Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9542 |
|---|---|
| ensemblid | ENSG00000158458.21 |
| hgncid | 7998 |
| symbol | NRG2 |
| name | neuregulin 2 |
| refseq_nuc | NM_004883.3 |
| refseq_prot | NP_004874.1 |
| ensembl_nuc | ENST00000361474.6 |
| ensembl_prot | ENSP00000354910.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 139846781 |
| end | 140043299 |
| strand | - |
| ver | v1.2 |
| region | chr5:139846781-140043299 |
| region5000 | chr5:139841781-140048299 |
| regionname0 | NRG2_chr5_139846781_140043299 |
| regionname5000 | NRG2_chr5_139841781_140048299 |
| 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 | 850 | 144 | 37 | 36 | 47 | 7 | 15 | 29 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002 | 0/0 | 848 | 32 | 18 | 7 | 4 | 1 | 2 | 3 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0003 | 0/0 | 850 | 5 | 0 | 1 | 0 | 0 | 4 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0004 | 0/0 | 850 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0005 | 0/0 | 850 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0006 | 0/0 | 850 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0007 | 0/0 | 850 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0008 | 0/0 | 850 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0009 | 0/0 | 848 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| 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 | 1/1 | 2553 | 133 | 32 | 34 | 46 | 5 | 14 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0002 | 0/0 | 2547 | 29 | 16 | 7 | 4 | 0 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0003 | 0/0 | 2553 | 5 | 0 | 1 | 0 | 0 | 4 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0004 | 0/0 | 2553 | 5 | 2 | 1 | 0 | 2 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0005 | 0/0 | 2553 | 3 | 3 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0006 | 0/0 | 2553 | 2 | 2 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0007 | 0/0 | 2547 | 2 | 1 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0008 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0009 | 0/0 | 2553 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0010 | 0/0 | 2553 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0011 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0012 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0013 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0014 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0015 | 0/0 | 2547 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| c0016 | 0/0 | 2553 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| 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 | 1367 | 149 | 37 | 38 | 47 | 7 | 18 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0002 | 0/0 | 1367 | 15 | 2 | 5 | 5 | 1 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0003 | 0/0 | 1366 | 13 | 10 | 1 | 1 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0004 | 0/0 | 1367 | 3 | 3 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0005 | 0/0 | 1367 | 3 | 3 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0006 | 0/0 | 1367 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0007 | 0/0 | 1367 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0008 | 0/0 | 1367 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0009 | 0/0 | 1367 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| t0010 | 0/0 | 1367 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| 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 | 1/1 | 2553 | 133 | 32 | 34 | 46 | 5 | 14 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0004 | 0/0 | 2553 | 5 | 2 | 1 | 0 | 2 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0005 | 0/0 | 2553 | 3 | 3 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0009 | 0/0 | 2553 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0010 | 0/0 | 2553 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0014 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0002 | 0/0 | 2547 | 29 | 16 | 7 | 4 | 0 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0007 | 0/0 | 2547 | 2 | 1 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0013 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0003c0003 | 0/0 | 2553 | 5 | 0 | 1 | 0 | 0 | 4 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0004c0006 | 0/0 | 2553 | 2 | 2 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0005c0016 | 0/0 | 2553 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0006c0008 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0007c0012 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0008c0011 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0009c0015 | 0/0 | 2547 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3919 | 128 | 31 | 34 | 44 | 5 | 12 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0001t0003 | 0/0 | 3918 | 2 | 0 | 0 | 1 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0001t0006 | 0/0 | 3919 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0001t0007 | 0/0 | 3919 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0001t0010 | 0/0 | 3919 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0004t0001 | 0/0 | 3919 | 5 | 2 | 1 | 0 | 2 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0005t0004 | 0/0 | 3919 | 3 | 3 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0009t0001 | 0/0 | 3919 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0010t0001 | 0/0 | 3919 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0001c0014t0001 | 0/0 | 3919 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0002t0001 | 0/0 | 3913 | 2 | 1 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0002t0002 | 0/0 | 3913 | 13 | 2 | 5 | 4 | 0 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0002t0003 | 0/0 | 3912 | 9 | 8 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0002t0005 | 0/0 | 3913 | 3 | 3 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0002t0008 | 0/0 | 3913 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0002t0009 | 0/0 | 3913 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0007t0002 | 0/0 | 3913 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0007t0003 | 0/0 | 3912 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0002c0013t0003 | 0/0 | 3912 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0003c0003t0001 | 0/0 | 3919 | 5 | 0 | 1 | 0 | 0 | 4 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0004c0006t0001 | 0/0 | 3919 | 2 | 2 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0005c0016t0001 | 0/0 | 3919 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0006c0008t0001 | 0/0 | 3919 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0007c0012t0001 | 0/0 | 3919 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0008c0011t0001 | 0/0 | 3919 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| a0009c0015t0002 | 0/0 | 3913 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | copy fasta | chr5 | 139841781 | 140048299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0005t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0005t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0005t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0009t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0010t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0001c0014t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0002t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0007t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0007t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0002c0013t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0003c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0003c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0004c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0004c0006t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0005c0016t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0006c0008t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0007c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0008c0011t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| a0009c0015t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0181 | EUR | GBR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0182 | EUR | FIN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0043 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01167 | hp2 | a0002 | c0002 | t0003 | g0150 | AMR | PUR | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01261 | hp2 | a0001 | c0009 | t0001 | g0063 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0179 | AMR | CLM | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01884 | hp2 | a0002 | c0007 | t0003 | g0180 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0085 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0041 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0160 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02056 | hp1 | a0006 | c0008 | t0001 | g0176 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02572 | hp1 | a0001 | c0005 | t0004 | g0156 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0170 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02602 | hp2 | a0001 | c0010 | t0001 | g0104 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0095 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0003 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02895 | hp2 | a0002 | c0002 | t0005 | g0138 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02965 | hp1 | a0002 | c0002 | t0003 | g0135 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02970 | hp1 | a0002 | c0013 | t0003 | g0083 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03195 | hp1 | a0001 | c0005 | t0004 | g0151 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03225 | hp1 | a0008 | c0011 | t0001 | g0106 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0173 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03486 | hp1 | a0002 | c0002 | t0005 | g0050 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0100 | AFR | GWD | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0169 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0171 | AFR | MSL | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0177 | SAS | BEB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG04115 | hp1 | a0005 | c0016 | t0001 | g0186 | SAS | STU | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0166 | SAS | STU | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18522 | hp1 | a0002 | c0002 | t0005 | g0141 | AFR | YRI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0148 | AFR | YRI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0038 | AFR | YRI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0184 | AFR | YRI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18988 | hp1 | a0009 | c0015 | t0002 | g0185 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0118 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19012 | hp2 | a0007 | c0012 | t0001 | g0121 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19030 | hp1 | a0002 | c0002 | t0003 | g0082 | AFR | LWK | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | LWK | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0167 | AFR | LWK | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19065 | hp2 | a0001 | c0014 | t0001 | g0117 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19240 | hp1 | a0004 | c0006 | t0001 | g0122 | AFR | YRI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA19240 | hp2 | a0001 | c0005 | t0004 | g0048 | AFR | YRI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA20129 | hp1 | a0002 | c0002 | t0009 | g0101 | AFR | ASW | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA20129 | hp2 | a0002 | c0002 | t0008 | g0143 | AFR | ASW | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA20805 | hp1 | a0002 | c0007 | t0002 | g0178 | EUR | TSI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0183 | AFR | USA | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| HG06807 | hp2 | a0004 | c0006 | t0001 | g0159 | AFR | USA | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0025 | REF | REF | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0037 | REF | REF | NRG2_chr5_139841781_140048299 | NRG2 | chr5 | 139841781 | 140048299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139848223
|
G | C | 1 | a0008 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2247C>G | p.Asn749Lys | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 2477/3919 | 2247/2553 | 749/850 | chr5 | 139848223 | ||
| chr5:139848487
|
CCCGGGT | C | 2 | a0002a0009 | 33 | HG01074.hp1 HG01081.hp2 HG01167.hp2 others(30): Show |
disruptive_inframe_deletion | MODERATE | c.1977_1982delACCCGG | p.Pro660_Gly661del | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 2212/3919 | 1977/2553 | 659/850 | chr5 | 139848487 | ||
| chr5:139851670
|
C | T | 1 | a0003 | 5 | HG01099.hp1 HG03490.hp1 HG03492.hp2 others(2): Show |
missense_variant | MODERATE | c.1706G>A | p.Arg569His | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/10 | 1936/3919 | 1706/2553 | 569/850 | chr5 | 139851670 | ||
| chr5:139852980
|
G | A | 1 | a0007 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1340C>T | p.Pro447Leu | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 7/10 | 1570/3919 | 1340/2553 | 447/850 | chr5 | 139852980 | ||
| chr5:139871761
|
C | T | 1 | a0006 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1072G>A | p.Val358Ile | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/10 | 1302/3919 | 1072/2553 | 358/850 | chr5 | 139871761 | ||
| chr5:139880879
|
C | T | 1 | a0004 | 2 | HG06807.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.968G>A | p.Arg323Gln | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/10 | 1198/3919 | 968/2553 | 323/850 | chr5 | 139880879 | ||
| chr5:140042808
|
C | A | 1 | a0009 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.262G>T | p.Ala88Ser | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/10 | 492/3919 | 262/2553 | 88/850 | chr5 | 140042808 | ||
| chr5:140042885
|
G | A | 1 | a0005 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.185C>T | p.Pro62Leu | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/10 | 415/3919 | 185/2553 | 62/850 | chr5 | 140042885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139847947
|
C | T | 1 | a0001c0009 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.2523G>A | p.Pro841Pro | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 2753/3919 | 2523/2553 | 841/850 | chr5 | 139847947 | ||
| chr5:139848187
|
G | A | 1 | a0001c0010 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2283C>T | p.Asp761Asp | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 2513/3919 | 2283/2553 | 761/850 | chr5 | 139848187 | ||
| chr5:139851690
|
G | A | 1 | a0001c0005 | 3 | HG02572.hp1 HG03195.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1686C>T | p.Ala562Ala | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/10 | 1916/3919 | 1686/2553 | 562/850 | chr5 | 139851690 | ||
| chr5:139855735
|
G | A | 1 | a0002c0013 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1233C>T | p.Gly411Gly | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/10 | 1463/3919 | 1233/2553 | 411/850 | chr5 | 139855735 | ||
| chr5:139871810
|
G | A | 1 | a0001c0014 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.1023C>T | p.His341His | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/10 | 1253/3919 | 1023/2553 | 341/850 | chr5 | 139871810 | ||
| chr5:140042647
|
G | A | 2 | a0001c0004a0002c0007 | 7 | HG00140.hp2 HG00323.hp1 HG01496.hp2 others(4): Show |
synonymous_variant | LOW | c.423C>T | p.Ala141Ala | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/10 | 653/3919 | 423/2553 | 141/850 | chr5 | 140042647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139846884
|
AT | A | 4 | a0001c0001t0003a0002c0002t0003a0002c0007t0003others(1): Show | 13 | HG01167.hp2 HG01884.hp2 HG02572.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1032delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 1032 | chr5 | 139846884 | |||||
| chr5:139846965
|
G | A | 1 | a0002c0002t0008 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 952 | chr5 | 139846965 | |||||
| chr5:139847079
|
G | A | 1 | a0002c0002t0009 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*838C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 838 | chr5 | 139847079 | |||||
| chr5:139847150
|
C | T | 1 | a0001c0005t0004 | 3 | HG02572.hp1 HG03195.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*767G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 767 | chr5 | 139847150 | |||||
| chr5:139847297
|
G | A | 1 | a0002c0002t0005 | 3 | HG02895.hp2 HG03486.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 620 | chr5 | 139847297 | |||||
| chr5:139847362
|
C | T | 1 | a0001c0001t0007 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*555G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 555 | chr5 | 139847362 | |||||
| chr5:139847408
|
T | C | 4 | a0002c0002t0002a0002c0002t0005a0002c0007t0002others(1): Show | 18 | HG01074.hp1 HG01081.hp2 HG01934.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*509A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 509 | chr5 | 139847408 | |||||
| chr5:139847734
|
G | A | 1 | a0001c0001t0010 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 10/10 | 183 | chr5 | 139847734 | |||||
| chr5:140043280
|
G | T | 1 | a0001c0001t0006 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-211C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/10 | 211 | chr5 | 140043280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:139848771
|
T | A | 8 | a0001c0001t0001g0047a0001c0001t0001g0065a0001c0001t0001g0072others(5): Show | 8 | HG02083.hp2 HG02523.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.1773-74A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139848771 | ||||||
| chr5:139848781
|
G | T | 1 | a0002c0007t0003g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1773-84C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139848781 | ||||||
| chr5:139849420
|
A | C | 4 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(1): Show | 4 | HG02647.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1773-723T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139849420 | ||||||
| chr5:139849661
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1773-964C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139849661 | ||||||
| chr5:139849706
|
T | C | 2 | a0002c0002t0002g0001a0002c0007t0002g0178 | 3 | HG03491.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1773-1009A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139849706 | ||||||
| chr5:139849736
|
C | G | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1773-1039G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139849736 | ||||||
| chr5:139850571
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1772+1033T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139850571 | ||||||
| chr5:139850734
|
G | A | 1 | a0006c0008t0001g0176 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1772+870C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139850734 | ||||||
| chr5:139850908
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1772+696C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139850908 | ||||||
| chr5:139851048
|
C | T | 1 | a0002c0002t0002g0171 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1772+556G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139851048 | ||||||
| chr5:139851279
|
G | T | 10 | a0002c0002t0001g0017a0002c0002t0001g0085a0002c0002t0003g0082others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1772+325C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139851279 | ||||||
| chr5:139851351
|
T | C | 6 | a0002c0002t0003g0082a0002c0002t0003g0169a0002c0002t0003g0170others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1772+253A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139851351 | ||||||
| chr5:139851362
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1772+242G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139851362 | ||||||
| chr5:139851415
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1772+189G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 9/9 | chr5 | 139851415 | ||||||
| chr5:139851909
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1545-78G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 8/9 | chr5 | 139851909 | ||||||
| chr5:139852087
|
C | A | 4 | a0002c0002t0003g0169a0002c0002t0003g0173a0002c0002t0008g0143others(1): Show | 4 | HG01884.hp2 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545-256G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 8/9 | chr5 | 139852087 | ||||||
| chr5:139852112
|
T | C | 16 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0108others(13): Show | 17 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1545-281A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 8/9 | chr5 | 139852112 | ||||||
| chr5:139852420
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0032 | 2 | HG00741.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1544+12C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 8/9 | chr5 | 139852420 | ||||||
| chr5:139852710
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1417-151G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 7/9 | chr5 | 139852710 | ||||||
| chr5:139852714
|
C | A | 16 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0108others(13): Show | 17 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1417-155G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 7/9 | chr5 | 139852714 | ||||||
| chr5:139852721
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1417-162T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 7/9 | chr5 | 139852721 | ||||||
| chr5:139852798
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1416+106C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 7/9 | chr5 | 139852798 | ||||||
| chr5:139852870
|
G | C | 7 | a0002c0002t0001g0017a0002c0002t0001g0085a0002c0002t0003g0150others(4): Show | 7 | HG01167.hp2 HG01884.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1416+34C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 7/9 | chr5 | 139852870 | ||||||
| chr5:139852891
|
G | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0066others(4): Show | 7 | HG00544.hp2 HG00673.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1416+13C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 7/9 | chr5 | 139852891 | ||||||
| chr5:139853208
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0144a0001c0001t0001g0172 | 3 | HG01884.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1293-181G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853208 | ||||||
| chr5:139853212
|
G | A | 4 | a0003c0003t0001g0002a0003c0003t0001g0043a0003c0003t0001g0166others(1): Show | 5 | HG01099.hp1 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1293-185C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853212 | ||||||
| chr5:139853518
|
G | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1293-491C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853518 | ||||||
| chr5:139853734
|
C | T | 5 | a0002c0002t0003g0150a0002c0002t0003g0169a0002c0002t0003g0173others(2): Show | 5 | HG01167.hp2 HG01884.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1293-707G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853734 | ||||||
| chr5:139853735
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0115 | 2 | NA18974.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1293-708C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853735 | ||||||
| chr5:139853802
|
G | A | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1293-775C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853802 | ||||||
| chr5:139853892
|
T | G | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1293-865A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853892 | ||||||
| chr5:139853908
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1293-881C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853908 | ||||||
| chr5:139853941
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1293-914G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139853941 | ||||||
| chr5:139854508
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1292+1168G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139854508 | ||||||
| chr5:139854580
|
C | T | 5 | a0002c0002t0003g0150a0002c0002t0003g0169a0002c0002t0003g0173others(2): Show | 5 | HG01167.hp2 HG01884.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292+1096G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139854580 | ||||||
| chr5:139855219
|
G | A | 21 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0108others(18): Show | 22 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292+457C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139855219 | ||||||
| chr5:139855259
|
G | A | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1292+417C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139855259 | ||||||
| chr5:139855278
|
C | T | 1 | a0002c0007t0003g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1292+398G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139855278 | ||||||
| chr5:139855300
|
A | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(49): Show | 53 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1292+376T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139855300 | ||||||
| chr5:139855372
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1292+304G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 6/9 | chr5 | 139855372 | ||||||
| chr5:139855854
|
G | T | 1 | a0005c0016t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1190-76C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139855854 | ||||||
| chr5:139855944
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1190-166A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139855944 | ||||||
| chr5:139856139
|
C | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1190-361G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856139 | ||||||
| chr5:139856226
|
T | C | 6 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190-448A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856226 | ||||||
| chr5:139856230
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1190-452T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856230 | ||||||
| chr5:139856375
|
C | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1190-597G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856375 | ||||||
| chr5:139856418
|
C | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1190-640G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856418 | ||||||
| chr5:139856426
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1190-648C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856426 | ||||||
| chr5:139856555
|
C | A | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1190-777G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856555 | ||||||
| chr5:139856626
|
A | G | 6 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190-848T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856626 | ||||||
| chr5:139856863
|
C | A | 4 | a0002c0002t0002g0100a0002c0002t0005g0050a0002c0002t0005g0138others(1): Show | 4 | HG02895.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1190-1085G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139856863 | ||||||
| chr5:139857377
|
C | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0016others(42): Show | 45 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1190-1599G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139857377 | ||||||
| chr5:139857413
|
C | T | 6 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190-1635G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139857413 | ||||||
| chr5:139857509
|
CT | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1190-1732delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139857509 | ||||||
| chr5:139857523
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1190-1745C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139857523 | ||||||
| chr5:139857756
|
A | G | 52 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(49): Show | 53 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1190-1978T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139857756 | ||||||
| chr5:139857794
|
T | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1190-2016A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139857794 | ||||||
| chr5:139857842
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1190-2064C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139857842 | ||||||
| chr5:139858235
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0165 | 2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1190-2457C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139858235 | ||||||
| chr5:139858397
|
A | G | 2 | a0002c0002t0003g0170a0008c0011t0001g0106 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1190-2619T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139858397 | ||||||
| chr5:139858560
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(10): Show | 13 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1190-2782G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139858560 | ||||||
| chr5:139858622
|
A | G | 1 | a0001c0010t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1190-2844T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139858622 | ||||||
| chr5:139858666
|
C | T | 21 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0108others(18): Show | 22 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1190-2888G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139858666 | ||||||
| chr5:139858786
|
C | T | 3 | a0001c0005t0004g0048a0001c0005t0004g0151a0001c0005t0004g0156 | 3 | HG02572.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1190-3008G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139858786 | ||||||
| chr5:139858873
|
T | C | 1 | a0002c0002t0003g0150 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1190-3095A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139858873 | ||||||
| chr5:139859137
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1190-3359T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859137 | ||||||
| chr5:139859231
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0157a0001c0004t0001g0179 | 3 | HG00642.hp1 HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1190-3453G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859231 | ||||||
| chr5:139859238
|
C | T | 6 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190-3460G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859238 | ||||||
| chr5:139859308
|
G | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(49): Show | 53 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1190-3530C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859308 | ||||||
| chr5:139859336
|
A | G | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1190-3558T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859336 | ||||||
| chr5:139859527
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1190-3749C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859527 | ||||||
| chr5:139859570
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | HG00323.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1190-3792G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859570 | ||||||
| chr5:139859830
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1190-4052G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859830 | ||||||
| chr5:139859930
|
C | CG | 52 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(49): Show | 53 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1190-4153dupC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139859930 | ||||||
| chr5:139860027
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0142 | 3 | HG02922.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1190-4249G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139860027 | ||||||
| chr5:139860141
|
AG | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0165 | 2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1190-4364delC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139860141 | ||||||
| chr5:139860334
|
T | C | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1190-4556A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139860334 | ||||||
| chr5:139860346
|
G | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1190-4568C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139860346 | ||||||
| chr5:139860605
|
A | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0108others(18): Show | 22 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1190-4827T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139860605 | ||||||
| chr5:139860615
|
C | T | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1190-4837G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139860615 | ||||||
| chr5:139861356
|
G | C | 7 | a0002c0002t0003g0038a0002c0002t0003g0082a0002c0002t0003g0095others(4): Show | 7 | HG02572.hp2 HG02647.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189+4193C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139861356 | ||||||
| chr5:139861374
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0165 | 2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1189+4175G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139861374 | ||||||
| chr5:139861438
|
G | A | 6 | a0002c0002t0003g0135a0002c0002t0003g0150a0002c0002t0003g0169others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189+4111C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139861438 | ||||||
| chr5:139861439
|
C | T | 6 | a0002c0002t0003g0135a0002c0002t0003g0150a0002c0002t0003g0169others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189+4110G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139861439 | ||||||
| chr5:139861947
|
G | A | 2 | a0002c0002t0003g0170a0008c0011t0001g0106 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1189+3602C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139861947 | ||||||
| chr5:139861955
|
G | T | 52 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(49): Show | 53 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1189+3594C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139861955 | ||||||
| chr5:139862142
|
G | T | 52 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(49): Show | 53 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1189+3407C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139862142 | ||||||
| chr5:139862150
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1189+3399T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139862150 | ||||||
| chr5:139862273
|
A | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1189+3276T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139862273 | ||||||
| chr5:139862390
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0145 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1189+3159C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139862390 | ||||||
| chr5:139862476
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1189+3073G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139862476 | ||||||
| chr5:139862705
|
T | C | 20 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0108others(17): Show | 21 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1189+2844A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139862705 | ||||||
| chr5:139862986
|
G | A | 6 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189+2563C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139862986 | ||||||
| chr5:139863182
|
C | G | 19 | a0001c0001t0001g0036a0001c0001t0001g0039a0002c0002t0002g0001others(16): Show | 20 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1189+2367G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139863182 | ||||||
| chr5:139863577
|
A | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(43): Show | 47 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1189+1972T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139863577 | ||||||
| chr5:139863805
|
C | T | 22 | a0001c0001t0001g0036a0001c0001t0001g0039a0002c0002t0001g0017others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1189+1744G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139863805 | ||||||
| chr5:139863857
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1189+1692G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139863857 | ||||||
| chr5:139864154
|
C | G | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1189+1395G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864154 | ||||||
| chr5:139864179
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1189+1370T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864179 | ||||||
| chr5:139864385
|
C | CT | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1189+1163dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864385 | ||||||
| chr5:139864385
|
CT | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1189+1163delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864385 | ||||||
| chr5:139864388
|
T | C | 2 | a0001c0001t0001g0065a0002c0002t0002g0081 | 2 | HG02083.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1189+1161A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864388 | ||||||
| chr5:139864495
|
TGAGA | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | HG00323.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1189+1050_1189+105 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864495 | ||||||
| chr5:139864601
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1189+948G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864601 | ||||||
| chr5:139864694
|
A | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1189+855T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864694 | ||||||
| chr5:139864752
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1189+797C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864752 | ||||||
| chr5:139864755
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1189+794C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864755 | ||||||
| chr5:139864756
|
G | GCA | 3 | a0001c0001t0001g0005a0001c0001t0001g0163a0007c0012t0001g0121 | 3 | HG01361.hp2 HG03195.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1189+791_1189+792d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864756 | ||||||
| chr5:139864756
|
GCA | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(61): Show | 66 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.1189+791_1189+792d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864756 | ||||||
| chr5:139864807
|
G | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1189+742C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864807 | ||||||
| chr5:139864830
|
G | T | 1 | a0001c0001t0003g0007 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1189+719C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139864830 | ||||||
| chr5:139865046
|
G | GC | 5 | a0002c0002t0003g0150a0002c0002t0003g0169a0002c0002t0003g0173others(2): Show | 5 | HG01167.hp2 HG01884.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189+502dupG | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139865046 | ||||||
| chr5:139865501
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(60): Show | 65 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.1189+48T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 5/9 | chr5 | 139865501 | ||||||
| chr5:139866039
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1113-414T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139866039 | ||||||
| chr5:139866159
|
TTTGACAA others(10): Show |
T | 1 | a0001c0001t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1113-551_1113-535d others(19): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139866159 | ||||||
| chr5:139866177
|
A | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(65): Show | 70 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1113-552T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139866177 | ||||||
| chr5:139866248
|
G | A | 3 | a0001c0001t0001g0086a0002c0002t0003g0170a0008c0011t0001g0106 | 3 | HG01099.hp2 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1113-623C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139866248 | ||||||
| chr5:139866632
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113-1007G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139866632 | ||||||
| chr5:139866777
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0089 | 2 | HG01978.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1113-1152C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139866777 | ||||||
| chr5:139866869
|
C | G | 41 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0047others(38): Show | 43 | HG00323.hp2 HG00609.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1113-1244G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139866869 | ||||||
| chr5:139867103
|
T | C | 3 | a0002c0002t0002g0081a0002c0002t0002g0162a0009c0015t0002g0185 | 3 | NA18942.hp2 NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1113-1478A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867103 | ||||||
| chr5:139867136
|
AGGCTTAC others(7): Show |
A | 3 | a0002c0002t0003g0169a0002c0002t0008g0143a0002c0007t0003g0180 | 3 | HG01884.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1113-1525_1113-151 others(18): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867136 | ||||||
| chr5:139867237
|
A | C | 3 | a0002c0002t0002g0171a0004c0006t0001g0122a0004c0006t0001g0159 | 3 | HG03579.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1113-1612T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867237 | ||||||
| chr5:139867405
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1113-1780C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867405 | ||||||
| chr5:139867425
|
T | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1113-1800A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867425 | ||||||
| chr5:139867761
|
C | CCT | 13 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0047others(10): Show | 13 | HG00323.hp2 HG01167.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113-2138_1113-213 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867761 | ||||||
| chr5:139867762
|
C | CTG | 24 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0029others(21): Show | 24 | HG00140.hp1 HG00639.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1113-2139_1113-213 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867762 | ||||||
| chr5:139867762
|
C | CTGTG | 51 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1113-2141_1113-213 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867762 | ||||||
| chr5:139867762
|
C | CTGTGTG | 9 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0079others(6): Show | 9 | HG00408.hp1 HG00735.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113-2143_1113-213 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867762 | ||||||
| chr5:139867762
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0090a0009c0015t0002g0185 | 3 | HG00673.hp2 HG01109.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1113-2145_1113-213 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867762 | ||||||
| chr5:139867762
|
C | CTGTGTGT others(3): Show |
1 | a0002c0002t0002g0081 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1113-2147_1113-213 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867762 | ||||||
| chr5:139867762
|
CTGTGTGT others(9): Show |
C | 7 | a0002c0002t0001g0017a0002c0002t0001g0085a0002c0002t0003g0082others(4): Show | 7 | HG01884.hp2 HG01934.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113-2153_1113-213 others(20): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867762 | ||||||
| chr5:139867764
|
G | C | 24 | a0001c0001t0001g0064a0001c0001t0001g0080a0001c0001t0001g0111others(21): Show | 26 | HG00609.hp1 HG01074.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1113-2139C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867764 | ||||||
| chr5:139867768
|
G | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1113-2143C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867768 | ||||||
| chr5:139867780
|
G | A | 4 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(1): Show | 4 | HG02647.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-2155C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867780 | ||||||
| chr5:139867782
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113-2157C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867782 | ||||||
| chr5:139867783
|
T | A | 4 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(1): Show | 4 | HG02647.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-2158A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867783 | ||||||
| chr5:139867783
|
T | TGTGC | 2 | a0001c0001t0001g0051a0001c0001t0001g0092 | 2 | HG00621.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1113-2159_1113-215 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867783 | ||||||
| chr5:139867785
|
T | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113-2160A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867785 | ||||||
| chr5:139867787
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1113-2176_1113-216 others(18): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867787 | ||||||
| chr5:139867789
|
T | TGTGTGTA others(3): Show |
3 | a0002c0002t0002g0021a0002c0002t0002g0040a0002c0002t0002g0041 | 3 | HG01074.hp1 HG01081.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1113-2165_1113-216 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867789 | ||||||
| chr5:139867789
|
TGTGTGTG others(5): Show |
T | 6 | a0001c0001t0001g0023a0002c0002t0002g0100a0002c0002t0003g0038others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113-2176_1113-216 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867789 | ||||||
| chr5:139867791
|
TGTGTGTA others(3): Show |
T | 2 | a0001c0001t0001g0144a0002c0002t0003g0170 | 2 | HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1113-2176_1113-216 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867791 | ||||||
| chr5:139867792
|
G | A | 3 | a0001c0004t0001g0183a0002c0002t0002g0001a0002c0007t0002g0178 | 4 | HG03491.hp1 HG03492.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113-2167C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867792 | ||||||
| chr5:139867793
|
T | TGTATGA | 5 | a0001c0014t0001g0117a0002c0002t0002g0009a0002c0002t0002g0087others(2): Show | 6 | HG01934.hp1 HG02056.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-2169_1113-216 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867793 | ||||||
| chr5:139867793
|
TGTGTATG others(1): Show |
T | 11 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0033others(8): Show | 11 | HG01099.hp2 HG01884.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113-2176_1113-216 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867793 | ||||||
| chr5:139867794
|
G | A | 13 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0047others(10): Show | 13 | HG00323.hp2 HG00609.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113-2169C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867794 | ||||||
| chr5:139867795
|
T | A | 3 | a0001c0004t0001g0183a0002c0002t0002g0001a0002c0007t0002g0178 | 4 | HG03491.hp1 HG03492.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113-2170A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867795 | ||||||
| chr5:139867795
|
T | TATGA | 3 | a0001c0001t0001g0125a0001c0001t0003g0103a0001c0004t0001g0184 | 3 | HG02735.hp1 HG02735.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1113-2171_1113-217 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867795 | ||||||
| chr5:139867796
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG01978.hp2 HG04115.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-2171C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867796 | ||||||
| chr5:139867796
|
GTA | G | 3 | a0001c0004t0001g0183a0002c0002t0002g0001a0002c0007t0002g0178 | 4 | HG03491.hp1 HG03492.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113-2173_1113-217 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867796 | ||||||
| chr5:139867797
|
T | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0047others(11): Show | 14 | HG00323.hp2 HG00609.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1113-2172A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867797 | ||||||
| chr5:139867797
|
TATGA | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01069.hp2 HG01071.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1113-2176_1113-217 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867797 | ||||||
| chr5:139867798
|
A | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0022others(39): Show | 43 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1113-2173T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867798 | ||||||
| chr5:139867799
|
T | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG01978.hp2 HG04115.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-2174A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867799 | ||||||
| chr5:139867800
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0130a0001c0001t0001g0142 | 3 | HG02922.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1113-2175C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867800 | ||||||
| chr5:139867800
|
G | GTA | 4 | a0001c0001t0001g0022a0001c0001t0001g0068a0001c0001t0001g0077others(1): Show | 4 | HG00609.hp2 HG01978.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-2176_1113-217 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867800 | ||||||
| chr5:139867801
|
A | AGT | 10 | a0001c0001t0001g0004a0001c0001t0001g0073a0001c0001t0001g0108others(7): Show | 10 | HG01433.hp1 HG01993.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1113-2178_1113-217 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867801 | ||||||
| chr5:139867801
|
A | AGTGT | 4 | a0001c0001t0001g0044a0001c0001t0001g0107a0001c0001t0001g0164others(1): Show | 4 | HG00639.hp2 HG01261.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-2180_1113-217 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867801 | ||||||
| chr5:139867801
|
A | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0022others(42): Show | 47 | HG00323.hp2 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1113-2176T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867801 | ||||||
| chr5:139867801
|
AGT | A | 5 | a0002c0002t0003g0082a0002c0002t0003g0169a0002c0002t0008g0143others(2): Show | 5 | HG01884.hp2 HG03579.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113-2178_1113-217 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867801 | ||||||
| chr5:139867801
|
AGTGT | A | 3 | a0002c0002t0002g0171a0004c0006t0001g0122a0004c0006t0001g0159 | 3 | HG03579.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1113-2180_1113-217 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867801 | ||||||
| chr5:139867801
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1113-2186_1113-217 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867801 | ||||||
| chr5:139867802
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1113-2177C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867802 | ||||||
| chr5:139867803
|
T | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0001g0077others(3): Show | 6 | HG00609.hp2 HG01978.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113-2178A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867803 | ||||||
| chr5:139867805
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0002c0002t0002g0162 | 3 | HG00639.hp1 HG00735.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1113-2180A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867805 | ||||||
| chr5:139867809
|
T | A | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113-2184A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867809 | ||||||
| chr5:139867938
|
GAACAATG others(2): Show |
G | 69 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(66): Show | 71 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1113-2322_1113-231 others(13): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139867938 | ||||||
| chr5:139868132
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1113-2507A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139868132 | ||||||
| chr5:139868386
|
T | C | 47 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0036others(44): Show | 49 | HG00323.hp2 HG00609.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.1113-2761A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139868386 | ||||||
| chr5:139868479
|
G | A | 7 | a0002c0002t0001g0017a0002c0002t0001g0085a0002c0002t0003g0038others(4): Show | 7 | HG01934.hp2 HG02647.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113-2854C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139868479 | ||||||
| chr5:139868516
|
A | G | 75 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(72): Show | 77 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.1113-2891T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139868516 | ||||||
| chr5:139868564
|
G | T | 1 | a0001c0005t0004g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1113-2939C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139868564 | ||||||
| chr5:139869163
|
G | A | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1112+2558C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139869163 | ||||||
| chr5:139869598
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1112+2123C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139869598 | ||||||
| chr5:139869855
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1112+1866T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139869855 | ||||||
| chr5:139869962
|
G | A | 1 | a0002c0002t0005g0141 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1112+1759C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139869962 | ||||||
| chr5:139870003
|
A | G | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1112+1718T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139870003 | ||||||
| chr5:139870139
|
G | C | 2 | a0002c0002t0005g0050a0002c0002t0005g0141 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1112+1582C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139870139 | ||||||
| chr5:139870229
|
C | CT | 18 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1112+1491dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139870229 | ||||||
| chr5:139870481
|
G | A | 4 | a0002c0002t0003g0038a0002c0002t0003g0095a0002c0002t0003g0148others(1): Show | 4 | HG02647.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112+1240C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139870481 | ||||||
| chr5:139870659
|
A | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1112+1062T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139870659 | ||||||
| chr5:139870830
|
T | A | 3 | a0002c0002t0003g0169a0002c0002t0008g0143a0002c0007t0003g0180 | 3 | HG01884.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1112+891A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139870830 | ||||||
| chr5:139871240
|
T | C | 18 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1112+481A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139871240 | ||||||
| chr5:139871257
|
G | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | NA18942.hp1 NA18983.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1112+464C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139871257 | ||||||
| chr5:139871283
|
T | C | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1112+438A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139871283 | ||||||
| chr5:139871414
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1112+307G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139871414 | ||||||
| chr5:139871491
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1112+230C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 4/9 | chr5 | 139871491 | ||||||
| chr5:139871851
|
T | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.992-10A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139871851 | ||||||
| chr5:139871884
|
T | G | 55 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.992-43A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139871884 | ||||||
| chr5:139871971
|
G | A | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.992-130C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139871971 | ||||||
| chr5:139872125
|
C | G | 18 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.992-284G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139872125 | ||||||
| chr5:139872241
|
G | A | 4 | a0002c0002t0002g0100a0002c0002t0003g0169a0002c0002t0008g0143others(1): Show | 4 | HG01884.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-400C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139872241 | ||||||
| chr5:139872359
|
C | T | 22 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(19): Show | 22 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.992-518G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139872359 | ||||||
| chr5:139872371
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.992-530T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139872371 | ||||||
| chr5:139872639
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(58): Show | 62 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.992-798T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139872639 | ||||||
| chr5:139872705
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.992-864A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139872705 | ||||||
| chr5:139872876
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.992-1035G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139872876 | ||||||
| chr5:139873188
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.992-1347C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139873188 | ||||||
| chr5:139873293
|
C | T | 1 | a0002c0002t0002g0009 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.992-1452G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139873293 | ||||||
| chr5:139873737
|
C | T | 22 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(19): Show | 22 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.992-1896G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139873737 | ||||||
| chr5:139873765
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.992-1924C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139873765 | ||||||
| chr5:139873813
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.992-1972C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139873813 | ||||||
| chr5:139873966
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(10): Show | 13 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.992-2125G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139873966 | ||||||
| chr5:139874083
|
A | G | 18 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.992-2242T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874083 | ||||||
| chr5:139874167
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.992-2326C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874167 | ||||||
| chr5:139874276
|
G | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.992-2435C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874276 | ||||||
| chr5:139874306
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.992-2465C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874306 | ||||||
| chr5:139874444
|
T | C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.992-2603A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874444 | ||||||
| chr5:139874644
|
A | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(18): Show | 21 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.992-2803T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874644 | ||||||
| chr5:139874805
|
T | G | 5 | a0002c0002t0002g0100a0002c0002t0003g0135a0002c0002t0003g0169others(2): Show | 5 | HG01884.hp2 HG02965.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-2964A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874805 | ||||||
| chr5:139874970
|
A | C | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.992-3129T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139874970 | ||||||
| chr5:139875123
|
T | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(18): Show | 21 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.992-3282A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139875123 | ||||||
| chr5:139875792
|
G | A | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.992-3951C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139875792 | ||||||
| chr5:139876185
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0139 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.992-4344T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876185 | ||||||
| chr5:139876215
|
C | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0036others(35): Show | 39 | HG00323.hp2 HG00609.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.992-4374G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876215 | ||||||
| chr5:139876243
|
G | A | 3 | a0002c0002t0003g0169a0002c0002t0008g0143a0002c0007t0003g0180 | 3 | HG01884.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.992-4402C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876243 | ||||||
| chr5:139876358
|
G | A | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.991+4498C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876358 | ||||||
| chr5:139876430
|
A | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.991+4426T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876430 | ||||||
| chr5:139876450
|
G | A | 1 | a0002c0002t0002g0171 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.991+4406C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876450 | ||||||
| chr5:139876530
|
G | A | 4 | a0002c0002t0002g0100a0002c0002t0003g0169a0002c0002t0008g0143others(1): Show | 4 | HG01884.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+4326C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876530 | ||||||
| chr5:139876637
|
A | G | 59 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(56): Show | 60 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.991+4219T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876637 | ||||||
| chr5:139876720
|
T | A | 1 | a0001c0001t0001g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.991+4136A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876720 | ||||||
| chr5:139876780
|
A | G | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.991+4076T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876780 | ||||||
| chr5:139876925
|
C | CTG | 23 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0024others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.991+3929_991+3930d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
C | CTGTG | 10 | a0001c0001t0001g0061a0001c0001t0001g0116a0001c0001t0001g0128others(7): Show | 10 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.991+3927_991+3930d others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
C | CTGTGTG | 6 | a0001c0001t0001g0086a0002c0002t0003g0038a0002c0002t0003g0095others(3): Show | 6 | HG01099.hp2 HG02056.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.991+3925_991+3930d others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
C | CTGTGTGT others(1): Show |
2 | a0001c0001t0001g0136a0002c0002t0003g0135 | 2 | HG02965.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.991+3923_991+3930d others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0019a0001c0001t0001g0056a0002c0002t0003g0082 | 3 | HG02602.hp1 HG03490.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.991+3921_991+3930d others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.991+3919_991+3930d others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.991+3917_991+3930d others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
CTG | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0014others(77): Show | 81 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.991+3929_991+3930d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
CTGTG | C | 30 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(27): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.991+3927_991+3930d others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876925
|
CTGTGTG | C | 4 | a0002c0002t0002g0100a0002c0002t0003g0169a0002c0002t0008g0143others(1): Show | 4 | HG01884.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+3925_991+3930d others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876925 | ||||||
| chr5:139876961
|
GTGT | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0113 | 2 | HG00741.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.991+3892_991+3894d others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876961 | ||||||
| chr5:139876963
|
GT | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0153 | 2 | HG01993.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.991+3892delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876963 | ||||||
| chr5:139876964
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.991+3891_991+3892i others(13): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139876964 | ||||||
| chr5:139877106
|
C | T | 17 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.991+3750G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139877106 | ||||||
| chr5:139877210
|
C | T | 7 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0102others(4): Show | 7 | HG00609.hp1 HG02735.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.991+3646G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139877210 | ||||||
| chr5:139877491
|
GACCACAG others(21): Show |
G | 1 | a0001c0001t0001g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.991+3337_991+3364d others(30): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139877491 | ||||||
| chr5:139877521
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.991+3335A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139877521 | ||||||
| chr5:139878018
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(58): Show | 62 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.991+2838T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139878018 | ||||||
| chr5:139878019
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.991+2837G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139878019 | ||||||
| chr5:139878256
|
A | G | 1 | a0001c0005t0004g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.991+2600T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139878256 | ||||||
| chr5:139878293
|
A | G | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.991+2563T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139878293 | ||||||
| chr5:139878477
|
AGAGAGGC others(973): Show |
A | 1 | a0001c0001t0001g0013 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.991+1399_991+2378d others(2): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139878477 | ||||||
| chr5:139878532
|
T | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(18): Show | 21 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.991+2324A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139878532 | ||||||
| chr5:139878757
|
G | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0115 | 2 | NA18974.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.991+2099C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139878757 | ||||||
| chr5:139879023
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.991+1833G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139879023 | ||||||
| chr5:139879029
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0109a0001c0001t0001g0165others(2): Show | 5 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+1827G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139879029 | ||||||
| chr5:139879260
|
GA | G | 16 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.991+1595delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139879260 | ||||||
| chr5:139879446
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(2): Show | 5 | HG02602.hp1 HG02976.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+1410G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139879446 | ||||||
| chr5:139879739
|
C | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0068 | 2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.991+1117G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139879739 | ||||||
| chr5:139879945
|
G | A | 1 | a0002c0007t0003g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.991+911C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139879945 | ||||||
| chr5:139880253
|
G | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.991+603C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139880253 | ||||||
| chr5:139880297
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.991+559C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139880297 | ||||||
| chr5:139880707
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.991+149C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139880707 | ||||||
| chr5:139880836
|
C | G | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.991+20G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139880836 | ||||||
| chr5:139880843
|
T | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(58): Show | 62 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.991+13A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 3/9 | chr5 | 139880843 | ||||||
| chr5:139881110
|
C | G | 16 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.873-136G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139881110 | ||||||
| chr5:139881181
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.873-207G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139881181 | ||||||
| chr5:139881251
|
G | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0034others(28): Show | 32 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.873-277C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139881251 | ||||||
| chr5:139881275
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0131 | 2 | HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.873-301C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139881275 | ||||||
| chr5:139881420
|
G | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0036others(34): Show | 38 | HG00323.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.873-446C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139881420 | ||||||
| chr5:139881572
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0163 | 2 | HG00642.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.873-598G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139881572 | ||||||
| chr5:139882009
|
C | A | 2 | a0002c0002t0003g0169a0002c0002t0008g0143 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.873-1035G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882009 | ||||||
| chr5:139882198
|
T | A | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.873-1224A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882198 | ||||||
| chr5:139882532
|
A | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(128): Show | 133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.873-1558T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882532 | ||||||
| chr5:139882561
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.873-1587C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882561 | ||||||
| chr5:139882635
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.873-1661T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882635 | ||||||
| chr5:139882705
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(2): Show | 5 | HG02602.hp1 HG02976.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-1731C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882705 | ||||||
| chr5:139882722
|
T | A | 1 | a0003c0003t0001g0043 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.873-1748A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882722 | ||||||
| chr5:139882722
|
T | C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.873-1748A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882722 | ||||||
| chr5:139882757
|
C | T | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.873-1783G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882757 | ||||||
| chr5:139882842
|
G | C | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.873-1868C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882842 | ||||||
| chr5:139882929
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.873-1955C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882929 | ||||||
| chr5:139882996
|
G | A | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.873-2022C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139882996 | ||||||
| chr5:139883352
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.873-2378C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139883352 | ||||||
| chr5:139883423
|
T | TG | 41 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0036others(38): Show | 42 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.873-2450dupC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139883423 | ||||||
| chr5:139883608
|
A | G | 20 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0056others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.873-2634T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139883608 | ||||||
| chr5:139883710
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.873-2736A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139883710 | ||||||
| chr5:139883832
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.873-2858C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139883832 | ||||||
| chr5:139883910
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.873-2936G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139883910 | ||||||
| chr5:139883970
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.873-2996C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139883970 | ||||||
| chr5:139884136
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.873-3162C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884136 | ||||||
| chr5:139884237
|
G | A | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.872+3103C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884237 | ||||||
| chr5:139884284
|
G | C | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.872+3056C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884284 | ||||||
| chr5:139884314
|
C | G | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.872+3026G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884314 | ||||||
| chr5:139884402
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+2938C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884402 | ||||||
| chr5:139884519
|
G | C | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.872+2821C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884519 | ||||||
| chr5:139884854
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.872+2486C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884854 | ||||||
| chr5:139884930
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.872+2410G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884930 | ||||||
| chr5:139884968
|
A | T | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.872+2372T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139884968 | ||||||
| chr5:139885352
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0158 | 2 | HG00741.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.872+1988G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139885352 | ||||||
| chr5:139885513
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1827C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139885513 | ||||||
| chr5:139885545
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.872+1795C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139885545 | ||||||
| chr5:139885743
|
G | A | 2 | a0003c0003t0001g0002a0003c0003t0001g0177 | 3 | HG03490.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.872+1597C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139885743 | ||||||
| chr5:139885755
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.872+1585C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139885755 | ||||||
| chr5:139885908
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0088 | 2 | NA18948.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.872+1432G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139885908 | ||||||
| chr5:139886002
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.872+1338C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139886002 | ||||||
| chr5:139886173
|
C | G | 1 | a0002c0002t0002g0160 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.872+1167G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139886173 | ||||||
| chr5:139886348
|
C | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.872+992G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139886348 | ||||||
| chr5:139886928
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.872+412A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139886928 | ||||||
| chr5:139887137
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.872+203G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 2/9 | chr5 | 139887137 | ||||||
| chr5:139887541
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.701-30G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139887541 | ||||||
| chr5:139887738
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.701-227G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139887738 | ||||||
| chr5:139887843
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.701-332C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139887843 | ||||||
| chr5:139888115
|
A | AAAACACA others(5): Show |
5 | a0002c0002t0001g0017a0002c0002t0001g0085a0002c0002t0002g0171others(2): Show | 5 | HG01934.hp2 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-605_701-604ins others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888115 | ||||||
| chr5:139888115
|
A | AAAACACA others(7): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0131 | 2 | HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.701-605_701-604ins others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888115 | ||||||
| chr5:139888115
|
A | AAAACACA others(9): Show |
1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-605_701-604ins others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888115 | ||||||
| chr5:139888115
|
A | AAC | 15 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0065others(12): Show | 15 | HG01109.hp2 HG01433.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-606_701-605dup others(2): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888115 | ||||||
| chr5:139888168
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.701-657C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888168 | ||||||
| chr5:139888280
|
C | T | 18 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0116others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.701-769G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888280 | ||||||
| chr5:139888325
|
A | T | 1 | a0002c0002t0002g0160 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.701-814T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888325 | ||||||
| chr5:139888649
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0024a0002c0002t0005g0050 | 3 | HG03453.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.701-1138T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888649 | ||||||
| chr5:139888680
|
G | A | 33 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0047others(30): Show | 33 | HG00609.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.701-1169C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888680 | ||||||
| chr5:139888717
|
A | G | 16 | a0001c0001t0001g0024a0001c0001t0001g0086a0001c0001t0001g0107others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.701-1206T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888717 | ||||||
| chr5:139888810
|
CAG | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0144others(5): Show | 9 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-1301_701-1300d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139888810 | ||||||
| chr5:139889007
|
C | A | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-1496G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889007 | ||||||
| chr5:139889070
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.701-1559C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889070 | ||||||
| chr5:139889272
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.701-1761A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889272 | ||||||
| chr5:139889277
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0130others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-1766C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889277 | ||||||
| chr5:139889393
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-1882A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889393 | ||||||
| chr5:139889577
|
T | C | 1 | a0007c0012t0001g0121 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.701-2066A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889577 | ||||||
| chr5:139889731
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.701-2220C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889731 | ||||||
| chr5:139889976
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.701-2465A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139889976 | ||||||
| chr5:139890172
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-2661T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890172 | ||||||
| chr5:139890414
|
T | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-2903A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890414 | ||||||
| chr5:139890473
|
CT | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.701-2963delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890473 | ||||||
| chr5:139890473
|
CTT | C | 9 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0131others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-2964_701-2963d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890473 | ||||||
| chr5:139890473
|
CTTT | C | 37 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(34): Show | 38 | HG00280.hp1 HG00609.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.701-2965_701-2963d others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890473 | ||||||
| chr5:139890478
|
T | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0129others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-2967A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890478 | ||||||
| chr5:139890479
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0131 | 2 | HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.701-2968A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890479 | ||||||
| chr5:139890620
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.701-3109G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890620 | ||||||
| chr5:139890736
|
A | G | 1 | a0001c0001t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.701-3225T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139890736 | ||||||
| chr5:139891035
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(57): Show | 61 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.701-3524A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891035 | ||||||
| chr5:139891137
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.701-3626G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891137 | ||||||
| chr5:139891144
|
C | A | 60 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(57): Show | 61 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.701-3633G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891144 | ||||||
| chr5:139891270
|
G | A | 48 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(45): Show | 49 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.701-3759C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891270 | ||||||
| chr5:139891333
|
A | C | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-3822T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891333 | ||||||
| chr5:139891347
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.701-3836G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891347 | ||||||
| chr5:139891494
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-3983G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891494 | ||||||
| chr5:139891629
|
T | TA | 33 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0022others(30): Show | 33 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.701-4119dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891629 | ||||||
| chr5:139891629
|
T | TAA | 19 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0054others(16): Show | 20 | HG00280.hp1 HG00544.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.701-4120_701-4119d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891629 | ||||||
| chr5:139891980
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-4469T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139891980 | ||||||
| chr5:139892786
|
C | T | 1 | a0001c0010t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.701-5275G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139892786 | ||||||
| chr5:139892981
|
CAA | C | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-5472_701-5471d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139892981 | ||||||
| chr5:139893259
|
A | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(51): Show | 55 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.701-5748T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893259 | ||||||
| chr5:139893330
|
G | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0108others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.701-5819C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893330 | ||||||
| chr5:139893562
|
G | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-6051C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893562 | ||||||
| chr5:139893626
|
G | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0130others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-6115C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893626 | ||||||
| chr5:139893707
|
A | AG | 60 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(57): Show | 61 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.701-6197_701-6196i others(3): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893707 | ||||||
| chr5:139893710
|
C | T | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-6199G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893710 | ||||||
| chr5:139893721
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.701-6210C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893721 | ||||||
| chr5:139893773
|
G | T | 2 | a0003c0003t0001g0002a0003c0003t0001g0177 | 3 | HG03490.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.701-6262C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893773 | ||||||
| chr5:139893828
|
A | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(46): Show | 50 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.701-6317T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893828 | ||||||
| chr5:139893851
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-6340G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893851 | ||||||
| chr5:139893964
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0088a0001c0001t0001g0090 | 3 | HG00408.hp2 HG00673.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.701-6453A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139893964 | ||||||
| chr5:139894066
|
GCC | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0108others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.701-6557_701-6556d others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894066 | ||||||
| chr5:139894242
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.701-6731T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894242 | ||||||
| chr5:139894363
|
C | T | 1 | a0005c0016t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.701-6852G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894363 | ||||||
| chr5:139894456
|
GA | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(53): Show | 57 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.701-6946delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894456 | ||||||
| chr5:139894468
|
A | C | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-6957T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894468 | ||||||
| chr5:139894729
|
C | T | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-7218G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894729 | ||||||
| chr5:139894774
|
G | A | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-7263C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894774 | ||||||
| chr5:139894774
|
G | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0131a0002c0002t0002g0171others(2): Show | 5 | HG02280.hp2 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-7263C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894774 | ||||||
| chr5:139894812
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.701-7301C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894812 | ||||||
| chr5:139894930
|
A | G | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-7419T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139894930 | ||||||
| chr5:139895208
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.701-7697C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895208 | ||||||
| chr5:139895290
|
G | A | 3 | a0002c0002t0002g0171a0004c0006t0001g0122a0004c0006t0001g0159 | 3 | HG03579.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.701-7779C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895290 | ||||||
| chr5:139895296
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.701-7785C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895296 | ||||||
| chr5:139895334
|
C | T | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-7823G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895334 | ||||||
| chr5:139895509
|
G | A | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-7998C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895509 | ||||||
| chr5:139895517
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.701-8006G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895517 | ||||||
| chr5:139895848
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.701-8337G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895848 | ||||||
| chr5:139895878
|
T | C | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-8367A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895878 | ||||||
| chr5:139895921
|
G | A | 15 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0054others(12): Show | 15 | HG00280.hp1 HG00544.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-8410C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139895921 | ||||||
| chr5:139896122
|
ACTGGCTT | A | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-8618_701-8612d others(9): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139896122 | ||||||
| chr5:139896441
|
C | T | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-8930G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139896441 | ||||||
| chr5:139896464
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.701-8953G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139896464 | ||||||
| chr5:139896464
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-8953G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139896464 | ||||||
| chr5:139896777
|
C | G | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701-9266G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139896777 | ||||||
| chr5:139896845
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-9334T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139896845 | ||||||
| chr5:139896907
|
C | T | 40 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(37): Show | 41 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.701-9396G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139896907 | ||||||
| chr5:139897062
|
T | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(43): Show | 47 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.701-9551A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897062 | ||||||
| chr5:139897079
|
G | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(36): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-9568C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897079 | ||||||
| chr5:139897163
|
A | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(88): Show | 92 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.701-9652T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897163 | ||||||
| chr5:139897173
|
T | A | 4 | a0001c0005t0004g0048a0001c0005t0004g0151a0001c0005t0004g0156others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-9662A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897173 | ||||||
| chr5:139897179
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0088a0001c0001t0001g0090 | 3 | HG00408.hp2 HG00673.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.701-9668C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897179 | ||||||
| chr5:139897278
|
G | A | 54 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(51): Show | 55 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.701-9767C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897278 | ||||||
| chr5:139897373
|
C | T | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-9862G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897373 | ||||||
| chr5:139897548
|
G | T | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-10037C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897548 | ||||||
| chr5:139897704
|
C | G | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701-10193G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897704 | ||||||
| chr5:139897725
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.701-10214A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897725 | ||||||
| chr5:139897833
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0131 | 2 | HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.701-10322T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897833 | ||||||
| chr5:139897940
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0110 | 3 | HG00642.hp2 HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.701-10429G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139897940 | ||||||
| chr5:139898113
|
G | A | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-10602C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139898113 | ||||||
| chr5:139898259
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.701-10748G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139898259 | ||||||
| chr5:139898260
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0131a0002c0002t0002g0171others(2): Show | 5 | HG02280.hp2 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-10749C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139898260 | ||||||
| chr5:139898309
|
G | A | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-10798C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139898309 | ||||||
| chr5:139898514
|
C | T | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-11003G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139898514 | ||||||
| chr5:139898723
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0130others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-11212C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139898723 | ||||||
| chr5:139899012
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0139 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.701-11501G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899012 | ||||||
| chr5:139899076
|
C | T | 1 | a0001c0010t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.701-11565G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899076 | ||||||
| chr5:139899276
|
AG | A | 5 | a0001c0001t0001g0107a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-11766delC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899276 | ||||||
| chr5:139899277
|
G | T | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-11766C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899277 | ||||||
| chr5:139899370
|
C | G | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-11859G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899370 | ||||||
| chr5:139899418
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.701-11907G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899418 | ||||||
| chr5:139899874
|
A | G | 55 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.701-12363T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899874 | ||||||
| chr5:139899881
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0004t0001g0184others(3): Show | 6 | HG02280.hp2 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-12370C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139899881 | ||||||
| chr5:139900136
|
A | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-12625T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900136 | ||||||
| chr5:139900528
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0153others(2): Show | 5 | HG01496.hp2 HG01943.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-13017C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900528 | ||||||
| chr5:139900583
|
G | GT | 5 | a0001c0001t0001g0107a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-13073dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900583 | ||||||
| chr5:139900693
|
A | G | 3 | a0001c0001t0001g0008a0002c0002t0002g0100a0002c0002t0009g0101 | 3 | HG01884.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-13182T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900693 | ||||||
| chr5:139900698
|
C | T | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-13187G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900698 | ||||||
| chr5:139900765
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-13254C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900765 | ||||||
| chr5:139900887
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.701-13376G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900887 | ||||||
| chr5:139900956
|
A | G | 8 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0004t0001g0184others(5): Show | 8 | HG02280.hp2 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-13445T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900956 | ||||||
| chr5:139900973
|
G | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.701-13462C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139900973 | ||||||
| chr5:139901040
|
C | T | 1 | a0008c0011t0001g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.701-13529G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139901040 | ||||||
| chr5:139901100
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.701-13589G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139901100 | ||||||
| chr5:139901146
|
G | A | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-13635C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139901146 | ||||||
| chr5:139901177
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(1): Show | 4 | HG01099.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-13666C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139901177 | ||||||
| chr5:139901203
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-13692G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139901203 | ||||||
| chr5:139901507
|
C | G | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-13996G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139901507 | ||||||
| chr5:139901902
|
C | T | 1 | a0002c0002t0003g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.701-14391G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139901902 | ||||||
| chr5:139902301
|
C | T | 8 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0004t0001g0184others(5): Show | 8 | HG02280.hp2 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-14790G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139902301 | ||||||
| chr5:139902378
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.701-14867T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139902378 | ||||||
| chr5:139902501
|
C | G | 46 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0020others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.701-14990G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139902501 | ||||||
| chr5:139902824
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.701-15313G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139902824 | ||||||
| chr5:139902891
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-15380C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139902891 | ||||||
| chr5:139902962
|
T | C | 8 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0004t0001g0184others(5): Show | 8 | HG02280.hp2 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-15451A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139902962 | ||||||
| chr5:139903142
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-15631G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139903142 | ||||||
| chr5:139903145
|
C | CA | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.701-15635dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139903145 | ||||||
| chr5:139903282
|
C | T | 61 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(58): Show | 62 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.701-15771G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139903282 | ||||||
| chr5:139903431
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.701-15920G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139903431 | ||||||
| chr5:139903721
|
C | G | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-16210G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139903721 | ||||||
| chr5:139903799
|
C | T | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-16288G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139903799 | ||||||
| chr5:139903925
|
C | A | 2 | a0001c0001t0001g0004a0002c0002t0005g0050 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.701-16414G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139903925 | ||||||
| chr5:139904023
|
C | T | 1 | a0001c0004t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.701-16512G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139904023 | ||||||
| chr5:139904162
|
A | G | 8 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0004t0001g0184others(5): Show | 8 | HG02280.hp2 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-16651T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139904162 | ||||||
| chr5:139904237
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0004t0001g0184 | 3 | HG02280.hp2 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.701-16726C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139904237 | ||||||
| chr5:139904412
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701-16901G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139904412 | ||||||
| chr5:139904570
|
G | T | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-17059C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139904570 | ||||||
| chr5:139904589
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-17078C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139904589 | ||||||
| chr5:139905167
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.701-17656A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905167 | ||||||
| chr5:139905607
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.701-18096C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905607 | ||||||
| chr5:139905631
|
G | A | 43 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(40): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-18120C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905631 | ||||||
| chr5:139905656
|
G | A | 38 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-18145C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905656 | ||||||
| chr5:139905683
|
TG | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(16): Show | 20 | HG01074.hp1 HG01081.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.701-18173delC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905683 | ||||||
| chr5:139905686
|
G | C | 1 | a0004c0006t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.701-18175C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905686 | ||||||
| chr5:139905687
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.701-18176C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905687 | ||||||
| chr5:139905896
|
T | TG | 38 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-18386dupC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139905896 | ||||||
| chr5:139906018
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-18507G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906018 | ||||||
| chr5:139906297
|
C | T | 38 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-18786G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906297 | ||||||
| chr5:139906395
|
C | G | 2 | a0001c0001t0001g0107a0008c0011t0001g0106 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-18884G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906395 | ||||||
| chr5:139906451
|
CACTTT | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0002t0003g0082others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-18945_701-1894 others(9): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906451 | ||||||
| chr5:139906500
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(7): Show | 10 | HG01099.hp2 HG02280.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-18989A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906500 | ||||||
| chr5:139906726
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.701-19215T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906726 | ||||||
| chr5:139906792
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0002t0003g0082others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-19281G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906792 | ||||||
| chr5:139906828
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-19317G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139906828 | ||||||
| chr5:139907081
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.701-19570C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907081 | ||||||
| chr5:139907151
|
C | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0015others(60): Show | 64 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.701-19640G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907151 | ||||||
| chr5:139907315
|
C | T | 2 | a0001c0001t0001g0107a0008c0011t0001g0106 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-19804G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907315 | ||||||
| chr5:139907424
|
G | C | 1 | a0001c0001t0010g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.701-19913C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907424 | ||||||
| chr5:139907678
|
G | A | 2 | a0001c0001t0001g0107a0008c0011t0001g0106 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-20167C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907678 | ||||||
| chr5:139907772
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0107a0002c0002t0009g0101others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-20261A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907772 | ||||||
| chr5:139907776
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-20265C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907776 | ||||||
| chr5:139907795
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.701-20284A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907795 | ||||||
| chr5:139907803
|
G | A | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.701-20292C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907803 | ||||||
| chr5:139907855
|
C | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(7): Show | 10 | HG01099.hp2 HG02280.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-20344G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907855 | ||||||
| chr5:139907901
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-20390C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907901 | ||||||
| chr5:139907920
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-20409G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907920 | ||||||
| chr5:139907964
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-20453G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907964 | ||||||
| chr5:139907991
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(7): Show | 10 | HG01099.hp2 HG02280.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-20480C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139907991 | ||||||
| chr5:139908049
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(11): Show | 14 | HG01099.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.701-20538T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908049 | ||||||
| chr5:139908050
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(12): Show | 15 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-20539G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908050 | ||||||
| chr5:139908109
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-20598G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908109 | ||||||
| chr5:139908138
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(11): Show | 14 | HG01099.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.701-20627A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908138 | ||||||
| chr5:139908412
|
G | T | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-20901C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908412 | ||||||
| chr5:139908443
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(12): Show | 15 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-20932C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908443 | ||||||
| chr5:139908742
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(12): Show | 15 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-21231A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908742 | ||||||
| chr5:139908744
|
G | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(12): Show | 15 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-21233C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908744 | ||||||
| chr5:139908798
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(7): Show | 10 | HG01099.hp2 HG02280.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-21287A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908798 | ||||||
| chr5:139908814
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-21303C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139908814 | ||||||
| chr5:139909119
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG00544.hp2 NA18747.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.701-21608C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139909119 | ||||||
| chr5:139909444
|
G | T | 2 | a0001c0001t0001g0107a0008c0011t0001g0106 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-21933C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139909444 | ||||||
| chr5:139909492
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.701-21981T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139909492 | ||||||
| chr5:139909525
|
T | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(15): Show | 18 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.701-22014A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139909525 | ||||||
| chr5:139909571
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701-22060C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139909571 | ||||||
| chr5:139909634
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(9): Show | 12 | HG01099.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.701-22123G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139909634 | ||||||
| chr5:139909946
|
G | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(16): Show | 19 | HG00738.hp1 HG01099.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-22435C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139909946 | ||||||
| chr5:139910154
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-22643T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139910154 | ||||||
| chr5:139910469
|
C | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(36): Show | 39 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-22958G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139910469 | ||||||
| chr5:139910491
|
C | T | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-22980G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139910491 | ||||||
| chr5:139910631
|
A | C | 41 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(38): Show | 42 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.701-23120T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139910631 | ||||||
| chr5:139910647
|
T | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0015others(60): Show | 64 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.701-23136A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139910647 | ||||||
| chr5:139910658
|
T | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-23147A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139910658 | ||||||
| chr5:139910969
|
G | A | 38 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0022others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-23458C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139910969 | ||||||
| chr5:139911221
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.701-23710G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139911221 | ||||||
| chr5:139911465
|
GC | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(7): Show | 10 | HG01099.hp2 HG02280.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-23955delG | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139911465 | ||||||
| chr5:139911604
|
G | A | 3 | a0002c0002t0001g0017a0002c0002t0003g0170a0002c0002t0005g0138 | 3 | HG02572.hp2 HG02895.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.701-24093C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139911604 | ||||||
| chr5:139911607
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.701-24096C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139911607 | ||||||
| chr5:139911656
|
A | G | 64 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0015others(61): Show | 65 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.701-24145T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139911656 | ||||||
| chr5:139911822
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0015others(55): Show | 58 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.701-24311C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139911822 | ||||||
| chr5:139911933
|
T | C | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-24422A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139911933 | ||||||
| chr5:139912006
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-24495G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139912006 | ||||||
| chr5:139912289
|
A | AG | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.701-24779dupC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139912289 | ||||||
| chr5:139912597
|
C | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-25086G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139912597 | ||||||
| chr5:139912832
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.701-25321C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139912832 | ||||||
| chr5:139913101
|
A | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0015others(62): Show | 66 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.701-25590T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139913101 | ||||||
| chr5:139913273
|
G | A | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.701-25762C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139913273 | ||||||
| chr5:139913562
|
C | T | 1 | a0005c0016t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.701-26051G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139913562 | ||||||
| chr5:139913581
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0015others(34): Show | 37 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.701-26070C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139913581 | ||||||
| chr5:139913592
|
C | T | 3 | a0002c0002t0002g0001a0002c0002t0003g0082a0002c0002t0009g0101 | 4 | HG03491.hp1 HG03492.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-26081G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139913592 | ||||||
| chr5:139913861
|
T | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-26350A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139913861 | ||||||
| chr5:139913989
|
C | CA | 9 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0129others(6): Show | 10 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-26479dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139913989 | ||||||
| chr5:139914182
|
T | C | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-26671A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139914182 | ||||||
| chr5:139914253
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0100 | 3 | HG02809.hp2 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.701-26742C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139914253 | ||||||
| chr5:139914555
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.701-27044G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139914555 | ||||||
| chr5:139914831
|
G | C | 1 | a0001c0005t0004g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.701-27320C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139914831 | ||||||
| chr5:139914915
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0165 | 2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.701-27404G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139914915 | ||||||
| chr5:139915024
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0157others(1): Show | 4 | HG00642.hp1 HG01257.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-27513G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139915024 | ||||||
| chr5:139915092
|
G | A | 45 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0025others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.701-27581C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139915092 | ||||||
| chr5:139915244
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0108a0001c0001t0001g0131others(7): Show | 10 | HG02280.hp2 HG02886.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-27733T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139915244 | ||||||
| chr5:139915544
|
A | C | 8 | a0001c0001t0001g0023a0002c0002t0001g0017a0002c0002t0002g0171others(5): Show | 8 | HG02572.hp2 HG02895.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-28033T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139915544 | ||||||
| chr5:139915676
|
A | G | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-28165T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139915676 | ||||||
| chr5:139916061
|
A | G | 54 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(51): Show | 55 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.701-28550T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916061 | ||||||
| chr5:139916070
|
A | G | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-28559T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916070 | ||||||
| chr5:139916136
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0056a0001c0001t0001g0058others(9): Show | 12 | HG00609.hp1 HG01071.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.701-28625C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916136 | ||||||
| chr5:139916153
|
T | C | 11 | a0001c0001t0001g0023a0001c0001t0001g0168a0002c0002t0001g0017others(8): Show | 11 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.701-28642A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916153 | ||||||
| chr5:139916182
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.701-28671G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916182 | ||||||
| chr5:139916190
|
C | T | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-28679G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916190 | ||||||
| chr5:139916236
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0137others(6): Show | 9 | HG00741.hp2 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-28725C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916236 | ||||||
| chr5:139916280
|
C | T | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-28769G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916280 | ||||||
| chr5:139916312
|
A | C | 11 | a0001c0001t0001g0023a0001c0001t0001g0168a0002c0002t0001g0017others(8): Show | 11 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.701-28801T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916312 | ||||||
| chr5:139916468
|
ACTGTGCA others(172): Show |
A | 1 | a0001c0001t0001g0136 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.701-29136_701-2895 others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916468 | ||||||
| chr5:139916585
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.701-29074A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916585 | ||||||
| chr5:139916621
|
A | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-29110T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916621 | ||||||
| chr5:139916989
|
C | A | 1 | a0001c0005t0004g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.701-29478G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139916989 | ||||||
| chr5:139917053
|
G | A | 7 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(4): Show | 7 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-29542C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917053 | ||||||
| chr5:139917108
|
TC | T | 7 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(4): Show | 7 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-29598delG | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917108 | ||||||
| chr5:139917202
|
T | C | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-29691A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917202 | ||||||
| chr5:139917254
|
T | A | 4 | a0001c0001t0001g0005a0001c0005t0004g0048a0001c0005t0004g0151others(1): Show | 4 | HG02572.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-29743A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917254 | ||||||
| chr5:139917336
|
T | C | 7 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(4): Show | 7 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-29825A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917336 | ||||||
| chr5:139917345
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.701-29834C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917345 | ||||||
| chr5:139917354
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | NA18942.hp1 NA18983.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.701-29843G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917354 | ||||||
| chr5:139917377
|
G | A | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-29866C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917377 | ||||||
| chr5:139917642
|
G | A | 7 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(4): Show | 7 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-30131C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139917642 | ||||||
| chr5:139918071
|
C | T | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-30560G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918071 | ||||||
| chr5:139918092
|
G | A | 6 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(3): Show | 6 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-30581C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918092 | ||||||
| chr5:139918473
|
C | A | 6 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(3): Show | 6 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-30962G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918473 | ||||||
| chr5:139918489
|
G | A | 2 | a0001c0001t0001g0105a0008c0011t0001g0106 | 2 | HG03225.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.701-30978C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918489 | ||||||
| chr5:139918610
|
G | A | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-31099C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918610 | ||||||
| chr5:139918933
|
C | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-31422G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918933 | ||||||
| chr5:139918938
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-31427C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918938 | ||||||
| chr5:139918973
|
A | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-31462T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139918973 | ||||||
| chr5:139919114
|
G | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0129others(5): Show | 8 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-31603C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919114 | ||||||
| chr5:139919299
|
T | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-31788A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919299 | ||||||
| chr5:139919332
|
C | T | 8 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0129others(5): Show | 8 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-31821G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919332 | ||||||
| chr5:139919766
|
G | A | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-32255C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919766 | ||||||
| chr5:139919800
|
T | C | 1 | a0002c0002t0005g0141 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.701-32289A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919800 | ||||||
| chr5:139919886
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701-32375G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919886 | ||||||
| chr5:139919911
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.701-32400C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919911 | ||||||
| chr5:139919928
|
T | A | 7 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(4): Show | 7 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-32417A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139919928 | ||||||
| chr5:139920143
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-32632C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139920143 | ||||||
| chr5:139920302
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0089 | 2 | HG01978.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.701-32791C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139920302 | ||||||
| chr5:139920322
|
A | G | 12 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0042others(9): Show | 12 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.701-32811T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139920322 | ||||||
| chr5:139920360
|
G | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(34): Show | 37 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.701-32849C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139920360 | ||||||
| chr5:139920724
|
C | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-33213G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139920724 | ||||||
| chr5:139920844
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.701-33333T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139920844 | ||||||
| chr5:139921031
|
A | G | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-33520T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921031 | ||||||
| chr5:139921204
|
C | T | 54 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(51): Show | 55 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.701-33693G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921204 | ||||||
| chr5:139921355
|
G | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-33844C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921355 | ||||||
| chr5:139921418
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.701-33907G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921418 | ||||||
| chr5:139921616
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.701-34105A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921616 | ||||||
| chr5:139921621
|
G | C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-34110C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921621 | ||||||
| chr5:139921787
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0164 | 3 | HG01255.hp1 HG01261.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.701-34276G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921787 | ||||||
| chr5:139921903
|
A | G | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-34392T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139921903 | ||||||
| chr5:139922070
|
CA | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-34560delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139922070 | ||||||
| chr5:139922070
|
CAA | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0056others(3): Show | 6 | HG01361.hp1 HG02970.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-34561_701-3456 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139922070 | ||||||
| chr5:139922070
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(3): Show | 6 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-34567_701-3456 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139922070 | ||||||
| chr5:139922115
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.701-34604C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139922115 | ||||||
| chr5:139923332
|
T | A | 6 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(3): Show | 6 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-35821A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139923332 | ||||||
| chr5:139923756
|
T | C | 48 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(45): Show | 49 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.701-36245A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139923756 | ||||||
| chr5:139923805
|
C | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-36294G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139923805 | ||||||
| chr5:139923959
|
T | TAGAAAGA others(315): Show |
4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-36449_701-3644 others(326): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139923959 | ||||||
| chr5:139924238
|
T | C | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-36727A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139924238 | ||||||
| chr5:139924502
|
T | A | 3 | a0002c0002t0001g0017a0002c0002t0003g0170a0002c0002t0005g0138 | 3 | HG02572.hp2 HG02895.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.701-36991A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139924502 | ||||||
| chr5:139924604
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-37093C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139924604 | ||||||
| chr5:139924729
|
G | A | 1 | a0002c0002t0003g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.701-37218C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139924729 | ||||||
| chr5:139924821
|
C | T | 2 | a0003c0003t0001g0002a0003c0003t0001g0177 | 3 | HG03490.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.701-37310G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139924821 | ||||||
| chr5:139925631
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0070 | 2 | NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.701-38120C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139925631 | ||||||
| chr5:139926000
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.701-38489G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139926000 | ||||||
| chr5:139926480
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.701-38969G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139926480 | ||||||
| chr5:139926481
|
G | A | 5 | a0001c0001t0001g0172a0002c0002t0002g0171a0002c0002t0003g0173others(2): Show | 5 | HG03225.hp2 HG03453.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-38970C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139926481 | ||||||
| chr5:139926734
|
A | G | 1 | a0001c0004t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.701-39223T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139926734 | ||||||
| chr5:139926787
|
T | G | 5 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(2): Show | 5 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-39276A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139926787 | ||||||
| chr5:139926853
|
G | C | 5 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(2): Show | 5 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-39342C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139926853 | ||||||
| chr5:139927027
|
A | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-39516T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927027 | ||||||
| chr5:139927186
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-39675A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927186 | ||||||
| chr5:139927242
|
G | C | 1 | a0001c0014t0001g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.701-39731C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927242 | ||||||
| chr5:139927539
|
G | A | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.701-40028C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927539 | ||||||
| chr5:139927547
|
T | C | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-40036A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927547 | ||||||
| chr5:139927593
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-40082C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927593 | ||||||
| chr5:139927674
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.701-40163C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927674 | ||||||
| chr5:139927700
|
G | A | 39 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(36): Show | 39 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-40189C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927700 | ||||||
| chr5:139927745
|
C | A | 11 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0123others(8): Show | 12 | HG01934.hp2 HG02145.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.701-40234G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927745 | ||||||
| chr5:139927764
|
CA | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0031others(15): Show | 18 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.701-40254delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927764 | ||||||
| chr5:139927764
|
CAA | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(43): Show | 47 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.701-40255_701-4025 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927764 | ||||||
| chr5:139927804
|
AC | A | 4 | a0001c0001t0001g0023a0002c0002t0002g0171a0004c0006t0001g0122others(1): Show | 4 | HG02976.hp2 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-40294delG | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927804 | ||||||
| chr5:139927857
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0107a0008c0011t0001g0106 | 3 | HG01884.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-40346T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927857 | ||||||
| chr5:139927904
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.701-40393G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139927904 | ||||||
| chr5:139928441
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.701-40930G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139928441 | ||||||
| chr5:139928484
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.701-40973A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139928484 | ||||||
| chr5:139928520
|
G | T | 43 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(40): Show | 43 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.701-41009C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139928520 | ||||||
| chr5:139928649
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-41138G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139928649 | ||||||
| chr5:139928660
|
G | A | 2 | a0001c0001t0001g0026a0001c0004t0001g0182 | 2 | HG00323.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.701-41149C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139928660 | ||||||
| chr5:139929135
|
G | A | 43 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(40): Show | 43 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.701-41624C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139929135 | ||||||
| chr5:139929403
|
G | A | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-41892C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139929403 | ||||||
| chr5:139929706
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701-42195C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139929706 | ||||||
| chr5:139929933
|
A | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-42422T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139929933 | ||||||
| chr5:139929979
|
T | C | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-42468A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139929979 | ||||||
| chr5:139930018
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.701-42507G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930018 | ||||||
| chr5:139930089
|
G | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-42578C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930089 | ||||||
| chr5:139930281
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.701-42770G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930281 | ||||||
| chr5:139930431
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.701-42920C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930431 | ||||||
| chr5:139930440
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0115 | 2 | NA18974.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.701-42929C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930440 | ||||||
| chr5:139930533
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.701-43022C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930533 | ||||||
| chr5:139930841
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.701-43330G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930841 | ||||||
| chr5:139930879
|
A | T | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-43368T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930879 | ||||||
| chr5:139930930
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.701-43419C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139930930 | ||||||
| chr5:139931246
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-43735A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139931246 | ||||||
| chr5:139931503
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.701-43992G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139931503 | ||||||
| chr5:139931774
|
A | G | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-44263T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139931774 | ||||||
| chr5:139931789
|
T | C | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.701-44278A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139931789 | ||||||
| chr5:139931890
|
A | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-44379T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139931890 | ||||||
| chr5:139931974
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.701-44463A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139931974 | ||||||
| chr5:139932003
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-44492G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932003 | ||||||
| chr5:139932143
|
T | C | 55 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.701-44632A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932143 | ||||||
| chr5:139932181
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-44670A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932181 | ||||||
| chr5:139932221
|
A | AGT | 13 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0039others(10): Show | 14 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.701-44712_701-4471 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932221 | ||||||
| chr5:139932221
|
A | AGTGT | 5 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0042others(2): Show | 5 | HG00642.hp1 HG01109.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-44714_701-4471 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932221 | ||||||
| chr5:139932221
|
AGT | A | 19 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0051others(16): Show | 19 | HG00408.hp2 HG00673.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-44712_701-4471 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932221 | ||||||
| chr5:139932221
|
AGTGT | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(24): Show | 28 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.701-44714_701-4471 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932221 | ||||||
| chr5:139932221
|
AGTGTGT | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0086others(3): Show | 6 | HG01099.hp2 HG02145.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-44716_701-4471 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932221 | ||||||
| chr5:139932260
|
G | A | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-44749C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932260 | ||||||
| chr5:139932260
|
G | GTGTA | 11 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0056others(8): Show | 11 | HG01978.hp2 HG02280.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.701-44750_701-4474 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932260 | ||||||
| chr5:139932260
|
G | GTGTGTA | 2 | a0001c0001t0001g0074a0001c0001t0007g0118 | 2 | NA19007.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.701-44750_701-4474 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932260 | ||||||
| chr5:139932260
|
G | GTGTGTGT others(5): Show |
1 | a0002c0002t0003g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.701-44750_701-4474 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932260 | ||||||
| chr5:139932260
|
G | GTGTGTGT others(7): Show |
2 | a0002c0002t0001g0017a0002c0002t0005g0138 | 2 | HG02895.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.701-44750_701-4474 others(18): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932260 | ||||||
| chr5:139932263
|
T | C | 17 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0056others(14): Show | 17 | HG01978.hp2 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.701-44752A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932263 | ||||||
| chr5:139932263
|
T | TAC | 27 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(24): Show | 27 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.701-44754_701-4475 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932263 | ||||||
| chr5:139932419
|
T | TA | 3 | a0001c0001t0007g0118a0002c0002t0003g0148a0002c0013t0003g0083 | 3 | HG02970.hp1 NA18522.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.701-44909_701-4490 others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932419 | ||||||
| chr5:139932420
|
T | A | 3 | a0001c0001t0007g0118a0002c0002t0003g0148a0002c0013t0003g0083 | 3 | HG02970.hp1 NA18522.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.701-44909A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932420 | ||||||
| chr5:139932420
|
T | TA | 34 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(31): Show | 34 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.701-44910_701-4490 others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932420 | ||||||
| chr5:139932421
|
T | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(38): Show | 42 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.701-44910A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932421 | ||||||
| chr5:139932421
|
T | TA | 6 | a0002c0002t0001g0017a0002c0002t0002g0100a0002c0002t0003g0082others(3): Show | 6 | HG02572.hp2 HG02895.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-44911dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139932421 | ||||||
| chr5:139933126
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-45615T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139933126 | ||||||
| chr5:139933269
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0107a0008c0011t0001g0106 | 3 | HG01884.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-45758G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139933269 | ||||||
| chr5:139933436
|
G | A | 55 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.701-45925C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139933436 | ||||||
| chr5:139934027
|
C | T | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.701-46516G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934027 | ||||||
| chr5:139934091
|
A | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(71): Show | 75 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.701-46580T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934091 | ||||||
| chr5:139934123
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-46612G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934123 | ||||||
| chr5:139934171
|
G | C | 55 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.701-46660C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934171 | ||||||
| chr5:139934279
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-46768T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934279 | ||||||
| chr5:139934421
|
T | C | 1 | a0001c0001t0003g0007 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.701-46910A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934421 | ||||||
| chr5:139934565
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-47054T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934565 | ||||||
| chr5:139934963
|
G | A | 2 | a0001c0001t0001g0153a0002c0002t0009g0101 | 2 | HG01993.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-47452C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139934963 | ||||||
| chr5:139935092
|
A | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-47581T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935092 | ||||||
| chr5:139935219
|
A | G | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-47708T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935219 | ||||||
| chr5:139935407
|
G | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-47896C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935407 | ||||||
| chr5:139935537
|
A | C | 1 | a0001c0001t0001g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.701-48026T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935537 | ||||||
| chr5:139935623
|
C | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0107a0008c0011t0001g0106 | 3 | HG01884.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-48112G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935623 | ||||||
| chr5:139935683
|
G | A | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-48172C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935683 | ||||||
| chr5:139935958
|
T | TA | 6 | a0001c0001t0001g0077a0002c0002t0001g0017a0002c0002t0003g0082others(3): Show | 6 | HG02572.hp2 HG02895.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-48448dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935958 | ||||||
| chr5:139935958
|
T | TAAA | 34 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(31): Show | 34 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.701-48450_701-4844 others(7): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935958 | ||||||
| chr5:139935958
|
TA | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0147others(5): Show | 8 | HG01255.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-48448delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935958 | ||||||
| chr5:139935976
|
G | A | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-48465C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139935976 | ||||||
| chr5:139936007
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.701-48496G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139936007 | ||||||
| chr5:139936194
|
T | C | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-48683A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139936194 | ||||||
| chr5:139936496
|
A | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-48985T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139936496 | ||||||
| chr5:139936796
|
A | T | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.701-49285T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139936796 | ||||||
| chr5:139936810
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701-49299T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139936810 | ||||||
| chr5:139936962
|
C | T | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701-49451G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139936962 | ||||||
| chr5:139937024
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-49513T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139937024 | ||||||
| chr5:139937345
|
G | A | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-49834C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139937345 | ||||||
| chr5:139937369
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-49858G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139937369 | ||||||
| chr5:139937916
|
G | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0123others(6): Show | 10 | HG01934.hp2 HG02145.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-50405C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139937916 | ||||||
| chr5:139938070
|
C | T | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-50559G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938070 | ||||||
| chr5:139938076
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.701-50565G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938076 | ||||||
| chr5:139938079
|
C | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-50568G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938079 | ||||||
| chr5:139938131
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.701-50620G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938131 | ||||||
| chr5:139938148
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-50637G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938148 | ||||||
| chr5:139938362
|
C | CT | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-50852dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938362 | ||||||
| chr5:139938460
|
A | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-50949T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938460 | ||||||
| chr5:139938538
|
A | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-51027T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938538 | ||||||
| chr5:139938834
|
T | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-51323A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938834 | ||||||
| chr5:139938850
|
A | AAG | 35 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0027others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.701-51341_701-5134 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938850 | ||||||
| chr5:139938850
|
A | AAGAG | 5 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0084others(2): Show | 5 | HG01943.hp2 HG02083.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-51343_701-5134 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938850 | ||||||
| chr5:139938850
|
AAG | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0107others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.701-51341_701-5134 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938850 | ||||||
| chr5:139938850
|
AAGAG | A | 7 | a0001c0001t0001g0108a0001c0001t0001g0129a0001c0001t0001g0140others(4): Show | 8 | HG02280.hp2 HG02886.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-51343_701-5134 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938850 | ||||||
| chr5:139938850
|
AAGAGAG | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0047others(23): Show | 26 | HG00280.hp1 HG00544.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.701-51345_701-5134 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938850 | ||||||
| chr5:139938850
|
AAGAGAGA others(1): Show |
A | 5 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0058others(2): Show | 5 | HG00609.hp1 HG02080.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-51347_701-5134 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938850 | ||||||
| chr5:139938872
|
GAGAGAGA others(22): Show |
G | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.701-51390_701-5136 others(33): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938872 | ||||||
| chr5:139938874
|
GAGAGAGA others(20): Show |
G | 4 | a0001c0001t0001g0074a0001c0001t0001g0105a0001c0001t0001g0114others(1): Show | 4 | NA18982.hp2 NA18988.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-51390_701-5136 others(31): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938874 | ||||||
| chr5:139938874
|
GAGAGAGA others(24): Show |
G | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.701-51394_701-5136 others(35): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938874 | ||||||
| chr5:139938875
|
A | AAG | 2 | a0001c0001t0001g0019a0001c0001t0001g0029 | 2 | HG01361.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.701-51365_701-5136 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938875 | ||||||
| chr5:139938877
|
AGAGAAGG others(12): Show |
A | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.701-51385_701-5136 others(23): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938877 | ||||||
| chr5:139938878
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0029a0005c0016t0001g0186 | 3 | HG01361.hp1 HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.701-51367C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938878 | ||||||
| chr5:139938878
|
GAGAAGGA others(22): Show |
G | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701-51396_701-5136 others(33): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938878 | ||||||
| chr5:139938879
|
A | G | 1 | a0005c0016t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.701-51368T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938879 | ||||||
| chr5:139938880
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.701-51369C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938880 | ||||||
| chr5:139938880
|
GAAGGAA | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0001g0116others(3): Show | 6 | HG01099.hp2 HG01255.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-51375_701-5137 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938880 | ||||||
| chr5:139938880
|
GAAGGAAA others(3): Show |
G | 6 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0128others(3): Show | 6 | HG00140.hp1 HG01167.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-51379_701-5137 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938880 | ||||||
| chr5:139938880
|
GAAGGAAA others(7): Show |
G | 2 | a0002c0002t0003g0038a0002c0002t0003g0169 | 2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.701-51383_701-5137 others(18): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938880 | ||||||
| chr5:139938881
|
A | AG | 7 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0078others(4): Show | 7 | HG00408.hp2 HG00673.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-51371_701-5137 others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938881 | ||||||
| chr5:139938881
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.701-51370T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938881 | ||||||
| chr5:139938881
|
AAG | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(21): Show | 25 | HG00408.hp1 HG00544.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.701-51372_701-5137 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938881 | ||||||
| chr5:139938882
|
A | G | 11 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0051others(8): Show | 11 | HG00642.hp2 HG00673.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.701-51371T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938882 | ||||||
| chr5:139938883
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(13): Show | 16 | HG00642.hp1 HG00642.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.701-51372C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938883 | ||||||
| chr5:139938883
|
G | GA | 8 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0078others(5): Show | 8 | HG00408.hp2 HG00673.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-51373_701-5137 others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938883 | ||||||
| chr5:139938886
|
A | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0097others(10): Show | 14 | HG00544.hp2 HG00642.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.701-51375T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938886 | ||||||
| chr5:139938887
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0031others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.701-51376T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938887 | ||||||
| chr5:139938888
|
GAAAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.701-51390_701-5137 others(17): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938888 | ||||||
| chr5:139938888
|
GAAAGAAA others(10): Show |
G | 12 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0091others(9): Show | 12 | HG00544.hp1 HG01074.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.701-51394_701-5137 others(21): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938888 | ||||||
| chr5:139938890
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0099a0003c0003t0001g0002 | 4 | HG01255.hp2 HG03490.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-51379T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938890 | ||||||
| chr5:139938891
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0086a0001c0001t0001g0097others(11): Show | 14 | HG00544.hp2 HG01081.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.701-51380T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938891 | ||||||
| chr5:139938892
|
GAAAGAAA others(6): Show |
G | 12 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0064others(9): Show | 12 | HG01071.hp2 HG01109.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.701-51394_701-5138 others(17): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938892 | ||||||
| chr5:139938894
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0128 | 2 | HG00140.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.701-51383T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938894 | ||||||
| chr5:139938895
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0046others(4): Show | 8 | HG01167.hp2 HG01255.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-51384T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938895 | ||||||
| chr5:139938896
|
GAAAGAAA others(2): Show |
G | 16 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0080others(13): Show | 17 | HG00609.hp1 HG01433.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.701-51394_701-5138 others(13): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938896 | ||||||
| chr5:139938898
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.701-51387T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938898 | ||||||
| chr5:139938899
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0128a0002c0002t0003g0038others(1): Show | 4 | HG00140.hp1 HG03491.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-51388T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938899 | ||||||
| chr5:139938900
|
GAAAGA | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(10): Show | 13 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.701-51394_701-5139 others(9): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938900 | ||||||
| chr5:139938904
|
G | A | 1 | a0002c0007t0003g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.701-51393C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938904 | ||||||
| chr5:139938904
|
GA | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 59 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.701-51394delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938904 | ||||||
| chr5:139938905
|
A | AAAAG | 12 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0036others(9): Show | 12 | HG00323.hp2 HG00621.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.701-51398_701-5139 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
A | AAAAGAAA others(1): Show |
5 | a0001c0001t0001g0065a0001c0001t0001g0126a0001c0001t0001g0139others(2): Show | 5 | HG00140.hp2 HG01943.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-51402_701-5139 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
A | AAAAGAAA others(5): Show |
2 | a0001c0001t0001g0149a0002c0002t0002g0075 | 2 | NA18977.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.701-51406_701-5139 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
A | AAAAGAAA others(13): Show |
1 | a0006c0008t0001g0176 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.701-51414_701-5139 others(24): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
A | AAAGAAAG others(4): Show |
1 | a0005c0016t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.701-51395_701-5139 others(15): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0074a0001c0001t0001g0096others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-51394T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
AAAAG | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0067others(2): Show | 5 | HG00280.hp2 HG00609.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-51398_701-5139 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
AAAAGAAA others(1): Show |
A | 8 | a0001c0001t0001g0035a0001c0001t0001g0060a0001c0001t0001g0076others(5): Show | 8 | HG01071.hp1 HG01361.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-51402_701-5139 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
AAAAGAAA others(5): Show |
A | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.701-51406_701-5139 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938905
|
AAAAGAAA others(17): Show |
A | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.701-51418_701-5139 others(28): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938905 | ||||||
| chr5:139938908
|
A | G | 11 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0061others(8): Show | 11 | HG00408.hp1 HG01978.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.701-51397T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938908 | ||||||
| chr5:139938909
|
G | A | 10 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0061others(7): Show | 10 | HG00408.hp1 HG01978.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.701-51398C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938909 | ||||||
| chr5:139938911
|
A | G | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701-51400T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938911 | ||||||
| chr5:139938915
|
A | G | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701-51404T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938915 | ||||||
| chr5:139938957
|
GAAA | G | 4 | a0001c0001t0001g0119a0001c0005t0004g0156a0002c0002t0001g0017others(1): Show | 4 | HG00544.hp2 HG02056.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-51449_701-5144 others(7): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938957 | ||||||
| chr5:139938958
|
A | G | 1 | a0001c0004t0001g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.701-51447T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938958 | ||||||
| chr5:139938960
|
A | AG | 2 | a0001c0001t0001g0096a0001c0001t0001g0105 | 2 | HG03041.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.701-51450_701-5144 others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938960 | ||||||
| chr5:139938961
|
AAAG | A | 2 | a0001c0001t0001g0123a0002c0002t0002g0001 | 3 | HG02809.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-51453_701-5145 others(7): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938961 | ||||||
| chr5:139938963
|
A | AGAAG | 3 | a0002c0002t0003g0082a0002c0002t0003g0170a0002c0002t0005g0138 | 3 | HG02572.hp2 HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.701-51456_701-5145 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938963 | ||||||
| chr5:139938963
|
A | G | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.701-51452T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938963 | ||||||
| chr5:139938964
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.701-51453C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938964 | ||||||
| chr5:139938986
|
A | AAAGG | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-51479_701-5147 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139938986 | ||||||
| chr5:139939204
|
T | TTTCC | 30 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0022others(27): Show | 30 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.701-51697_701-5169 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939204 | ||||||
| chr5:139939204
|
T | TTTCCTTC others(1): Show |
8 | a0001c0001t0001g0062a0001c0001t0001g0067a0001c0001t0001g0105others(5): Show | 8 | HG00280.hp2 HG01071.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-51701_701-5169 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939204 | ||||||
| chr5:139939204
|
T | TTTCCTTC others(17): Show |
1 | a0001c0001t0001g0054 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.701-51717_701-5169 others(28): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939204 | ||||||
| chr5:139939204
|
TTTCC | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.701-51697_701-5169 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939204 | ||||||
| chr5:139939204
|
TTTCCTTC others(1): Show |
T | 13 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0057others(10): Show | 13 | HG00408.hp1 HG00621.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.701-51701_701-5169 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939204 | ||||||
| chr5:139939204
|
TTTCCTTC others(5): Show |
T | 3 | a0002c0002t0001g0017a0002c0002t0003g0170a0002c0002t0005g0138 | 3 | HG02572.hp2 HG02895.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.701-51705_701-5169 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939204 | ||||||
| chr5:139939235
|
CCTTCCTT others(5): Show |
C | 5 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0145others(2): Show | 5 | HG02970.hp2 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-51736_701-5172 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939235 | ||||||
| chr5:139939243
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.701-51732G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939243 | ||||||
| chr5:139939243
|
CCTTT | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0168a0002c0002t0001g0085 | 3 | HG01109.hp1 HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-51736_701-5173 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939243 | ||||||
| chr5:139939247
|
T | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(43): Show | 46 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.701-51736A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939247 | ||||||
| chr5:139939251
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0074others(8): Show | 11 | HG01934.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.701-51740A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939251 | ||||||
| chr5:139939260
|
C | T | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-51749G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939260 | ||||||
| chr5:139939262
|
T | C | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-51751A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939262 | ||||||
| chr5:139939264
|
T | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(36): Show | 39 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-51753A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939264 | ||||||
| chr5:139939266
|
C | T | 39 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(36): Show | 39 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-51755G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939266 | ||||||
| chr5:139939413
|
T | C | 3 | a0002c0002t0002g0171a0004c0006t0001g0122a0004c0006t0001g0159 | 3 | HG03579.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.701-51902A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939413 | ||||||
| chr5:139939603
|
G | A | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-52092C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939603 | ||||||
| chr5:139939793
|
T | C | 4 | a0001c0001t0001g0023a0002c0002t0002g0171a0004c0006t0001g0122others(1): Show | 4 | HG02976.hp2 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-52282A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139939793 | ||||||
| chr5:139940260
|
A | G | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-52749T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940260 | ||||||
| chr5:139940420
|
T | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-52909A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940420 | ||||||
| chr5:139940421
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.701-52910A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940421 | ||||||
| chr5:139940534
|
T | A | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-53023A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940534 | ||||||
| chr5:139940598
|
A | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-53087T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940598 | ||||||
| chr5:139940645
|
A | C | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-53134T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940645 | ||||||
| chr5:139940784
|
G | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-53273C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940784 | ||||||
| chr5:139940859
|
A | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-53348T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940859 | ||||||
| chr5:139940876
|
A | T | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701-53365T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940876 | ||||||
| chr5:139940927
|
G | A | 39 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(36): Show | 39 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-53416C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139940927 | ||||||
| chr5:139941056
|
A | C | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-53545T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139941056 | ||||||
| chr5:139941239
|
A | G | 5 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0153others(2): Show | 5 | HG01496.hp2 HG01943.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-53728T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139941239 | ||||||
| chr5:139941377
|
G | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-53866C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139941377 | ||||||
| chr5:139941393
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-53882G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139941393 | ||||||
| chr5:139942482
|
A | G | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-54971T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139942482 | ||||||
| chr5:139942495
|
G | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(39): Show | 42 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.701-54984C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139942495 | ||||||
| chr5:139942584
|
T | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-55073A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139942584 | ||||||
| chr5:139942744
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.701-55233G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139942744 | ||||||
| chr5:139942820
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0089 | 2 | HG01978.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.701-55309A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139942820 | ||||||
| chr5:139943169
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.701-55658G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943169 | ||||||
| chr5:139943445
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0145others(4): Show | 7 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-55934C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943445 | ||||||
| chr5:139943596
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-56085A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943596 | ||||||
| chr5:139943672
|
G | A | 46 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0020others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.701-56161C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943672 | ||||||
| chr5:139943702
|
C | G | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-56191G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943702 | ||||||
| chr5:139943755
|
T | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0144 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.701-56244A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943755 | ||||||
| chr5:139943779
|
A | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-56268T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943779 | ||||||
| chr5:139943796
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.701-56285T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943796 | ||||||
| chr5:139943852
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-56341A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943852 | ||||||
| chr5:139943879
|
G | GCAAA | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-56372_701-5636 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943879 | ||||||
| chr5:139943962
|
G | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.701-56451C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139943962 | ||||||
| chr5:139944164
|
TA | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-56654delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139944164 | ||||||
| chr5:139944421
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0137 | 3 | HG00741.hp2 HG01109.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.701-56910G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139944421 | ||||||
| chr5:139944825
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0174 | 2 | HG01257.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.701-57314G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139944825 | ||||||
| chr5:139944951
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-57440C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139944951 | ||||||
| chr5:139945022
|
A | G | 1 | a0002c0002t0002g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.701-57511T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945022 | ||||||
| chr5:139945165
|
G | C | 3 | a0002c0002t0001g0017a0002c0002t0003g0170a0002c0002t0005g0138 | 3 | HG02572.hp2 HG02895.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.701-57654C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945165 | ||||||
| chr5:139945243
|
C | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-57732G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945243 | ||||||
| chr5:139945298
|
C | T | 2 | a0001c0001t0001g0154a0006c0008t0001g0176 | 2 | HG02056.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.701-57787G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945298 | ||||||
| chr5:139945354
|
C | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-57843G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945354 | ||||||
| chr5:139945493
|
T | C | 1 | a0001c0014t0001g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.701-57982A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945493 | ||||||
| chr5:139945670
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-58159A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945670 | ||||||
| chr5:139945728
|
C | T | 2 | a0001c0001t0001g0026a0001c0004t0001g0182 | 2 | HG00323.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.701-58217G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139945728 | ||||||
| chr5:139946041
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0070 | 2 | NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.701-58530G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139946041 | ||||||
| chr5:139946085
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-58574G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139946085 | ||||||
| chr5:139946562
|
G | A | 55 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.701-59051C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139946562 | ||||||
| chr5:139946582
|
CTT | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-59073_701-5907 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139946582 | ||||||
| chr5:139946603
|
G | GA | 5 | a0001c0001t0001g0023a0002c0002t0002g0075a0002c0002t0002g0171others(2): Show | 5 | HG02976.hp2 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-59093dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139946603 | ||||||
| chr5:139947004
|
T | TA | 5 | a0001c0001t0001g0008a0001c0001t0001g0042a0002c0002t0002g0021others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-59494dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947004 | ||||||
| chr5:139947031
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-59520C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947031 | ||||||
| chr5:139947182
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.701-59671G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947182 | ||||||
| chr5:139947271
|
C | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-59760G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947271 | ||||||
| chr5:139947432
|
A | G | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-59921T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947432 | ||||||
| chr5:139947433
|
AT | A | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-59923delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947433 | ||||||
| chr5:139947447
|
T | A | 3 | a0002c0002t0002g0171a0004c0006t0001g0122a0004c0006t0001g0159 | 3 | HG03579.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.701-59936A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947447 | ||||||
| chr5:139947552
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-60041C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947552 | ||||||
| chr5:139947558
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0137 | 3 | HG00741.hp2 HG01109.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.701-60047C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947558 | ||||||
| chr5:139947569
|
C | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0168a0001c0001t0001g0172others(5): Show | 8 | HG01934.hp2 HG02145.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-60058G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947569 | ||||||
| chr5:139947570
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.701-60059C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947570 | ||||||
| chr5:139947749
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.701-60238T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947749 | ||||||
| chr5:139947777
|
C | T | 55 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.701-60266G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947777 | ||||||
| chr5:139947832
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0142 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.701-60321A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947832 | ||||||
| chr5:139947842
|
T | G | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701-60331A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947842 | ||||||
| chr5:139947919
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.701-60408T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139947919 | ||||||
| chr5:139948215
|
G | GAGTT | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-60705_701-6070 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948215 | ||||||
| chr5:139948236
|
A | C | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-60725T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948236 | ||||||
| chr5:139948281
|
C | T | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-60770G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948281 | ||||||
| chr5:139948407
|
T | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-60896A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948407 | ||||||
| chr5:139948477
|
C | A | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701-60966G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948477 | ||||||
| chr5:139948946
|
A | T | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-61435T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948946 | ||||||
| chr5:139948947
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.701-61436G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948947 | ||||||
| chr5:139948984
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.701-61473G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139948984 | ||||||
| chr5:139949153
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-61642C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949153 | ||||||
| chr5:139949177
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-61666A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949177 | ||||||
| chr5:139949292
|
C | A | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-61781G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949292 | ||||||
| chr5:139949406
|
G | A | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-61895C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949406 | ||||||
| chr5:139949458
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG00140.hp1 HG01081.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-61947A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949458 | ||||||
| chr5:139949464
|
T | C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-61953A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949464 | ||||||
| chr5:139949480
|
C | T | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-61969G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949480 | ||||||
| chr5:139949481
|
A | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-61970T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949481 | ||||||
| chr5:139949581
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-62070A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949581 | ||||||
| chr5:139949699
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.701-62188G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139949699 | ||||||
| chr5:139950291
|
G | A | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-62780C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139950291 | ||||||
| chr5:139950377
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-62866G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139950377 | ||||||
| chr5:139950410
|
T | C | 9 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0123others(6): Show | 10 | HG01934.hp2 HG02145.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-62899A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139950410 | ||||||
| chr5:139950582
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0088a0001c0001t0001g0168others(4): Show | 7 | HG01934.hp2 HG02145.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-63071C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139950582 | ||||||
| chr5:139950625
|
G | A | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-63114C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139950625 | ||||||
| chr5:139950853
|
G | A | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-63342C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139950853 | ||||||
| chr5:139950906
|
G | A | 1 | a0007c0012t0001g0121 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.701-63395C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139950906 | ||||||
| chr5:139951083
|
G | A | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701-63572C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951083 | ||||||
| chr5:139951447
|
G | T | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-63936C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951447 | ||||||
| chr5:139951581
|
T | TCCTTTTT others(1): Show |
58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-64071_701-6407 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951581 | ||||||
| chr5:139951624
|
C | T | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-64113G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951624 | ||||||
| chr5:139951804
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.701-64293G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951804 | ||||||
| chr5:139951893
|
T | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-64382A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951893 | ||||||
| chr5:139951952
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-64441C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951952 | ||||||
| chr5:139951966
|
A | G | 3 | a0002c0002t0002g0171a0004c0006t0001g0122a0004c0006t0001g0159 | 3 | HG03579.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.701-64455T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139951966 | ||||||
| chr5:139952029
|
A | T | 4 | a0001c0001t0001g0023a0002c0002t0002g0171a0004c0006t0001g0122others(1): Show | 4 | HG02976.hp2 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-64518T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952029 | ||||||
| chr5:139952083
|
A | G | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-64572T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952083 | ||||||
| chr5:139952124
|
G | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-64613C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952124 | ||||||
| chr5:139952145
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.701-64634A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952145 | ||||||
| chr5:139952198
|
T | C | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-64687A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952198 | ||||||
| chr5:139952343
|
T | C | 1 | a0002c0002t0005g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.701-64832A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952343 | ||||||
| chr5:139952376
|
C | T | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-64865G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952376 | ||||||
| chr5:139952449
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-64938G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952449 | ||||||
| chr5:139952615
|
T | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-65104A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952615 | ||||||
| chr5:139952621
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0056a0001c0001t0001g0058others(9): Show | 12 | HG00609.hp1 HG01071.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.701-65110G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952621 | ||||||
| chr5:139952632
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.701-65121G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952632 | ||||||
| chr5:139952773
|
G | A | 2 | a0002c0002t0002g0009a0002c0002t0002g0087 | 2 | HG01934.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.701-65262C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952773 | ||||||
| chr5:139952900
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(11): Show | 14 | HG00642.hp1 HG00741.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.701-65389G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139952900 | ||||||
| chr5:139953223
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(2): Show | 5 | HG01167.hp1 HG01361.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-65712C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953223 | ||||||
| chr5:139953413
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-65902G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953413 | ||||||
| chr5:139953473
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-65962A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953473 | ||||||
| chr5:139953478
|
C | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-65967G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953478 | ||||||
| chr5:139953579
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0092 | 3 | HG00621.hp1 HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.701-66068C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953579 | ||||||
| chr5:139953843
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.701-66332G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953843 | ||||||
| chr5:139953929
|
C | T | 1 | a0002c0002t0002g0040 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.701-66418G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953929 | ||||||
| chr5:139953944
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.701-66433G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953944 | ||||||
| chr5:139953993
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.701-66482G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139953993 | ||||||
| chr5:139954052
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.701-66541C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954052 | ||||||
| chr5:139954296
|
C | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-66785G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954296 | ||||||
| chr5:139954329
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.701-66818A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954329 | ||||||
| chr5:139954388
|
G | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-66877C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954388 | ||||||
| chr5:139954594
|
G | A | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-67083C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954594 | ||||||
| chr5:139954621
|
C | T | 5 | a0001c0001t0001g0168a0002c0002t0001g0085a0002c0002t0002g0171others(2): Show | 5 | HG01934.hp2 HG02145.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-67110G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954621 | ||||||
| chr5:139954648
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0123others(1): Show | 5 | HG02809.hp2 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-67137G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954648 | ||||||
| chr5:139954836
|
G | C | 1 | a0001c0001t0001g0054 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.701-67325C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954836 | ||||||
| chr5:139954876
|
G | T | 39 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(36): Show | 39 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-67365C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954876 | ||||||
| chr5:139954894
|
ATTG | A | 9 | a0001c0001t0001g0168a0002c0002t0001g0017a0002c0002t0001g0085others(6): Show | 9 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-67386_701-6738 others(7): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139954894 | ||||||
| chr5:139955233
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.701-67722C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139955233 | ||||||
| chr5:139955280
|
G | A | 2 | a0001c0001t0001g0004a0002c0002t0005g0050 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.701-67769C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139955280 | ||||||
| chr5:139955324
|
A | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-67813T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139955324 | ||||||
| chr5:139955463
|
T | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-67952A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139955463 | ||||||
| chr5:139955681
|
A | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0137 | 2 | HG01109.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.701-68170T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139955681 | ||||||
| chr5:139955903
|
C | T | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701-68392G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139955903 | ||||||
| chr5:139956005
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.701-68494G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139956005 | ||||||
| chr5:139956315
|
C | G | 2 | a0001c0001t0001g0107a0008c0011t0001g0106 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-68804G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139956315 | ||||||
| chr5:139956363
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-68852G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139956363 | ||||||
| chr5:139956370
|
A | G | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-68859T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139956370 | ||||||
| chr5:139956761
|
G | A | 4 | a0002c0002t0001g0017a0002c0002t0003g0082a0002c0002t0003g0170others(1): Show | 4 | HG02572.hp2 HG02895.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-69250C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139956761 | ||||||
| chr5:139956890
|
G | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-69379C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139956890 | ||||||
| chr5:139956892
|
C | T | 1 | a0002c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.701-69381G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139956892 | ||||||
| chr5:139957307
|
C | CTG | 4 | a0001c0001t0001g0015a0001c0001t0001g0074a0001c0001t0001g0175others(1): Show | 4 | HG00280.hp1 HG01099.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-69798_701-6979 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957307
|
C | CTGTG | 3 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0007g0118 | 3 | HG00738.hp1 NA19007.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.701-69800_701-6979 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957307
|
CTG | C | 39 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 40 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-69798_701-6979 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957307
|
CTGTG | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0023others(24): Show | 27 | HG00544.hp2 HG00673.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.701-69800_701-6979 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957307
|
CTGTGTG | C | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.701-69802_701-6979 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957307
|
CTGTGTGT others(1): Show |
C | 27 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0001g0060others(24): Show | 28 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.701-69804_701-6979 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957307
|
CTGTGTGT others(3): Show |
C | 12 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0042others(9): Show | 12 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.701-69806_701-6979 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957307
|
CTGTGTGT others(7): Show |
C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-69810_701-6979 others(18): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957307 | ||||||
| chr5:139957309
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.701-69798C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957309 | ||||||
| chr5:139957311
|
G | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0107a0001c0014t0001g0117others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-69800C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957311 | ||||||
| chr5:139957313
|
G | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0107a0008c0011t0001g0106 | 3 | HG01884.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.701-69802C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957313 | ||||||
| chr5:139957315
|
G | C | 2 | a0001c0001t0001g0008a0008c0011t0001g0106 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.701-69804C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957315 | ||||||
| chr5:139957673
|
A | G | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-70162T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957673 | ||||||
| chr5:139957834
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG01081.hp1 HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.701-70323T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957834 | ||||||
| chr5:139957901
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-70390C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957901 | ||||||
| chr5:139957921
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0029 | 2 | HG00738.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.701-70410G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139957921 | ||||||
| chr5:139958021
|
G | A | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-70510C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958021 | ||||||
| chr5:139958026
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-70515C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958026 | ||||||
| chr5:139958047
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.701-70536G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958047 | ||||||
| chr5:139958473
|
G | C | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-70962C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958473 | ||||||
| chr5:139958599
|
A | G | 4 | a0001c0001t0001g0042a0002c0002t0002g0021a0002c0002t0002g0040others(1): Show | 4 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-71088T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958599 | ||||||
| chr5:139958780
|
C | T | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.701-71269G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958780 | ||||||
| chr5:139958781
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01255.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.701-71270C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958781 | ||||||
| chr5:139958826
|
A | ACATC | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-71319_701-7131 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958826 | ||||||
| chr5:139958896
|
C | T | 5 | a0001c0001t0001g0168a0002c0002t0001g0085a0002c0002t0002g0171others(2): Show | 5 | HG01934.hp2 HG02145.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-71385G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139958896 | ||||||
| chr5:139959042
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-71531C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959042 | ||||||
| chr5:139959182
|
TTTTG | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-71675_701-7167 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959182 | ||||||
| chr5:139959285
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.701-71774G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959285 | ||||||
| chr5:139959325
|
G | A | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-71814C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959325 | ||||||
| chr5:139959415
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 40 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.701-71904G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959415 | ||||||
| chr5:139959470
|
A | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-71959T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959470 | ||||||
| chr5:139959667
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.701-72156G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959667 | ||||||
| chr5:139959674
|
C | CT | 13 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0123others(10): Show | 14 | HG01934.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.701-72164dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959674 | ||||||
| chr5:139959793
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.701-72282C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959793 | ||||||
| chr5:139959802
|
C | T | 2 | a0001c0001t0001g0069a0002c0002t0009g0101 | 2 | NA19012.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.701-72291G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959802 | ||||||
| chr5:139959963
|
C | T | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-72452G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139959963 | ||||||
| chr5:139960102
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.701-72591C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139960102 | ||||||
| chr5:139960479
|
G | C | 53 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(50): Show | 54 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.701-72968C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139960479 | ||||||
| chr5:139960531
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.701-73020T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139960531 | ||||||
| chr5:139960754
|
A | ACAGGTAG others(12): Show |
1 | a0009c0015t0002g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.701-73262_701-7324 others(23): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139960754 | ||||||
| chr5:139960869
|
C | T | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-73358G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139960869 | ||||||
| chr5:139960975
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.701-73464C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139960975 | ||||||
| chr5:139961124
|
G | A | 1 | a0005c0016t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.701-73613C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961124 | ||||||
| chr5:139961194
|
C | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 113 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.701-73683G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961194 | ||||||
| chr5:139961277
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.701-73766C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961277 | ||||||
| chr5:139961351
|
C | T | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.701-73840G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961351 | ||||||
| chr5:139961406
|
A | G | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-73895T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961406 | ||||||
| chr5:139961535
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.701-74024G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961535 | ||||||
| chr5:139961542
|
A | G | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-74031T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961542 | ||||||
| chr5:139961543
|
A | G | 2 | a0002c0002t0003g0148a0002c0013t0003g0083 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.701-74032T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961543 | ||||||
| chr5:139961715
|
C | A | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-74204G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961715 | ||||||
| chr5:139961779
|
G | A | 1 | a0002c0002t0002g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-74268C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961779 | ||||||
| chr5:139961842
|
G | A | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-74331C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961842 | ||||||
| chr5:139961846
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0163 | 2 | HG01167.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.701-74335C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961846 | ||||||
| chr5:139961927
|
C | A | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-74416G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961927 | ||||||
| chr5:139961927
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.701-74416G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139961927 | ||||||
| chr5:139962004
|
CA | C | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-74494delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139962004 | ||||||
| chr5:139962609
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-75098C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139962609 | ||||||
| chr5:139962833
|
T | C | 49 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(46): Show | 50 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.701-75322A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139962833 | ||||||
| chr5:139962864
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.701-75353T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139962864 | ||||||
| chr5:139962868
|
A | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(51): Show | 55 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.701-75357T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139962868 | ||||||
| chr5:139962954
|
T | C | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-75443A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139962954 | ||||||
| chr5:139963022
|
C | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-75511G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963022 | ||||||
| chr5:139963031
|
A | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0073a0001c0004t0001g0183others(4): Show | 7 | HG01069.hp1 HG03195.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-75520T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963031 | ||||||
| chr5:139963082
|
A | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(51): Show | 55 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.701-75571T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963082 | ||||||
| chr5:139963361
|
C | T | 1 | a0001c0001t0003g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.701-75850G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963361 | ||||||
| chr5:139963362
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.701-75851C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963362 | ||||||
| chr5:139963589
|
A | G | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.701-76078T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963589 | ||||||
| chr5:139963716
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.701-76205C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963716 | ||||||
| chr5:139963804
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(35): Show | 38 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.701-76293G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963804 | ||||||
| chr5:139963994
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.701-76483T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139963994 | ||||||
| chr5:139964013
|
G | C | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701-76502C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964013 | ||||||
| chr5:139964236
|
G | A | 2 | a0002c0002t0002g0100a0002c0002t0009g0101 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.701-76725C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964236 | ||||||
| chr5:139964341
|
T | C | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701-76830A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964341 | ||||||
| chr5:139964356
|
A | G | 1 | a0002c0002t0009g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.701-76845T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964356 | ||||||
| chr5:139964357
|
T | TAC | 19 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0070others(16): Show | 19 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.701-76848_701-7684 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964357 | ||||||
| chr5:139964357
|
T | TACAC | 7 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(4): Show | 7 | HG00741.hp2 HG01109.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-76850_701-7684 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964357 | ||||||
| chr5:139964357
|
TAC | T | 4 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0005t0004g0048others(1): Show | 4 | HG01934.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-76848_701-7684 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964357 | ||||||
| chr5:139964357
|
TACAC | T | 4 | a0002c0002t0002g0171a0004c0006t0001g0122a0004c0006t0001g0159others(1): Show | 4 | HG03579.hp2 HG04115.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-76850_701-7684 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964357 | ||||||
| chr5:139964357
|
TACACAC | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(37): Show | 41 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.701-76852_701-7684 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964357 | ||||||
| chr5:139964357
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0008a0001c0001t0001g0107a0002c0002t0009g0101others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-76854_701-7684 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964357 | ||||||
| chr5:139964357
|
TACACACA others(3): Show |
T | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-76856_701-7684 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964357 | ||||||
| chr5:139964359
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.701-76848G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964359 | ||||||
| chr5:139964420
|
CA | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0015others(50): Show | 54 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.701-76910delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964420 | ||||||
| chr5:139964737
|
C | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-77226G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964737 | ||||||
| chr5:139964800
|
C | A | 2 | a0001c0001t0001g0168a0002c0002t0001g0085 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.701-77289G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964800 | ||||||
| chr5:139964887
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.701-77376C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139964887 | ||||||
| chr5:139965310
|
G | C | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.700+77060C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139965310 | ||||||
| chr5:139965599
|
C | T | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.700+76771G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139965599 | ||||||
| chr5:139965836
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+76534C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139965836 | ||||||
| chr5:139966178
|
C | T | 1 | a0002c0002t0002g0075 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.700+76192G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139966178 | ||||||
| chr5:139966183
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0002c0002t0002g0001 | 4 | HG02809.hp2 HG03041.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+76187C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139966183 | ||||||
| chr5:139966570
|
G | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0107a0008c0011t0001g0106 | 3 | HG01884.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.700+75800C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139966570 | ||||||
| chr5:139966653
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0107a0008c0011t0001g0106 | 3 | HG01884.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.700+75717G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139966653 | ||||||
| chr5:139966741
|
G | A | 1 | a0002c0002t0003g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.700+75629C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139966741 | ||||||
| chr5:139967506
|
C | T | 1 | a0001c0010t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.700+74864G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967506 | ||||||
| chr5:139967570
|
T | C | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.700+74800A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967570 | ||||||
| chr5:139967578
|
G | C | 1 | a0003c0003t0001g0043 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.700+74792C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967578 | ||||||
| chr5:139967827
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0080 | 3 | HG00609.hp1 HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.700+74543G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967827 | ||||||
| chr5:139967832
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0107a0002c0002t0003g0038others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+74538C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967832 | ||||||
| chr5:139967914
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.700+74456C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967914 | ||||||
| chr5:139967942
|
G | C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+74428C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967942 | ||||||
| chr5:139967945
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.700+74425G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967945 | ||||||
| chr5:139967974
|
A | AAAAT | 61 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0023others(58): Show | 62 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.700+74392_700+7439 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967974 | ||||||
| chr5:139967974
|
A | AAAATAAA others(1): Show |
19 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0056others(16): Show | 20 | HG00609.hp1 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.700+74388_700+7439 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967974 | ||||||
| chr5:139967974
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0013 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.700+74384_700+7439 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967974 | ||||||
| chr5:139967974
|
AAAAT | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0022others(27): Show | 30 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.700+74392_700+7439 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967974 | ||||||
| chr5:139967974
|
AAAATAAA others(5): Show |
A | 2 | a0001c0004t0001g0179a0002c0002t0002g0100 | 2 | HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.700+74384_700+7439 others(16): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139967974 | ||||||
| chr5:139968263
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.700+74107C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968263 | ||||||
| chr5:139968318
|
C | T | 1 | a0002c0002t0005g0141 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.700+74052G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968318 | ||||||
| chr5:139968522
|
G | C | 1 | a0002c0002t0005g0141 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.700+73848C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968522 | ||||||
| chr5:139968617
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.700+73753G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968617 | ||||||
| chr5:139968898
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.700+73472G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968898 | ||||||
| chr5:139968908
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.700+73462C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968908 | ||||||
| chr5:139968914
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.700+73456T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968914 | ||||||
| chr5:139968987
|
G | T | 1 | a0003c0003t0001g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.700+73383C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139968987 | ||||||
| chr5:139969023
|
C | T | 20 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(17): Show | 20 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.700+73347G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139969023 | ||||||
| chr5:139969330
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.700+73040A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139969330 | ||||||
| chr5:139969330
|
T | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(88): Show | 93 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.700+73040A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139969330 | ||||||
| chr5:139969457
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.700+72913G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139969457 | ||||||
| chr5:139969586
|
G | C | 21 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0058others(18): Show | 21 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.700+72784C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139969586 | ||||||
| chr5:139970120
|
C | T | 1 | a0002c0002t0003g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.700+72250G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139970120 | ||||||
| chr5:139970347
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+72023C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139970347 | ||||||
| chr5:139970405
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+71965A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139970405 | ||||||
| chr5:139970448
|
G | A | 1 | a0002c0002t0005g0141 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.700+71922C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139970448 | ||||||
| chr5:139970885
|
C | G | 10 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0073others(7): Show | 10 | HG01361.hp1 HG02809.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.700+71485G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139970885 | ||||||
| chr5:139971212
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+71158C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139971212 | ||||||
| chr5:139971439
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.700+70931G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139971439 | ||||||
| chr5:139971835
|
C | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | NA18942.hp1 NA18983.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.700+70535G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139971835 | ||||||
| chr5:139972451
|
A | G | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(70): Show | 73 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.700+69919T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139972451 | ||||||
| chr5:139972500
|
G | A | 25 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0031others(22): Show | 25 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.700+69870C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139972500 | ||||||
| chr5:139972593
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(39): Show | 42 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.700+69777C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139972593 | ||||||
| chr5:139972616
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+69754G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139972616 | ||||||
| chr5:139972639
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+69731C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139972639 | ||||||
| chr5:139972672
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0001c0001t0001g0140 | 3 | HG02809.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.700+69698G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139972672 | ||||||
| chr5:139972957
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.700+69413G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139972957 | ||||||
| chr5:139973045
|
A | G | 2 | a0001c0001t0001g0008a0002c0002t0003g0038 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+69325T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973045 | ||||||
| chr5:139973156
|
C | CA | 41 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.700+69213dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973156 | ||||||
| chr5:139973156
|
CAAA | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0073a0001c0001t0001g0094others(6): Show | 9 | HG01361.hp1 HG02809.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+69211_700+6921 others(7): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973156 | ||||||
| chr5:139973156
|
CAAAA | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(40): Show | 43 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.700+69210_700+6921 others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973156 | ||||||
| chr5:139973156
|
CAAAAA | C | 19 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(16): Show | 19 | HG00609.hp1 HG01071.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+69209_700+6921 others(9): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973156 | ||||||
| chr5:139973214
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+69156A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973214 | ||||||
| chr5:139973394
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG00642.hp1 HG00741.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.700+68976C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973394 | ||||||
| chr5:139973543
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.700+68827C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973543 | ||||||
| chr5:139973778
|
G | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0073others(5): Show | 8 | HG01361.hp1 HG03017.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+68592C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973778 | ||||||
| chr5:139973917
|
T | C | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.700+68453A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973917 | ||||||
| chr5:139973972
|
GATTATGA others(8): Show |
G | 1 | a0002c0002t0005g0138 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.700+68383_700+6839 others(19): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139973972 | ||||||
| chr5:139974138
|
A | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(66): Show | 69 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.700+68232T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974138 | ||||||
| chr5:139974272
|
G | A | 34 | a0001c0001t0001g0013a0001c0001t0001g0045a0001c0001t0001g0046others(31): Show | 36 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.700+68098C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974272 | ||||||
| chr5:139974433
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.700+67937C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974433 | ||||||
| chr5:139974435
|
G | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0073others(5): Show | 8 | HG01361.hp1 HG03017.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+67935C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974435 | ||||||
| chr5:139974602
|
A | T | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+67768T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974602 | ||||||
| chr5:139974606
|
GT | G | 8 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0073others(5): Show | 8 | HG01361.hp1 HG03017.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+67763delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974606 | ||||||
| chr5:139974705
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0001c0001t0001g0140 | 3 | HG02809.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.700+67665C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974705 | ||||||
| chr5:139974966
|
A | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+67404T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139974966 | ||||||
| chr5:139975347
|
A | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+67023T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139975347 | ||||||
| chr5:139975471
|
A | G | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.700+66899T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139975471 | ||||||
| chr5:139975667
|
C | T | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.700+66703G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139975667 | ||||||
| chr5:139975859
|
T | C | 3 | a0002c0002t0001g0017a0002c0002t0003g0170a0002c0002t0005g0138 | 3 | HG02572.hp2 HG02895.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.700+66511A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139975859 | ||||||
| chr5:139975991
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.700+66379G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139975991 | ||||||
| chr5:139975998
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.700+66372A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139975998 | ||||||
| chr5:139976096
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG01069.hp1 HG01255.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+66274A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139976096 | ||||||
| chr5:139976154
|
C | T | 22 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(19): Show | 22 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.700+66216G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139976154 | ||||||
| chr5:139976181
|
G | A | 1 | a0002c0002t0005g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.700+66189C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139976181 | ||||||
| chr5:139976960
|
T | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+65410A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139976960 | ||||||
| chr5:139977693
|
ATAC | A | 22 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(19): Show | 22 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.700+64674_700+6467 others(7): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139977693 | ||||||
| chr5:139977699
|
C | A | 22 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(19): Show | 22 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.700+64671G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139977699 | ||||||
| chr5:139978028
|
A | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+64342T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978028 | ||||||
| chr5:139978063
|
G | A | 19 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(16): Show | 19 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.700+64307C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978063 | ||||||
| chr5:139978149
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.700+64221C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978149 | ||||||
| chr5:139978311
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+64059T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978311 | ||||||
| chr5:139978373
|
T | C | 27 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0058others(24): Show | 27 | HG00609.hp1 HG01071.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.700+63997A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978373 | ||||||
| chr5:139978568
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0139 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.700+63802G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978568 | ||||||
| chr5:139978579
|
G | A | 1 | a0001c0004t0001g0181 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.700+63791C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978579 | ||||||
| chr5:139978722
|
A | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+63648T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978722 | ||||||
| chr5:139978723
|
G | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+63647C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978723 | ||||||
| chr5:139978739
|
C | T | 22 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(19): Show | 22 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.700+63631G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978739 | ||||||
| chr5:139978765
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0145others(4): Show | 7 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.700+63605G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978765 | ||||||
| chr5:139978766
|
G | GCAGCCAC others(3): Show |
1 | a0001c0001t0001g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.700+63594_700+6360 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139978766 | ||||||
| chr5:139979097
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.700+63273T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979097 | ||||||
| chr5:139979099
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.700+63271C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979099 | ||||||
| chr5:139979144
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.700+63226C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979144 | ||||||
| chr5:139979278
|
G | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0057 | 2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.700+63092C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979278 | ||||||
| chr5:139979432
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.700+62938G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979432 | ||||||
| chr5:139979439
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+62931C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979439 | ||||||
| chr5:139979554
|
G | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(75): Show | 78 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.700+62816C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979554 | ||||||
| chr5:139979672
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.700+62698A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979672 | ||||||
| chr5:139979806
|
A | G | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.700+62564T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979806 | ||||||
| chr5:139979895
|
T | G | 23 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0058others(20): Show | 23 | HG00609.hp1 HG01071.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.700+62475A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139979895 | ||||||
| chr5:139980153
|
T | C | 2 | a0001c0001t0001g0008a0002c0002t0003g0038 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+62217A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139980153 | ||||||
| chr5:139980349
|
C | CA | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(50): Show | 53 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.700+62020dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139980349 | ||||||
| chr5:139980349
|
C | CAA | 26 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0058others(23): Show | 26 | HG00609.hp1 HG01071.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.700+62019_700+6202 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139980349 | ||||||
| chr5:139980462
|
C | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0089a0001c0001t0001g0126 | 3 | HG01943.hp2 HG01978.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.700+61908G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139980462 | ||||||
| chr5:139980715
|
A | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+61655T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139980715 | ||||||
| chr5:139981005
|
T | C | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(120): Show | 125 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.700+61365A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139981005 | ||||||
| chr5:139981209
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.700+61161G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139981209 | ||||||
| chr5:139981279
|
C | T | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(74): Show | 77 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+61091G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139981279 | ||||||
| chr5:139981511
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.700+60859A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139981511 | ||||||
| chr5:139981618
|
G | A | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.700+60752C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139981618 | ||||||
| chr5:139982094
|
T | C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+60276A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982094 | ||||||
| chr5:139982233
|
C | T | 1 | a0002c0007t0003g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.700+60137G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982233 | ||||||
| chr5:139982361
|
C | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.700+60009G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982361 | ||||||
| chr5:139982499
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.700+59871G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982499 | ||||||
| chr5:139982555
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.700+59815G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982555 | ||||||
| chr5:139982607
|
C | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(1): Show | 4 | HG00280.hp1 HG02602.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+59763G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982607 | ||||||
| chr5:139982615
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.700+59755C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982615 | ||||||
| chr5:139982616
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.700+59754G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982616 | ||||||
| chr5:139982736
|
T | C | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(72): Show | 75 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.700+59634A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982736 | ||||||
| chr5:139982969
|
C | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.700+59401G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139982969 | ||||||
| chr5:139983662
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+58708A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139983662 | ||||||
| chr5:139983957
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.700+58413G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139983957 | ||||||
| chr5:139983978
|
C | A | 1 | a0002c0002t0005g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.700+58392G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139983978 | ||||||
| chr5:139983998
|
G | A | 19 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(16): Show | 19 | HG00609.hp1 HG01071.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.700+58372C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139983998 | ||||||
| chr5:139984194
|
G | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(2): Show | 5 | HG00609.hp1 HG01071.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+58176C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139984194 | ||||||
| chr5:139984208
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.700+58162C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139984208 | ||||||
| chr5:139984225
|
T | G | 1 | a0002c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.700+58145A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139984225 | ||||||
| chr5:139984471
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.700+57899C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139984471 | ||||||
| chr5:139985110
|
T | C | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(72): Show | 75 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.700+57260A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139985110 | ||||||
| chr5:139985332
|
T | C | 1 | a0001c0004t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.700+57038A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139985332 | ||||||
| chr5:139985506
|
T | C | 2 | a0001c0004t0001g0184a0002c0002t0003g0082 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.700+56864A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139985506 | ||||||
| chr5:139985631
|
G | A | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(72): Show | 75 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.700+56739C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139985631 | ||||||
| chr5:139985867
|
C | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(43): Show | 46 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.700+56503G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139985867 | ||||||
| chr5:139985969
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+56401C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139985969 | ||||||
| chr5:139986191
|
T | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0073others(5): Show | 8 | HG01361.hp1 HG03017.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+56179A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139986191 | ||||||
| chr5:139986228
|
C | A | 25 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0031others(22): Show | 25 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.700+56142G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139986228 | ||||||
| chr5:139986387
|
A | T | 2 | a0001c0001t0001g0102a0002c0002t0002g0075 | 2 | NA18747.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.700+55983T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139986387 | ||||||
| chr5:139986701
|
T | C | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.700+55669A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139986701 | ||||||
| chr5:139986875
|
C | T | 1 | a0002c0002t0003g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.700+55495G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139986875 | ||||||
| chr5:139987110
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0054 | 2 | NA18971.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.700+55260C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987110 | ||||||
| chr5:139987216
|
C | CA | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(41): Show | 44 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.700+55153dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987216 | ||||||
| chr5:139987216
|
C | CAA | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+55152_700+5515 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987216 | ||||||
| chr5:139987367
|
C | CA | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0013others(58): Show | 61 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.700+55002dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987367 | ||||||
| chr5:139987367
|
C | CAA | 5 | a0001c0001t0001g0093a0001c0001t0001g0107a0002c0002t0001g0017others(2): Show | 5 | HG00735.hp2 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+55001_700+5500 others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987367 | ||||||
| chr5:139987421
|
C | G | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+54949G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987421 | ||||||
| chr5:139987603
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0145others(4): Show | 7 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.700+54767G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987603 | ||||||
| chr5:139987772
|
G | GT | 15 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0034others(12): Show | 15 | HG00741.hp1 HG01109.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.700+54597dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987772 | ||||||
| chr5:139987772
|
GT | G | 23 | a0001c0001t0001g0047a0001c0001t0001g0056a0001c0001t0001g0058others(20): Show | 23 | HG00609.hp1 HG01071.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.700+54597delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987772 | ||||||
| chr5:139987867
|
C | G | 1 | a0002c0002t0003g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700+54503G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987867 | ||||||
| chr5:139987899
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+54471G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139987899 | ||||||
| chr5:139988021
|
GCCTCGGC others(2007): Show |
G | 2 | a0001c0001t0001g0109a0001c0001t0001g0165 | 2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.700+52335_700+5434 others(4): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988021 | ||||||
| chr5:139988026
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(33): Show | 36 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.700+54344C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988026 | ||||||
| chr5:139988053
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.700+54317G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988053 | ||||||
| chr5:139988159
|
GT | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0147 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.700+54210delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988159 | ||||||
| chr5:139988491
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+53879T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988491 | ||||||
| chr5:139988596
|
T | C | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.700+53774A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988596 | ||||||
| chr5:139988874
|
T | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02738.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.700+53496A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988874 | ||||||
| chr5:139988881
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | HG00323.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.700+53489C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139988881 | ||||||
| chr5:139989129
|
G | T | 1 | a0009c0015t0002g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.700+53241C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989129 | ||||||
| chr5:139989158
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.700+53212G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989158 | ||||||
| chr5:139989230
|
T | C | 1 | a0002c0002t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+53140A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989230 | ||||||
| chr5:139989397
|
A | G | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.700+52973T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989397 | ||||||
| chr5:139989409
|
G | A | 1 | a0003c0003t0001g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.700+52961C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989409 | ||||||
| chr5:139989478
|
A | G | 1 | a0005c0016t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.700+52892T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989478 | ||||||
| chr5:139989593
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.700+52777C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989593 | ||||||
| chr5:139989758
|
T | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG01167.hp1 HG01361.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+52612A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989758 | ||||||
| chr5:139989758
|
T | TTTA | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.700+52609_700+5261 others(7): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989758 | ||||||
| chr5:139989829
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0073others(5): Show | 8 | HG01361.hp1 HG03017.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+52541G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989829 | ||||||
| chr5:139989881
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.700+52489A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989881 | ||||||
| chr5:139989889
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.700+52481A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989889 | ||||||
| chr5:139989937
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.700+52433G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989937 | ||||||
| chr5:139989938
|
A | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(98): Show | 101 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.700+52432T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989938 | ||||||
| chr5:139989946
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.700+52424C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989946 | ||||||
| chr5:139989950
|
A | G | 1 | a0003c0003t0001g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.700+52420T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989950 | ||||||
| chr5:139989955
|
A | AT | 4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG01167.hp1 HG01361.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+52414dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989955 | ||||||
| chr5:139989978
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.700+52392G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989978 | ||||||
| chr5:139989990
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.700+52380T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989990 | ||||||
| chr5:139989990
|
A | G | 9 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(6): Show | 10 | HG00140.hp1 HG01081.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.700+52380T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139989990 | ||||||
| chr5:139990009
|
T | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(37): Show | 40 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.700+52361A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990009 | ||||||
| chr5:139990031
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG00544.hp1 HG00544.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.700+52339C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990031 | ||||||
| chr5:139990039
|
C | T | 63 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(60): Show | 65 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.700+52331G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990039 | ||||||
| chr5:139990273
|
A | ATATTT | 14 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.700+52092_700+5209 others(9): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990273 | ||||||
| chr5:139990273
|
ATATTT | A | 26 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0023others(23): Show | 26 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.700+52092_700+5209 others(9): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990273 | ||||||
| chr5:139990273
|
ATATTTTA others(3): Show |
A | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(70): Show | 73 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.700+52087_700+5209 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990273 | ||||||
| chr5:139990290
|
ATTTTATT others(1): Show |
A | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.700+52072_700+5207 others(12): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990290 | ||||||
| chr5:139990339
|
A | G | 2 | a0001c0001t0001g0125a0002c0002t0002g0160 | 2 | HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.700+52031T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990339 | ||||||
| chr5:139990882
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.700+51488C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139990882 | ||||||
| chr5:139991120
|
A | G | 1 | a0003c0003t0001g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.700+51250T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139991120 | ||||||
| chr5:139991320
|
G | A | 2 | a0001c0001t0001g0172a0002c0002t0003g0173 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.700+51050C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139991320 | ||||||
| chr5:139991406
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.700+50964T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139991406 | ||||||
| chr5:139991804
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0027 | 2 | HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.700+50566T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139991804 | ||||||
| chr5:139991911
|
G | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(86): Show | 89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.700+50459C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139991911 | ||||||
| chr5:139991960
|
C | T | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.700+50410G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139991960 | ||||||
| chr5:139992006
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+50364A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139992006 | ||||||
| chr5:139992284
|
T | A | 2 | a0001c0001t0001g0107a0008c0011t0001g0106 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.700+50086A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139992284 | ||||||
| chr5:139992564
|
G | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(84): Show | 87 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.700+49806C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139992564 | ||||||
| chr5:139992819
|
G | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(84): Show | 87 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.700+49551C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139992819 | ||||||
| chr5:139992936
|
T | C | 36 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(33): Show | 36 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.700+49434A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139992936 | ||||||
| chr5:139992957
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.700+49413C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139992957 | ||||||
| chr5:139993139
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+49231C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139993139 | ||||||
| chr5:139993795
|
T | TA | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.700+48574dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139993795 | ||||||
| chr5:139994046
|
T | C | 1 | a0004c0006t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.700+48324A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139994046 | ||||||
| chr5:139994050
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.700+48320A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139994050 | ||||||
| chr5:139994175
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+48195T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139994175 | ||||||
| chr5:139994260
|
T | C | 1 | a0001c0010t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.700+48110A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139994260 | ||||||
| chr5:139994698
|
T | C | 1 | a0001c0005t0004g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.700+47672A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139994698 | ||||||
| chr5:139994776
|
G | A | 1 | a0001c0004t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.700+47594C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139994776 | ||||||
| chr5:139995091
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.700+47279C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139995091 | ||||||
| chr5:139995432
|
G | T | 1 | a0001c0009t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.700+46938C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139995432 | ||||||
| chr5:139995440
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+46930G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139995440 | ||||||
| chr5:139995472
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+46898A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139995472 | ||||||
| chr5:139995485
|
T | C | 25 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0031others(22): Show | 25 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.700+46885A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139995485 | ||||||
| chr5:139995597
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+46773G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139995597 | ||||||
| chr5:139996060
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.700+46310A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139996060 | ||||||
| chr5:139996107
|
T | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.700+46263A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139996107 | ||||||
| chr5:139996347
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.700+46023G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139996347 | ||||||
| chr5:139996495
|
T | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(90): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.700+45875A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139996495 | ||||||
| chr5:139996563
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.700+45807C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139996563 | ||||||
| chr5:139996670
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+45700G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139996670 | ||||||
| chr5:139996851
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.700+45519A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139996851 | ||||||
| chr5:139997103
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.700+45267G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139997103 | ||||||
| chr5:139997153
|
A | T | 1 | a0003c0003t0001g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.700+45217T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139997153 | ||||||
| chr5:139997178
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+45192T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139997178 | ||||||
| chr5:139997179
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+45191A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139997179 | ||||||
| chr5:139997234
|
T | C | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.700+45136A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139997234 | ||||||
| chr5:139997993
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+44377G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139997993 | ||||||
| chr5:139998243
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+44127G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998243 | ||||||
| chr5:139998244
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+44126A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998244 | ||||||
| chr5:139998245
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+44125C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998245 | ||||||
| chr5:139998250
|
G | A | 33 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(30): Show | 33 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.700+44120C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998250 | ||||||
| chr5:139998558
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+43812C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998558 | ||||||
| chr5:139998587
|
G | A | 1 | a0002c0002t0003g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700+43783C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998587 | ||||||
| chr5:139998616
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.700+43754G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998616 | ||||||
| chr5:139998651
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.700+43719C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998651 | ||||||
| chr5:139998767
|
AG | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.700+43602delC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139998767 | ||||||
| chr5:139999080
|
C | G | 1 | a0009c0015t0002g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.700+43290G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999080 | ||||||
| chr5:139999095
|
G | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01255.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.700+43275C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999095 | ||||||
| chr5:139999108
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+43262G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999108 | ||||||
| chr5:139999140
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.700+43230C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999140 | ||||||
| chr5:139999185
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.700+43185T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999185 | ||||||
| chr5:139999213
|
AG | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0145others(4): Show | 7 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.700+43156delC | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999213 | ||||||
| chr5:139999228
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+43142G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999228 | ||||||
| chr5:139999239
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+43131G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999239 | ||||||
| chr5:139999347
|
A | T | 1 | a0004c0006t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.700+43023T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999347 | ||||||
| chr5:139999401
|
A | C | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.700+42969T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 139999401 | ||||||
| chr5:140000122
|
C | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(41): Show | 44 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.700+42248G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140000122 | ||||||
| chr5:140000384
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+41986C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140000384 | ||||||
| chr5:140000544
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.700+41826G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140000544 | ||||||
| chr5:140001160
|
T | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.700+41210A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001160 | ||||||
| chr5:140001247
|
C | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(42): Show | 45 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.700+41123G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001247 | ||||||
| chr5:140001406
|
A | G | 31 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(28): Show | 31 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.700+40964T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001406 | ||||||
| chr5:140001530
|
T | C | 1 | a0002c0002t0002g0009 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.700+40840A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001530 | ||||||
| chr5:140001641
|
C | T | 1 | a0002c0002t0002g0160 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.700+40729G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001641 | ||||||
| chr5:140001699
|
CA | C | 28 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.700+40670delT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001699 | ||||||
| chr5:140001800
|
C | T | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.700+40570G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001800 | ||||||
| chr5:140001911
|
A | G | 31 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(28): Show | 31 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.700+40459T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001911 | ||||||
| chr5:140001937
|
C | T | 1 | a0001c0001t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.700+40433G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140001937 | ||||||
| chr5:140002123
|
A | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.700+40247T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140002123 | ||||||
| chr5:140002243
|
A | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0144a0002c0007t0003g0180 | 3 | HG01884.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.700+40127T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140002243 | ||||||
| chr5:140002292
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.700+40078G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140002292 | ||||||
| chr5:140002379
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+39991T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140002379 | ||||||
| chr5:140002663
|
T | C | 23 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0045others(20): Show | 23 | HG00544.hp2 HG01255.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.700+39707A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140002663 | ||||||
| chr5:140002768
|
G | A | 48 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(45): Show | 48 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.700+39602C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140002768 | ||||||
| chr5:140003097
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.700+39273G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140003097 | ||||||
| chr5:140003134
|
A | C | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+39236T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140003134 | ||||||
| chr5:140003220
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.700+39150G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140003220 | ||||||
| chr5:140003664
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.700+38706A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140003664 | ||||||
| chr5:140003685
|
T | C | 2 | a0001c0001t0001g0008a0002c0002t0003g0038 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+38685A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140003685 | ||||||
| chr5:140003835
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.700+38535G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140003835 | ||||||
| chr5:140003944
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+38426C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140003944 | ||||||
| chr5:140004328
|
CT | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+38041delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140004328 | ||||||
| chr5:140004405
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+37965G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140004405 | ||||||
| chr5:140004414
|
T | C | 8 | a0001c0001t0001g0125a0001c0001t0010g0167a0001c0004t0001g0179others(5): Show | 9 | HG00323.hp1 HG01496.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+37956A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140004414 | ||||||
| chr5:140004652
|
G | A | 2 | a0001c0004t0001g0184a0002c0002t0003g0082 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.700+37718C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140004652 | ||||||
| chr5:140004905
|
T | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.700+37465A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140004905 | ||||||
| chr5:140005017
|
C | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.700+37353G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140005017 | ||||||
| chr5:140005121
|
T | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0114a0001c0001t0007g0118others(2): Show | 5 | HG00735.hp2 NA18982.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+37249A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140005121 | ||||||
| chr5:140005336
|
C | T | 2 | a0002c0002t0002g0081a0002c0002t0002g0162 | 2 | NA18942.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.700+37034G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140005336 | ||||||
| chr5:140005337
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.700+37033C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140005337 | ||||||
| chr5:140005616
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+36754C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140005616 | ||||||
| chr5:140005810
|
C | A | 1 | a0002c0002t0002g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.700+36560G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140005810 | ||||||
| chr5:140006013
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0096a0001c0001t0001g0123others(2): Show | 5 | HG01884.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+36357A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140006013 | ||||||
| chr5:140006361
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.700+36009C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140006361 | ||||||
| chr5:140006573
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+35797T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140006573 | ||||||
| chr5:140006735
|
A | G | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+35635T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140006735 | ||||||
| chr5:140006879
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.700+35491G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140006879 | ||||||
| chr5:140007030
|
A | G | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.700+35340T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140007030 | ||||||
| chr5:140007037
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.700+35333G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140007037 | ||||||
| chr5:140007074
|
C | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(48): Show | 51 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.700+35296G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140007074 | ||||||
| chr5:140007136
|
C | T | 1 | a0002c0002t0003g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.700+35234G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140007136 | ||||||
| chr5:140007472
|
T | C | 1 | a0001c0009t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.700+34898A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140007472 | ||||||
| chr5:140007593
|
C | T | 1 | a0001c0004t0001g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.700+34777G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140007593 | ||||||
| chr5:140008090
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+34280C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140008090 | ||||||
| chr5:140008148
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+34222A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140008148 | ||||||
| chr5:140008208
|
A | C | 5 | a0001c0004t0001g0179a0001c0004t0001g0182a0001c0004t0001g0183others(2): Show | 6 | HG00323.hp1 HG01496.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.700+34162T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140008208 | ||||||
| chr5:140008412
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.700+33958A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140008412 | ||||||
| chr5:140008543
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.700+33827A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140008543 | ||||||
| chr5:140008750
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0096a0001c0001t0001g0123others(2): Show | 5 | HG01884.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+33620A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140008750 | ||||||
| chr5:140009272
|
T | C | 25 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0045others(22): Show | 25 | HG00544.hp2 HG01255.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.700+33098A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140009272 | ||||||
| chr5:140009370
|
C | G | 27 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.700+33000G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140009370 | ||||||
| chr5:140009498
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.700+32872T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140009498 | ||||||
| chr5:140009557
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+32813T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140009557 | ||||||
| chr5:140009604
|
T | C | 1 | a0002c0002t0005g0141 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.700+32766A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140009604 | ||||||
| chr5:140010017
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.700+32353C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010017 | ||||||
| chr5:140010019
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0096a0001c0001t0001g0123others(2): Show | 5 | HG01884.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+32351G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010019 | ||||||
| chr5:140010284
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.700+32086G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010284 | ||||||
| chr5:140010295
|
C | CA | 19 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0039others(16): Show | 20 | HG00140.hp1 HG00323.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.700+32074dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010295 | ||||||
| chr5:140010383
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+31987C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010383 | ||||||
| chr5:140010422
|
C | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.700+31948G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010422 | ||||||
| chr5:140010507
|
T | C | 24 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0031others(21): Show | 24 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.700+31863A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010507 | ||||||
| chr5:140010528
|
G | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+31842C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010528 | ||||||
| chr5:140010792
|
T | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(46): Show | 49 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.700+31578A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010792 | ||||||
| chr5:140010831
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+31539T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010831 | ||||||
| chr5:140010882
|
G | A | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.700+31488C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140010882 | ||||||
| chr5:140011134
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+31236G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140011134 | ||||||
| chr5:140011167
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(51): Show | 54 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.700+31203T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140011167 | ||||||
| chr5:140011329
|
A | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(53): Show | 56 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.700+31041T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140011329 | ||||||
| chr5:140011418
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.700+30952C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140011418 | ||||||
| chr5:140011637
|
G | A | 1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.700+30733C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140011637 | ||||||
| chr5:140011762
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0139a0002c0002t0002g0100 | 3 | HG02647.hp2 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.700+30608G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140011762 | ||||||
| chr5:140011901
|
A | G | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.700+30469T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140011901 | ||||||
| chr5:140012116
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0142 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.700+30254A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140012116 | ||||||
| chr5:140012231
|
A | AC | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.700+30138_700+3013 others(5): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140012231 | ||||||
| chr5:140012241
|
G | A | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+30129C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140012241 | ||||||
| chr5:140012337
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+30033G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140012337 | ||||||
| chr5:140012484
|
T | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.700+29886A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140012484 | ||||||
| chr5:140012790
|
T | C | 28 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.700+29580A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140012790 | ||||||
| chr5:140012909
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+29461G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140012909 | ||||||
| chr5:140013279
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.700+29091G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140013279 | ||||||
| chr5:140013480
|
C | T | 8 | a0001c0001t0001g0125a0001c0001t0010g0167a0001c0004t0001g0179others(5): Show | 9 | HG00323.hp1 HG01496.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+28890G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140013480 | ||||||
| chr5:140013832
|
T | C | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(51): Show | 54 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.700+28538A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140013832 | ||||||
| chr5:140014234
|
A | AT | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(51): Show | 54 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.700+28135dupA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140014234 | ||||||
| chr5:140014685
|
G | C | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.700+27685C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140014685 | ||||||
| chr5:140014761
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.700+27609G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140014761 | ||||||
| chr5:140014829
|
A | C | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+27541T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140014829 | ||||||
| chr5:140014830
|
G | C | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+27540C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140014830 | ||||||
| chr5:140015001
|
C | G | 104 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.700+27369G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015001 | ||||||
| chr5:140015016
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01255.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.700+27354A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015016 | ||||||
| chr5:140015049
|
C | T | 76 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.700+27321G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015049 | ||||||
| chr5:140015155
|
AT | A | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(51): Show | 54 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.700+27214delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015155 | ||||||
| chr5:140015356
|
T | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(46): Show | 49 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.700+27014A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015356 | ||||||
| chr5:140015375
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0049others(3): Show | 6 | HG00741.hp1 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.700+26995A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015375 | ||||||
| chr5:140015455
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.700+26915C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015455 | ||||||
| chr5:140015466
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.700+26904A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015466 | ||||||
| chr5:140015507
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+26863G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015507 | ||||||
| chr5:140015514
|
T | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(10): Show | 13 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.700+26856A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015514 | ||||||
| chr5:140015648
|
T | A | 27 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.700+26722A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140015648 | ||||||
| chr5:140016012
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.700+26358G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016012 | ||||||
| chr5:140016176
|
G | A | 1 | a0003c0003t0001g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.700+26194C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016176 | ||||||
| chr5:140016336
|
C | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+26034G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016336 | ||||||
| chr5:140016451
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0071a0001c0001t0001g0137 | 3 | HG01109.hp1 HG04115.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.700+25919G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016451 | ||||||
| chr5:140016511
|
C | T | 1 | a0002c0002t0002g0171 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.700+25859G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016511 | ||||||
| chr5:140016587
|
G | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(11): Show | 14 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.700+25783C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016587 | ||||||
| chr5:140016599
|
C | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.700+25771G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016599 | ||||||
| chr5:140016790
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(44): Show | 47 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+25580C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016790 | ||||||
| chr5:140016877
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+25493C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140016877 | ||||||
| chr5:140017023
|
A | G | 4 | a0001c0001t0001g0107a0002c0002t0003g0169a0004c0006t0001g0122others(1): Show | 4 | HG02145.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+25347T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140017023 | ||||||
| chr5:140017413
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(44): Show | 47 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+24957G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140017413 | ||||||
| chr5:140017481
|
A | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(46): Show | 49 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.700+24889T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140017481 | ||||||
| chr5:140017570
|
T | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(44): Show | 47 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+24800A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140017570 | ||||||
| chr5:140017665
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(44): Show | 47 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+24705C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140017665 | ||||||
| chr5:140017747
|
G | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(46): Show | 49 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.700+24623C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140017747 | ||||||
| chr5:140017776
|
T | C | 2 | a0003c0003t0001g0043a0003c0003t0001g0166 | 2 | HG01099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.700+24594A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140017776 | ||||||
| chr5:140018465
|
T | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(44): Show | 47 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+23905A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140018465 | ||||||
| chr5:140018629
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.700+23741G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140018629 | ||||||
| chr5:140018738
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.700+23632G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140018738 | ||||||
| chr5:140019821
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+22549A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140019821 | ||||||
| chr5:140020430
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+21940C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020430 | ||||||
| chr5:140020472
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+21898A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020472 | ||||||
| chr5:140020508
|
C | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.700+21862G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020508 | ||||||
| chr5:140020707
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700+21663G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020707 | ||||||
| chr5:140020777
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+21593G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020777 | ||||||
| chr5:140020947
|
T | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(44): Show | 47 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+21423A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020947 | ||||||
| chr5:140020990
|
C | T | 1 | a0001c0001t0003g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.700+21380G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020990 | ||||||
| chr5:140020991
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+21379G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140020991 | ||||||
| chr5:140021194
|
T | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(46): Show | 49 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.700+21176A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140021194 | ||||||
| chr5:140021289
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+21081C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140021289 | ||||||
| chr5:140021431
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.700+20939C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140021431 | ||||||
| chr5:140021498
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0172a0002c0002t0003g0173others(2): Show | 5 | HG03225.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+20872G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140021498 | ||||||
| chr5:140021544
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.700+20826C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140021544 | ||||||
| chr5:140021935
|
C | T | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0119others(5): Show | 8 | HG00544.hp2 HG01255.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.700+20435G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140021935 | ||||||
| chr5:140022306
|
G | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0022others(41): Show | 44 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.700+20064C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140022306 | ||||||
| chr5:140022757
|
T | C | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.700+19613A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140022757 | ||||||
| chr5:140022763
|
A | C | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.700+19607T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140022763 | ||||||
| chr5:140023012
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0023others(17): Show | 21 | HG00323.hp1 HG00741.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.700+19358G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023012 | ||||||
| chr5:140023016
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+19354T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023016 | ||||||
| chr5:140023150
|
C | A | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+19220G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023150 | ||||||
| chr5:140023284
|
A | G | 1 | a0002c0002t0002g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.700+19086T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023284 | ||||||
| chr5:140023718
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.700+18652A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023718 | ||||||
| chr5:140023750
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.700+18620A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023750 | ||||||
| chr5:140023802
|
A | C | 2 | a0002c0002t0005g0138a0002c0013t0003g0083 | 2 | HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.700+18568T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023802 | ||||||
| chr5:140023886
|
T | C | 2 | a0001c0001t0001g0004a0004c0006t0001g0159 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.700+18484A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023886 | ||||||
| chr5:140023932
|
A | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0022others(43): Show | 46 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.700+18438T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140023932 | ||||||
| chr5:140024019
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+18351G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140024019 | ||||||
| chr5:140024406
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.700+17964G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140024406 | ||||||
| chr5:140024441
|
G | C | 2 | a0002c0002t0003g0135a0002c0002t0009g0101 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.700+17929C>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140024441 | ||||||
| chr5:140024803
|
G | A | 1 | a0001c0005t0004g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.700+17567C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140024803 | ||||||
| chr5:140025067
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+17303C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140025067 | ||||||
| chr5:140025267
|
C | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0022others(45): Show | 48 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.700+17103G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140025267 | ||||||
| chr5:140025487
|
A | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.700+16883T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140025487 | ||||||
| chr5:140025830
|
G | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0086a0001c0001t0001g0108others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+16540C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140025830 | ||||||
| chr5:140025896
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.700+16474G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140025896 | ||||||
| chr5:140026116
|
C | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0023others(16): Show | 20 | HG00323.hp1 HG00741.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.700+16254G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026116 | ||||||
| chr5:140026347
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.700+16023T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026347 | ||||||
| chr5:140026573
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0023others(17): Show | 21 | HG00323.hp1 HG00741.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.700+15797G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026573 | ||||||
| chr5:140026676
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.700+15694T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026676 | ||||||
| chr5:140026753
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.700+15617A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026753 | ||||||
| chr5:140026777
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0123 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700+15593A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026777 | ||||||
| chr5:140026812
|
T | C | 1 | a0001c0005t0004g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.700+15558A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026812 | ||||||
| chr5:140026858
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0140a0002c0002t0003g0038 | 3 | HG01884.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.700+15512A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026858 | ||||||
| chr5:140026953
|
G | A | 1 | a0002c0002t0003g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.700+15417C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026953 | ||||||
| chr5:140026962
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0144 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.700+15408T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140026962 | ||||||
| chr5:140027371
|
C | A | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+14999G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140027371 | ||||||
| chr5:140027459
|
G | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0022others(58): Show | 61 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.700+14911C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140027459 | ||||||
| chr5:140027522
|
G | A | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+14848C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140027522 | ||||||
| chr5:140027766
|
C | T | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+14604G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140027766 | ||||||
| chr5:140027780
|
A | C | 1 | a0002c0002t0008g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+14590T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140027780 | ||||||
| chr5:140028519
|
C | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(62): Show | 65 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.700+13851G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028519 | ||||||
| chr5:140028545
|
A | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0018others(62): Show | 65 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.700+13825T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028545 | ||||||
| chr5:140028630
|
C | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0023others(16): Show | 20 | HG00323.hp1 HG00741.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.700+13740G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028630 | ||||||
| chr5:140028706
|
C | T | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.700+13664G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028706 | ||||||
| chr5:140028799
|
T | G | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+13571A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028799 | ||||||
| chr5:140028811
|
G | A | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+13559C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028811 | ||||||
| chr5:140028982
|
T | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 17 | HG00544.hp2 HG01255.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.700+13388A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028982 | ||||||
| chr5:140028990
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0006c0008t0001g0176 | 3 | HG00544.hp2 HG02056.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.700+13380C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140028990 | ||||||
| chr5:140029331
|
T | C | 1 | a0002c0002t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.700+13039A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029331 | ||||||
| chr5:140029468
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.700+12902G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029468 | ||||||
| chr5:140029553
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.700+12817C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029553 | ||||||
| chr5:140029637
|
G | A | 1 | a0002c0002t0003g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.700+12733C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029637 | ||||||
| chr5:140029687
|
C | CAAAAAA | 6 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0172others(3): Show | 6 | HG00741.hp2 HG03225.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.700+12677_700+1268 others(10): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(2): Show |
14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+12674_700+1268 others(13): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(3): Show |
1 | a0002c0002t0003g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.700+12673_700+1268 others(14): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0168 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.700+12668_700+1268 others(19): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0108 | 2 | HG01069.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(22): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0131 | 2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(23): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(15): Show |
3 | a0002c0002t0002g0021a0002c0002t0002g0040a0002c0002t0002g0041 | 3 | HG01074.hp1 HG01081.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(26): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0174a0002c0002t0003g0095 | 3 | HG01257.hp1 HG01496.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(27): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0157 | 2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(28): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(20): Show |
1 | a0001c0014t0001g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.700+12682_700+1268 others(31): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(22): Show |
1 | a0007c0012t0001g0121 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.700+12682_700+1268 others(33): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.700+12682_700+1268 others(35): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.700+12682_700+1268 others(36): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(27): Show |
2 | a0001c0001t0001g0107a0008c0011t0001g0106 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(38): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(28): Show |
2 | a0002c0002t0003g0169a0004c0006t0001g0122 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(39): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0092 | 2 | HG00621.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(40): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.700+12682_700+1268 others(41): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(32): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0071a0002c0002t0002g0009others(1): Show | 4 | HG01099.hp1 HG01934.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+12682_700+1268 others(43): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(33): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0137others(1): Show | 4 | HG00735.hp2 HG01109.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+12682_700+1268 others(44): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(35): Show |
1 | a0001c0001t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.700+12682_700+1268 others(46): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140029687
|
C | CAAAAAAA others(36): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0115 | 2 | HG00639.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.700+12682_700+1268 others(47): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140029687 | ||||||
| chr5:140030313
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.700+12057G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140030313 | ||||||
| chr5:140030460
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0086a0001c0001t0001g0108others(3): Show | 6 | HG01099.hp2 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.700+11910G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140030460 | ||||||
| chr5:140030473
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.700+11897A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140030473 | ||||||
| chr5:140030925
|
T | C | 43 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0045others(40): Show | 44 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.700+11445A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140030925 | ||||||
| chr5:140031102
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(71): Show | 74 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.700+11268G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140031102 | ||||||
| chr5:140031360
|
T | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 114 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.700+11010A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140031360 | ||||||
| chr5:140031449
|
T | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 5 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+10921A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140031449 | ||||||
| chr5:140031561
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 43 | HG00544.hp2 HG01109.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.700+10809A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140031561 | ||||||
| chr5:140031652
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | NA18974.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.700+10718G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140031652 | ||||||
| chr5:140031711
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.700+10659A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140031711 | ||||||
| chr5:140031721
|
A | T | 3 | a0001c0001t0001g0168a0002c0002t0003g0150a0002c0002t0003g0170 | 3 | HG01167.hp2 HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.700+10649T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140031721 | ||||||
| chr5:140032118
|
G | A | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 124 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.700+10252C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032118 | ||||||
| chr5:140032245
|
T | C | 1 | a0009c0015t0002g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.700+10125A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032245 | ||||||
| chr5:140032414
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.700+9956C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032414 | ||||||
| chr5:140032587
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0168a0001c0001t0001g0172others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+9783G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032587 | ||||||
| chr5:140032593
|
A | G | 9 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+9777T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032593 | ||||||
| chr5:140032759
|
A | G | 2 | a0001c0001t0001g0049a0002c0002t0005g0050 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.700+9611T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032759 | ||||||
| chr5:140032845
|
T | C | 1 | a0002c0002t0002g0160 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.700+9525A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032845 | ||||||
| chr5:140032914
|
G | A | 5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0142others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+9456C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140032914 | ||||||
| chr5:140033326
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0168a0001c0001t0001g0172others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+9044T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140033326 | ||||||
| chr5:140033336
|
C | G | 2 | a0001c0005t0004g0048a0002c0002t0003g0038 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.700+9034G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140033336 | ||||||
| chr5:140033579
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0123a0001c0001t0001g0124others(11): Show | 14 | HG01167.hp2 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.700+8791C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140033579 | ||||||
| chr5:140033583
|
C | G | 1 | a0001c0001t0010g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.700+8787G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140033583 | ||||||
| chr5:140033772
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.700+8598G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140033772 | ||||||
| chr5:140033814
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.700+8556T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140033814 | ||||||
| chr5:140034000
|
C | T | 17 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0044others(14): Show | 18 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.700+8370G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140034000 | ||||||
| chr5:140034331
|
CT | C | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01257.hp1 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.700+8038delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140034331 | ||||||
| chr5:140034749
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.700+7621T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140034749 | ||||||
| chr5:140034803
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.700+7567G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140034803 | ||||||
| chr5:140035146
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0168a0001c0001t0001g0172others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+7224A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140035146 | ||||||
| chr5:140035167
|
G | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.700+7203C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140035167 | ||||||
| chr5:140035910
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.700+6460G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140035910 | ||||||
| chr5:140035947
|
C | T | 153 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.700+6423G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140035947 | ||||||
| chr5:140036612
|
C | T | 1 | a0002c0002t0003g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.700+5758G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140036612 | ||||||
| chr5:140036680
|
C | A | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(157): Show | 162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.700+5690G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140036680 | ||||||
| chr5:140036833
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.700+5537A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140036833 | ||||||
| chr5:140036850
|
T | C | 1 | a0002c0002t0003g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.700+5520A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140036850 | ||||||
| chr5:140036902
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.700+5468T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140036902 | ||||||
| chr5:140037341
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.700+5029A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037341 | ||||||
| chr5:140037762
|
A | G | 2 | a0001c0005t0004g0151a0002c0002t0003g0150 | 2 | HG01167.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.700+4608T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037762 | ||||||
| chr5:140037907
|
C | CA | 11 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0110others(8): Show | 11 | HG00639.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+4462dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037907 | ||||||
| chr5:140037907
|
C | CAAAAAA | 23 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0152others(20): Show | 24 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.700+4457_700+4462d others(8): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037907 | ||||||
| chr5:140037926
|
AAGACTGC others(4): Show |
A | 3 | a0001c0001t0001g0168a0002c0002t0003g0169a0002c0002t0003g0170 | 3 | HG02145.hp1 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.700+4433_700+4443d others(13): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037926 | ||||||
| chr5:140037936
|
TGAAAAAC others(12): Show |
T | 6 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0172others(3): Show | 6 | HG01884.hp1 HG03225.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.700+4415_700+4433d others(21): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037936 | ||||||
| chr5:140037943
|
C | G | 3 | a0001c0001t0001g0168a0002c0002t0003g0169a0002c0002t0003g0170 | 3 | HG02145.hp1 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.700+4427G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037943 | ||||||
| chr5:140037945
|
T | C | 3 | a0001c0001t0001g0168a0002c0002t0003g0169a0002c0002t0003g0170 | 3 | HG02145.hp1 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.700+4425A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037945 | ||||||
| chr5:140037947
|
GTGTT | G | 3 | a0001c0001t0001g0168a0002c0002t0003g0169a0002c0002t0003g0170 | 3 | HG02145.hp1 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.700+4419_700+4422d others(6): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037947 | ||||||
| chr5:140037952
|
T | C | 3 | a0001c0001t0001g0168a0002c0002t0003g0169a0002c0002t0003g0170 | 3 | HG02145.hp1 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.700+4418A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037952 | ||||||
| chr5:140037955
|
A | T | 3 | a0001c0001t0001g0168a0002c0002t0003g0169a0002c0002t0003g0170 | 3 | HG02145.hp1 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.700+4415T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140037955 | ||||||
| chr5:140038106
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+4264C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140038106 | ||||||
| chr5:140038227
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127 | 3 | HG01496.hp1 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.700+4143G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140038227 | ||||||
| chr5:140038470
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | NA19002.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.700+3900T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140038470 | ||||||
| chr5:140038564
|
G | A | 7 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0175others(4): Show | 7 | HG00544.hp2 HG02056.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.700+3806C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140038564 | ||||||
| chr5:140038801
|
G | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127 | 3 | HG01496.hp1 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.700+3569C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140038801 | ||||||
| chr5:140039000
|
T | C | 1 | a0004c0006t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.700+3370A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140039000 | ||||||
| chr5:140039448
|
G | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.700+2922C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140039448 | ||||||
| chr5:140039595
|
A | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.700+2775T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140039595 | ||||||
| chr5:140039648
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.700+2722C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140039648 | ||||||
| chr5:140039868
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG00639.hp1 HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.700+2502G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140039868 | ||||||
| chr5:140040083
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.700+2287T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140040083 | ||||||
| chr5:140040377
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0168others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+1993G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140040377 | ||||||
| chr5:140040390
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.700+1980G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140040390 | ||||||
| chr5:140040400
|
C | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0123others(36): Show | 40 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.700+1970G>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140040400 | ||||||
| chr5:140040525
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0127 | 3 | HG01496.hp1 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.700+1845T>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140040525 | ||||||
| chr5:140040890
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0172a0002c0002t0002g0171others(1): Show | 4 | HG03225.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+1480C>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140040890 | ||||||
| chr5:140041002
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.700+1368A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041002 | ||||||
| chr5:140041041
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.700+1329C>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041041 | ||||||
| chr5:140041069
|
C | T | 1 | a0002c0002t0002g0009 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.700+1301G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041069 | ||||||
| chr5:140041142
|
C | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0168others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+1228G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041142 | ||||||
| chr5:140041355
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.700+1015A>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041355 | ||||||
| chr5:140041360
|
T | A | 28 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0149others(25): Show | 29 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.700+1010A>T | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041360 | ||||||
| chr5:140041405
|
A | T | 1 | a0001c0001t0003g0007 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.700+965T>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041405 | ||||||
| chr5:140041564
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.700+806G>A | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041564 | ||||||
| chr5:140041666
|
T | TA | 39 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(36): Show | 40 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.700+703dupT | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041666 | ||||||
| chr5:140041666
|
T | TAA | 11 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0161others(8): Show | 11 | HG01261.hp1 HG01361.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.700+702_700+703dup others(2): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041666 | ||||||
| chr5:140041666
|
T | TAAA | 9 | a0001c0001t0001g0004a0001c0001t0001g0168a0001c0001t0001g0172others(6): Show | 9 | HG01257.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+701_700+703dup others(3): Show |
NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041666 | ||||||
| chr5:140041690
|
T | C | 2 | a0001c0001t0001g0175a0006c0008t0001g0176 | 2 | HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.700+680A>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041690 | ||||||
| chr5:140041769
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.700+601G>C | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041769 | ||||||
| chr5:140041863
|
A | C | 1 | a0001c0001t0001g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.700+507T>G | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140041863 | ||||||
| chr5:140042163
|
CT | C | 2 | a0003c0003t0001g0002a0003c0003t0001g0177 | 3 | HG03490.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.700+206delA | NRG2 | ENSG00000158458.21 | transcript | ENST00000361474.6 | protein_coding | 1/9 | chr5 | 140042163 |