others(3): Show | 6 | HG02080.hp2 HG03239.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+21874_1110+21 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200070679 | |||||
| chr1:200070723
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1110+21905T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070723 | ||||||
| chr1:200070835
|
C | T | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+22017C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070835 | ||||||
| chr1:200070959
|
A | G | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+22141A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200070959 | ||||||
| chr1:200071037
|
C | T | 1 | a0001c0003t0002g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1110+22219C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200071037 | ||||||
| chr1:200071596
|
T | G | 12 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0003g0105others(9): Show | 12 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+22778T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200071596 | ||||||
| chr1:200071717
|
C | T | 125 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(122): Show | 125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1110+22899C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200071717 | ||||||
| chr1:200071823
|
A | G | 5 | a0001c0001t0006g0040a0001c0003t0031g0039a0002c0008t0012g0084others(2): Show | 5 | HG01884.hp2 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+23005A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200071823 | ||||||
| chr1:200071920
|
C | G | 1 | a0001c0001t0001g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1110+23102C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200071920 | ||||||
| chr1:200072076
|
A | G | 125 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(122): Show | 125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1110+23258A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200072076 | ||||||
| chr1:200072095
|
C | T | 8 | a0001c0002t0021g0046a0001c0003t0006g0036a0001c0003t0006g0061others(5): Show | 8 | HG01074.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+23277C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200072095 | ||||||
| chr1:200072216
|
A | G | 133 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(130): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1110+23398A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200072216 | ||||||
| chr1:200072251
|
A | AT | 5 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(2): Show | 5 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+23439dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200072251 | |||||
| chr1:200072735
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1110+23917C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200072735 | ||||||
| chr1:200072903
|
T | C | 68 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1110+24085T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200072903 | ||||||
| chr1:200072921
|
A | G | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+24103A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200072921 | ||||||
| chr1:200073038
|
T | C | 1 | a0001c0004t0001g0047 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1110+24220T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200073038 | ||||||
| chr1:200073235
|
C | CAT | 22 | a0001c0001t0002g0165a0001c0001t0002g0280a0001c0001t0003g0122others(19): Show | 22 | HG00621.hp2 HG00738.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1110+24442_1110+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073235 | |||||
| chr1:200073235
|
C | CATATATA others(13): Show |
1 | a0001c0001t0010g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1110+24424_1110+24 others(26): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073235 | |||||
| chr1:200073235
|
C | CATATATA others(15): Show |
1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+24422_1110+24 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073235 | |||||
| chr1:200073235
|
CAT | C | 37 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0068others(34): Show | 37 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110+24442_1110+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073235 | |||||
| chr1:200073235
|
CATAT | C | 93 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(90): Show | 93 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1110+24440_1110+24 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073235 | |||||
| chr1:200073235
|
CATATAT | C | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0007g0016others(2): Show | 5 | HG01074.hp2 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+24438_1110+24 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073235 | |||||
| chr1:200073238
|
ATATATAT others(77): Show |
A | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1110+24438_1110+24 others(90): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073238 | |||||
| chr1:200073268
|
T | TTA | 7 | a0001c0001t0001g0216a0001c0001t0005g0214a0001c0001t0008g0166others(4): Show | 7 | HG03098.hp1 HG03704.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+24472_1110+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
T | TTATATA | 16 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(13): Show | 16 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1110+24468_1110+24 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0003g0234a0001c0002t0001g0082 | 2 | NA18947.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1110+24464_1110+24 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0003g0235 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1110+24462_1110+24 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
T | TTATATAT others(7): Show |
5 | a0001c0002t0007g0026a0001c0003t0002g0056a0001c0004t0004g0037others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+24460_1110+24 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0006g0017a0001c0007t0006g0283 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1110+24456_1110+24 others(24): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
T | TTATATAT others(13): Show |
1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1110+24454_1110+24 others(26): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
TTA | T | 8 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0010g0092others(5): Show | 8 | HG01255.hp2 HG03704.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+24472_1110+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073268
|
TTATATAT others(3): Show |
T | 3 | a0001c0005t0004g0021a0001c0005t0004g0022a0001c0005t0004g0023 | 3 | HG02965.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1110+24464_1110+24 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073268 | |||||
| chr1:200073270
|
ATATATAT others(21): Show |
A | 86 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(83): Show | 86 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1110+24470_1110+24 others(34): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073270 | |||||
| chr1:200073272
|
ATATATAT others(19): Show |
A | 44 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(41): Show | 44 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1110+24472_1110+24 others(32): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073272 | |||||
| chr1:200073274
|
ATATATAT others(17): Show |
A | 1 | a0001c0004t0001g0273 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1110+24516_1110+24 others(30): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073274 | |||||
| chr1:200073276
|
ATATATAT others(15): Show |
A | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1110+24474_1110+24 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073276 | |||||
| chr1:200073298
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0008g0195 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1110+24496_1110+24 others(32): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073298 | |||||
| chr1:200073322
|
TTA | T | 131 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(128): Show | 131 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1110+24520_1110+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073322 | |||||
| chr1:200073358
|
G | A | 127 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(124): Show | 127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1110+24540G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200073358 | ||||||
| chr1:200073486
|
T | G | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+24668T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200073486 | ||||||
| chr1:200073645
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1110+24827G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200073645 | ||||||
| chr1:200073684
|
AAC | A | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+24881_1110+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200073684 | |||||
| chr1:200073800
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1110+24982A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200073800 | ||||||
| chr1:200073860
|
G | A | 1 | a0001c0001t0003g0259 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1110+25042G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200073860 | ||||||
| chr1:200073904
|
A | G | 5 | a0001c0001t0005g0094a0001c0003t0006g0035a0001c0004t0004g0276others(2): Show | 5 | HG02630.hp2 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+25086A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200073904 | ||||||
| chr1:200074156
|
A | G | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+25338A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074156 | ||||||
| chr1:200074384
|
C | T | 1 | a0001c0004t0004g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1110+25566C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074384 | ||||||
| chr1:200074391
|
T | A | 30 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(27): Show | 30 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1110+25573T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074391 | ||||||
| chr1:200074401
|
GAAAAGAA others(4): Show |
G | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+25598_1110+25 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074401 | |||||
| chr1:200074417
|
G | GA | 5 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(2): Show | 5 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+25608dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074417 | |||||
| chr1:200074476
|
G | A | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1110+25658G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074476 | ||||||
| chr1:200074564
|
C | T | 133 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(130): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1110+25746C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074564 | ||||||
| chr1:200074598
|
T | G | 141 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(138): Show | 141 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1110+25780T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074598 | ||||||
| chr1:200074608
|
G | A | 128 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(125): Show | 128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1110+25790G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074608 | ||||||
| chr1:200074653
|
C | T | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+25835C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074653 | ||||||
| chr1:200074654
|
G | A | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1110+25836G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074654 | ||||||
| chr1:200074718
|
C | A | 2 | a0001c0003t0006g0036a0001c0003t0009g0013 | 2 | HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+25900C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074718 | ||||||
| chr1:200074736
|
C | CA | 9 | a0001c0001t0001g0071a0001c0001t0001g0163a0001c0001t0003g0113others(6): Show | 9 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1110+25938dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA | 44 | a0001c0001t0001g0137a0001c0001t0002g0069a0001c0001t0002g0117others(41): Show | 44 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1110+25932_1110+25 others(13): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(1): Show |
20 | a0001c0001t0002g0068a0001c0001t0002g0207a0001c0001t0002g0254others(17): Show | 20 | HG00621.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1110+25931_1110+25 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1110+25929_1110+25 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(4): Show |
2 | a0001c0002t0001g0187a0001c0002t0007g0026 | 2 | HG02647.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1110+25928_1110+25 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1110+25925_1110+25 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0252a0001c0002t0001g0070 | 2 | HG03710.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1110+25924_1110+25 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0005g0159a0001c0003t0002g0167 | 2 | HG00609.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1110+25922_1110+25 others(23): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(11): Show |
5 | a0001c0001t0002g0150a0001c0001t0002g0173a0001c0001t0005g0020others(2): Show | 5 | HG01517.hp2 HG01934.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+25921_1110+25 others(24): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(12): Show |
8 | a0001c0001t0002g0034a0001c0001t0002g0151a0001c0001t0003g0030others(5): Show | 8 | HG01358.hp1 HG01496.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+25920_1110+25 others(25): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(13): Show |
8 | a0001c0001t0002g0280a0001c0001t0003g0234a0001c0002t0007g0093others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+25919_1110+25 others(26): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(14): Show |
6 | a0001c0001t0003g0235a0001c0001t0005g0031a0001c0001t0005g0032others(3): Show | 6 | HG00639.hp1 HG01099.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(27): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(15): Show |
3 | a0001c0001t0003g0147a0001c0001t0011g0078a0001c0002t0001g0082 | 3 | HG00544.hp2 NA18947.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0005g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1110+25938_1110+25 others(29): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0002g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1110+25938_1110+25 others(33): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(21): Show |
7 | a0001c0001t0001g0201a0001c0001t0002g0199a0001c0001t0005g0214others(4): Show | 7 | HG01981.hp2 HG02027.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(34): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(22): Show |
11 | a0001c0001t0001g0202a0001c0001t0001g0261a0001c0001t0002g0081others(8): Show | 11 | HG02155.hp1 HG02293.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(35): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(23): Show |
3 | a0001c0001t0007g0176a0001c0002t0001g0236a0001c0002t0029g0142 | 3 | HG02040.hp1 HG03492.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(36): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(25): Show |
1 | a0001c0002t0001g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1110+25938_1110+25 others(38): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(26): Show |
3 | a0001c0001t0002g0213a0001c0001t0003g0191a0001c0001t0003g0263 | 3 | HG01943.hp2 NA18981.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(39): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(27): Show |
2 | a0001c0001t0005g0146a0001c0002t0001g0127 | 2 | HG02027.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(40): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0216 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1110+25938_1110+25 others(41): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(29): Show |
3 | a0001c0001t0002g0212a0001c0001t0008g0005a0001c0002t0001g0233 | 3 | HG01928.hp1 NA18945.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1110+25938_1110+25 others(42): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(30): Show |
1 | a0001c0002t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1110+25938_1110+25 others(43): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1110+25936_1110+25 others(35): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
CAAAAA | C | 8 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0006g0075others(5): Show | 8 | HG00408.hp1 HG00408.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+25934_1110+25 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074736
|
CAAAAAA | C | 58 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(55): Show | 58 | HG00558.hp2 HG00609.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1110+25933_1110+25 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074736 | |||||
| chr1:200074755
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0010g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1110+25938_1110+25 others(27): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074755 | |||||
| chr1:200074759
|
C | T | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+25941C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074759 | ||||||
| chr1:200074782
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1110+25964A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074782 | ||||||
| chr1:200074788
|
A | AT | 128 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(125): Show | 128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1110+25982dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200074788 | |||||
| chr1:200074937
|
T | C | 1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1110+26119T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074937 | ||||||
| chr1:200074995
|
G | A | 5 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(2): Show | 5 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+26177G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200074995 | ||||||
| chr1:200075200
|
T | C | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+26382T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200075200 | ||||||
| chr1:200075758
|
A | G | 129 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1110+26940A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200075758 | ||||||
| chr1:200075860
|
A | C | 5 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(2): Show | 5 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+27042A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200075860 | ||||||
| chr1:200075886
|
G | GTTTTC | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0003g0238others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1110+27078_1110+27 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200075886 | |||||
| chr1:200075886
|
G | GTTTTCTT others(3): Show |
8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+27073_1110+27 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200075886 | |||||
| chr1:200075886
|
G | GTTTTCTT others(8): Show |
109 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(106): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1110+27082_1110+27 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200075886 | |||||
| chr1:200075896
|
C | CTTTTCTT others(4): Show |
1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1110+27082_1110+27 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200075896 | |||||
| chr1:200075896
|
C | CTTTTCTT others(9): Show |
7 | a0001c0001t0005g0025a0001c0002t0001g0200a0001c0004t0001g0052others(4): Show | 7 | HG02109.hp2 HG02129.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+27082_1110+27 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200075896 | |||||
| chr1:200076455
|
A | AT | 122 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(119): Show | 122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1110+27652dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200076455 | |||||
| chr1:200076455
|
A | ATT | 7 | a0001c0001t0002g0251a0001c0001t0002g0254a0001c0002t0001g0130others(4): Show | 7 | HG01074.hp2 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+27651_1110+27 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200076455 | |||||
| chr1:200076626
|
T | C | 1 | a0001c0001t0003g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1110+27808T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200076626 | ||||||
| chr1:200076933
|
T | TAC | 4 | a0001c0002t0001g0200a0001c0004t0001g0052a0001c0004t0001g0053others(1): Show | 4 | HG02129.hp1 NA18942.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+28115_1110+28 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200076933 | ||||||
| chr1:200077005
|
T | G | 1 | a0001c0004t0006g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1110+28187T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077005 | ||||||
| chr1:200077077
|
C | T | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+28259C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077077 | ||||||
| chr1:200077078
|
G | A | 1 | a0001c0003t0006g0035 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1110+28260G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077078 | ||||||
| chr1:200077147
|
C | G | 53 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(50): Show | 53 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1110+28329C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077147 | ||||||
| chr1:200077193
|
T | C | 4 | a0001c0002t0001g0200a0001c0004t0001g0052a0001c0004t0001g0053others(1): Show | 4 | HG02129.hp1 NA18942.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+28375T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077193 | ||||||
| chr1:200077228
|
A | T | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+28410A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077228 | ||||||
| chr1:200077301
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1110+28483A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077301 | ||||||
| chr1:200077316
|
T | G | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+28498T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077316 | ||||||
| chr1:200077362
|
C | T | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+28544C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077362 | ||||||
| chr1:200077406
|
G | A | 5 | a0001c0001t0002g0114a0001c0001t0002g0262a0001c0001t0005g0115others(2): Show | 5 | HG00738.hp1 HG01109.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+28588G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077406 | ||||||
| chr1:200077406
|
G | T | 129 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1110+28588G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077406 | ||||||
| chr1:200077449
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1110+28631C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077449 | ||||||
| chr1:200077727
|
A | AAC | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+28911_1110+28 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200077727 | |||||
| chr1:200077738
|
T | C | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+28920T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077738 | ||||||
| chr1:200077779
|
G | C | 285 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(282): Show | 285 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1110+28961G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077779 | ||||||
| chr1:200077819
|
G | A | 2 | a0001c0004t0007g0016a0001c0005t0006g0060 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1110+29001G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077819 | ||||||
| chr1:200077877
|
C | A | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+29059C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077877 | ||||||
| chr1:200077978
|
A | G | 3 | a0001c0001t0011g0100a0001c0001t0026g0255a0001c0002t0001g0125 | 3 | HG02015.hp1 HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1110+29160A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200077978 | ||||||
| chr1:200078031
|
G | T | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+29213G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200078031 | ||||||
| chr1:200078066
|
T | A | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+29248T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200078066 | ||||||
| chr1:200078475
|
A | G | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+29657A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200078475 | ||||||
| chr1:200078597
|
TTTC | T | 60 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(57): Show | 60 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1110+29783_1110+29 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200078597 | |||||
| chr1:200078728
|
C | T | 1 | a0001c0002t0001g0134 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1110+29910C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200078728 | ||||||
| chr1:200078730
|
T | C | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1110+29912T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200078730 | ||||||
| chr1:200079026
|
G | A | 1 | a0001c0003t0002g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1110+30208G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079026 | ||||||
| chr1:200079060
|
G | A | 2 | a0001c0004t0007g0016a0001c0005t0006g0060 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1110+30242G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079060 | ||||||
| chr1:200079236
|
T | C | 1 | a0001c0003t0002g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1110+30418T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079236 | ||||||
| chr1:200079264
|
A | G | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1110+30446A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079264 | ||||||
| chr1:200079382
|
G | C | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+30564G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079382 | ||||||
| chr1:200079505
|
C | T | 5 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(2): Show | 5 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+30687C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079505 | ||||||
| chr1:200079534
|
G | C | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+30716G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079534 | ||||||
| chr1:200079678
|
A | G | 1 | a0001c0002t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1110+30860A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079678 | ||||||
| chr1:200079734
|
C | T | 2 | a0001c0003t0002g0279a0001c0005t0007g0281 | 2 | HG02148.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1110+30916C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200079734 | ||||||
| chr1:200079868
|
TA | T | 134 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(131): Show | 134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1110+31062delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200079868 | |||||
| chr1:200080012
|
T | G | 1 | a0001c0001t0005g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1111-31190T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200080012 | ||||||
| chr1:200080174
|
T | A | 69 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1111-31028T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200080174 | ||||||
| chr1:200080303
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1111-30899C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200080303 | ||||||
| chr1:200080320
|
A | T | 1 | a0001c0002t0001g0145 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1111-30882A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200080320 | ||||||
| chr1:200080496
|
G | C | 4 | a0001c0002t0021g0046a0001c0004t0004g0285a0001c0004t0007g0016others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-30706G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200080496 | ||||||
| chr1:200080846
|
T | C | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-30356T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200080846 | ||||||
| chr1:200080978
|
T | C | 1 | a0001c0002t0001g0233 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1111-30224T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200080978 | ||||||
| chr1:200081076
|
G | A | 142 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(139): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1111-30126G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081076 | ||||||
| chr1:200081143
|
A | G | 5 | a0001c0001t0003g0191a0001c0001t0005g0146a0001c0001t0005g0159others(2): Show | 5 | HG00609.hp1 HG02027.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-30059A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081143 | ||||||
| chr1:200081217
|
G | A | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-29985G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081217 | ||||||
| chr1:200081441
|
T | C | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1111-29761T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081441 | ||||||
| chr1:200081657
|
A | C | 6 | a0001c0001t0006g0024a0001c0001t0006g0075a0001c0003t0005g0055others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-29545A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081657 | ||||||
| chr1:200081766
|
C | G | 35 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(32): Show | 35 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1111-29436C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081766 | ||||||
| chr1:200081767
|
C | T | 2 | a0001c0002t0004g0090a0001c0004t0004g0037 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1111-29435C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081767 | ||||||
| chr1:200081767
|
CT | C | 39 | a0001c0001t0001g0216a0001c0001t0002g0034a0001c0001t0002g0150others(36): Show | 39 | HG00639.hp1 HG01070.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1111-29421delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200081767 | |||||
| chr1:200081767
|
CTT | C | 60 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(57): Show | 60 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1111-29422_1111-29 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200081767 | |||||
| chr1:200081862
|
G | A | 228 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(225): Show | 228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1111-29340G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081862 | ||||||
| chr1:200081896
|
T | TA | 7 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0010g0092others(4): Show | 7 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111-29296dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200081896 | |||||
| chr1:200081909
|
C | T | 129 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1111-29293C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081909 | ||||||
| chr1:200081979
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1111-29223C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200081979 | ||||||
| chr1:200082146
|
G | A | 129 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1111-29056G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082146 | ||||||
| chr1:200082247
|
T | C | 1 | a0001c0001t0005g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1111-28955T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082247 | ||||||
| chr1:200082425
|
T | C | 2 | a0001c0001t0006g0017a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1111-28777T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082425 | ||||||
| chr1:200082707
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1111-28495C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082707 | ||||||
| chr1:200082728
|
G | A | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-28474G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082728 | ||||||
| chr1:200082813
|
A | C | 1 | a0001c0002t0001g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1111-28389A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082813 | ||||||
| chr1:200082853
|
G | A | 135 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(132): Show | 135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1111-28349G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082853 | ||||||
| chr1:200082863
|
C | T | 135 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(132): Show | 135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1111-28339C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082863 | ||||||
| chr1:200082937
|
A | G | 135 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(132): Show | 135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1111-28265A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200082937 | ||||||
| chr1:200083052
|
C | T | 11 | a0001c0003t0009g0223a0001c0003t0009g0224a0001c0003t0009g0257others(8): Show | 11 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-28150C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083052 | ||||||
| chr1:200083081
|
CAT | C | 5 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(2): Show | 5 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-28118_1111-28 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083081 | |||||
| chr1:200083111
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0003g0113a0001c0001t0003g0122others(2): Show | 5 | HG00621.hp2 NA18979.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-28091A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083111 | ||||||
| chr1:200083341
|
A | G | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1111-27861A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083341 | ||||||
| chr1:200083407
|
C | T | 7 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0010g0092others(4): Show | 7 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111-27795C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083407 | ||||||
| chr1:200083587
|
G | T | 5 | a0001c0001t0005g0094a0001c0003t0006g0035a0001c0004t0004g0276others(2): Show | 5 | HG02630.hp2 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-27615G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083587 | ||||||
| chr1:200083603
|
T | C | 135 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(132): Show | 135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1111-27599T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083603 | ||||||
| chr1:200083631
|
ATATACAG others(3): Show |
A | 36 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(33): Show | 36 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1111-27569_1111-27 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083631 | |||||
| chr1:200083633
|
A | G | 100 | a0001c0001t0001g0137a0001c0001t0002g0011a0001c0001t0002g0012others(97): Show | 100 | HG00280.hp2 HG00621.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.1111-27569A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083633 | ||||||
| chr1:200083738
|
A | G | 174 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(171): Show | 174 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.1111-27464A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083738 | ||||||
| chr1:200083848
|
C | T | 1 | a0001c0001t0011g0126 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1111-27354C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083848 | ||||||
| chr1:200083895
|
G | T | 1 | a0001c0003t0022g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111-27307G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200083895 | ||||||
| chr1:200083967
|
A | AAAT | 25 | a0001c0001t0001g0261a0001c0001t0002g0117a0001c0001t0002g0133others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1111-27196_1111-27 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200083967
|
A | AAATAAT | 17 | a0001c0001t0002g0034a0001c0001t0003g0171a0001c0001t0005g0097others(14): Show | 17 | HG00642.hp1 HG01070.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1111-27199_1111-27 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200083967
|
A | AAATAATA others(2): Show |
10 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0006g0059others(7): Show | 10 | HG01074.hp1 HG01243.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1111-27202_1111-27 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200083967
|
AAAT | A | 105 | a0001c0001t0001g0095a0001c0001t0001g0163a0001c0001t0001g0192others(102): Show | 105 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1111-27196_1111-27 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200083967
|
AAATAAT | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0114others(17): Show | 20 | HG00738.hp1 HG01109.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-27199_1111-27 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200083967
|
AAATAATA others(2): Show |
A | 19 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(16): Show | 19 | HG00741.hp1 HG01109.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1111-27202_1111-27 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200083967
|
AAATAATA others(8): Show |
A | 2 | a0001c0004t0007g0049a0001c0004t0007g0050 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1111-27208_1111-27 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200083967
|
AAATAATA others(11): Show |
A | 1 | a0001c0001t0005g0177 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1111-27211_1111-27 others(24): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200083967 | |||||
| chr1:200084016
|
T | C | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-27186T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084016 | ||||||
| chr1:200084032
|
T | C | 1 | a0001c0004t0004g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1111-27170T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084032 | ||||||
| chr1:200084039
|
G | A | 4 | a0001c0001t0005g0025a0001c0001t0006g0059a0003c0006t0016g0001others(1): Show | 4 | HG02109.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-27163G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084039 | ||||||
| chr1:200084091
|
C | T | 136 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1111-27111C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084091 | ||||||
| chr1:200084094
|
A | G | 4 | a0001c0002t0021g0046a0001c0004t0004g0285a0001c0004t0007g0016others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-27108A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084094 | ||||||
| chr1:200084119
|
G | T | 129 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1111-27083G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084119 | ||||||
| chr1:200084354
|
T | C | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1111-26848T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084354 | ||||||
| chr1:200084515
|
G | A | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-26687G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084515 | ||||||
| chr1:200084537
|
G | A | 1 | a0001c0001t0028g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1111-26665G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084537 | ||||||
| chr1:200084541
|
TTTCACAC others(7): Show |
T | 1 | a0001c0002t0001g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1111-26660_1111-26 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084541 | ||||||
| chr1:200084557
|
A | T | 1 | a0001c0002t0001g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1111-26645A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084557 | ||||||
| chr1:200084608
|
A | T | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-26594A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084608 | ||||||
| chr1:200084692
|
A | C | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1111-26510A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084692 | ||||||
| chr1:200084760
|
A | T | 2 | a0001c0002t0001g0249a0001c0002t0001g0265 | 2 | HG00621.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1111-26442A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084760 | ||||||
| chr1:200084765
|
A | T | 1 | a0001c0001t0025g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1111-26437A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084765 | ||||||
| chr1:200084947
|
C | T | 1 | a0003c0006t0006g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1111-26255C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084947 | ||||||
| chr1:200084958
|
G | A | 2 | a0001c0001t0005g0146a0001c0001t0005g0159 | 2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1111-26244G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200084958 | ||||||
| chr1:200085263
|
C | T | 1 | a0001c0003t0002g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1111-25939C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085263 | ||||||
| chr1:200085294
|
A | G | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1111-25908A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085294 | ||||||
| chr1:200085331
|
G | C | 1 | a0001c0001t0003g0234 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1111-25871G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085331 | ||||||
| chr1:200085353
|
A | G | 1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1111-25849A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085353 | ||||||
| chr1:200085500
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1111-25702G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085500 | ||||||
| chr1:200085551
|
G | A | 5 | a0001c0002t0021g0046a0001c0003t0006g0061a0001c0004t0004g0285others(2): Show | 5 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-25651G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085551 | ||||||
| chr1:200085561
|
A | G | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-25641A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085561 | ||||||
| chr1:200085662
|
C | CA | 21 | a0001c0001t0001g0229a0001c0001t0002g0011a0001c0001t0002g0012others(18): Show | 21 | HG00544.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1111-25525dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200085662 | |||||
| chr1:200085662
|
CA | C | 8 | a0001c0001t0001g0137a0001c0001t0005g0025a0001c0001t0006g0059others(5): Show | 8 | HG01074.hp1 HG01361.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-25525delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200085662 | |||||
| chr1:200085683
|
G | GA | 129 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1111-25516dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200085683 | |||||
| chr1:200085864
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1111-25338A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085864 | ||||||
| chr1:200085949
|
G | T | 142 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(139): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1111-25253G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085949 | ||||||
| chr1:200085982
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1111-25220G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200085982 | ||||||
| chr1:200086115
|
G | A | 1 | a0001c0004t0004g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1111-25087G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086115 | ||||||
| chr1:200086174
|
T | C | 3 | a0001c0001t0002g0104a0001c0003t0002g0152a0001c0003t0014g0272 | 3 | HG00741.hp1 HG01361.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1111-25028T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086174 | ||||||
| chr1:200086229
|
C | T | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-24973C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086229 | ||||||
| chr1:200086305
|
T | G | 5 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(2): Show | 5 | HG01255.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-24897T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086305 | ||||||
| chr1:200086362
|
G | A | 1 | a0001c0001t0008g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1111-24840G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086362 | ||||||
| chr1:200086381
|
G | A | 129 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1111-24821G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086381 | ||||||
| chr1:200086407
|
T | G | 136 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1111-24795T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086407 | ||||||
| chr1:200086411
|
C | A | 1 | a0001c0001t0003g0206 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1111-24791C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086411 | ||||||
| chr1:200086600
|
C | T | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1111-24602C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086600 | ||||||
| chr1:200086616
|
T | G | 1 | a0001c0001t0005g0177 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1111-24586T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086616 | ||||||
| chr1:200086656
|
G | T | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1111-24546G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086656 | ||||||
| chr1:200086739
|
T | G | 142 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(139): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1111-24463T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086739 | ||||||
| chr1:200086776
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1111-24426C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086776 | ||||||
| chr1:200086809
|
C | T | 1 | a0001c0004t0020g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1111-24393C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086809 | ||||||
| chr1:200086865
|
C | T | 1 | a0001c0002t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1111-24337C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086865 | ||||||
| chr1:200086954
|
A | G | 2 | a0001c0001t0002g0254a0001c0001t0023g0225 | 2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1111-24248A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200086954 | ||||||
| chr1:200087110
|
G | A | 142 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(139): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1111-24092G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087110 | ||||||
| chr1:200087148
|
T | TTGTTGCA | 60 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(57): Show | 60 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1111-24054_1111-24 others(13): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087148 | ||||||
| chr1:200087241
|
A | AACACACA others(3): Show |
1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1111-23944_1111-23 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200087241 | |||||
| chr1:200087241
|
A | AACACACA others(5): Show |
3 | a0001c0001t0003g0238a0001c0001t0024g0029a0001c0002t0001g0240 | 3 | HG01255.hp2 HG04115.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1111-23946_1111-23 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200087241 | |||||
| chr1:200087241
|
AAC | A | 14 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0204others(11): Show | 14 | HG00280.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-23936_1111-23 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200087241 | |||||
| chr1:200087241
|
AACAC | A | 122 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(119): Show | 122 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.1111-23938_1111-23 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200087241 | |||||
| chr1:200087327
|
C | T | 1 | a0001c0001t0005g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1111-23875C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087327 | ||||||
| chr1:200087376
|
C | G | 8 | a0001c0001t0002g0104a0001c0001t0002g0204a0001c0001t0002g0227others(5): Show | 8 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-23826C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087376 | ||||||
| chr1:200087630
|
C | T | 11 | a0001c0003t0009g0223a0001c0003t0009g0224a0001c0003t0009g0257others(8): Show | 11 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-23572C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087630 | ||||||
| chr1:200087646
|
C | T | 56 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(53): Show | 56 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1111-23556C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087646 | ||||||
| chr1:200087691
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1111-23511G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087691 | ||||||
| chr1:200087719
|
C | A | 1 | a0001c0004t0004g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1111-23483C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087719 | ||||||
| chr1:200087770
|
G | T | 1 | a0001c0002t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1111-23432G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087770 | ||||||
| chr1:200087848
|
T | C | 1 | a0001c0003t0006g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-23354T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200087848 | ||||||
| chr1:200088076
|
G | T | 1 | a0001c0001t0002g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1111-23126G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088076 | ||||||
| chr1:200088216
|
T | G | 6 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0024g0029others(3): Show | 6 | HG01255.hp2 HG03704.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-22986T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088216 | ||||||
| chr1:200088218
|
T | G | 2 | a0001c0004t0007g0049a0001c0004t0007g0050 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1111-22984T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088218 | ||||||
| chr1:200088231
|
T | G | 8 | a0001c0001t0003g0238a0001c0001t0008g0103a0001c0001t0010g0092others(5): Show | 8 | HG01255.hp2 HG03704.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-22971T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088231 | ||||||
| chr1:200088319
|
G | T | 18 | a0001c0001t0002g0110a0001c0001t0002g0133a0001c0001t0005g0009others(15): Show | 18 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1111-22883G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088319 | ||||||
| chr1:200088332
|
A | G | 125 | a0001c0001t0001g0095a0001c0001t0001g0137a0001c0001t0001g0192others(122): Show | 125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1111-22870A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088332 | ||||||
| chr1:200088375
|
C | T | 42 | a0001c0001t0002g0104a0001c0001t0002g0110a0001c0001t0002g0133others(39): Show | 42 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.1111-22827C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088375 | ||||||
| chr1:200088376
|
G | A | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1111-22826G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088376 | ||||||
| chr1:200088384
|
A | G | 2 | a0001c0002t0001g0130a0001c0002t0001g0164 | 2 | NA18981.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1111-22818A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088384 | ||||||
| chr1:200088617
|
T | G | 2 | a0001c0001t0006g0017a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1111-22585T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088617 | ||||||
| chr1:200088733
|
G | T | 11 | a0001c0001t0002g0280a0001c0003t0002g0102a0001c0003t0002g0279others(8): Show | 11 | HG02148.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-22469G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088733 | ||||||
| chr1:200088875
|
C | T | 1 | a0001c0003t0002g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111-22327C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088875 | ||||||
| chr1:200088963
|
C | G | 2 | a0001c0001t0006g0270a0001c0001t0006g0271 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1111-22239C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200088963 | ||||||
| chr1:200089113
|
C | T | 4 | a0001c0002t0021g0046a0001c0004t0004g0285a0001c0004t0007g0016others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-22089C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200089113 | ||||||
| chr1:200089239
|
G | C | 4 | a0001c0002t0021g0046a0001c0004t0004g0285a0001c0004t0007g0016others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-21963G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200089239 | ||||||
| chr1:200089363
|
T | G | 44 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(41): Show | 44 | HG00639.hp1 HG01070.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1111-21839T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200089363 | ||||||
| chr1:200089614
|
C | T | 1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1111-21588C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200089614 | ||||||
| chr1:200089749
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1111-21453C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200089749 | ||||||
| chr1:200089993
|
C | CATGGGGA others(9): Show |
1 | a0001c0001t0002g0133 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1111-21181_1111-21 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200089993 | |||||
| chr1:200090010
|
A | G | 2 | a0001c0001t0005g0106a0001c0001t0005g0107 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1111-21192A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090010 | ||||||
| chr1:200090062
|
A | T | 44 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(41): Show | 44 | HG00639.hp1 HG01070.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1111-21140A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090062 | ||||||
| chr1:200090269
|
C | T | 44 | a0001c0001t0001g0202a0001c0001t0001g0216a0001c0001t0001g0261others(41): Show | 44 | HG00544.hp2 HG00609.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.1111-20933C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090269 | ||||||
| chr1:200090540
|
C | A | 1 | a0001c0004t0001g0047 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1111-20662C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090540 | ||||||
| chr1:200090580
|
A | G | 44 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(41): Show | 44 | HG00639.hp1 HG01070.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1111-20622A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090580 | ||||||
| chr1:200090614
|
G | A | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1111-20588G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090614 | ||||||
| chr1:200090682
|
G | A | 17 | a0001c0001t0002g0110a0001c0001t0002g0133a0001c0001t0005g0009others(14): Show | 17 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1111-20520G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090682 | ||||||
| chr1:200090787
|
A | G | 1 | a0001c0004t0001g0052 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1111-20415A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090787 | ||||||
| chr1:200090848
|
C | A | 2 | a0001c0002t0007g0026a0001c0003t0002g0056 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1111-20354C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090848 | ||||||
| chr1:200090925
|
G | A | 1 | a0001c0001t0005g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1111-20277G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090925 | ||||||
| chr1:200090967
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1111-20235C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200090967 | ||||||
| chr1:200091241
|
C | T | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1111-19961C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091241 | ||||||
| chr1:200091440
|
C | T | 1 | a0001c0003t0001g0027 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1111-19762C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091440 | ||||||
| chr1:200091484
|
C | CT | 77 | a0001c0001t0001g0137a0001c0001t0002g0068a0001c0001t0002g0069others(74): Show | 77 | HG00280.hp2 HG00621.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1111-19700dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200091484 | |||||
| chr1:200091484
|
C | CTT | 22 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(19): Show | 22 | HG00639.hp1 HG01070.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1111-19701_1111-19 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200091484 | |||||
| chr1:200091484
|
CT | C | 11 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0005g0214others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-19700delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200091484 | |||||
| chr1:200091545
|
C | T | 3 | a0001c0001t0002g0262a0001c0002t0005g0141a0001c0004t0001g0273 | 3 | HG00738.hp1 HG01109.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1111-19657C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091545 | ||||||
| chr1:200091548
|
G | A | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1111-19654G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091548 | ||||||
| chr1:200091578
|
A | G | 47 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(44): Show | 47 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.1111-19624A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091578 | ||||||
| chr1:200091700
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111-19502G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091700 | ||||||
| chr1:200091853
|
T | G | 6 | a0001c0001t0002g0104a0001c0002t0004g0091a0001c0003t0002g0152others(3): Show | 6 | HG00741.hp1 HG01361.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-19349T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091853 | ||||||
| chr1:200091928
|
C | T | 178 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(175): Show | 178 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.1111-19274C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200091928 | ||||||
| chr1:200092366
|
C | T | 1 | a0001c0001t0025g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1111-18836C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200092366 | ||||||
| chr1:200092407
|
G | A | 4 | a0001c0001t0006g0059a0001c0002t0021g0046a0001c0004t0004g0285others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-18795G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200092407 | ||||||
| chr1:200092691
|
A | ATCAGTTA others(1): Show |
3 | a0001c0001t0005g0025a0001c0001t0010g0092a0001c0002t0007g0093 | 3 | HG02109.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-18506_1111-18 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092691 | |||||
| chr1:200092703
|
G | GA | 13 | a0001c0001t0002g0034a0001c0001t0002g0150a0001c0001t0002g0151others(10): Show | 13 | HG00639.hp1 HG01099.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1111-18489dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092703 | |||||
| chr1:200092703
|
G | GAA | 116 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(113): Show | 116 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.1111-18490_1111-18 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092703 | |||||
| chr1:200092703
|
G | GAAA | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0280others(17): Show | 20 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1111-18491_1111-18 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092703 | |||||
| chr1:200092745
|
A | G | 64 | a0001c0001t0001g0163a0001c0001t0001g0202a0001c0001t0001g0216others(61): Show | 64 | HG00544.hp2 HG00735.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.1111-18457A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200092745 | ||||||
| chr1:200092829
|
T | C | 3 | a0001c0004t0007g0016a0001c0005t0006g0060a0003c0006t0006g0003 | 3 | HG02145.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1111-18373T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200092829 | ||||||
| chr1:200092831
|
A | T | 2 | a0001c0004t0007g0049a0001c0004t0007g0050 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1111-18371A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200092831 | ||||||
| chr1:200092873
|
C | CT | 23 | a0001c0001t0001g0071a0001c0001t0002g0034a0001c0001t0003g0235others(20): Show | 23 | HG00642.hp2 HG01106.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.1111-18301dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092873 | |||||
| chr1:200092873
|
C | CTT | 25 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0002g0110others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1111-18302_1111-18 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092873 | |||||
| chr1:200092873
|
C | CTTT | 9 | a0001c0001t0001g0201a0001c0001t0001g0221a0001c0001t0001g0229others(6): Show | 9 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111-18303_1111-18 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092873 | |||||
| chr1:200092873
|
CTTT | C | 18 | a0001c0001t0001g0163a0001c0001t0001g0202a0001c0001t0002g0197others(15): Show | 18 | HG00741.hp2 HG01168.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1111-18303_1111-18 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092873 | |||||
| chr1:200092873
|
CTTTT | C | 121 | a0001c0001t0001g0137a0001c0001t0001g0216a0001c0001t0001g0261others(118): Show | 121 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1111-18304_1111-18 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200092873 | |||||
| chr1:200092922
|
C | T | 1 | a0001c0002t0029g0142 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1111-18280C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200092922 | ||||||
| chr1:200093145
|
C | A | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-18057C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093145 | ||||||
| chr1:200093261
|
G | A | 130 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(127): Show | 130 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.1111-17941G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093261 | ||||||
| chr1:200093382
|
A | G | 136 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(133): Show | 136 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.1111-17820A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093382 | ||||||
| chr1:200093508
|
C | G | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1111-17694C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093508 | ||||||
| chr1:200093520
|
C | G | 1 | a0001c0001t0003g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111-17682C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093520 | ||||||
| chr1:200093538
|
C | T | 4 | a0001c0001t0002g0069a0001c0001t0002g0161a0001c0001t0003g0148others(1): Show | 4 | HG01261.hp2 HG01993.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-17664C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093538 | ||||||
| chr1:200093730
|
T | G | 128 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(125): Show | 128 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.1111-17472T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093730 | ||||||
| chr1:200093765
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-17437G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093765 | ||||||
| chr1:200093783
|
C | T | 2 | a0001c0001t0005g0025a0001c0001t0006g0271 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1111-17419C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093783 | ||||||
| chr1:200093895
|
G | A | 3 | a0001c0001t0005g0025a0001c0001t0006g0271a0001c0003t0006g0061 | 3 | HG01074.hp2 HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1111-17307G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093895 | ||||||
| chr1:200093986
|
C | G | 1 | a0001c0001t0023g0225 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1111-17216C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093986 | ||||||
| chr1:200093991
|
C | T | 1 | a0001c0004t0007g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1111-17211C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200093991 | ||||||
| chr1:200094072
|
G | A | 3 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0011g0078 | 3 | NA18977.hp1 NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1111-17130G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094072 | ||||||
| chr1:200094100
|
C | T | 2 | a0001c0001t0008g0166a0001c0002t0029g0142 | 2 | NA19065.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1111-17102C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094100 | ||||||
| chr1:200094179
|
T | A | 2 | a0001c0001t0011g0100a0001c0001t0026g0255 | 2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1111-17023T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094179 | ||||||
| chr1:200094180
|
TG | T | 126 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(123): Show | 126 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.1111-17020delG | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200094180 | |||||
| chr1:200094181
|
G | T | 2 | a0001c0001t0011g0100a0001c0001t0026g0255 | 2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1111-17021G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094181 | ||||||
| chr1:200094182
|
G | T | 5 | a0001c0002t0001g0215a0001c0002t0004g0090a0001c0005t0004g0021others(2): Show | 5 | HG00408.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-17020G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094182 | ||||||
| chr1:200094194
|
C | A | 131 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(128): Show | 131 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.1111-17008C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094194 | ||||||
| chr1:200094195
|
T | G | 131 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(128): Show | 131 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.1111-17007T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094195 | ||||||
| chr1:200094246
|
G | A | 128 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(125): Show | 128 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.1111-16956G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094246 | ||||||
| chr1:200094364
|
T | C | 3 | a0001c0004t0007g0016a0001c0005t0006g0060a0003c0006t0006g0003 | 3 | HG02145.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1111-16838T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094364 | ||||||
| chr1:200094443
|
C | T | 4 | a0001c0001t0006g0059a0001c0002t0021g0046a0001c0004t0004g0285others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-16759C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094443 | ||||||
| chr1:200094524
|
C | CT | 52 | a0001c0001t0001g0202a0001c0001t0001g0221a0001c0001t0002g0150others(49): Show | 52 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1111-16652dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200094524 | |||||
| chr1:200094524
|
C | CTT | 68 | a0001c0001t0001g0163a0001c0001t0001g0216a0001c0001t0001g0261others(65): Show | 68 | HG00544.hp2 HG00738.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1111-16653_1111-16 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200094524 | |||||
| chr1:200094524
|
C | CTTT | 55 | a0001c0001t0001g0137a0001c0001t0002g0117a0001c0001t0002g0197others(52): Show | 55 | HG00621.hp1 HG00735.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1111-16654_1111-16 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200094524 | |||||
| chr1:200094524
|
C | CTTTT | 13 | a0001c0001t0002g0243a0001c0001t0002g0280a0001c0001t0003g0030others(10): Show | 13 | HG00280.hp2 HG01074.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1111-16655_1111-16 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200094524 | |||||
| chr1:200094524
|
CT | C | 14 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0017others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-16652delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200094524 | |||||
| chr1:200094571
|
C | T | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-16631C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094571 | ||||||
| chr1:200094593
|
T | C | 2 | a0001c0003t0016g0153a0003c0006t0016g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1111-16609T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094593 | ||||||
| chr1:200094595
|
C | T | 2 | a0001c0003t0002g0279a0001c0005t0007g0281 | 2 | HG02148.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1111-16607C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094595 | ||||||
| chr1:200094690
|
G | A | 1 | a0001c0002t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1111-16512G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094690 | ||||||
| chr1:200094731
|
G | A | 1 | a0001c0002t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1111-16471G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094731 | ||||||
| chr1:200094780
|
C | T | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1111-16422C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094780 | ||||||
| chr1:200094792
|
A | G | 2 | a0001c0002t0001g0190a0001c0002t0001g0217 | 2 | NA18612.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1111-16410A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094792 | ||||||
| chr1:200094798
|
C | T | 2 | a0001c0004t0007g0016a0003c0006t0006g0003 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1111-16404C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094798 | ||||||
| chr1:200094892
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1111-16310A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094892 | ||||||
| chr1:200094958
|
A | G | 1 | a0001c0001t0005g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1111-16244A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200094958 | ||||||
| chr1:200095080
|
A | G | 1 | a0001c0001t0006g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1111-16122A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095080 | ||||||
| chr1:200095129
|
GA | G | 126 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0192others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1111-16059delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200095129 | |||||
| chr1:200095129
|
GAAA | G | 126 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(123): Show | 126 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.1111-16061_1111-16 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200095129 | |||||
| chr1:200095288
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1111-15914T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095288 | ||||||
| chr1:200095304
|
A | G | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111-15898A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095304 | ||||||
| chr1:200095709
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1111-15493T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095709 | ||||||
| chr1:200095714
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1111-15488A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095714 | ||||||
| chr1:200095728
|
AT | A | 254 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(251): Show | 254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.1111-15469delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200095728 | |||||
| chr1:200095756
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1111-15446G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095756 | ||||||
| chr1:200095834
|
G | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1111-15368G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095834 | ||||||
| chr1:200095843
|
C | T | 8 | a0001c0001t0005g0019a0001c0001t0005g0020a0001c0001t0005g0115others(5): Show | 8 | HG01109.hp1 HG01168.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-15359C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095843 | ||||||
| chr1:200095844
|
G | A | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1111-15358G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095844 | ||||||
| chr1:200095870
|
A | C | 60 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(57): Show | 60 | HG00280.hp2 HG00735.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1111-15332A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200095870 | ||||||
| chr1:200096009
|
C | A | 1 | a0001c0003t0022g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111-15193C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096009 | ||||||
| chr1:200096087
|
C | T | 144 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(141): Show | 144 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(141): Show |
intron_variant | MODIFIER | c.1111-15115C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096087 | ||||||
| chr1:200096179
|
T | C | 1 | a0001c0003t0002g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1111-15023T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096179 | ||||||
| chr1:200096242
|
C | A | 15 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(12): Show | 15 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1111-14960C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096242 | ||||||
| chr1:200096272
|
G | A | 1 | a0001c0003t0009g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1111-14930G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096272 | ||||||
| chr1:200096489
|
A | G | 174 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(171): Show | 174 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(171): Show |
intron_variant | MODIFIER | c.1111-14713A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096489 | ||||||
| chr1:200096585
|
A | C | 268 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(265): Show | 268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1111-14617A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096585 | ||||||
| chr1:200096659
|
G | A | 1 | a0001c0002t0004g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1111-14543G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096659 | ||||||
| chr1:200096711
|
A | T | 5 | a0001c0001t0006g0040a0001c0005t0006g0060a0002c0008t0012g0084others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-14491A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096711 | ||||||
| chr1:200096809
|
G | A | 11 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(8): Show | 11 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-14393G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200096809 | ||||||
| chr1:200097125
|
C | T | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-14077C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097125 | ||||||
| chr1:200097126
|
G | A | 1 | a0001c0001t0011g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1111-14076G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097126 | ||||||
| chr1:200097234
|
A | T | 3 | a0001c0001t0006g0024a0001c0004t0004g0044a0001c0005t0004g0083 | 3 | HG02559.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1111-13968A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097234 | ||||||
| chr1:200097236
|
C | A | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1111-13966C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097236 | ||||||
| chr1:200097350
|
C | T | 264 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1111-13852C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097350 | ||||||
| chr1:200097395
|
A | G | 5 | a0001c0003t0006g0061a0001c0003t0009g0223a0001c0003t0009g0224others(2): Show | 5 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-13807A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097395 | ||||||
| chr1:200097397
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1111-13805C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097397 | ||||||
| chr1:200097624
|
C | T | 169 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(166): Show | 169 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.1111-13578C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097624 | ||||||
| chr1:200097686
|
A | C | 7 | a0001c0004t0004g0008a0001c0004t0004g0010a0001c0004t0004g0015others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111-13516A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097686 | ||||||
| chr1:200097765
|
G | A | 161 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(158): Show | 161 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1111-13437G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097765 | ||||||
| chr1:200097938
|
A | G | 2 | a0001c0001t0002g0173a0001c0001t0008g0005 | 2 | HG03654.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1111-13264A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200097938 | ||||||
| chr1:200098120
|
C | T | 267 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.1111-13082C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200098120 | ||||||
| chr1:200098312
|
G | A | 2 | a0001c0001t0002g0254a0001c0001t0023g0225 | 2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1111-12890G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200098312 | ||||||
| chr1:200098572
|
T | A | 2 | a0001c0004t0007g0049a0001c0004t0007g0050 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1111-12630T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200098572 | ||||||
| chr1:200098715
|
G | A | 6 | a0001c0001t0003g0238a0001c0001t0008g0166a0001c0001t0024g0029others(3): Show | 6 | HG04115.hp1 NA19001.hp2 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-12487G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200098715 | ||||||
| chr1:200098717
|
G | T | 264 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1111-12485G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200098717 | ||||||
| chr1:200098897
|
A | C | 6 | a0001c0002t0007g0026a0001c0003t0006g0061a0001c0003t0009g0223others(3): Show | 6 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-12305A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200098897 | ||||||
| chr1:200098941
|
T | C | 155 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1111-12261T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200098941 | ||||||
| chr1:200099343
|
CT | C | 257 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(254): Show | 257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1111-11846delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200099343 | |||||
| chr1:200099427
|
C | G | 65 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(62): Show | 65 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1111-11775C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200099427 | ||||||
| chr1:200099466
|
T | C | 257 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(254): Show | 257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1111-11736T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200099466 | ||||||
| chr1:200099530
|
C | T | 83 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1111-11672C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200099530 | ||||||
| chr1:200099587
|
T | A | 264 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1111-11615T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200099587 | ||||||
| chr1:200099843
|
C | T | 124 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(121): Show | 124 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.1111-11359C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200099843 | ||||||
| chr1:200100073
|
T | C | 267 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.1111-11129T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200100073 | ||||||
| chr1:200100088
|
A | G | 120 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1111-11114A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200100088 | ||||||
| chr1:200100266
|
G | A | 1 | a0001c0001t0010g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1111-10936G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200100266 | ||||||
| chr1:200100320
|
C | CTTTA | 67 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(64): Show | 67 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1111-10866_1111-10 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200100320 | |||||
| chr1:200100342
|
ATTTCAG | A | 3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-10856_1111-10 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200100342 | |||||
| chr1:200100434
|
G | C | 4 | a0001c0003t0006g0061a0001c0003t0009g0223a0001c0003t0009g0257others(1): Show | 4 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-10768G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200100434 | ||||||
| chr1:200100500
|
T | C | 1 | a0001c0001t0003g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1111-10702T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200100500 | ||||||
| chr1:200100558
|
G | T | 258 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(255): Show | 258 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1111-10644G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200100558 | ||||||
| chr1:200100662
|
C | T | 2 | a0001c0001t0010g0092a0001c0002t0007g0093 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-10540C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200100662 | ||||||
| chr1:200101247
|
A | T | 1 | a0001c0002t0001g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1111-9955A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101247 | ||||||
| chr1:200101254
|
A | T | 12 | a0001c0001t0009g0181a0001c0001t0010g0092a0001c0001t0012g0182others(9): Show | 12 | HG02145.hp1 HG02717.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.1111-9948A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101254 | ||||||
| chr1:200101536
|
A | T | 1 | a0001c0002t0001g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1111-9666A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101536 | ||||||
| chr1:200101551
|
C | T | 1 | a0001c0003t0002g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1111-9651C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101551 | ||||||
| chr1:200101637
|
A | C | 122 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(119): Show | 122 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1111-9565A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101637 | ||||||
| chr1:200101692
|
C | T | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1111-9510C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101692 | ||||||
| chr1:200101753
|
C | T | 1 | a0001c0001t0003g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1111-9449C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101753 | ||||||
| chr1:200101841
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1111-9361G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101841 | ||||||
| chr1:200101976
|
C | G | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1111-9226C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200101976 | ||||||
| chr1:200102033
|
T | C | 2 | a0001c0003t0009g0064a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1111-9169T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102033 | ||||||
| chr1:200102135
|
T | C | 3 | a0001c0001t0010g0116a0001c0001t0010g0140a0001c0002t0001g0139 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1111-9067T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102135 | ||||||
| chr1:200102158
|
G | A | 117 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(114): Show | 117 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.1111-9044G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102158 | ||||||
| chr1:200102217
|
T | G | 138 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(135): Show | 138 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.1111-8985T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102217 | ||||||
| chr1:200102220
|
A | T | 5 | a0001c0001t0006g0075a0001c0002t0021g0046a0001c0003t0005g0055others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-8982A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102220 | ||||||
| chr1:200102229
|
G | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1111-8973G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102229 | ||||||
| chr1:200102364
|
C | T | 1 | a0001c0003t0009g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1111-8838C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102364 | ||||||
| chr1:200102508
|
T | C | 258 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(255): Show | 258 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1111-8694T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102508 | ||||||
| chr1:200102734
|
T | A | 1 | a0001c0001t0003g0235 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1111-8468T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102734 | ||||||
| chr1:200102805
|
T | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1111-8397T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102805 | ||||||
| chr1:200102869
|
C | G | 2 | a0001c0001t0002g0204a0001c0001t0002g0227 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1111-8333C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200102869 | ||||||
| chr1:200103040
|
C | T | 137 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(134): Show | 137 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(134): Show |
intron_variant | MODIFIER | c.1111-8162C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103040 | ||||||
| chr1:200103122
|
C | CT | 8 | a0001c0001t0008g0103a0001c0001t0011g0100a0001c0001t0026g0255others(5): Show | 8 | HG02015.hp1 HG02080.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-8061dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200103122 | |||||
| chr1:200103122
|
C | CTT | 17 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0068others(14): Show | 17 | HG00735.hp1 HG00735.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.1111-8062_1111-806 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200103122 | |||||
| chr1:200103122
|
C | CTTT | 79 | a0001c0001t0001g0202a0001c0001t0002g0110a0001c0001t0002g0114others(76): Show | 79 | HG00544.hp2 HG00741.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.1111-8063_1111-806 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200103122 | |||||
| chr1:200103122
|
C | CTTTT | 22 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(19): Show | 22 | HG00621.hp2 HG00738.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1111-8064_1111-806 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200103122 | |||||
| chr1:200103122
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1111-8080C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103122 | ||||||
| chr1:200103122
|
CT | C | 14 | a0001c0001t0001g0095a0001c0001t0006g0075a0001c0001t0008g0231others(11): Show | 14 | HG01981.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-8061delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200103122 | |||||
| chr1:200103522
|
A | C | 3 | a0001c0001t0005g0106a0001c0001t0005g0107a0001c0001t0005g0177 | 3 | HG01256.hp1 HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1111-7680A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103522 | ||||||
| chr1:200103697
|
C | T | 32 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(29): Show | 32 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1111-7505C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103697 | ||||||
| chr1:200103832
|
G | A | 3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-7370G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103832 | ||||||
| chr1:200103838
|
A | G | 133 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(130): Show | 133 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(130): Show |
intron_variant | MODIFIER | c.1111-7364A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103838 | ||||||
| chr1:200103925
|
G | T | 1 | a0001c0002t0001g0260 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1111-7277G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103925 | ||||||
| chr1:200103956
|
C | T | 2 | a0001c0003t0002g0279a0001c0005t0007g0281 | 2 | HG02148.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1111-7246C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200103956 | ||||||
| chr1:200104054
|
C | T | 15 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(12): Show | 15 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1111-7148C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104054 | ||||||
| chr1:200104100
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1111-7102G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104100 | ||||||
| chr1:200104252
|
G | A | 1 | a0001c0004t0001g0273 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1111-6950G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104252 | ||||||
| chr1:200104345
|
C | A | 2 | a0001c0003t0016g0153a0003c0006t0016g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1111-6857C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104345 | ||||||
| chr1:200104602
|
A | C | 134 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(131): Show | 134 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.1111-6600A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104602 | ||||||
| chr1:200104699
|
G | A | 2 | a0001c0003t0009g0064a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1111-6503G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104699 | ||||||
| chr1:200104725
|
C | T | 78 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1111-6477C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104725 | ||||||
| chr1:200104748
|
C | T | 1 | a0001c0004t0004g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1111-6454C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104748 | ||||||
| chr1:200104879
|
T | G | 1 | a0001c0002t0001g0082 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1111-6323T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104879 | ||||||
| chr1:200104883
|
G | A | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1111-6319G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104883 | ||||||
| chr1:200104890
|
C | T | 259 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(256): Show | 259 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1111-6312C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104890 | ||||||
| chr1:200104925
|
A | T | 2 | a0001c0003t0006g0061a0001c0003t0017g0042 | 2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1111-6277A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104925 | ||||||
| chr1:200104943
|
G | A | 1 | a0001c0001t0003g0238 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1111-6259G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104943 | ||||||
| chr1:200104985
|
G | A | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1111-6217G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200104985 | ||||||
| chr1:200105001
|
G | A | 110 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(107): Show | 110 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.1111-6201G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200105001 | ||||||
| chr1:200105188
|
G | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1111-6014G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200105188 | ||||||
| chr1:200105392
|
C | T | 2 | a0001c0001t0006g0270a0003c0010t0001g0002 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1111-5810C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200105392 | ||||||
| chr1:200105537
|
A | G | 1 | a0001c0002t0001g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1111-5665A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200105537 | ||||||
| chr1:200105680
|
C | T | 7 | a0001c0001t0005g0094a0001c0002t0004g0178a0001c0003t0006g0014others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111-5522C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200105680 | ||||||
| chr1:200105758
|
T | G | 266 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(263): Show | 266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1111-5444T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200105758 | ||||||
| chr1:200106017
|
C | T | 1 | a0001c0004t0001g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1111-5185C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106017 | ||||||
| chr1:200106061
|
C | CCTCTGT | 30 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(27): Show | 30 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1111-5141_1111-514 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106061 | ||||||
| chr1:200106061
|
C | CCTCTGTT | 19 | a0001c0001t0002g0280a0001c0001t0006g0017a0001c0003t0006g0061others(16): Show | 19 | HG01074.hp2 HG01109.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1111-5141_1111-514 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106061 | ||||||
| chr1:200106061
|
C | CCTCTGTT others(1): Show |
76 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(73): Show | 76 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1111-5141_1111-514 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106061 | ||||||
| chr1:200106064
|
C | CT | 112 | a0001c0001t0001g0202a0001c0001t0002g0034a0001c0001t0002g0068others(109): Show | 112 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.1111-5127dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200106064 | |||||
| chr1:200106064
|
C | CTT | 24 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0005g0025others(21): Show | 24 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111-5128_1111-512 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200106064 | |||||
| chr1:200106064
|
C | T | 128 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1111-5138C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106064 | ||||||
| chr1:200106213
|
A | C | 70 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(67): Show | 70 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1111-4989A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106213 | ||||||
| chr1:200106215
|
G | A | 20 | a0001c0001t0005g0025a0001c0001t0009g0181a0001c0001t0012g0182others(17): Show | 20 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-4987G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106215 | ||||||
| chr1:200106225
|
T | G | 4 | a0001c0003t0006g0061a0001c0003t0009g0223a0001c0003t0009g0257others(1): Show | 4 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-4977T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106225 | ||||||
| chr1:200106534
|
T | C | 6 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0002t0007g0093others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-4668T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106534 | ||||||
| chr1:200106594
|
G | A | 1 | a0001c0002t0001g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1111-4608G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106594 | ||||||
| chr1:200106770
|
C | T | 266 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(263): Show | 266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1111-4432C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106770 | ||||||
| chr1:200106788
|
G | A | 3 | a0001c0001t0003g0239a0001c0002t0001g0208a0001c0002t0001g0242 | 3 | HG01258.hp2 HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1111-4414G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200106788 | ||||||
| chr1:200107176
|
TACAA | T | 266 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(263): Show | 266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1111-4017_1111-401 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200107176 | |||||
| chr1:200107196
|
G | T | 1 | a0001c0001t0003g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1111-4006G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107196 | ||||||
| chr1:200107245
|
C | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1111-3957C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107245 | ||||||
| chr1:200107303
|
C | CT | 260 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(257): Show | 260 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1111-3886dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200107303 | |||||
| chr1:200107310
|
T | TG | 3 | a0001c0003t0009g0224a0001c0004t0007g0049a0001c0004t0007g0050 | 3 | HG02622.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1111-3892_1111-389 others(5): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107310 | ||||||
| chr1:200107362
|
G | A | 1 | a0001c0001t0010g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1111-3840G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107362 | ||||||
| chr1:200107478
|
G | T | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1111-3724G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107478 | ||||||
| chr1:200107518
|
AACAG | A | 30 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(27): Show | 30 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1111-3679_1111-367 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200107518 | |||||
| chr1:200107524
|
C | T | 115 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(112): Show | 115 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1111-3678C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107524 | ||||||
| chr1:200107658
|
G | C | 1 | a0001c0001t0005g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1111-3544G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107658 | ||||||
| chr1:200107749
|
C | T | 117 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(114): Show | 117 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.1111-3453C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107749 | ||||||
| chr1:200107812
|
T | TTTTTTTT others(172): Show |
1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1111-3390_1111-338 others(183): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107812 | ||||||
| chr1:200107812
|
T | TTTTTTTT others(173): Show |
1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1111-3390_1111-338 others(184): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107812 | ||||||
| chr1:200107813
|
A | T | 2 | a0001c0003t0009g0064a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1111-3389A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107813 | ||||||
| chr1:200107819
|
C | T | 26 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(23): Show | 26 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1111-3383C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107819 | ||||||
| chr1:200107820
|
G | A | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1111-3382G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107820 | ||||||
| chr1:200107831
|
A | T | 2 | a0001c0003t0009g0064a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1111-3371A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107831 | ||||||
| chr1:200107836
|
G | A | 2 | a0001c0003t0009g0064a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1111-3366G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107836 | ||||||
| chr1:200107842
|
A | G | 2 | a0001c0003t0009g0064a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1111-3360A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107842 | ||||||
| chr1:200107843
|
C | A | 2 | a0001c0003t0009g0064a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1111-3359C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107843 | ||||||
| chr1:200107915
|
G | T | 146 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(143): Show | 146 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.1111-3287G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200107915 | ||||||
| chr1:200108025
|
C | T | 2 | a0002c0008t0012g0084a0002c0009t0006g0086 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1111-3177C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200108025 | ||||||
| chr1:200108049
|
G | A | 2 | a0001c0001t0002g0165a0001c0002t0001g0268 | 2 | HG00738.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1111-3153G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200108049 | ||||||
| chr1:200108081
|
C | CGT | 4 | a0001c0001t0002g0243a0001c0001t0003g0171a0001c0002t0001g0096others(1): Show | 4 | HG00280.hp2 HG01361.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-3088_1111-308 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(3): Show |
3 | a0001c0001t0002g0213a0001c0005t0001g0282a0001c0005t0001g0284 | 3 | HG01943.hp2 HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1111-3096_1111-308 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(5): Show |
1 | a0006c0011t0030g0218 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1111-3098_1111-308 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(7): Show |
14 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(11): Show | 14 | HG00558.hp2 HG00609.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1111-3100_1111-308 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(9): Show |
3 | a0001c0002t0001g0160a0001c0002t0001g0200a0001c0004t0001g0052 | 3 | HG02129.hp1 HG02155.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1111-3102_1111-308 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(11): Show |
10 | a0001c0001t0003g0191a0001c0001t0005g0146a0001c0001t0005g0159others(7): Show | 10 | HG00408.hp2 HG00609.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111-3104_1111-308 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(13): Show |
6 | a0001c0001t0005g0009a0001c0002t0001g0118a0001c0002t0001g0130others(3): Show | 6 | HG03239.hp2 NA18966.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-3106_1111-308 others(24): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(15): Show |
2 | a0001c0002t0001g0072a0001c0003t0017g0042 | 2 | NA18973.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1111-3108_1111-308 others(26): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(17): Show |
1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1111-3110_1111-308 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
C | CGTGTGTG others(25): Show |
1 | a0001c0001t0001g0229 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1111-3118_1111-308 others(36): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
CGT | C | 78 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(75): Show | 78 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1111-3088_1111-308 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
CGTGT | C | 8 | a0001c0001t0005g0094a0001c0002t0004g0178a0001c0003t0006g0014others(5): Show | 8 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-3090_1111-308 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
CGTGTGT | C | 14 | a0001c0001t0005g0025a0001c0001t0006g0271a0001c0003t0002g0043others(11): Show | 14 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1111-3092_1111-308 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
CGTGTGTG others(1): Show |
C | 119 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(116): Show | 119 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.1111-3094_1111-308 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108081
|
CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1111-3096_1111-308 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 200108081 | |||||
| chr1:200108126
|
C | T | 6 | a0001c0001t0005g0025a0001c0003t0009g0064a0001c0003t0009g0224others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-3076C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200108126 | ||||||
| chr1:200108564
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1111-2638C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200108564 | ||||||
| chr1:200108645
|
C | T | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1111-2557C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200108645 | ||||||
| chr1:200108878
|
G | A | 123 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1111-2324G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200108878 | ||||||
| chr1:200108907
|
G | T | 270 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(267): Show | 270 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.1111-2295G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200108907 | ||||||
| chr1:200109059
|
G | A | 1 | a0001c0001t0003g0263 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1111-2143G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200109059 | ||||||
| chr1:200109151
|
G | T | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1111-2051G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200109151 | ||||||
| chr1:200109632
|
G | A | 1 | a0001c0001t0003g0238 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1111-1570G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200109632 | ||||||
| chr1:200109645
|
A | G | 91 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(88): Show | 91 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1111-1557A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200109645 | ||||||
| chr1:200109672
|
A | G | 16 | a0001c0001t0005g0025a0001c0003t0002g0043a0001c0003t0009g0064others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111-1530A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200109672 | ||||||
| chr1:200109725
|
C | T | 6 | a0001c0001t0005g0025a0001c0003t0009g0064a0001c0003t0009g0224others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-1477C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200109725 | ||||||
| chr1:200110000
|
G | A | 269 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(266): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1111-1202G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110000 | ||||||
| chr1:200110165
|
T | C | 269 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(266): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1111-1037T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110165 | ||||||
| chr1:200110374
|
A | G | 1 | a0001c0002t0001g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1111-828A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110374 | ||||||
| chr1:200110385
|
T | C | 1 | a0001c0003t0002g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1111-817T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110385 | ||||||
| chr1:200110458
|
A | G | 269 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(266): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1111-744A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110458 | ||||||
| chr1:200110496
|
A | T | 5 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0002t0007g0093others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-706A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110496 | ||||||
| chr1:200110531
|
G | A | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1111-671G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110531 | ||||||
| chr1:200110652
|
C | A | 16 | a0001c0001t0005g0025a0001c0003t0002g0043a0001c0003t0009g0064others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111-550C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110652 | ||||||
| chr1:200110735
|
T | C | 16 | a0001c0001t0005g0025a0001c0003t0002g0043a0001c0003t0009g0064others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111-467T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110735 | ||||||
| chr1:200110820
|
A | G | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1111-382A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110820 | ||||||
| chr1:200110831
|
T | A | 11 | a0001c0001t0002g0280a0001c0001t0006g0017a0001c0003t0006g0061others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-371T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110831 | ||||||
| chr1:200110836
|
A | G | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1111-366A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 5/7 | chr1 | 200110836 | ||||||
| chr1:200111334
|
A | AT | 94 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(91): Show | 94 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1230+13_1230+14ins others(1): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200111334 | ||||||
| chr1:200111335
|
C | T | 54 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(51): Show | 54 | HG00738.hp1 HG01109.hp2 HG01358.hp1 others(51): Show |
intron_variant | MODIFIER | c.1230+14C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200111335 | ||||||
| chr1:200111336
|
C | A | 94 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(91): Show | 94 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1230+15C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200111336 | ||||||
| chr1:200111336
|
C | CAA | 32 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(29): Show | 32 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.1230+29_1230+30dup others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200111336 | |||||
| chr1:200111336
|
C | CAAAAA | 8 | a0001c0001t0002g0011a0001c0001t0006g0040a0001c0001t0015g0041others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1230+26_1230+30dup others(5): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200111336 | |||||
| chr1:200111422
|
A | G | 1 | a0001c0001t0003g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1230+101A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200111422 | ||||||
| chr1:200111486
|
T | G | 285 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(282): Show | 285 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1230+165T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200111486 | ||||||
| chr1:200111828
|
TAGAG | T | 8 | a0001c0001t0006g0270a0001c0002t0021g0046a0001c0004t0004g0015others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1230+511_1230+514d others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200111828 | |||||
| chr1:200111893
|
A | T | 128 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1230+572A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200111893 | ||||||
| chr1:200112019
|
A | G | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1230+698A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112019 | ||||||
| chr1:200112031
|
A | G | 128 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1230+710A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112031 | ||||||
| chr1:200112057
|
G | T | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1230+736G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112057 | ||||||
| chr1:200112161
|
G | C | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1230+840G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112161 | ||||||
| chr1:200112232
|
A | G | 3 | a0001c0001t0006g0075a0001c0003t0005g0055a0001c0004t0007g0016 | 3 | HG02145.hp2 HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1230+911A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112232 | ||||||
| chr1:200112421
|
C | T | 5 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+1100C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112421 | ||||||
| chr1:200112582
|
T | C | 81 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1230+1261T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112582 | ||||||
| chr1:200112681
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0003g0143a0001c0001t0003g0220others(2): Show | 5 | NA18945.hp1 NA18947.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+1360C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112681 | ||||||
| chr1:200112774
|
A | G | 2 | a0001c0004t0004g0044a0001c0005t0004g0083 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1230+1453A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112774 | ||||||
| chr1:200112783
|
A | G | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1230+1462A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112783 | ||||||
| chr1:200112829
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1230+1508G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112829 | ||||||
| chr1:200112923
|
G | A | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+1602G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112923 | ||||||
| chr1:200112975
|
T | G | 1 | a0001c0001t0008g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1230+1654T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200112975 | ||||||
| chr1:200113072
|
C | T | 1 | a0001c0002t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1230+1751C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113072 | ||||||
| chr1:200113176
|
T | G | 1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1230+1855T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113176 | ||||||
| chr1:200113188
|
TATATGTT others(43): Show |
T | 1 | a0001c0001t0001g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1230+1911_1230+196 others(54): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200113188 | |||||
| chr1:200113232
|
T | C | 263 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1230+1911T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113232 | ||||||
| chr1:200113282
|
C | A | 4 | a0001c0001t0005g0019a0001c0001t0005g0020a0001c0002t0001g0267others(1): Show | 4 | HG01192.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230+1961C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113282 | ||||||
| chr1:200113336
|
A | G | 81 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1230+2015A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113336 | ||||||
| chr1:200113459
|
T | A | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1230+2138T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113459 | ||||||
| chr1:200113558
|
G | C | 127 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1230+2237G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113558 | ||||||
| chr1:200113575
|
T | C | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1230+2254T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113575 | ||||||
| chr1:200113727
|
T | G | 116 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(113): Show | 116 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.1230+2406T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113727 | ||||||
| chr1:200113827
|
G | A | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+2506G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113827 | ||||||
| chr1:200113902
|
C | T | 4 | a0001c0001t0002g0189a0001c0001t0002g0199a0001c0001t0003g0198others(1): Show | 4 | HG00741.hp2 HG01168.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230+2581C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113902 | ||||||
| chr1:200113936
|
T | C | 3 | a0001c0001t0006g0270a0001c0002t0021g0046a0001c0004t0004g0285 | 3 | HG03098.hp2 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1230+2615T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200113936 | ||||||
| chr1:200114056
|
G | A | 81 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1230+2735G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114056 | ||||||
| chr1:200114108
|
G | A | 2 | a0001c0003t0006g0061a0001c0003t0017g0042 | 2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1230+2787G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114108 | ||||||
| chr1:200114187
|
A | AAACT | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+2868_1230+286 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114187 | |||||
| chr1:200114191
|
T | A | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+2870T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114191 | ||||||
| chr1:200114191
|
T | TAAAA | 129 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 129 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.1230+2872_1230+287 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114191 | |||||
| chr1:200114231
|
T | TAC | 4 | a0001c0001t0006g0040a0001c0005t0006g0060a0002c0008t0012g0084others(1): Show | 4 | HG02451.hp1 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230+2911_1230+291 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114231 | |||||
| chr1:200114231
|
TATACAC | T | 128 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1230+2912_1230+291 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114231 | |||||
| chr1:200114233
|
T | C | 8 | a0001c0001t0006g0040a0001c0004t0004g0037a0001c0005t0004g0021others(5): Show | 8 | HG02451.hp1 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+2912T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114233 | ||||||
| chr1:200114233
|
T | TAC | 103 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 103 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.1230+2924_1230+292 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114233 | |||||
| chr1:200114233
|
T | TATAC | 18 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0234others(15): Show | 18 | HG02559.hp2 HG02723.hp1 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.1230+2913_1230+291 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114233 | |||||
| chr1:200114271
|
TACATATA others(5): Show |
T | 1 | a0001c0002t0001g0028 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1230+2966_1230+297 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114271 | |||||
| chr1:200114301
|
CAT | C | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+2987_1230+298 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114301 | |||||
| chr1:200114317
|
A | AAGT | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+2997_1230+299 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114317 | |||||
| chr1:200114332
|
GAAAAAAA others(3): Show |
G | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1230+3018_1230+302 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200114332 | |||||
| chr1:200114413
|
C | T | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+3092C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114413 | ||||||
| chr1:200114526
|
G | A | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+3205G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114526 | ||||||
| chr1:200114545
|
G | A | 10 | a0001c0001t0002g0280a0001c0001t0006g0024a0001c0002t0001g0096others(7): Show | 10 | HG01361.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1230+3224G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114545 | ||||||
| chr1:200114736
|
T | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1230+3415T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114736 | ||||||
| chr1:200114786
|
G | T | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1230+3465G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114786 | ||||||
| chr1:200114903
|
A | C | 1 | a0001c0002t0029g0142 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1230+3582A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200114903 | ||||||
| chr1:200115036
|
C | CT | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+3722dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200115036 | |||||
| chr1:200115039
|
T | C | 129 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 129 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.1230+3718T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115039 | ||||||
| chr1:200115048
|
T | TTTAG | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+3737_1230+374 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200115048 | |||||
| chr1:200115090
|
G | A | 1 | a0001c0001t0008g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1230+3769G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115090 | ||||||
| chr1:200115323
|
G | A | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1230+4002G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115323 | ||||||
| chr1:200115506
|
T | G | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1230+4185T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115506 | ||||||
| chr1:200115597
|
G | A | 1 | a0001c0001t0007g0176 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1230+4276G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115597 | ||||||
| chr1:200115615
|
C | G | 127 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1230+4294C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115615 | ||||||
| chr1:200115765
|
G | A | 130 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1230+4444G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115765 | ||||||
| chr1:200115781
|
G | A | 1 | a0004c0013t0032g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1230+4460G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115781 | ||||||
| chr1:200115837
|
G | A | 1 | a0001c0003t0002g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1230+4516G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115837 | ||||||
| chr1:200115876
|
A | G | 264 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1230+4555A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115876 | ||||||
| chr1:200115912
|
C | T | 1 | a0001c0002t0005g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1230+4591C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115912 | ||||||
| chr1:200115967
|
C | T | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1230+4646C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115967 | ||||||
| chr1:200115988
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1230+4667T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200115988 | ||||||
| chr1:200116248
|
G | A | 255 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(252): Show | 255 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1231-4560G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116248 | ||||||
| chr1:200116274
|
G | A | 4 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-4534G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116274 | ||||||
| chr1:200116289
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0004t0004g0066others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-4519G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116289 | ||||||
| chr1:200116317
|
G | A | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-4491G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116317 | ||||||
| chr1:200116407
|
C | T | 2 | a0001c0004t0007g0049a0001c0004t0007g0050 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1231-4401C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116407 | ||||||
| chr1:200116432
|
T | A | 279 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(276): Show | 279 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1231-4376T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116432 | ||||||
| chr1:200116490
|
G | GTT | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1231-4316_1231-431 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200116490 | |||||
| chr1:200116507
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1231-4301A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116507 | ||||||
| chr1:200116521
|
T | C | 2 | a0001c0002t0001g0200a0001c0004t0001g0052 | 2 | HG02129.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1231-4287T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116521 | ||||||
| chr1:200116575
|
C | T | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1231-4233C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116575 | ||||||
| chr1:200116586
|
T | A | 127 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1231-4222T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116586 | ||||||
| chr1:200116664
|
G | A | 15 | a0001c0001t0002g0110a0001c0001t0005g0031a0001c0001t0005g0032others(12): Show | 15 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1231-4144G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116664 | ||||||
| chr1:200116813
|
C | T | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1231-3995C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116813 | ||||||
| chr1:200116946
|
G | A | 127 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1231-3862G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200116946 | ||||||
| chr1:200117000
|
A | G | 1 | a0001c0004t0006g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1231-3808A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117000 | ||||||
| chr1:200117004
|
T | C | 72 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(69): Show | 72 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1231-3804T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117004 | ||||||
| chr1:200117268
|
A | G | 10 | a0001c0001t0002g0280a0001c0001t0006g0017a0001c0001t0006g0024others(7): Show | 10 | HG02258.hp1 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-3540A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117268 | ||||||
| chr1:200117275
|
G | A | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1231-3533G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117275 | ||||||
| chr1:200117296
|
A | C | 26 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(23): Show | 26 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1231-3512A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117296 | ||||||
| chr1:200117319
|
C | G | 3 | a0001c0001t0006g0270a0001c0002t0021g0046a0001c0004t0004g0285 | 3 | HG03098.hp2 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1231-3489C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117319 | ||||||
| chr1:200117636
|
T | C | 1 | a0001c0003t0002g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1231-3172T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117636 | ||||||
| chr1:200117711
|
T | C | 79 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(76): Show | 79 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1231-3097T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117711 | ||||||
| chr1:200117721
|
C | CT | 32 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(29): Show | 32 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1231-3077dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200117721 | |||||
| chr1:200117799
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1231-3009C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117799 | ||||||
| chr1:200117823
|
C | G | 4 | a0001c0001t0005g0019a0001c0001t0005g0020a0001c0002t0001g0267others(1): Show | 4 | HG01192.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-2985C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117823 | ||||||
| chr1:200117828
|
C | T | 1 | a0001c0001t0008g0231 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1231-2980C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117828 | ||||||
| chr1:200117870
|
C | T | 1 | a0001c0002t0001g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1231-2938C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117870 | ||||||
| chr1:200117914
|
A | G | 72 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(69): Show | 72 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1231-2894A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117914 | ||||||
| chr1:200117960
|
C | T | 2 | a0001c0003t0006g0061a0001c0003t0017g0042 | 2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1231-2848C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200117960 | ||||||
| chr1:200118019
|
C | CT | 94 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(91): Show | 94 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1231-2772dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200118019 | |||||
| chr1:200118019
|
C | CTT | 75 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(72): Show | 75 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1231-2773_1231-277 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200118019 | |||||
| chr1:200118019
|
C | CTTTT | 6 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-2775_1231-277 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200118019 | |||||
| chr1:200118022
|
T | TC | 4 | a0001c0001t0002g0069a0001c0001t0002g0161a0001c0001t0003g0148others(1): Show | 4 | HG01261.hp2 HG01993.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-2786_1231-278 others(5): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118022 | ||||||
| chr1:200118094
|
G | A | 71 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(68): Show | 71 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.1231-2714G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118094 | ||||||
| chr1:200118167
|
C | T | 2 | a0001c0004t0004g0044a0001c0005t0004g0083 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1231-2641C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118167 | ||||||
| chr1:200118174
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1231-2634G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118174 | ||||||
| chr1:200118191
|
A | T | 1 | a0001c0003t0022g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1231-2617A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118191 | ||||||
| chr1:200118226
|
A | G | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1231-2582A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118226 | ||||||
| chr1:200118295
|
G | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1231-2513G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118295 | ||||||
| chr1:200118406
|
T | A | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1231-2402T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118406 | ||||||
| chr1:200118522
|
A | T | 1 | a0001c0001t0009g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1231-2286A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118522 | ||||||
| chr1:200118564
|
G | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1231-2244G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118564 | ||||||
| chr1:200118694
|
T | C | 1 | a0001c0001t0003g0113 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1231-2114T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118694 | ||||||
| chr1:200118760
|
G | A | 8 | a0001c0001t0002g0280a0001c0001t0006g0024a0001c0003t0016g0153others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-2048G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118760 | ||||||
| chr1:200118798
|
C | T | 116 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(113): Show | 116 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.1231-2010C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118798 | ||||||
| chr1:200118913
|
C | T | 79 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(76): Show | 79 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1231-1895C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118913 | ||||||
| chr1:200118947
|
C | T | 11 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(8): Show | 11 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1231-1861C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200118947 | ||||||
| chr1:200119112
|
T | A | 264 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1231-1696T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119112 | ||||||
| chr1:200119138
|
GA | G | 11 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(8): Show | 11 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1231-1665delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 200119138 | |||||
| chr1:200119158
|
C | T | 15 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(12): Show | 15 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1231-1650C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119158 | ||||||
| chr1:200119159
|
A | G | 15 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(12): Show | 15 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1231-1649A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119159 | ||||||
| chr1:200119431
|
C | A | 127 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1231-1377C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119431 | ||||||
| chr1:200119515
|
T | C | 1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1231-1293T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119515 | ||||||
| chr1:200119524
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1231-1284C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119524 | ||||||
| chr1:200119709
|
C | A | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1231-1099C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119709 | ||||||
| chr1:200119787
|
C | A | 1 | a0003c0006t0006g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1231-1021C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119787 | ||||||
| chr1:200119846
|
C | T | 5 | a0001c0004t0004g0015a0001c0004t0004g0057a0001c0004t0004g0058others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-962C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119846 | ||||||
| chr1:200119872
|
G | A | 1 | a0001c0002t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1231-936G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200119872 | ||||||
| chr1:200120146
|
G | A | 72 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(69): Show | 72 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1231-662G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120146 | ||||||
| chr1:200120198
|
A | G | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1231-610A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120198 | ||||||
| chr1:200120225
|
T | C | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1231-583T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120225 | ||||||
| chr1:200120475
|
A | G | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1231-333A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120475 | ||||||
| chr1:200120540
|
A | C | 119 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(116): Show | 119 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.1231-268A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120540 | ||||||
| chr1:200120572
|
T | C | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1231-236T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120572 | ||||||
| chr1:200120735
|
T | C | 5 | a0001c0002t0007g0093a0001c0003t0009g0224a0001c0004t0007g0049others(2): Show | 5 | HG02622.hp2 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-73T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120735 | ||||||
| chr1:200120740
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1231-68C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120740 | ||||||
| chr1:200120743
|
A | C | 1 | a0001c0007t0015g0278 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1231-65A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120743 | ||||||
| chr1:200120744
|
C | T | 113 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1231-64C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 6/7 | chr1 | 200120744 | ||||||
| chr1:200120992
|
G | A | 85 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(82): Show | 85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1378+37G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200120992 | ||||||
| chr1:200121091
|
C | T | 113 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1378+136C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121091 | ||||||
| chr1:200121147
|
T | C | 7 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+192T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121147 | ||||||
| chr1:200121213
|
A | G | 5 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+258A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121213 | ||||||
| chr1:200121333
|
C | T | 2 | a0001c0004t0004g0044a0001c0005t0004g0083 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1378+378C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121333 | ||||||
| chr1:200121334
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1378+379G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121334 | ||||||
| chr1:200121753
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1378+798G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121753 | ||||||
| chr1:200121857
|
G | A | 262 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(259): Show | 262 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1378+902G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121857 | ||||||
| chr1:200121859
|
G | A | 1 | a0001c0001t0008g0128 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1378+904G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200121859 | ||||||
| chr1:200122060
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1378+1105G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122060 | ||||||
| chr1:200122127
|
C | T | 7 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+1172C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122127 | ||||||
| chr1:200122420
|
G | C | 93 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(90): Show | 93 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1378+1465G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122420 | ||||||
| chr1:200122483
|
A | G | 7 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+1528A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122483 | ||||||
| chr1:200122588
|
A | G | 1 | a0002c0008t0012g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1378+1633A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122588 | ||||||
| chr1:200122712
|
C | T | 1 | a0001c0001t0005g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1378+1757C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122712 | ||||||
| chr1:200122736
|
C | T | 93 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(90): Show | 93 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1378+1781C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122736 | ||||||
| chr1:200122746
|
C | T | 4 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+1791C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122746 | ||||||
| chr1:200122901
|
G | A | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+1946G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200122901 | ||||||
| chr1:200123115
|
G | T | 4 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+2160G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123115 | ||||||
| chr1:200123224
|
A | G | 262 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(259): Show | 262 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1378+2269A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123224 | ||||||
| chr1:200123316
|
A | G | 3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+2361A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123316 | ||||||
| chr1:200123320
|
G | A | 139 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(136): Show | 139 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1378+2365G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123320 | ||||||
| chr1:200123324
|
G | A | 46 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(43): Show | 46 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1378+2369G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123324 | ||||||
| chr1:200123397
|
C | T | 1 | a0001c0002t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1378+2442C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123397 | ||||||
| chr1:200123487
|
G | T | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+2532G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123487 | ||||||
| chr1:200123635
|
C | T | 2 | a0001c0003t0006g0036a0001c0003t0009g0013 | 2 | HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1378+2680C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123635 | ||||||
| chr1:200123636
|
G | A | 1 | a0001c0001t0003g0226 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1378+2681G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123636 | ||||||
| chr1:200123706
|
A | G | 1 | a0001c0002t0001g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1378+2751A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123706 | ||||||
| chr1:200123744
|
T | A | 113 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1378+2789T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123744 | ||||||
| chr1:200123746
|
T | A | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+2791T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123746 | ||||||
| chr1:200123747
|
TTAA | T | 104 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(101): Show | 104 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.1378+2794_1378+279 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200123747 | |||||
| chr1:200123748
|
TAA | T | 4 | a0001c0001t0008g0166a0001c0002t0001g0111a0001c0002t0029g0142others(1): Show | 4 | HG02630.hp1 NA18953.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+2794_1378+279 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123748 | ||||||
| chr1:200123750
|
A | AT | 47 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(44): Show | 47 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1378+2810dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200123750 | |||||
| chr1:200123750
|
A | ATT | 6 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+2809_1378+281 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200123750 | |||||
| chr1:200123750
|
A | T | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+2795A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123750 | ||||||
| chr1:200123806
|
G | GT | 6 | a0001c0001t0001g0071a0001c0001t0002g0069a0001c0001t0002g0161others(3): Show | 6 | HG01261.hp2 HG01993.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+2863dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200123806 | |||||
| chr1:200123823
|
C | T | 146 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(143): Show | 146 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1378+2868C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123823 | ||||||
| chr1:200123887
|
C | T | 11 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(8): Show | 11 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+2932C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123887 | ||||||
| chr1:200123888
|
G | A | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+2933G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123888 | ||||||
| chr1:200123894
|
T | G | 1 | a0001c0001t0003g0235 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1378+2939T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123894 | ||||||
| chr1:200123996
|
G | A | 1 | a0001c0001t0007g0176 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1378+3041G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200123996 | ||||||
| chr1:200124092
|
C | A | 46 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(43): Show | 46 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1378+3137C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200124092 | ||||||
| chr1:200124125
|
A | C | 92 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1378+3170A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200124125 | ||||||
| chr1:200124223
|
C | T | 264 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1378+3268C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200124223 | ||||||
| chr1:200124631
|
T | C | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+3676T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200124631 | ||||||
| chr1:200124759
|
G | T | 145 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1378+3804G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200124759 | ||||||
| chr1:200124836
|
G | A | 46 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(43): Show | 46 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1378+3881G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200124836 | ||||||
| chr1:200124856
|
C | G | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1378+3901C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200124856 | ||||||
| chr1:200125158
|
G | A | 1 | a0001c0003t0002g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1378+4203G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125158 | ||||||
| chr1:200125177
|
A | G | 14 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1378+4222A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125177 | ||||||
| chr1:200125219
|
C | T | 79 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(76): Show | 79 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1378+4264C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125219 | ||||||
| chr1:200125603
|
A | G | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+4648A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125603 | ||||||
| chr1:200125658
|
T | C | 263 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1378+4703T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125658 | ||||||
| chr1:200125659
|
G | T | 3 | a0001c0001t0024g0029a0001c0002t0001g0236a0001c0002t0001g0237 | 3 | HG03490.hp1 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1378+4704G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125659 | ||||||
| chr1:200125677
|
T | A | 263 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1378+4722T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125677 | ||||||
| chr1:200125724
|
C | T | 262 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(259): Show | 262 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1378+4769C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125724 | ||||||
| chr1:200125727
|
T | C | 7 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+4772T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125727 | ||||||
| chr1:200125951
|
T | C | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378+4996T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200125951 | ||||||
| chr1:200126116
|
G | A | 113 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1378+5161G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200126116 | ||||||
| chr1:200126123
|
C | T | 113 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1378+5168C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200126123 | ||||||
| chr1:200126271
|
G | A | 2 | a0001c0003t0006g0061a0001c0003t0017g0042 | 2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1378+5316G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200126271 | ||||||
| chr1:200126683
|
AT | A | 6 | a0001c0001t0003g0205a0001c0001t0005g0009a0001c0001t0005g0019others(3): Show | 6 | HG01516.hp1 HG01516.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+5745delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200126683 | |||||
| chr1:200126683
|
ATT | A | 34 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(31): Show | 34 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1378+5744_1378+574 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200126683 | |||||
| chr1:200126683
|
ATTT | A | 108 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1378+5743_1378+574 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200126683 | |||||
| chr1:200126700
|
T | A | 2 | a0001c0004t0004g0066a0001c0004t0004g0067 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1378+5745T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200126700 | ||||||
| chr1:200126807
|
C | G | 150 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1378+5852C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200126807 | ||||||
| chr1:200126864
|
C | T | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1378+5909C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200126864 | ||||||
| chr1:200127054
|
C | T | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+6099C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127054 | ||||||
| chr1:200127072
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1378+6117G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127072 | ||||||
| chr1:200127099
|
T | TA | 140 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1378+6151dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127099 | |||||
| chr1:200127149
|
G | A | 3 | a0001c0002t0001g0118a0001c0002t0001g0200a0001c0004t0001g0052 | 3 | HG02129.hp1 NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1378+6194G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127149 | ||||||
| chr1:200127424
|
C | T | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1378+6469C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127424 | ||||||
| chr1:200127469
|
G | C | 4 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+6514G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127469 | ||||||
| chr1:200127597
|
A | C | 1 | a0001c0001t0011g0124 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1378+6642A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127597 | ||||||
| chr1:200127608
|
C | T | 112 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(109): Show | 112 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.1378+6653C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127608 | ||||||
| chr1:200127676
|
CA | C | 8 | a0001c0001t0006g0271a0001c0002t0001g0028a0001c0002t0001g0096others(5): Show | 8 | HG00642.hp1 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+6755delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAA | C | 9 | a0001c0001t0006g0040a0001c0002t0001g0018a0001c0002t0001g0033others(6): Show | 9 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+6754_1378+675 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAA | C | 23 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(20): Show | 23 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1378+6753_1378+675 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAAA | C | 18 | a0001c0001t0002g0068a0001c0001t0002g0204a0001c0001t0003g0196others(15): Show | 18 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1378+6752_1378+675 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAAAA | C | 14 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(11): Show | 14 | HG00544.hp2 HG01070.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1378+6751_1378+675 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAAAAA | C | 11 | a0001c0001t0002g0110a0001c0001t0003g0226a0001c0001t0005g0031others(8): Show | 11 | HG00639.hp1 HG01099.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+6750_1378+675 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0003t0009g0064a0001c0003t0009g0224a0001c0003t0014g0272 | 3 | HG01361.hp2 HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1378+6746_1378+675 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0002t0007g0093a0001c0003t0002g0154a0001c0003t0002g0275 | 3 | HG01256.hp2 HG01346.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1378+6745_1378+675 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0005g0025a0001c0007t0006g0062 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1378+6744_1378+675 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127676
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0007t0006g0283 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1378+6743_1378+675 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127676 | |||||
| chr1:200127693
|
A | AATATATA others(5): Show |
1 | a0001c0002t0001g0082 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1378+6739_1378+674 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127693 | |||||
| chr1:200127693
|
A | AATATATA others(9): Show |
1 | a0001c0001t0028g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1378+6739_1378+674 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127693 | |||||
| chr1:200127693
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0005g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1378+6738_1378+673 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127693 | ||||||
| chr1:200127695
|
A | AATATATA others(3): Show |
5 | a0001c0001t0003g0143a0001c0001t0008g0128a0001c0002t0001g0211others(2): Show | 5 | NA18612.hp2 NA18942.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+6741_1378+674 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127695 | |||||
| chr1:200127695
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0137a0001c0001t0007g0176 | 2 | HG02040.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1378+6741_1378+674 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127695 | |||||
| chr1:200127695
|
A | AATATATA others(9): Show |
1 | a0001c0002t0001g0188 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1378+6741_1378+674 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127695 | |||||
| chr1:200127695
|
A | AATATATA others(19): Show |
1 | a0001c0002t0001g0268 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1378+6741_1378+674 others(30): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127695 | |||||
| chr1:200127695
|
A | ATATATAT | 3 | a0001c0001t0003g0030a0001c0001t0011g0126a0001c0002t0001g0125 | 3 | HG02129.hp2 NA18948.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1378+6740_1378+674 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127695 | ||||||
| chr1:200127695
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0070 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1378+6740_1378+674 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127695 | ||||||
| chr1:200127695
|
A | ATATATAT others(6): Show |
4 | a0001c0001t0002g0069a0001c0001t0002g0165a0001c0001t0005g0175others(1): Show | 4 | HG00738.hp2 HG03579.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+6740_1378+674 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127695 | ||||||
| chr1:200127695
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0161a0001c0003t0001g0027a0001c0003t0002g0155 | 3 | HG00558.hp1 HG01993.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1378+6740_1378+674 others(23): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127695 | ||||||
| chr1:200127695
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0148 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1378+6740_1378+674 others(25): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127695 | ||||||
| chr1:200127695
|
A | T | 5 | a0001c0001t0001g0163a0001c0001t0003g0220a0001c0001t0005g0186others(2): Show | 5 | HG03927.hp2 NA18947.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+6740A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127695 | ||||||
| chr1:200127696
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1378+6743_1378+675 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127696 | |||||
| chr1:200127697
|
A | AATATATA others(5): Show |
1 | a0001c0002t0001g0190 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1378+6743_1378+674 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127697 | |||||
| chr1:200127697
|
A | AATATATA others(7): Show |
3 | a0001c0001t0019g0209a0002c0009t0006g0086a0004c0013t0032g0149 | 3 | HG00639.hp2 HG01884.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1378+6743_1378+674 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127697 | |||||
| chr1:200127697
|
A | AATATATA others(9): Show |
1 | a0001c0001t0003g0113 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1378+6743_1378+674 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127697 | |||||
| chr1:200127697
|
A | ATATATAT | 3 | a0001c0001t0001g0216a0001c0001t0001g0261a0001c0002t0001g0215 | 3 | HG00408.hp1 NA18979.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1378+6742_1378+674 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127697 | ||||||
| chr1:200127697
|
A | ATATATAT others(2): Show |
3 | a0001c0004t0001g0053a0001c0004t0001g0054a0003c0006t0006g0003 | 3 | NA18942.hp2 NA19005.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1378+6742_1378+674 others(13): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127697 | ||||||
| chr1:200127697
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0071a0001c0002t0001g0101 | 2 | HG01346.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1378+6742_1378+674 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127697 | ||||||
| chr1:200127697
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1378+6742_1378+674 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127697 | ||||||
| chr1:200127697
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0010g0203a0001c0002t0001g0185 | 2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1378+6742_1378+674 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127697 | ||||||
| chr1:200127697
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0002g0168a0001c0001t0002g0169 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1378+6742_1378+674 others(25): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127697 | ||||||
| chr1:200127697
|
A | T | 30 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0002g0069others(27): Show | 30 | HG00558.hp1 HG00738.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1378+6742A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127697 | ||||||
| chr1:200127698
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0023g0225 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1378+6745_1378+675 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127698 | |||||
| chr1:200127699
|
A | AATATATA others(3): Show |
1 | a0001c0003t0009g0223 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1378+6745_1378+674 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127699 | |||||
| chr1:200127699
|
A | AATATATA others(11): Show |
1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1378+6745_1378+674 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127699 | |||||
| chr1:200127699
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1378+6744_1378+674 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127699 | ||||||
| chr1:200127699
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0002g0133a0001c0003t0002g0152a0001c0003t0002g0274 | 3 | HG00741.hp1 HG01070.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1378+6744_1378+674 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127699 | ||||||
| chr1:200127699
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1378+6744_1378+674 others(23): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127699 | ||||||
| chr1:200127699
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1378+6744_1378+674 others(27): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127699 | ||||||
| chr1:200127699
|
A | T | 63 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1378+6744A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127699 | ||||||
| chr1:200127701
|
A | AATATATA others(9): Show |
1 | a0001c0005t0001g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1378+6747_1378+674 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127701 | |||||
| chr1:200127701
|
A | AATATATA others(11): Show |
1 | a0001c0002t0005g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1378+6747_1378+674 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127701 | |||||
| chr1:200127701
|
A | ATATATAT others(4): Show |
2 | a0001c0003t0009g0013a0001c0004t0004g0276 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1378+6746_1378+674 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127701 | ||||||
| chr1:200127701
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0008g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1378+6746_1378+674 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127701 | ||||||
| chr1:200127701
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1378+6746_1378+674 others(25): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127701 | ||||||
| chr1:200127701
|
A | T | 79 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(76): Show | 79 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1378+6746A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127701 | ||||||
| chr1:200127703
|
A | AATATATA others(9): Show |
1 | a0001c0005t0001g0282 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1378+6749_1378+675 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127703 | |||||
| chr1:200127703
|
A | ATATATAT others(12): Show |
1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1378+6748_1378+674 others(23): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127703 | ||||||
| chr1:200127703
|
A | T | 92 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1378+6748A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127703 | ||||||
| chr1:200127705
|
A | AATATATA others(3): Show |
2 | a0001c0001t0008g0005a0001c0002t0001g0193 | 2 | NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1378+6751_1378+675 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127705 | |||||
| chr1:200127705
|
A | AATATATA others(7): Show |
1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378+6751_1378+675 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127705 | |||||
| chr1:200127705
|
A | AATATATA others(9): Show |
2 | a0001c0001t0006g0024a0001c0004t0004g0008 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1378+6751_1378+675 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127705 | |||||
| chr1:200127705
|
A | ATATATAT others(8): Show |
1 | a0001c0004t0004g0010 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1378+6750_1378+675 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127705 | ||||||
| chr1:200127705
|
A | T | 105 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(102): Show | 105 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1378+6750A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127705 | ||||||
| chr1:200127705
|
AAAAAAT | A | 10 | a0001c0001t0003g0198a0001c0001t0003g0210a0001c0001t0005g0019others(7): Show | 10 | HG01081.hp2 HG01168.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1378+6752_1378+675 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127705 | |||||
| chr1:200127706
|
AAAAAT | A | 21 | a0001c0001t0002g0114a0001c0001t0002g0189a0001c0001t0002g0199others(18): Show | 21 | HG00741.hp2 HG01192.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1378+6753_1378+675 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127706 | |||||
| chr1:200127707
|
A | AATATAT | 8 | a0001c0001t0001g0095a0001c0001t0001g0201a0001c0001t0001g0229others(5): Show | 8 | HG00544.hp1 HG00558.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+6753_1378+675 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127707 | |||||
| chr1:200127707
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0192 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1378+6753_1378+675 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127707 | |||||
| chr1:200127707
|
A | ATATAT | 10 | a0001c0001t0002g0081a0001c0001t0003g0191a0001c0001t0005g0009others(7): Show | 10 | HG02129.hp1 HG02293.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.1378+6752_1378+675 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127707 | ||||||
| chr1:200127707
|
A | ATATATAT others(8): Show |
2 | a0001c0003t0016g0153a0003c0006t0016g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1378+6752_1378+675 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127707 | ||||||
| chr1:200127707
|
A | T | 140 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1378+6752A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127707 | ||||||
| chr1:200127707
|
AAAAT | A | 7 | a0001c0001t0003g0122a0001c0001t0003g0239a0001c0001t0003g0263others(4): Show | 7 | HG00621.hp1 HG00621.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+6754_1378+675 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127707 | |||||
| chr1:200127709
|
A | AAATATAT others(10): Show |
1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1378+6755_1378+675 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127709 | |||||
| chr1:200127709
|
A | AT | 6 | a0001c0001t0010g0116a0001c0001t0010g0140a0001c0001t0027g0245others(3): Show | 6 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+6754_1378+675 others(5): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127709 | ||||||
| chr1:200127709
|
A | T | 189 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1378+6754A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127709 | ||||||
| chr1:200127899
|
CTATT | C | 113 | a0001c0001t0001g0202a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1378+6961_1378+696 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200127899 | |||||
| chr1:200127963
|
G | A | 99 | a0001c0001t0001g0202a0001c0001t0002g0034a0001c0001t0002g0068others(96): Show | 99 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.1378+7008G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200127963 | ||||||
| chr1:200128002
|
A | G | 31 | a0001c0001t0002g0069a0001c0001t0002g0112a0001c0001t0002g0133others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1378+7047A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128002 | ||||||
| chr1:200128085
|
C | T | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+7130C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128085 | ||||||
| chr1:200128099
|
A | G | 15 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(12): Show | 15 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1378+7144A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128099 | ||||||
| chr1:200128269
|
G | A | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1378+7314G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128269 | ||||||
| chr1:200128520
|
G | A | 145 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1378+7565G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128520 | ||||||
| chr1:200128615
|
A | G | 264 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(261): Show | 264 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1378+7660A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128615 | ||||||
| chr1:200128665
|
T | G | 1 | a0001c0001t0003g0226 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1378+7710T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128665 | ||||||
| chr1:200128713
|
G | A | 1 | a0001c0001t0008g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1378+7758G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128713 | ||||||
| chr1:200128767
|
G | A | 4 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+7812G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128767 | ||||||
| chr1:200128826
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1378+7871T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128826 | ||||||
| chr1:200128931
|
C | A | 259 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(256): Show | 259 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.1378+7976C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128931 | ||||||
| chr1:200128933
|
A | G | 3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+7978A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200128933 | ||||||
| chr1:200129174
|
A | G | 3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+8219A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129174 | ||||||
| chr1:200129227
|
A | ACT | 12 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(9): Show | 12 | HG02280.hp2 HG02723.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1378+8285_1378+828 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200129227 | |||||
| chr1:200129259
|
TACATACA others(3): Show |
T | 84 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(81): Show | 84 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.1378+8308_1378+831 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200129259 | |||||
| chr1:200129330
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1378+8375G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129330 | ||||||
| chr1:200129360
|
G | T | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+8405G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129360 | ||||||
| chr1:200129374
|
G | A | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+8419G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129374 | ||||||
| chr1:200129380
|
AT | A | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+8427delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200129380 | |||||
| chr1:200129409
|
G | A | 155 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1378+8454G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129409 | ||||||
| chr1:200129437
|
C | A | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+8482C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129437 | ||||||
| chr1:200129456
|
C | T | 3 | a0001c0001t0002g0251a0001c0002t0001g0127a0001c0002t0005g0141 | 3 | HG01109.hp1 HG03669.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1378+8501C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129456 | ||||||
| chr1:200129491
|
A | C | 7 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+8536A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129491 | ||||||
| chr1:200129507
|
C | T | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+8552C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129507 | ||||||
| chr1:200129663
|
T | C | 4 | a0001c0001t0002g0112a0001c0003t0002g0152a0001c0003t0002g0274others(1): Show | 4 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+8708T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129663 | ||||||
| chr1:200129879
|
T | A | 161 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(158): Show | 161 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1378+8924T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129879 | ||||||
| chr1:200129895
|
C | T | 14 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(11): Show | 14 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1378+8940C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129895 | ||||||
| chr1:200129922
|
T | C | 5 | a0001c0001t0011g0100a0001c0001t0026g0255a0001c0002t0001g0070others(2): Show | 5 | HG02015.hp1 HG02080.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+8967T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200129922 | ||||||
| chr1:200130087
|
T | G | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+9132T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130087 | ||||||
| chr1:200130090
|
T | C | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+9135T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130090 | ||||||
| chr1:200130091
|
T | C | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+9136T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130091 | ||||||
| chr1:200130255
|
G | T | 1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1378+9300G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130255 | ||||||
| chr1:200130278
|
G | GGAA | 5 | a0001c0001t0010g0116a0001c0001t0010g0140a0001c0002t0001g0028others(2): Show | 5 | HG01192.hp2 HG03017.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+9366_1378+936 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130278 | |||||
| chr1:200130278
|
GGAAGAA | G | 13 | a0001c0001t0003g0105a0001c0001t0006g0040a0001c0001t0027g0245others(10): Show | 13 | HG01243.hp1 HG02451.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.1378+9363_1378+936 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130278 | |||||
| chr1:200130278
|
GGAAGAAG others(2): Show |
G | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0015g0041others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+9360_1378+936 others(13): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130278 | |||||
| chr1:200130278
|
GGAAGAAG others(5): Show |
G | 1 | a0001c0001t0005g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1378+9357_1378+936 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130278 | |||||
| chr1:200130278
|
GGAAGAAG others(8): Show |
G | 7 | a0001c0001t0006g0017a0001c0001t0006g0075a0001c0001t0010g0092others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+9354_1378+936 others(19): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130278 | |||||
| chr1:200130278
|
GGAAGAAG others(11): Show |
G | 163 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1378+9351_1378+936 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130278 | |||||
| chr1:200130278
|
GGAAGAAG others(23): Show |
G | 83 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(80): Show | 83 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1378+9339_1378+936 others(34): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130278 | |||||
| chr1:200130291
|
GAAGAAGA others(24): Show |
G | 1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1378+9339_1378+936 others(35): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130291 | |||||
| chr1:200130321
|
G | A | 108 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1378+9366G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130321 | ||||||
| chr1:200130346
|
T | G | 1 | a0001c0003t0002g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1378+9391T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130346 | ||||||
| chr1:200130393
|
C | T | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1378+9438C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130393 | ||||||
| chr1:200130610
|
TA | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0190a0001c0002t0001g0217 | 3 | NA18612.hp2 NA18939.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1378+9657delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200130610 | |||||
| chr1:200130626
|
A | G | 1 | a0001c0002t0001g0208 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1378+9671A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130626 | ||||||
| chr1:200130665
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1378+9710G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130665 | ||||||
| chr1:200130801
|
G | T | 1 | a0001c0001t0005g0108 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1378+9846G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130801 | ||||||
| chr1:200130909
|
G | C | 13 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(10): Show | 13 | HG02559.hp2 HG02723.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+9954G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130909 | ||||||
| chr1:200130919
|
A | C | 1 | a0001c0002t0001g0241 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1378+9964A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130919 | ||||||
| chr1:200130970
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1378+10015T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200130970 | ||||||
| chr1:200131031
|
G | A | 84 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(81): Show | 84 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.1378+10076G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200131031 | ||||||
| chr1:200131156
|
T | C | 1 | a0001c0004t0007g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1378+10201T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200131156 | ||||||
| chr1:200131228
|
GTTGTGGA others(1): Show |
G | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+10276_1378+10 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200131228 | |||||
| chr1:200131252
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1378+10297G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200131252 | ||||||
| chr1:200131516
|
A | G | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+10561A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200131516 | ||||||
| chr1:200131593
|
C | T | 8 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+10638C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200131593 | ||||||
| chr1:200131871
|
A | G | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+10916A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200131871 | ||||||
| chr1:200132008
|
C | T | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+11053C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132008 | ||||||
| chr1:200132095
|
C | T | 149 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(146): Show | 149 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1378+11140C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132095 | ||||||
| chr1:200132209
|
C | T | 1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1378+11254C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132209 | ||||||
| chr1:200132305
|
C | T | 103 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1378+11350C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132305 | ||||||
| chr1:200132353
|
G | A | 259 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(256): Show | 259 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.1378+11398G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132353 | ||||||
| chr1:200132644
|
T | C | 1 | a0001c0003t0002g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1378+11689T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132644 | ||||||
| chr1:200132771
|
T | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+11816T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132771 | ||||||
| chr1:200132792
|
A | G | 250 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(247): Show | 250 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1378+11837A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132792 | ||||||
| chr1:200132800
|
AC | A | 157 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(154): Show | 157 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1378+11847delC | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200132800 | |||||
| chr1:200132829
|
T | C | 1 | a0003c0006t0002g0004 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1378+11874T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200132829 | ||||||
| chr1:200133028
|
T | C | 1 | a0003c0006t0006g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1378+12073T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133028 | ||||||
| chr1:200133050
|
C | T | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378+12095C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133050 | ||||||
| chr1:200133421
|
C | G | 103 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(100): Show | 103 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1378+12466C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133421 | ||||||
| chr1:200133505
|
C | CTA | 65 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(62): Show | 65 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1378+12571_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
C | CTATA | 5 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0249others(2): Show | 5 | HG00621.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+12569_1378+12 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
C | CTATATA | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0015g0041others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+12567_1378+12 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
C | CTATATAT others(5): Show |
2 | a0001c0002t0004g0091a0001c0004t0004g0066 | 2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1378+12561_1378+12 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
C | CTATATAT others(7): Show |
3 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0004t0004g0067 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1378+12559_1378+12 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
C | CTATATAT others(13): Show |
2 | a0001c0001t0008g0166a0001c0002t0001g0230 | 2 | NA19065.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1378+12553_1378+12 others(26): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
C | CTATATAT others(15): Show |
2 | a0001c0002t0029g0142a0005c0012t0001g0194 | 2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1378+12551_1378+12 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
C | CTATATAT others(17): Show |
1 | a0001c0001t0003g0238 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1378+12572_1378+12 others(30): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133505
|
CTA | C | 7 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0004g0285others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378+12571_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133505 | |||||
| chr1:200133518
|
TATATATA others(9): Show |
T | 12 | a0001c0001t0002g0280a0001c0001t0006g0017a0001c0001t0006g0024others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1378+12573_1378+12 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133518 | |||||
| chr1:200133520
|
TATATATA others(7): Show |
T | 3 | a0001c0001t0005g0186a0001c0002t0001g0073a0001c0003t0002g0170 | 3 | HG00642.hp2 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1378+12573_1378+12 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133520 | |||||
| chr1:200133522
|
TATATACA others(5): Show |
T | 1 | a0003c0006t0006g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1378+12573_1378+12 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133522 | |||||
| chr1:200133524
|
T | C | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+12569T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133524 | ||||||
| chr1:200133526
|
T | C | 6 | a0001c0001t0006g0270a0001c0003t0002g0279a0001c0003t0013g0048others(3): Show | 6 | HG02148.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+12571T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133526 | ||||||
| chr1:200133526
|
T | TAC | 4 | a0001c0001t0008g0128a0001c0005t0004g0021a0001c0005t0004g0022others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+12579_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133526 | |||||
| chr1:200133526
|
T | TATATATA others(17): Show |
1 | a0001c0002t0001g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1378+12572_1378+12 others(30): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133526 | |||||
| chr1:200133528
|
C | T | 92 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(89): Show | 92 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1378+12573C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133528 | ||||||
| chr1:200133530
|
C | T | 6 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0002t0007g0093others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+12575C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133530 | ||||||
| chr1:200133532
|
C | T | 1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1378+12577C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133532 | ||||||
| chr1:200133534
|
C | T | 1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1378+12579C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133534 | ||||||
| chr1:200133535
|
AT | A | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+12581delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133535 | ||||||
| chr1:200133536
|
T | C | 16 | a0001c0001t0006g0059a0001c0001t0006g0075a0001c0001t0009g0181others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1378+12581T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133536 | ||||||
| chr1:200133536
|
TATATATA others(7): Show |
T | 87 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(84): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1378+12589_1378+12 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133536 | |||||
| chr1:200133537
|
A | AC | 5 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+12582_1378+12 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133537 | ||||||
| chr1:200133537
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1378+12590_1378+12 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133537 | |||||
| chr1:200133537
|
A | C | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+12582A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133537 | ||||||
| chr1:200133542
|
TATATACA others(1): Show |
T | 8 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+12593_1378+12 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133542 | |||||
| chr1:200133546
|
T | C | 6 | a0001c0001t0005g0186a0001c0002t0001g0073a0001c0002t0021g0046others(3): Show | 6 | HG00642.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+12591T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133546 | ||||||
| chr1:200133550
|
CATATATA others(9): Show |
C | 3 | a0001c0003t0013g0048a0001c0003t0013g0051a0001c0003t0013g0269 | 3 | HG02970.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1378+12607_1378+12 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133550 | |||||
| chr1:200133556
|
T | C | 87 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(84): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1378+12601T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133556 | ||||||
| chr1:200133560
|
CACATAT | C | 8 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+12607_1378+12 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133560 | |||||
| chr1:200133562
|
C | CAT | 16 | a0001c0001t0002g0280a0001c0001t0005g0186a0001c0001t0006g0017others(13): Show | 16 | HG00642.hp2 HG01074.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1378+12617_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133562 | |||||
| chr1:200133562
|
C | T | 87 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(84): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1378+12607C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133562 | ||||||
| chr1:200133562
|
CAT | C | 14 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0196others(11): Show | 14 | HG01243.hp2 HG02647.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1378+12617_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133562 | |||||
| chr1:200133572
|
T | C | 2 | a0001c0001t0003g0030a0001c0002t0021g0046 | 2 | HG03098.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1378+12617T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133572 | ||||||
| chr1:200133574
|
C | T | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+12619C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133574 | ||||||
| chr1:200133576
|
CAT | C | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+12629_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133576 | |||||
| chr1:200133578
|
T | C | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+12623T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133578 | ||||||
| chr1:200133586
|
C | T | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+12631C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133586 | ||||||
| chr1:200133588
|
C | A | 1 | a0001c0001t0014g0264 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1378+12633C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133588 | ||||||
| chr1:200133590
|
T | C | 6 | a0001c0001t0005g0025a0001c0003t0009g0224a0001c0004t0007g0049others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+12635T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133590 | ||||||
| chr1:200133600
|
T | C | 19 | a0001c0001t0005g0009a0001c0001t0006g0075a0001c0001t0006g0270others(16): Show | 19 | HG02145.hp1 HG02148.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1378+12645T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133600 | ||||||
| chr1:200133600
|
T | TAC | 3 | a0001c0001t0010g0092a0001c0004t0007g0016a0001c0005t0006g0060 | 3 | HG02145.hp2 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1378+12649_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133600 | |||||
| chr1:200133604
|
C | T | 13 | a0001c0001t0005g0009a0001c0001t0009g0181a0001c0001t0012g0182others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1378+12649C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133604 | ||||||
| chr1:200133608
|
T | C | 3 | a0001c0003t0013g0048a0001c0003t0013g0051a0001c0003t0013g0269 | 3 | HG02970.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1378+12653T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133608 | ||||||
| chr1:200133610
|
T | C | 13 | a0001c0001t0005g0009a0001c0001t0009g0181a0001c0001t0012g0182others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1378+12655T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133610 | ||||||
| chr1:200133610
|
T | TAC | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+12670_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133610 | |||||
| chr1:200133610
|
TAC | T | 126 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1378+12670_1378+12 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133610 | |||||
| chr1:200133610
|
TACAC | T | 4 | a0001c0001t0008g0103a0001c0001t0008g0138a0001c0003t0006g0036others(1): Show | 4 | HG02970.hp1 HG03225.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+12668_1378+12 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200133610 | |||||
| chr1:200133646
|
C | T | 1 | a0001c0002t0001g0268 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1378+12691C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133646 | ||||||
| chr1:200133752
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1378+12797A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133752 | ||||||
| chr1:200133915
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1378+12960G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200133915 | ||||||
| chr1:200134256
|
A | C | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+13301A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134256 | ||||||
| chr1:200134341
|
C | T | 4 | a0001c0004t0004g0037a0001c0005t0004g0021a0001c0005t0004g0022others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+13386C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134341 | ||||||
| chr1:200134436
|
T | C | 250 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(247): Show | 250 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1378+13481T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134436 | ||||||
| chr1:200134439
|
A | G | 1 | a0001c0003t0002g0170 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1378+13484A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134439 | ||||||
| chr1:200134510
|
G | T | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+13555G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134510 | ||||||
| chr1:200134549
|
A | G | 3 | a0001c0001t0002g0081a0001c0001t0002g0212a0001c0001t0002g0213 | 3 | HG01928.hp1 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1378+13594A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134549 | ||||||
| chr1:200134593
|
A | C | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378+13638A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134593 | ||||||
| chr1:200134604
|
T | C | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+13649T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134604 | ||||||
| chr1:200134761
|
T | C | 1 | a0001c0001t0005g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1378+13806T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200134761 | ||||||
| chr1:200135026
|
C | T | 2 | a0001c0004t0004g0044a0001c0005t0004g0083 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1378+14071C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135026 | ||||||
| chr1:200135071
|
A | G | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378+14116A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135071 | ||||||
| chr1:200135183
|
C | T | 1 | a0001c0004t0001g0047 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1378+14228C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135183 | ||||||
| chr1:200135212
|
C | T | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+14257C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135212 | ||||||
| chr1:200135242
|
C | T | 53 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0114others(50): Show | 53 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1378+14287C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135242 | ||||||
| chr1:200135252
|
G | A | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+14297G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135252 | ||||||
| chr1:200135310
|
C | T | 1 | a0001c0003t0002g0157 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1378+14355C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135310 | ||||||
| chr1:200135345
|
A | AC | 9 | a0001c0001t0002g0068a0001c0001t0002g0117a0001c0001t0002g0197others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+14394dupC | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200135345 | |||||
| chr1:200135359
|
A | G | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+14404A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135359 | ||||||
| chr1:200135414
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1378+14459G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135414 | ||||||
| chr1:200135475
|
T | G | 1 | a0001c0001t0011g0126 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1378+14520T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135475 | ||||||
| chr1:200135521
|
C | CA | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(13): Show | 16 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1378+14579dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200135521 | |||||
| chr1:200135531
|
AAAAG | A | 13 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(10): Show | 13 | HG02559.hp2 HG02723.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+14579_1378+14 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200135531 | |||||
| chr1:200135532
|
A | AAAG | 10 | a0001c0001t0005g0025a0001c0002t0001g0119a0001c0002t0001g0120others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1378+14598_1378+14 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200135532 | |||||
| chr1:200135627
|
A | T | 1 | a0001c0001t0003g0238 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1378+14672A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135627 | ||||||
| chr1:200135634
|
C | T | 13 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(10): Show | 13 | HG02559.hp2 HG02723.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+14679C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135634 | ||||||
| chr1:200135844
|
A | C | 71 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(68): Show | 71 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.1378+14889A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135844 | ||||||
| chr1:200135860
|
C | T | 1 | a0001c0001t0008g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1378+14905C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135860 | ||||||
| chr1:200135864
|
A | T | 149 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(146): Show | 149 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1378+14909A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135864 | ||||||
| chr1:200135867
|
T | C | 85 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(82): Show | 85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1378+14912T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135867 | ||||||
| chr1:200135942
|
C | T | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+14987C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135942 | ||||||
| chr1:200135968
|
T | G | 1 | a0001c0001t0005g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1378+15013T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200135968 | ||||||
| chr1:200136125
|
G | A | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+15170G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136125 | ||||||
| chr1:200136295
|
C | T | 16 | a0001c0001t0002g0110a0001c0001t0005g0031a0001c0001t0005g0032others(13): Show | 16 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1378+15340C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136295 | ||||||
| chr1:200136432
|
C | T | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378+15477C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136432 | ||||||
| chr1:200136584
|
A | G | 2 | a0001c0003t0016g0153a0003c0006t0016g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1378+15629A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136584 | ||||||
| chr1:200136595
|
G | A | 1 | a0001c0002t0004g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1378+15640G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136595 | ||||||
| chr1:200136600
|
G | A | 2 | a0001c0001t0008g0138a0001c0002t0001g0184 | 2 | NA18948.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1378+15645G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136600 | ||||||
| chr1:200136618
|
T | A | 246 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(243): Show | 246 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.1378+15663T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136618 | ||||||
| chr1:200136774
|
G | A | 1 | a0001c0002t0001g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1378+15819G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136774 | ||||||
| chr1:200136863
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0263a0001c0003t0009g0064 | 3 | HG02630.hp1 NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1378+15908C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136863 | ||||||
| chr1:200136911
|
C | T | 3 | a0001c0001t0002g0068a0001c0002t0001g0079a0001c0002t0001g0080 | 3 | HG00735.hp1 HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1378+15956C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200136911 | ||||||
| chr1:200137004
|
C | A | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1378+16049C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137004 | ||||||
| chr1:200137142
|
A | ATTTT | 82 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(79): Show | 82 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.1378+16188_1378+16 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200137142 | |||||
| chr1:200137143
|
T | TTTTA | 3 | a0001c0001t0006g0271a0001c0002t0004g0091a0001c0003t0002g0167 | 3 | HG01070.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1378+16208_1378+16 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200137143 | |||||
| chr1:200137191
|
C | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378+16236C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137191 | ||||||
| chr1:200137276
|
G | A | 2 | a0001c0001t0003g0191a0001c0001t0005g0175 | 2 | HG03579.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1378+16321G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137276 | ||||||
| chr1:200137317
|
A | AT | 41 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0221others(38): Show | 41 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1378+16382dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200137317 | |||||
| chr1:200137317
|
A | ATT | 17 | a0001c0001t0001g0201a0001c0001t0002g0011a0001c0001t0002g0012others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1378+16381_1378+16 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200137317 | |||||
| chr1:200137317
|
AT | A | 7 | a0001c0001t0002g0133a0001c0001t0003g0239a0001c0001t0005g0106others(4): Show | 7 | HG01070.hp2 HG01256.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378+16382delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200137317 | |||||
| chr1:200137317
|
ATT | A | 11 | a0001c0001t0002g0280a0001c0001t0006g0017a0001c0001t0006g0024others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+16381_1378+16 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200137317 | |||||
| chr1:200137337
|
T | A | 2 | a0001c0003t0002g0279a0001c0005t0007g0281 | 2 | HG02148.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1378+16382T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137337 | ||||||
| chr1:200137543
|
T | C | 1 | a0001c0002t0001g0268 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1378+16588T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137543 | ||||||
| chr1:200137596
|
A | G | 6 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+16641A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137596 | ||||||
| chr1:200137793
|
A | T | 4 | a0001c0001t0002g0069a0001c0001t0002g0161a0001c0001t0003g0148others(1): Show | 4 | HG01261.hp2 HG01993.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+16838A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137793 | ||||||
| chr1:200137983
|
G | A | 1 | a0001c0002t0004g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1378+17028G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200137983 | ||||||
| chr1:200138297
|
G | A | 31 | a0001c0001t0002g0069a0001c0001t0002g0112a0001c0001t0002g0133others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1378+17342G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200138297 | ||||||
| chr1:200138422
|
A | G | 123 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1378+17467A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200138422 | ||||||
| chr1:200138450
|
T | C | 122 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(119): Show | 122 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1378+17495T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200138450 | ||||||
| chr1:200138482
|
C | A | 99 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(96): Show | 99 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1378+17527C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200138482 | ||||||
| chr1:200138599
|
T | C | 1 | a0001c0002t0004g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1378+17644T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200138599 | ||||||
| chr1:200138966
|
T | C | 34 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(31): Show | 34 | HG00408.hp1 HG01346.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378+18011T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200138966 | ||||||
| chr1:200139035
|
T | A | 5 | a0001c0002t0001g0188a0001c0002t0001g0190a0001c0002t0001g0217others(2): Show | 5 | NA18612.hp2 NA18939.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+18080T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139035 | ||||||
| chr1:200139243
|
A | G | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1378+18288A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139243 | ||||||
| chr1:200139299
|
T | C | 85 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(82): Show | 85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1378+18344T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139299 | ||||||
| chr1:200139418
|
T | C | 257 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(254): Show | 257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1378+18463T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139418 | ||||||
| chr1:200139423
|
T | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+18468T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139423 | ||||||
| chr1:200139466
|
T | C | 1 | a0001c0002t0001g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1378+18511T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139466 | ||||||
| chr1:200139487
|
T | G | 1 | a0001c0007t0015g0278 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1378+18532T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139487 | ||||||
| chr1:200139593
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1378+18638T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139593 | ||||||
| chr1:200139678
|
C | CTTTTG | 5 | a0001c0001t0002g0189a0001c0001t0002g0199a0001c0001t0003g0198others(2): Show | 5 | HG00741.hp2 HG01168.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+18742_1378+18 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200139678 | |||||
| chr1:200139678
|
CTTTTG | C | 15 | a0001c0001t0002g0110a0001c0001t0005g0031a0001c0001t0005g0032others(12): Show | 15 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1378+18742_1378+18 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200139678 | |||||
| chr1:200139790
|
C | T | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+18835C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139790 | ||||||
| chr1:200139935
|
T | C | 1 | a0001c0002t0004g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1378+18980T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139935 | ||||||
| chr1:200139963
|
G | A | 1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1378+19008G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200139963 | ||||||
| chr1:200140040
|
G | A | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+19085G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140040 | ||||||
| chr1:200140061
|
T | C | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+19106T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140061 | ||||||
| chr1:200140075
|
A | T | 114 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1378+19120A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140075 | ||||||
| chr1:200140150
|
GTATT | G | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+19201_1378+19 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200140150 | |||||
| chr1:200140209
|
C | T | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+19254C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140209 | ||||||
| chr1:200140216
|
T | A | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+19261T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140216 | ||||||
| chr1:200140247
|
C | T | 1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378+19292C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140247 | ||||||
| chr1:200140355
|
G | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378+19400G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140355 | ||||||
| chr1:200140757
|
G | A | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+19802G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140757 | ||||||
| chr1:200140768
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1378+19813C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140768 | ||||||
| chr1:200140788
|
T | A | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378+19833T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140788 | ||||||
| chr1:200140845
|
A | G | 1 | a0001c0002t0001g0082 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1378+19890A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140845 | ||||||
| chr1:200140989
|
C | G | 158 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(155): Show | 158 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1378+20034C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140989 | ||||||
| chr1:200140990
|
C | A | 158 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(155): Show | 158 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1378+20035C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200140990 | ||||||
| chr1:200141031
|
T | TAAACAAA others(1): Show |
14 | a0001c0001t0003g0147a0001c0001t0003g0239a0001c0001t0003g0263others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1378+20092_1378+20 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200141031 | |||||
| chr1:200141031
|
TAAAC | T | 100 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1378+20096_1378+20 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200141031 | |||||
| chr1:200141055
|
A | C | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+20100A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141055 | ||||||
| chr1:200141150
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1378+20195G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141150 | ||||||
| chr1:200141174
|
T | C | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+20219T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141174 | ||||||
| chr1:200141269
|
A | G | 4 | a0001c0003t0009g0224a0001c0004t0007g0049a0001c0004t0007g0050others(1): Show | 4 | HG02622.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+20314A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141269 | ||||||
| chr1:200141271
|
C | T | 5 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0003t0005g0055others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+20316C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141271 | ||||||
| chr1:200141364
|
G | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+20409G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141364 | ||||||
| chr1:200141460
|
G | T | 1 | a0001c0003t0031g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1378+20505G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141460 | ||||||
| chr1:200141597
|
A | G | 1 | a0001c0001t0005g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1378+20642A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141597 | ||||||
| chr1:200141934
|
C | T | 36 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(33): Show | 36 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1378+20979C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200141934 | ||||||
| chr1:200142063
|
A | G | 1 | a0001c0005t0006g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1378+21108A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142063 | ||||||
| chr1:200142187
|
T | C | 1 | a0001c0003t0006g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1378+21232T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142187 | ||||||
| chr1:200142188
|
C | CT | 8 | a0001c0001t0003g0105a0001c0001t0015g0041a0001c0001t0025g0074others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+21262dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200142188 | |||||
| chr1:200142188
|
CT | C | 9 | a0001c0001t0005g0025a0001c0001t0005g0146a0001c0001t0006g0059others(6): Show | 9 | HG02027.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378+21262delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200142188 | |||||
| chr1:200142188
|
CTT | C | 37 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(34): Show | 37 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1378+21261_1378+21 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200142188 | |||||
| chr1:200142188
|
CTTT | C | 41 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0161others(38): Show | 41 | HG00738.hp1 HG01074.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.1378+21260_1378+21 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200142188 | |||||
| chr1:200142188
|
CTTTT | C | 82 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1378+21259_1378+21 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200142188 | |||||
| chr1:200142188
|
CTTTTT | C | 77 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(74): Show | 77 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1378+21258_1378+21 others(11): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200142188 | |||||
| chr1:200142188
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1378+21252_1378+21 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200142188 | |||||
| chr1:200142360
|
C | T | 2 | a0001c0001t0003g0210a0001c0001t0003g0263 | 2 | NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1378+21405C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142360 | ||||||
| chr1:200142417
|
C | T | 1 | a0001c0001t0007g0176 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1378+21462C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142417 | ||||||
| chr1:200142494
|
C | A | 83 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(80): Show | 83 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1378+21539C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142494 | ||||||
| chr1:200142494
|
C | G | 2 | a0001c0003t0006g0061a0001c0003t0017g0042 | 2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1378+21539C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142494 | ||||||
| chr1:200142512
|
T | TA | 3 | a0001c0002t0001g0265a0001c0002t0021g0046a0001c0004t0004g0285 | 3 | HG03098.hp2 HG03453.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1378+21557_1378+21 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142512 | ||||||
| chr1:200142513
|
T | A | 170 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1378+21558T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142513 | ||||||
| chr1:200142514
|
A | T | 9 | a0001c0001t0005g0025a0001c0001t0006g0075a0001c0001t0010g0092others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+21559A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142514 | ||||||
| chr1:200142569
|
C | T | 4 | a0001c0001t0006g0059a0001c0002t0007g0026a0001c0002t0021g0046others(1): Show | 4 | HG02647.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+21614C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142569 | ||||||
| chr1:200142718
|
T | C | 261 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(258): Show | 261 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1378+21763T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142718 | ||||||
| chr1:200142801
|
A | G | 53 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0114others(50): Show | 53 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1378+21846A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142801 | ||||||
| chr1:200142808
|
T | G | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+21853T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200142808 | ||||||
| chr1:200143045
|
A | ATG | 6 | a0001c0002t0021g0046a0001c0003t0002g0043a0001c0003t0006g0014others(3): Show | 6 | HG02055.hp2 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+22105_1378+22 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200143045 | |||||
| chr1:200143045
|
ATGTG | A | 34 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(31): Show | 34 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1378+22103_1378+22 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200143045 | |||||
| chr1:200143054
|
T | A | 2 | a0001c0001t0006g0059a0001c0002t0007g0026 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1378+22099T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143054 | ||||||
| chr1:200143126
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1378+22171G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143126 | ||||||
| chr1:200143424
|
G | T | 4 | a0001c0001t0002g0189a0001c0001t0002g0199a0001c0001t0003g0198others(1): Show | 4 | HG00741.hp2 HG01168.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+22469G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143424 | ||||||
| chr1:200143425
|
T | G | 1 | a0001c0001t0005g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1378+22470T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143425 | ||||||
| chr1:200143435
|
C | T | 232 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(229): Show | 232 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1378+22480C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143435 | ||||||
| chr1:200143510
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1378+22555C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143510 | ||||||
| chr1:200143638
|
A | AT | 22 | a0001c0001t0001g0163a0001c0001t0002g0150a0001c0001t0012g0182others(19): Show | 22 | HG01243.hp1 HG01361.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.1378+22705dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200143638 | |||||
| chr1:200143638
|
AT | A | 137 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(134): Show | 137 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.1378+22705delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200143638 | |||||
| chr1:200143712
|
G | A | 99 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(96): Show | 99 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1378+22757G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143712 | ||||||
| chr1:200143786
|
C | T | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+22831C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143786 | ||||||
| chr1:200143788
|
C | T | 72 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(69): Show | 72 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1378+22833C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143788 | ||||||
| chr1:200143790
|
C | T | 10 | a0001c0001t0002g0243a0001c0001t0002g0252a0001c0001t0003g0171others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1378+22835C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143790 | ||||||
| chr1:200143875
|
A | G | 257 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(254): Show | 257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1378+22920A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143875 | ||||||
| chr1:200143949
|
G | A | 149 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1378+22994G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200143949 | ||||||
| chr1:200144116
|
A | T | 247 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1378+23161A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144116 | ||||||
| chr1:200144214
|
TTC | T | 20 | a0001c0001t0001g0202a0001c0001t0002g0110a0001c0001t0002g0197others(17): Show | 20 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1378+23278_1378+23 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144214 | |||||
| chr1:200144214
|
TTCTC | T | 34 | a0001c0001t0002g0068a0001c0001t0002g0114a0001c0001t0002g0117others(31): Show | 34 | HG00544.hp2 HG00639.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1378+23276_1378+23 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144214 | |||||
| chr1:200144214
|
TTCTCTC | T | 13 | a0001c0001t0003g0196a0001c0001t0003g0205a0001c0001t0003g0247others(10): Show | 13 | HG01070.hp1 HG01081.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+23274_1378+23 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144214 | |||||
| chr1:200144214
|
TTCTCTCT others(5): Show |
T | 2 | a0001c0001t0006g0271a0001c0003t0002g0286 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1378+23268_1378+23 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144214 | |||||
| chr1:200144221
|
TCTCTCTC others(15): Show |
T | 11 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0238others(8): Show | 11 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+23268_1378+23 others(28): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144221 | |||||
| chr1:200144223
|
T | A | 3 | a0001c0001t0002g0110a0001c0002t0001g0111a0001c0002t0001g0136 | 3 | HG02015.hp2 HG02257.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1378+23268T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144223 | ||||||
| chr1:200144225
|
T | A | 22 | a0001c0001t0001g0202a0001c0001t0002g0110a0001c0001t0002g0197others(19): Show | 22 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+23270T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144225 | ||||||
| chr1:200144227
|
T | A | 57 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(54): Show | 57 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1378+23272T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144227 | ||||||
| chr1:200144227
|
TCTCTCTC others(3): Show |
T | 1 | a0001c0007t0015g0278 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1378+23274_1378+23 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144227 | |||||
| chr1:200144229
|
T | A | 70 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(67): Show | 70 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1378+23274T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144229 | ||||||
| chr1:200144229
|
T | TCA | 9 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(6): Show | 9 | HG02148.hp2 HG02717.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378+23275_1378+23 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144229 | |||||
| chr1:200144229
|
TCTCTCA | T | 4 | a0001c0001t0007g0176a0001c0002t0001g0096a0001c0003t0002g0170others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+23276_1378+23 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144229 | |||||
| chr1:200144229
|
TCTCTCAC others(1): Show |
T | 92 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1378+23276_1378+23 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144229 | |||||
| chr1:200144229
|
TCTCTCAC others(3): Show |
T | 16 | a0001c0001t0001g0229a0001c0001t0002g0280a0001c0001t0005g0146others(13): Show | 16 | HG00544.hp1 HG02027.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1378+23276_1378+23 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144229 | |||||
| chr1:200144229
|
TCTCTCAC others(5): Show |
T | 28 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(25): Show | 28 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1378+23276_1378+23 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144229 | |||||
| chr1:200144229
|
TCTCTCAC others(7): Show |
T | 1 | a0001c0001t0002g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1378+23276_1378+23 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144229 | |||||
| chr1:200144231
|
T | A | 85 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(82): Show | 85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1378+23276T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144231 | ||||||
| chr1:200144231
|
TCTCACAC others(1): Show |
T | 5 | a0001c0001t0003g0148a0001c0003t0006g0061a0001c0003t0009g0223others(2): Show | 5 | HG01074.hp2 HG01261.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+23278_1378+23 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144231 | |||||
| chr1:200144231
|
TCTCACAC others(5): Show |
T | 1 | a0001c0004t0001g0052 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1378+23278_1378+23 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144231 | |||||
| chr1:200144231
|
TCTCACAC others(9): Show |
T | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+23278_1378+23 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144231 | |||||
| chr1:200144233
|
T | A | 85 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(82): Show | 85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1378+23278T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144233 | ||||||
| chr1:200144233
|
T | TCACA | 6 | a0001c0001t0003g0105a0001c0003t0002g0056a0001c0004t0004g0015others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+23313_1378+23 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCACACAC others(1): Show |
3 | a0001c0001t0010g0116a0001c0002t0001g0139a0003c0010t0001g0002 | 3 | HG02965.hp2 HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1378+23309_1378+23 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0010g0140 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1378+23307_1378+23 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCTCA | 3 | a0001c0001t0006g0040a0002c0008t0012g0084a0002c0008t0012g0085 | 3 | HG02922.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1378+23279_1378+23 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCTCACA | 11 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0075others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+23279_1378+23 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCTCACAC others(5): Show |
1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1378+23279_1378+23 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCTCACAC others(7): Show |
1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1378+23279_1378+23 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCTCTCAC others(3): Show |
3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+23279_1378+23 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144233
|
T | TCTCTCAC others(5): Show |
1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1378+23279_1378+23 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200144233 | |||||
| chr1:200144272
|
G | C | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1378+23317G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144272 | ||||||
| chr1:200144384
|
A | G | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+23429A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144384 | ||||||
| chr1:200144385
|
A | G | 85 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(82): Show | 85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1378+23430A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144385 | ||||||
| chr1:200144424
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1378+23469A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144424 | ||||||
| chr1:200144535
|
T | C | 247 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1378+23580T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144535 | ||||||
| chr1:200144708
|
G | A | 1 | a0001c0002t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1378+23753G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144708 | ||||||
| chr1:200144744
|
G | A | 1 | a0001c0002t0001g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1378+23789G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144744 | ||||||
| chr1:200144746
|
T | C | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+23791T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144746 | ||||||
| chr1:200144773
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1378+23818C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144773 | ||||||
| chr1:200144835
|
C | T | 13 | a0001c0001t0002g0280a0001c0001t0006g0017a0001c0001t0006g0024others(10): Show | 13 | HG01074.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+23880C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200144835 | ||||||
| chr1:200145141
|
C | G | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1378+24186C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145141 | ||||||
| chr1:200145250
|
C | T | 114 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1378+24295C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145250 | ||||||
| chr1:200145293
|
G | A | 1 | a0001c0001t0008g0128 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1378+24338G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145293 | ||||||
| chr1:200145334
|
A | G | 2 | a0001c0002t0001g0130a0001c0002t0001g0164 | 2 | NA18981.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1378+24379A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145334 | ||||||
| chr1:200145360
|
A | AT | 11 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(8): Show | 11 | HG02145.hp1 HG02717.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+24415dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145360 | |||||
| chr1:200145399
|
G | A | 3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+24444G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145399 | ||||||
| chr1:200145467
|
TTTGTGTG others(4): Show |
T | 1 | a0001c0001t0001g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1378+24514_1378+24 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145467 | |||||
| chr1:200145467
|
TTTGTGTG others(8): Show |
T | 1 | a0001c0001t0003g0147 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1378+24514_1378+24 others(21): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145467 | |||||
| chr1:200145468
|
T | TG | 3 | a0001c0001t0002g0151a0001c0001t0002g0165a0001c0002t0001g0268 | 3 | HG00738.hp2 HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1378+24513_1378+24 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145468 | ||||||
| chr1:200145468
|
T | TGTG | 3 | a0001c0001t0003g0030a0001c0001t0011g0100a0001c0001t0028g0099 | 3 | HG02015.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1378+24513_1378+24 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145468 | ||||||
| chr1:200145468
|
T | TTG | 27 | a0001c0001t0001g0216a0001c0001t0002g0104a0001c0001t0002g0173others(24): Show | 27 | HG00280.hp2 HG00642.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1378+24559_1378+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
T | TTGTG | 17 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1378+24557_1378+24 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
T | TTGTGTG | 6 | a0001c0001t0002g0262a0001c0001t0003g0235a0001c0002t0001g0070others(3): Show | 6 | HG00738.hp1 NA18612.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+24555_1378+24 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
T | TTGTGTGT others(1): Show |
4 | a0001c0001t0003g0143a0001c0001t0003g0234a0001c0001t0005g0186others(1): Show | 4 | NA18977.hp1 NA18977.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+24553_1378+24 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTG | T | 21 | a0001c0001t0002g0112a0001c0001t0002g0133a0001c0001t0002g0254others(18): Show | 21 | HG00280.hp1 HG01070.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1378+24559_1378+24 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTG | T | 20 | a0001c0001t0003g0113a0001c0001t0005g0106a0001c0001t0005g0107others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1378+24557_1378+24 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTGTG | T | 15 | a0001c0001t0002g0110a0001c0001t0002g0204a0001c0001t0002g0227others(12): Show | 15 | HG00639.hp1 HG01081.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1378+24555_1378+24 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0006g0017a0001c0001t0006g0024a0001c0003t0006g0061others(6): Show | 9 | HG01074.hp2 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+24553_1378+24 others(14): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTGTGT others(3): Show |
T | 8 | a0001c0001t0002g0012a0001c0002t0001g0132a0001c0002t0007g0026others(5): Show | 8 | HG01515.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+24551_1378+24 others(16): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTGTGT others(5): Show |
T | 10 | a0001c0001t0002g0011a0001c0001t0006g0040a0001c0001t0015g0041others(7): Show | 10 | HG01255.hp2 HG02559.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1378+24549_1378+24 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTGTGT others(7): Show |
T | 18 | a0001c0001t0001g0202a0001c0001t0002g0069a0001c0001t0002g0161others(15): Show | 18 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.1378+24547_1378+24 others(20): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTGTGT others(9): Show |
T | 50 | a0001c0001t0002g0068a0001c0001t0002g0114a0001c0001t0002g0117others(47): Show | 50 | HG00621.hp1 HG00621.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1378+24545_1378+24 others(22): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145468
|
TTGTGTGT others(21): Show |
T | 34 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(31): Show | 34 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1378+24533_1378+24 others(34): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200145468 | |||||
| chr1:200145514
|
G | A | 73 | a0001c0001t0001g0202a0001c0001t0002g0068a0001c0001t0002g0110others(70): Show | 73 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1378+24559G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145514 | ||||||
| chr1:200145522
|
G | A | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+24567G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145522 | ||||||
| chr1:200145575
|
T | A | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1378+24620T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145575 | ||||||
| chr1:200145595
|
G | A | 2 | a0001c0004t0001g0053a0001c0004t0001g0054 | 2 | NA18942.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1378+24640G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145595 | ||||||
| chr1:200145689
|
A | G | 11 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(8): Show | 11 | HG02145.hp1 HG02717.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378+24734A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145689 | ||||||
| chr1:200145740
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1378+24785C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145740 | ||||||
| chr1:200145760
|
A | T | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1378+24805A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145760 | ||||||
| chr1:200145866
|
C | T | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+24911C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145866 | ||||||
| chr1:200145905
|
G | A | 248 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1378+24950G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200145905 | ||||||
| chr1:200146099
|
GACT | G | 5 | a0001c0003t0009g0224a0001c0004t0007g0049a0001c0004t0007g0050others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+25149_1378+25 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200146099 | |||||
| chr1:200146227
|
TAAAG | T | 6 | a0001c0001t0006g0075a0001c0001t0010g0092a0001c0002t0007g0026others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+25276_1378+25 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200146227 | |||||
| chr1:200146243
|
C | T | 236 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(233): Show | 236 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1378+25288C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200146243 | ||||||
| chr1:200146279
|
A | G | 222 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1378+25324A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200146279 | ||||||
| chr1:200146283
|
G | A | 13 | a0001c0001t0009g0181a0001c0001t0012g0182a0001c0001t0018g0179others(10): Show | 13 | HG02145.hp1 HG02148.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378+25328G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200146283 | ||||||
| chr1:200146450
|
T | C | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+25495T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200146450 | ||||||
| chr1:200146789
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0015g0041 | 3 | HG01891.hp2 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1378+25834C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200146789 | ||||||
| chr1:200146815
|
G | A | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1378+25860G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200146815 | ||||||
| chr1:200146961
|
C | CTTT | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+26016_1378+26 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200146961 | |||||
| chr1:200146961
|
CT | C | 115 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(112): Show | 115 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1378+26018delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200146961 | |||||
| chr1:200147272
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1378+26317A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200147272 | ||||||
| chr1:200147273
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1378+26318G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200147273 | ||||||
| chr1:200147278
|
G | A | 1 | a0001c0002t0001g0240 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1378+26323G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200147278 | ||||||
| chr1:200147364
|
C | A | 2 | a0001c0002t0001g0200a0001c0004t0001g0052 | 2 | HG02129.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1378+26409C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200147364 | ||||||
| chr1:200147761
|
C | T | 3 | a0001c0005t0004g0021a0001c0005t0004g0022a0001c0005t0004g0023 | 3 | HG02965.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1379-26202C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200147761 | ||||||
| chr1:200147765
|
AATGCCGG others(5): Show |
A | 248 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1379-26185_1379-26 others(18): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200147765 | |||||
| chr1:200147826
|
C | G | 109 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(106): Show | 109 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1379-26137C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200147826 | ||||||
| chr1:200147894
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1379-26069C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200147894 | ||||||
| chr1:200148179
|
C | G | 34 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(31): Show | 34 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1379-25784C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148179 | ||||||
| chr1:200148182
|
C | T | 272 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(269): Show | 272 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.1379-25781C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148182 | ||||||
| chr1:200148325
|
A | T | 34 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(31): Show | 34 | HG00639.hp1 HG00738.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1379-25638A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148325 | ||||||
| chr1:200148461
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1379-25502C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148461 | ||||||
| chr1:200148502
|
A | G | 1 | a0001c0001t0008g0138 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1379-25461A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148502 | ||||||
| chr1:200148610
|
T | G | 1 | a0001c0001t0001g0071 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1379-25353T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148610 | ||||||
| chr1:200148798
|
T | C | 42 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(39): Show | 42 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1379-25165T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148798 | ||||||
| chr1:200148901
|
C | A | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1379-25062C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200148901 | ||||||
| chr1:200148906
|
C | CT | 57 | a0001c0001t0001g0261a0001c0001t0002g0034a0001c0001t0002g0069others(54): Show | 57 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1379-25037dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200148906 | |||||
| chr1:200148906
|
CTT | C | 39 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(36): Show | 39 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1379-25038_1379-25 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200148906 | |||||
| chr1:200149003
|
C | A | 1 | a0001c0001t0005g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1379-24960C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149003 | ||||||
| chr1:200149027
|
C | T | 6 | a0001c0001t0006g0017a0001c0004t0004g0015a0001c0004t0004g0057others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-24936C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149027 | ||||||
| chr1:200149112
|
T | C | 237 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(234): Show | 237 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1379-24851T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149112 | ||||||
| chr1:200149204
|
A | G | 43 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(40): Show | 43 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1379-24759A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149204 | ||||||
| chr1:200149216
|
G | C | 1 | a0001c0002t0001g0190 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1379-24747G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149216 | ||||||
| chr1:200149311
|
C | T | 27 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(24): Show | 27 | HG00639.hp1 HG00738.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1379-24652C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149311 | ||||||
| chr1:200149595
|
G | T | 1 | a0001c0002t0001g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1379-24368G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149595 | ||||||
| chr1:200149682
|
C | T | 4 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0004t0004g0066others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-24281C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149682 | ||||||
| chr1:200149834
|
C | T | 1 | a0001c0001t0005g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1379-24129C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149834 | ||||||
| chr1:200149839
|
T | C | 1 | a0001c0002t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1379-24124T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149839 | ||||||
| chr1:200149873
|
TC | T | 4 | a0001c0003t0006g0061a0001c0003t0009g0223a0001c0003t0009g0257others(1): Show | 4 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-24089delC | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149873 | ||||||
| chr1:200149920
|
G | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1379-24043G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149920 | ||||||
| chr1:200149951
|
A | T | 44 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(41): Show | 44 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1379-24012A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149951 | ||||||
| chr1:200149986
|
A | G | 1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1379-23977A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200149986 | ||||||
| chr1:200150041
|
A | AATGG | 46 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(43): Show | 46 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1379-23897_1379-23 others(10): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200150041 | |||||
| chr1:200150066
|
A | T | 157 | a0001c0001t0001g0071a0001c0001t0001g0137a0001c0001t0001g0163others(154): Show | 157 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1379-23897A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200150066 | ||||||
| chr1:200150449
|
T | C | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1379-23514T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200150449 | ||||||
| chr1:200150541
|
C | T | 4 | a0001c0003t0006g0061a0001c0003t0009g0223a0001c0003t0009g0257others(1): Show | 4 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-23422C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200150541 | ||||||
| chr1:200150766
|
T | G | 1 | a0001c0003t0002g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1379-23197T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200150766 | ||||||
| chr1:200150905
|
C | T | 24 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1379-23058C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200150905 | ||||||
| chr1:200150943
|
A | G | 1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1379-23020A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200150943 | ||||||
| chr1:200151163
|
GA | G | 5 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0002t0004g0091others(2): Show | 5 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-22793delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200151163 | |||||
| chr1:200151186
|
T | C | 2 | a0001c0003t0016g0153a0003c0006t0016g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1379-22777T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151186 | ||||||
| chr1:200151215
|
G | A | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1379-22748G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151215 | ||||||
| chr1:200151236
|
A | G | 5 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0002t0004g0091others(2): Show | 5 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-22727A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151236 | ||||||
| chr1:200151345
|
G | A | 45 | a0001c0001t0002g0110a0001c0001t0002g0280a0001c0001t0003g0105others(42): Show | 45 | HG01081.hp2 HG01109.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.1379-22618G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151345 | ||||||
| chr1:200151564
|
T | C | 4 | a0001c0001t0002g0069a0001c0001t0002g0161a0001c0001t0003g0148others(1): Show | 4 | HG01261.hp2 HG01993.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-22399T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151564 | ||||||
| chr1:200151587
|
A | C | 1 | a0001c0004t0001g0054 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1379-22376A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151587 | ||||||
| chr1:200151777
|
A | G | 5 | a0001c0003t0006g0061a0001c0003t0009g0223a0001c0003t0009g0257others(2): Show | 5 | HG01074.hp2 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1379-22186A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151777 | ||||||
| chr1:200151827
|
G | A | 1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1379-22136G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151827 | ||||||
| chr1:200151863
|
G | A | 3 | a0001c0001t0002g0104a0001c0001t0002g0262a0001c0003t0014g0272 | 3 | HG00738.hp1 HG01361.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1379-22100G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151863 | ||||||
| chr1:200151899
|
A | G | 43 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(40): Show | 43 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1379-22064A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200151899 | ||||||
| chr1:200152016
|
G | C | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-21947G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152016 | ||||||
| chr1:200152212
|
A | G | 4 | a0001c0001t0002g0069a0001c0001t0002g0161a0001c0001t0003g0148others(1): Show | 4 | HG01261.hp2 HG01993.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-21751A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152212 | ||||||
| chr1:200152362
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1379-21601G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152362 | ||||||
| chr1:200152401
|
C | A | 5 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0002t0004g0091others(2): Show | 5 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-21562C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152401 | ||||||
| chr1:200152551
|
G | C | 4 | a0001c0001t0003g0105a0001c0001t0027g0245a0001c0003t0002g0098others(1): Show | 4 | HG02698.hp2 HG03927.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-21412G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152551 | ||||||
| chr1:200152578
|
A | G | 48 | a0001c0001t0002g0110a0001c0001t0002g0280a0001c0001t0005g0025others(45): Show | 48 | HG01081.hp2 HG01109.hp2 HG01256.hp1 others(45): Show |
intron_variant | MODIFIER | c.1379-21385A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152578 | ||||||
| chr1:200152624
|
A | G | 1 | a0001c0005t0004g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1379-21339A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152624 | ||||||
| chr1:200152647
|
G | A | 1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1379-21316G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152647 | ||||||
| chr1:200152786
|
A | G | 1 | a0001c0007t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1379-21177A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200152786 | ||||||
| chr1:200153078
|
C | T | 141 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(138): Show | 141 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1379-20885C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200153078 | ||||||
| chr1:200153270
|
G | A | 5 | a0001c0001t0005g0094a0001c0002t0004g0178a0001c0003t0006g0035others(2): Show | 5 | HG02630.hp2 HG03139.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-20693G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200153270 | ||||||
| chr1:200153783
|
G | GGA | 4 | a0001c0004t0004g0037a0001c0005t0004g0021a0001c0005t0004g0022others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-20178_1379-20 others(8): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200153783 | |||||
| chr1:200153832
|
G | A | 1 | a0001c0001t0025g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1379-20131G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200153832 | ||||||
| chr1:200154302
|
T | C | 145 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(142): Show | 145 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.1379-19661T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200154302 | ||||||
| chr1:200154604
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1379-19359A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200154604 | ||||||
| chr1:200154608
|
A | G | 4 | a0001c0001t0002g0112a0001c0003t0002g0152a0001c0003t0002g0274others(1): Show | 4 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-19355A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200154608 | ||||||
| chr1:200154726
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0004t0004g0066others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-19237G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200154726 | ||||||
| chr1:200154823
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1379-19140C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200154823 | ||||||
| chr1:200154850
|
T | C | 144 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(141): Show | 144 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.1379-19113T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200154850 | ||||||
| chr1:200155010
|
C | T | 1 | a0001c0002t0001g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1379-18953C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155010 | ||||||
| chr1:200155011
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1379-18952G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155011 | ||||||
| chr1:200155126
|
C | A | 3 | a0001c0004t0007g0049a0001c0004t0007g0050a0002c0009t0007g0089 | 3 | HG02622.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1379-18837C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155126 | ||||||
| chr1:200155171
|
T | C | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1379-18792T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155171 | ||||||
| chr1:200155231
|
AT | A | 48 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(45): Show | 48 | HG00738.hp1 HG01074.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.1379-18731delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155231 | ||||||
| chr1:200155244
|
T | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1379-18719T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155244 | ||||||
| chr1:200155256
|
C | G | 1 | a0001c0003t0001g0027 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1379-18707C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155256 | ||||||
| chr1:200155351
|
T | G | 3 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224 | 3 | HG02109.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1379-18612T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155351 | ||||||
| chr1:200155680
|
AT | A | 15 | a0001c0001t0003g0105a0001c0001t0003g0234a0001c0001t0003g0238others(12): Show | 15 | HG01168.hp1 HG01243.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1379-18269delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200155680 | |||||
| chr1:200155681
|
T | A | 24 | a0001c0001t0002g0110a0001c0001t0005g0097a0001c0001t0005g0106others(21): Show | 24 | HG01081.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1379-18282T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155681 | ||||||
| chr1:200155727
|
G | A | 15 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(12): Show | 15 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1379-18236G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155727 | ||||||
| chr1:200155728
|
C | A | 15 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(12): Show | 15 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1379-18235C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155728 | ||||||
| chr1:200155736
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1379-18227C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155736 | ||||||
| chr1:200155837
|
C | A | 48 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(45): Show | 48 | HG00738.hp1 HG01074.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.1379-18126C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155837 | ||||||
| chr1:200155870
|
C | T | 46 | a0001c0001t0002g0110a0001c0001t0002g0280a0001c0001t0005g0094others(43): Show | 46 | HG01081.hp2 HG01109.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.1379-18093C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155870 | ||||||
| chr1:200155871
|
G | A | 3 | a0001c0003t0006g0061a0001c0003t0017g0042a0001c0007t0015g0278 | 3 | HG01074.hp2 HG02895.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-18092G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200155871 | ||||||
| chr1:200155890
|
TCTCGAAC others(14169): Show |
T | 2 | a0001c0002t0001g0236a0001c0002t0001g0237 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1379-18069_1379-38 others(5): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200155890 | |||||
| chr1:200156225
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1379-17738A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156225 | ||||||
| chr1:200156261
|
G | A | 1 | a0001c0004t0004g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1379-17702G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156261 | ||||||
| chr1:200156361
|
C | G | 1 | a0001c0001t0006g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1379-17602C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156361 | ||||||
| chr1:200156385
|
C | G | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1379-17578C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156385 | ||||||
| chr1:200156420
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1379-17543C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156420 | ||||||
| chr1:200156546
|
C | A | 11 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1379-17417C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156546 | ||||||
| chr1:200156574
|
T | TTTTTAGT others(35): Show |
1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1379-17386_1379-17 others(48): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200156574 | |||||
| chr1:200156584
|
A | G | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1379-17379A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156584 | ||||||
| chr1:200156648
|
C | T | 1 | a0001c0002t0001g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1379-17315C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156648 | ||||||
| chr1:200156657
|
A | C | 1 | a0001c0002t0001g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1379-17306A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156657 | ||||||
| chr1:200156770
|
T | C | 1 | a0001c0001t0008g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1379-17193T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156770 | ||||||
| chr1:200156844
|
A | T | 1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1379-17119A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156844 | ||||||
| chr1:200156855
|
T | C | 2 | a0001c0001t0002g0251a0001c0002t0005g0141 | 2 | HG01109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1379-17108T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156855 | ||||||
| chr1:200156864
|
T | G | 1 | a0001c0003t0005g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1379-17099T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156864 | ||||||
| chr1:200156974
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1379-16989G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156974 | ||||||
| chr1:200156997
|
A | T | 1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1379-16966A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156997 | ||||||
| chr1:200156999
|
A | G | 43 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(40): Show | 43 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1379-16964A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200156999 | ||||||
| chr1:200157374
|
GGTCACCA others(4): Show |
G | 1 | a0001c0001t0006g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-16585_1379-16 others(17): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200157374 | |||||
| chr1:200157509
|
A | C | 3 | a0001c0001t0005g0025a0001c0002t0007g0093a0001c0003t0009g0224 | 3 | HG02109.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1379-16454A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200157509 | ||||||
| chr1:200157514
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1379-16449T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200157514 | ||||||
| chr1:200157644
|
A | G | 39 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(36): Show | 39 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1379-16319A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200157644 | ||||||
| chr1:200158225
|
G | A | 3 | a0001c0003t0002g0043a0001c0004t0004g0088a0001c0005t0004g0277 | 3 | HG02886.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1379-15738G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158225 | ||||||
| chr1:200158414
|
G | A | 142 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(139): Show | 142 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1379-15549G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158414 | ||||||
| chr1:200158578
|
A | G | 1 | a0001c0003t0002g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1379-15385A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158578 | ||||||
| chr1:200158648
|
T | C | 53 | a0001c0001t0002g0110a0001c0001t0002g0204a0001c0001t0002g0227others(50): Show | 53 | HG01081.hp2 HG01109.hp2 HG01256.hp1 others(50): Show |
intron_variant | MODIFIER | c.1379-15315T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158648 | ||||||
| chr1:200158696
|
T | C | 18 | a0001c0001t0002g0280a0001c0001t0005g0094a0001c0001t0006g0017others(15): Show | 18 | HG01109.hp2 HG02451.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1379-15267T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158696 | ||||||
| chr1:200158827
|
C | G | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1379-15136C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158827 | ||||||
| chr1:200158843
|
C | A | 1 | a0001c0001t0002g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1379-15120C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158843 | ||||||
| chr1:200158900
|
T | G | 16 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(13): Show | 16 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1379-15063T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158900 | ||||||
| chr1:200158901
|
C | CT | 142 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(139): Show | 142 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1379-15049dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200158901 | |||||
| chr1:200158920
|
T | C | 1 | a0001c0002t0007g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1379-15043T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200158920 | ||||||
| chr1:200159007
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1379-14956G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159007 | ||||||
| chr1:200159048
|
AT | A | 27 | a0001c0001t0002g0110a0001c0001t0005g0097a0001c0001t0005g0106others(24): Show | 27 | HG01081.hp2 HG01256.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1379-14904delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200159048 | |||||
| chr1:200159526
|
C | A | 1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1379-14437C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159526 | ||||||
| chr1:200159548
|
A | G | 53 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(50): Show | 53 | HG00738.hp1 HG01074.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.1379-14415A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159548 | ||||||
| chr1:200159603
|
G | A | 1 | a0003c0010t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1379-14360G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159603 | ||||||
| chr1:200159640
|
T | TTTA | 90 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0202others(87): Show | 90 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.1379-14299_1379-14 others(9): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200159640 | |||||
| chr1:200159640
|
T | TTTATTA | 3 | a0001c0002t0001g0188a0001c0002t0001g0190a0001c0002t0001g0217 | 3 | NA18612.hp2 NA18939.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1379-14302_1379-14 others(12): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200159640 | |||||
| chr1:200159640
|
TTTATTAT others(2): Show |
T | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0040others(13): Show | 16 | HG01074.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1379-14305_1379-14 others(15): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200159640 | |||||
| chr1:200159679
|
T | C | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1379-14284T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159679 | ||||||
| chr1:200159714
|
C | T | 3 | a0001c0001t0006g0024a0001c0004t0004g0008a0001c0004t0004g0010 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1379-14249C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159714 | ||||||
| chr1:200159794
|
G | C | 1 | a0001c0002t0001g0134 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1379-14169G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159794 | ||||||
| chr1:200159797
|
G | A | 1 | a0001c0002t0001g0230 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1379-14166G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159797 | ||||||
| chr1:200159799
|
G | A | 31 | a0001c0001t0002g0110a0001c0001t0005g0097a0001c0001t0005g0106others(28): Show | 31 | HG01081.hp2 HG01109.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1379-14164G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159799 | ||||||
| chr1:200159813
|
C | T | 33 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(30): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1379-14150C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200159813 | ||||||
| chr1:200159819
|
A | AT | 16 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(13): Show | 16 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1379-14139dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200159819 | |||||
| chr1:200160066
|
G | C | 1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1379-13897G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160066 | ||||||
| chr1:200160095
|
G | C | 2 | a0001c0002t0021g0046a0001c0004t0004g0285 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1379-13868G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160095 | ||||||
| chr1:200160130
|
G | A | 146 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(143): Show | 146 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.1379-13833G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160130 | ||||||
| chr1:200160157
|
C | T | 6 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0002t0001g0073others(3): Show | 6 | HG02723.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1379-13806C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160157 | ||||||
| chr1:200160174
|
A | G | 76 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0034others(73): Show | 76 | HG00738.hp1 HG01081.hp2 HG01109.hp2 others(73): Show |
intron_variant | MODIFIER | c.1379-13789A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160174 | ||||||
| chr1:200160493
|
C | T | 1 | a0001c0001t0003g0234 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1379-13470C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160493 | ||||||
| chr1:200160651
|
G | A | 1 | a0001c0003t0009g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1379-13312G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160651 | ||||||
| chr1:200160695
|
C | T | 1 | a0001c0001t0005g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1379-13268C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160695 | ||||||
| chr1:200160712
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1379-13251G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160712 | ||||||
| chr1:200160723
|
G | A | 1 | a0001c0002t0004g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1379-13240G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160723 | ||||||
| chr1:200160839
|
T | A | 1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1379-13124T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160839 | ||||||
| chr1:200160899
|
T | C | 12 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(9): Show | 12 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1379-13064T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160899 | ||||||
| chr1:200160941
|
A | C | 19 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0003g0105others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1379-13022A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160941 | ||||||
| chr1:200160974
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379-12989C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200160974 | ||||||
| chr1:200160982
|
CA | C | 116 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(113): Show | 116 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.1379-12968delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200160982 | |||||
| chr1:200161229
|
G | A | 1 | a0005c0012t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1379-12734G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200161229 | ||||||
| chr1:200161527
|
A | T | 2 | a0001c0003t0006g0061a0001c0003t0017g0042 | 2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-12436A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200161527 | ||||||
| chr1:200161603
|
G | T | 280 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(277): Show | 280 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1379-12360G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200161603 | ||||||
| chr1:200161898
|
T | C | 1 | a0001c0002t0001g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1379-12065T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200161898 | ||||||
| chr1:200162079
|
C | T | 1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1379-11884C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162079 | ||||||
| chr1:200162107
|
C | T | 34 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(31): Show | 34 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1379-11856C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162107 | ||||||
| chr1:200162158
|
G | A | 3 | a0001c0001t0006g0270a0001c0003t0006g0061a0001c0003t0017g0042 | 3 | HG01074.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-11805G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162158 | ||||||
| chr1:200162180
|
G | T | 127 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(124): Show | 127 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.1379-11783G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162180 | ||||||
| chr1:200162305
|
C | T | 9 | a0001c0001t0003g0234a0001c0001t0003g0238a0001c0002t0001g0129others(6): Show | 9 | HG03130.hp1 NA18612.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-11658C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162305 | ||||||
| chr1:200162387
|
G | GC | 46 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(43): Show | 46 | HG00738.hp1 HG01243.hp1 HG01358.hp1 others(43): Show |
intron_variant | MODIFIER | c.1379-11574dupC | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200162387 | |||||
| chr1:200162523
|
A | T | 142 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(139): Show | 142 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.1379-11440A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162523 | ||||||
| chr1:200162910
|
G | A | 50 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(47): Show | 50 | HG00738.hp1 HG01243.hp1 HG01358.hp1 others(47): Show |
intron_variant | MODIFIER | c.1379-11053G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162910 | ||||||
| chr1:200162926
|
C | T | 1 | a0001c0001t0002g0280 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1379-11037C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162926 | ||||||
| chr1:200162956
|
C | T | 124 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(121): Show | 124 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1379-11007C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200162956 | ||||||
| chr1:200163018
|
G | A | 2 | a0001c0001t0006g0059a0001c0002t0021g0046 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1379-10945G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163018 | ||||||
| chr1:200163147
|
A | G | 1 | a0001c0001t0003g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1379-10816A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163147 | ||||||
| chr1:200163259
|
C | T | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0017others(6): Show | 9 | HG01891.hp2 HG02559.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1379-10704C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163259 | ||||||
| chr1:200163265
|
C | CA | 36 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0114others(33): Show | 36 | HG01168.hp1 HG01891.hp2 HG02148.hp1 others(33): Show |
intron_variant | MODIFIER | c.1379-10683dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200163265 | |||||
| chr1:200163265
|
CA | C | 36 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(33): Show | 36 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.1379-10683delA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200163265 | |||||
| chr1:200163275
|
A | T | 1 | a0001c0001t0008g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1379-10688A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163275 | ||||||
| chr1:200163278
|
A | G | 2 | a0001c0001t0006g0270a0001c0003t0017g0042 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-10685A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163278 | ||||||
| chr1:200163486
|
G | GT | 6 | a0001c0001t0002g0112a0001c0001t0002g0161a0001c0001t0024g0029others(3): Show | 6 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-10464dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200163486 | |||||
| chr1:200163736
|
T | A | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1379-10227T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163736 | ||||||
| chr1:200163773
|
C | T | 5 | a0001c0004t0007g0049a0001c0004t0007g0050a0001c0007t0006g0062others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1379-10190C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163773 | ||||||
| chr1:200163882
|
A | G | 10 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0002t0001g0073others(7): Show | 10 | HG02258.hp1 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1379-10081A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163882 | ||||||
| chr1:200163933
|
A | G | 58 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(55): Show | 58 | HG00738.hp1 HG01243.hp1 HG01358.hp1 others(55): Show |
intron_variant | MODIFIER | c.1379-10030A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200163933 | ||||||
| chr1:200164127
|
C | G | 2 | a0001c0002t0001g0183a0001c0002t0001g0244 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1379-9836C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164127 | ||||||
| chr1:200164138
|
C | T | 1 | a0001c0003t0002g0157 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1379-9825C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164138 | ||||||
| chr1:200164463
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1379-9500A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164463 | ||||||
| chr1:200164549
|
C | CT | 34 | a0001c0001t0002g0069a0001c0001t0002g0161a0001c0001t0003g0171others(31): Show | 34 | HG00408.hp1 HG01081.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1379-9398dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200164549 | |||||
| chr1:200164549
|
C | CTT | 19 | a0001c0001t0003g0105a0001c0001t0003g0234a0001c0001t0003g0238others(16): Show | 19 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1379-9399_1379-939 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200164549 | |||||
| chr1:200164549
|
C | CTTT | 6 | a0001c0004t0007g0049a0001c0004t0007g0050a0001c0007t0006g0062others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-9400_1379-939 others(7): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200164549 | |||||
| chr1:200164582
|
C | G | 5 | a0001c0004t0007g0049a0001c0004t0007g0050a0001c0007t0006g0062others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1379-9381C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164582 | ||||||
| chr1:200164633
|
C | T | 1 | a0001c0001t0006g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1379-9330C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164633 | ||||||
| chr1:200164639
|
G | A | 45 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(42): Show | 45 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.1379-9324G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164639 | ||||||
| chr1:200164850
|
C | G | 52 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(49): Show | 52 | HG00738.hp1 HG01243.hp1 HG01358.hp1 others(49): Show |
intron_variant | MODIFIER | c.1379-9113C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164850 | ||||||
| chr1:200164867
|
G | GT | 37 | a0001c0001t0001g0071a0001c0001t0001g0202a0001c0001t0001g0261others(34): Show | 37 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1379-9069dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200164867 | |||||
| chr1:200164867
|
GT | G | 81 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(78): Show | 81 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1379-9069delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200164867 | |||||
| chr1:200164867
|
GTT | G | 10 | a0001c0001t0002g0204a0001c0001t0002g0213a0001c0001t0002g0227others(7): Show | 10 | HG01943.hp2 HG02258.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1379-9070_1379-906 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200164867 | |||||
| chr1:200164906
|
T | C | 138 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(135): Show | 138 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.1379-9057T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200164906 | ||||||
| chr1:200165238
|
C | A | 1 | a0003c0006t0006g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1379-8725C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200165238 | ||||||
| chr1:200165337
|
T | A | 2 | a0001c0001t0006g0270a0001c0003t0017g0042 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-8626T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200165337 | ||||||
| chr1:200165364
|
G | A | 45 | a0001c0001t0002g0034a0001c0001t0002g0104a0001c0001t0002g0150others(42): Show | 45 | HG00738.hp1 HG01358.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.1379-8599G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200165364 | ||||||
| chr1:200165636
|
A | G | 7 | a0001c0001t0003g0105a0001c0001t0027g0245a0001c0003t0002g0056others(4): Show | 7 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-8327A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200165636 | ||||||
| chr1:200165650
|
C | T | 2 | a0001c0007t0006g0062a0002c0008t0002g0087 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1379-8313C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200165650 | ||||||
| chr1:200165681
|
G | A | 2 | a0001c0001t0011g0124a0001c0001t0023g0225 | 2 | HG00408.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1379-8282G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200165681 | ||||||
| chr1:200165929
|
C | T | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1379-8034C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200165929 | ||||||
| chr1:200166047
|
A | T | 131 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(128): Show | 131 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.1379-7916A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166047 | ||||||
| chr1:200166197
|
C | T | 2 | a0001c0001t0006g0075a0001c0003t0006g0036 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1379-7766C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166197 | ||||||
| chr1:200166210
|
T | C | 32 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(29): Show | 32 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1379-7753T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166210 | ||||||
| chr1:200166369
|
G | A | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0017others(6): Show | 9 | HG01891.hp2 HG02559.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1379-7594G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166369 | ||||||
| chr1:200166436
|
C | T | 62 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(59): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1379-7527C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166436 | ||||||
| chr1:200166442
|
G | C | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1379-7521G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166442 | ||||||
| chr1:200166537
|
C | G | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1379-7426C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166537 | ||||||
| chr1:200166619
|
A | G | 75 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(72): Show | 75 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1379-7344A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166619 | ||||||
| chr1:200166657
|
G | A | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1379-7306G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166657 | ||||||
| chr1:200166665
|
A | T | 1 | a0001c0001t0006g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1379-7298A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166665 | ||||||
| chr1:200166672
|
C | G | 30 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(27): Show | 30 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1379-7291C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166672 | ||||||
| chr1:200166680
|
G | A | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1379-7283G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166680 | ||||||
| chr1:200166749
|
T | C | 1 | a0001c0001t0005g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1379-7214T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166749 | ||||||
| chr1:200166940
|
G | A | 126 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(123): Show | 126 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1379-7023G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200166940 | ||||||
| chr1:200167020
|
C | A | 1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1379-6943C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167020 | ||||||
| chr1:200167030
|
T | A | 1 | a0001c0002t0021g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1379-6933T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167030 | ||||||
| chr1:200167033
|
G | A | 1 | a0001c0001t0006g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1379-6930G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167033 | ||||||
| chr1:200167037
|
A | T | 1 | a0001c0001t0025g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1379-6926A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167037 | ||||||
| chr1:200167135
|
C | G | 1 | a0001c0007t0015g0278 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1379-6828C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167135 | ||||||
| chr1:200167255
|
C | A | 2 | a0001c0001t0005g0019a0001c0001t0005g0020 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1379-6708C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167255 | ||||||
| chr1:200167296
|
A | G | 134 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(131): Show | 134 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1379-6667A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167296 | ||||||
| chr1:200167429
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379-6534G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167429 | ||||||
| chr1:200167451
|
G | A | 3 | a0001c0001t0003g0105a0001c0001t0027g0245a0001c0003t0002g0098 | 3 | HG02698.hp2 HG03927.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1379-6512G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167451 | ||||||
| chr1:200167454
|
G | A | 130 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(127): Show | 130 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.1379-6509G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167454 | ||||||
| chr1:200167632
|
G | C | 21 | a0001c0001t0002g0110a0001c0001t0003g0171a0001c0001t0005g0097others(18): Show | 21 | HG01081.hp2 HG01109.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1379-6331G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167632 | ||||||
| chr1:200167663
|
T | C | 2 | a0001c0003t0009g0064a0001c0004t0004g0285 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1379-6300T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167663 | ||||||
| chr1:200167673
|
T | G | 11 | a0001c0001t0002g0280a0001c0001t0005g0094a0001c0001t0006g0024others(8): Show | 11 | HG02451.hp2 HG02630.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1379-6290T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167673 | ||||||
| chr1:200167821
|
G | A | 1 | a0001c0005t0004g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1379-6142G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167821 | ||||||
| chr1:200167976
|
G | T | 1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1379-5987G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200167976 | ||||||
| chr1:200168182
|
C | G | 1 | a0001c0002t0001g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1379-5781C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168182 | ||||||
| chr1:200168210
|
C | CT | 32 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0104others(29): Show | 32 | HG00738.hp1 HG01070.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1379-5736dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200168210 | |||||
| chr1:200168210
|
C | CTT | 22 | a0001c0001t0002g0110a0001c0001t0002g0204a0001c0001t0002g0227others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-5737_1379-573 others(6): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200168210 | |||||
| chr1:200168210
|
C | T | 69 | a0001c0001t0001g0095a0001c0001t0001g0192a0001c0001t0001g0201others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1379-5753C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168210 | ||||||
| chr1:200168221
|
T | A | 1 | a0001c0003t0017g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1379-5742T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168221 | ||||||
| chr1:200168397
|
G | T | 1 | a0001c0002t0001g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1379-5566G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168397 | ||||||
| chr1:200168459
|
C | T | 9 | a0001c0001t0005g0025a0001c0001t0005g0094a0001c0001t0006g0075others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-5504C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168459 | ||||||
| chr1:200168510
|
T | C | 1 | a0002c0008t0002g0087 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1379-5453T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168510 | ||||||
| chr1:200168521
|
A | C | 121 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0163others(118): Show | 121 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1379-5442A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168521 | ||||||
| chr1:200168678
|
C | A | 9 | a0001c0002t0004g0065a0001c0002t0004g0180a0001c0002t0007g0026others(6): Show | 9 | HG02257.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1379-5285C>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168678 | ||||||
| chr1:200168855
|
T | C | 24 | a0001c0001t0005g0009a0001c0001t0005g0019a0001c0001t0005g0020others(21): Show | 24 | HG00408.hp2 HG00639.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1379-5108T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168855 | ||||||
| chr1:200168921
|
T | C | 1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1379-5042T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200168921 | ||||||
| chr1:200169150
|
A | G | 1 | a0001c0001t0014g0264 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1379-4813A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169150 | ||||||
| chr1:200169174
|
T | A | 7 | a0001c0001t0006g0024a0001c0001t0006g0059a0001c0001t0006g0075others(4): Show | 7 | HG01074.hp2 HG01891.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-4789T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169174 | ||||||
| chr1:200169186
|
G | A | 2 | a0001c0001t0003g0171a0001c0001t0003g0247 | 2 | HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1379-4777G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169186 | ||||||
| chr1:200169195
|
C | T | 1 | a0001c0002t0001g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1379-4768C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169195 | ||||||
| chr1:200169216
|
T | TA | 6 | a0001c0001t0006g0024a0001c0001t0006g0059a0001c0001t0006g0075others(3): Show | 6 | HG01074.hp2 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-4738dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200169216 | |||||
| chr1:200169341
|
T | A | 1 | a0001c0002t0007g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1379-4622T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169341 | ||||||
| chr1:200169435
|
A | T | 6 | a0001c0001t0006g0024a0001c0001t0006g0059a0001c0001t0006g0075others(3): Show | 6 | HG01074.hp2 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-4528A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169435 | ||||||
| chr1:200169484
|
A | T | 36 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0104others(33): Show | 36 | HG00738.hp1 HG01070.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1379-4479A>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169484 | ||||||
| chr1:200169646
|
T | C | 36 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0104others(33): Show | 36 | HG00738.hp1 HG01070.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1379-4317T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169646 | ||||||
| chr1:200169680
|
G | T | 1 | a0001c0001t0002g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1379-4283G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169680 | ||||||
| chr1:200169721
|
C | T | 66 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(63): Show | 66 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1379-4242C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169721 | ||||||
| chr1:200169773
|
T | C | 1 | a0001c0002t0004g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1379-4190T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169773 | ||||||
| chr1:200169835
|
T | C | 1 | a0001c0003t0005g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1379-4128T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169835 | ||||||
| chr1:200169900
|
C | T | 1 | a0001c0001t0003g0234 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1379-4063C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200169900 | ||||||
| chr1:200170100
|
G | T | 57 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(54): Show | 57 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1379-3863G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170100 | ||||||
| chr1:200170218
|
A | G | 6 | a0001c0001t0006g0024a0001c0001t0006g0059a0001c0001t0006g0075others(3): Show | 6 | HG01074.hp2 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-3745A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170218 | ||||||
| chr1:200170222
|
C | T | 103 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(100): Show | 103 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1379-3741C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170222 | ||||||
| chr1:200170316
|
T | C | 110 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(107): Show | 110 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1379-3647T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170316 | ||||||
| chr1:200170361
|
T | A | 110 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(107): Show | 110 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1379-3602T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170361 | ||||||
| chr1:200170410
|
C | T | 2 | a0001c0001t0003g0234a0001c0001t0003g0235 | 2 | NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1379-3553C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170410 | ||||||
| chr1:200170632
|
T | G | 2 | a0001c0002t0007g0026a0001c0005t0007g0281 | 2 | HG02148.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1379-3331T>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170632 | ||||||
| chr1:200170643
|
G | C | 1 | a0001c0004t0004g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1379-3320G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170643 | ||||||
| chr1:200170664
|
G | A | 122 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(119): Show | 122 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1379-3299G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170664 | ||||||
| chr1:200170736
|
G | A | 122 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(119): Show | 122 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1379-3227G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170736 | ||||||
| chr1:200170988
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1379-2975G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200170988 | ||||||
| chr1:200171095
|
C | CA | 3 | a0001c0003t0002g0152a0001c0003t0002g0274a0004c0013t0032g0149 | 3 | HG00639.hp2 HG00741.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1379-2867dupA | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200171095 | |||||
| chr1:200171297
|
C | T | 132 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(129): Show | 132 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1379-2666C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171297 | ||||||
| chr1:200171298
|
T | C | 117 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(114): Show | 117 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1379-2665T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171298 | ||||||
| chr1:200171304
|
A | G | 66 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0104others(63): Show | 66 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1379-2659A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171304 | ||||||
| chr1:200171388
|
G | A | 2 | a0001c0001t0019g0209a0001c0001t0024g0029 | 2 | HG03239.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1379-2575G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171388 | ||||||
| chr1:200171454
|
A | C | 1 | a0001c0002t0001g0082 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1379-2509A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171454 | ||||||
| chr1:200171578
|
A | G | 164 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(161): Show | 164 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.1379-2385A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171578 | ||||||
| chr1:200171645
|
T | A | 123 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(120): Show | 123 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1379-2318T>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171645 | ||||||
| chr1:200171775
|
A | G | 7 | a0001c0001t0009g0181a0001c0003t0009g0013a0001c0003t0009g0064others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-2188A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171775 | ||||||
| chr1:200171865
|
G | C | 8 | a0001c0001t0006g0024a0001c0001t0006g0059a0001c0001t0006g0075others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1379-2098G>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171865 | ||||||
| chr1:200171944
|
A | G | 124 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(121): Show | 124 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1379-2019A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171944 | ||||||
| chr1:200171990
|
A | C | 27 | a0001c0002t0004g0065a0001c0002t0004g0090a0001c0002t0004g0091others(24): Show | 27 | HG01109.hp2 HG02109.hp1 HG02148.hp2 others(24): Show |
intron_variant | MODIFIER | c.1379-1973A>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200171990 | ||||||
| chr1:200172029
|
A | G | 1 | a0001c0002t0001g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1379-1934A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172029 | ||||||
| chr1:200172273
|
C | T | 274 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(271): Show | 274 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.1379-1690C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172273 | ||||||
| chr1:200172365
|
C | T | 2 | a0001c0002t0001g0183a0001c0002t0001g0244 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1379-1598C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172365 | ||||||
| chr1:200172520
|
A | G | 128 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(125): Show | 128 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1379-1443A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172520 | ||||||
| chr1:200172538
|
A | G | 1 | a0001c0002t0001g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1379-1425A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172538 | ||||||
| chr1:200172673
|
C | T | 113 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(110): Show | 113 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1379-1290C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172673 | ||||||
| chr1:200172799
|
C | G | 1 | a0001c0003t0009g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1379-1164C>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172799 | ||||||
| chr1:200172951
|
C | T | 20 | a0001c0001t0005g0009a0001c0001t0005g0094a0001c0001t0005g0106others(17): Show | 20 | HG00408.hp2 HG00609.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1379-1012C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200172951 | ||||||
| chr1:200173024
|
C | T | 6 | a0001c0001t0002g0104a0001c0001t0002g0168a0001c0001t0002g0169others(3): Show | 6 | HG00738.hp1 HG01070.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379-939C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173024 | ||||||
| chr1:200173049
|
G | A | 111 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(108): Show | 111 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1379-914G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173049 | ||||||
| chr1:200173176
|
A | G | 9 | a0001c0001t0006g0270a0001c0001t0008g0005a0001c0001t0008g0123others(6): Show | 9 | HG01358.hp2 HG01981.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-787A>G | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173176 | ||||||
| chr1:200173189
|
C | T | 110 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(107): Show | 110 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1379-774C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173189 | ||||||
| chr1:200173289
|
G | T | 1 | a0001c0001t0023g0225 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1379-674G>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173289 | ||||||
| chr1:200173404
|
C | T | 7 | a0001c0001t0009g0181a0001c0003t0009g0013a0001c0003t0009g0064others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-559C>T | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173404 | ||||||
| chr1:200173435
|
G | A | 7 | a0001c0001t0008g0005a0001c0001t0008g0123a0001c0001t0008g0128others(4): Show | 7 | HG01358.hp2 HG01981.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379-528G>A | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173435 | ||||||
| chr1:200173882
|
T | C | 1 | a0001c0001t0006g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1379-81T>C | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | chr1 | 200173882 | ||||||
| chr1:200173936
|
C | CT | 34 | a0001c0001t0002g0213a0001c0002t0001g0145a0001c0002t0001g0250others(31): Show | 34 | HG01109.hp2 HG01943.hp2 HG02109.hp1 others(31): Show |
splice_region_variant&intron_variant | LOW | c.1379-8dupT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200173936 | |||||
| chr1:200173936
|
CT | C | 6 | a0001c0001t0002g0081a0001c0001t0002g0212a0001c0001t0002g0227others(3): Show | 6 | HG00558.hp2 HG01884.hp2 HG01928.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1379-8delT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200173936 | |||||
| chr1:200173936
|
CTT | C | 8 | a0001c0001t0009g0181a0001c0001t0019g0209a0001c0003t0009g0013others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1379-9_1379-8delTT | NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200173936 | |||||
| chr1:200173936
|
CTTT | C | 13 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0003g0238others(10): Show | 13 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1379-10_1379-8delT others(2): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200173936 | |||||
| chr1:200173936
|
CTTTT | C | 104 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0001g0137others(101): Show | 104 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(101): Show |
splice_region_variant&intron_variant | LOW | c.1379-11_1379-8delT others(3): Show |
NR5A2 | ENSG00000116833.14 | transcript | ENST00000367362.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 200173936 |