Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4771 |
|---|---|
| ensemblid | ENSG00000186575.19 |
| hgncid | 7773 |
| symbol | NF2 |
| name | NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor |
| refseq_nuc | NM_000268.4 |
| refseq_prot | NP_000259.1 |
| ensembl_nuc | ENST00000338641.10 |
| ensembl_prot | ENSP00000344666.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 29603633 |
| end | 29698598 |
| strand | + |
| ver | v1.2 |
| region | chr22:29603633-29698598 |
| region5000 | chr22:29598633-29703598 |
| regionname0 | NF2_chr22_29603633_29698598 |
| regionname5000 | NF2_chr22_29598633_29703598 |
| 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 | 595 | 342 | 90 | 62 | 137 | 16 | 35 | 96 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0002 | 0/0 | 595 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0003 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| 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 | 1788 | 331 | 87 | 62 | 129 | 16 | 35 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| c0002 | 0/0 | 1788 | 8 | 0 | 0 | 8 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| c0003 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| c0004 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| c0005 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| c0006 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| c0007 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4164 | 54 | 9 | 5 | 32 | 3 | 5 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0002 | 0/1 | 4163 | 45 | 2 | 14 | 17 | 3 | 8 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0003 | 0/0 | 4164 | 39 | 13 | 1 | 20 | 0 | 5 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0004 | 0/0 | 4164 | 27 | 0 | 1 | 23 | 0 | 3 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0005 | 0/0 | 4165 | 23 | 1 | 8 | 5 | 4 | 5 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0006 | 0/0 | 4164 | 17 | 16 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0007 | 0/0 | 4164 | 11 | 2 | 5 | 3 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0008 | 0/0 | 4165 | 11 | 10 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0009 | 0/0 | 4164 | 11 | 0 | 3 | 7 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0010 | 0/0 | 4164 | 10 | 0 | 8 | 0 | 2 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0011 | 0/0 | 4164 | 7 | 3 | 2 | 1 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0012 | 0/0 | 4165 | 5 | 0 | 0 | 4 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0013 | 0/0 | 4164 | 5 | 5 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0014 | 0/0 | 4165 | 5 | 2 | 1 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0015 | 0/0 | 4164 | 4 | 4 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0016 | 0/0 | 4158 | 4 | 0 | 0 | 2 | 0 | 2 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0017 | 0/0 | 4164 | 4 | 0 | 1 | 2 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0018 | 0/0 | 4165 | 3 | 0 | 0 | 2 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0019 | 0/0 | 4162 | 3 | 1 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0020 | 0/0 | 4165 | 3 | 0 | 0 | 3 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0021 | 0/0 | 4165 | 3 | 1 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0022 | 0/0 | 4165 | 2 | 0 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0023 | 0/0 | 4154 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0024 | 0/0 | 4163 | 2 | 1 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0025 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0026 | 0/0 | 4164 | 2 | 0 | 2 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0027 | 0/0 | 4165 | 2 | 0 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0028 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0029 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0030 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0031 | 0/0 | 4163 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0032 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0033 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0034 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0035 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0036 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0037 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0038 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0039 | 0/0 | 4163 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0040 | 0/0 | 4163 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0041 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0042 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0043 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0044 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0045 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0046 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0047 | 0/0 | 4163 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0048 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0049 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0050 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0051 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0052 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0053 | 0/0 | 4165 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0054 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0055 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0056 | 0/0 | 4165 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0057 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0058 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0059 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0060 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0061 | 1/0 | 4163 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0062 | 0/0 | 4163 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0063 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0064 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| t0065 | 0/0 | 4165 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| 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 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0320 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| 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 | 1788 | 331 | 87 | 62 | 129 | 16 | 35 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0002 | 0/0 | 1788 | 8 | 0 | 0 | 8 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0004 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0006 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0007 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0002c0003 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0003c0005 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5951 | 53 | 9 | 5 | 32 | 3 | 4 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0002 | 0/1 | 5950 | 44 | 1 | 14 | 17 | 3 | 8 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0003 | 0/0 | 5951 | 31 | 13 | 1 | 12 | 0 | 5 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0004 | 0/0 | 5951 | 27 | 0 | 1 | 23 | 0 | 3 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0005 | 0/0 | 5952 | 23 | 1 | 8 | 5 | 4 | 5 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0006 | 0/0 | 5951 | 17 | 16 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0007 | 0/0 | 5951 | 11 | 2 | 5 | 3 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0008 | 0/0 | 5952 | 11 | 10 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0009 | 0/0 | 5951 | 11 | 0 | 3 | 7 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0010 | 0/0 | 5951 | 10 | 0 | 8 | 0 | 2 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0011 | 0/0 | 5951 | 7 | 3 | 2 | 1 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0012 | 0/0 | 5952 | 5 | 0 | 0 | 4 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0013 | 0/0 | 5951 | 5 | 5 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0014 | 0/0 | 5952 | 5 | 2 | 1 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0015 | 0/0 | 5951 | 4 | 4 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0016 | 0/0 | 5945 | 4 | 0 | 0 | 2 | 0 | 2 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0017 | 0/0 | 5951 | 3 | 0 | 1 | 1 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0018 | 0/0 | 5952 | 3 | 0 | 0 | 2 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0019 | 0/0 | 5949 | 3 | 1 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0020 | 0/0 | 5952 | 3 | 0 | 0 | 3 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0021 | 0/0 | 5952 | 3 | 1 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0022 | 0/0 | 5952 | 2 | 0 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0023 | 0/0 | 5941 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0024 | 0/0 | 5950 | 2 | 1 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0025 | 0/0 | 5951 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0026 | 0/0 | 5951 | 2 | 0 | 2 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0027 | 0/0 | 5952 | 2 | 0 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0028 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0029 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0030 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0031 | 0/0 | 5950 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0032 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0033 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0034 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0035 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0036 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0037 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0038 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0039 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0040 | 0/0 | 5950 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0041 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0042 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0043 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0045 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0046 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0047 | 0/0 | 5950 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0048 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0049 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0050 | 0/0 | 5951 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0051 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0053 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0054 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0055 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0056 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0057 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0058 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0059 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0060 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0061 | 1/0 | 5950 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0062 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0063 | 0/0 | 5951 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0064 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0001t0065 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0002t0003 | 0/0 | 5951 | 8 | 0 | 0 | 8 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0004t0002 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0006t0044 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0001c0007t0052 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0002c0003t0001 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| a0003c0005t0017 | 0/0 | 5951 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | copy fasta | chr22 | 29598633 | 29703598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0015g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0015g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0016g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0016g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0016g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0016g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0017g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0017g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0018g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0018g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0018g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0019g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0019g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0019g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0020g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0020g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0020g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0021g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0021g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0021g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0022g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0022g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0023g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0023g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0024g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0024g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0025g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0025g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0026g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0026g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0027g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0027g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0028g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0029g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0030g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0031g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0032g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0033g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0034g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0035g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0036g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0037g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0038g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0039g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0040g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0041g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0042g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0043g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0045g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0046g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0047g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0048g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0049g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0050g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0051g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0053g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0054g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0055g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0056g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0057g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0058g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0059g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0060g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0061g0320 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0062g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0063g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0064g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0065g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0004t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0006t0044g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0007t0052g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0002c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0003c0005t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0041 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0318 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0321 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00280 | hp2 | a0001 | c0001 | t0028 | g0219 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0252 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0093 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00438 | hp2 | a0001 | c0001 | t0020 | g0136 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00558 | hp1 | a0001 | c0001 | t0009 | g0089 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00558 | hp2 | a0001 | c0001 | t0034 | g0229 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00609 | hp1 | a0001 | c0001 | t0016 | g0329 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00621 | hp1 | a0001 | c0001 | t0014 | g0059 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00639 | hp2 | a0001 | c0001 | t0038 | g0034 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00673 | hp2 | a0001 | c0001 | t0018 | g0223 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00735 | hp1 | a0001 | c0001 | t0053 | g0128 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0303 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00738 | hp2 | a0001 | c0001 | t0057 | g0148 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0319 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01070 | hp1 | a0001 | c0001 | t0026 | g0067 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01070 | hp2 | a0001 | c0001 | t0011 | g0074 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01071 | hp1 | a0001 | c0001 | t0026 | g0132 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0032 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0324 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01081 | hp1 | a0001 | c0001 | t0049 | g0131 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0033 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01099 | hp2 | a0001 | c0001 | t0024 | g0014 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0077 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0315 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0327 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0290 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01175 | hp2 | a0001 | c0001 | t0056 | g0008 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01192 | hp1 | a0001 | c0001 | t0040 | g0035 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01243 | hp2 | a0001 | c0001 | t0029 | g0151 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0030 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0313 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0028 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01257 | hp2 | a0001 | c0001 | t0017 | g0323 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0322 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0029 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0053 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0309 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01346 | hp2 | a0001 | c0001 | t0009 | g0233 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01358 | hp1 | a0001 | c0001 | t0065 | g0234 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0007 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0113 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01515 | hp1 | a0001 | c0001 | t0047 | g0142 | EUR | IBS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01515 | hp2 | a0001 | c0001 | t0017 | g0317 | EUR | IBS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0299 | EUR | IBS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01517 | hp2 | a0001 | c0001 | t0031 | g0071 | EUR | IBS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0016 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01884 | hp2 | a0001 | c0001 | t0058 | g0254 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0208 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0083 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0326 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0106 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01978 | hp1 | a0001 | c0001 | t0009 | g0284 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0207 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0087 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02015 | hp1 | a0003 | c0005 | t0017 | g0002 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0296 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0114 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02056 | hp1 | a0001 | c0001 | t0018 | g0169 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02056 | hp2 | a0001 | c0001 | t0021 | g0066 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02080 | hp1 | a0001 | c0001 | t0021 | g0075 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02083 | hp1 | a0001 | c0001 | t0017 | g0002 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0090 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0314 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02148 | hp1 | a0001 | c0001 | t0014 | g0186 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0213 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | CDX | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | CDX | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0258 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0082 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02280 | hp2 | a0001 | c0001 | t0023 | g0231 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02451 | hp1 | a0001 | c0001 | t0033 | g0152 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02451 | hp2 | a0001 | c0001 | t0043 | g0047 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02523 | hp1 | a0001 | c0001 | t0009 | g0088 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02572 | hp2 | a0001 | c0001 | t0060 | g0248 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0130 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02622 | hp1 | a0001 | c0001 | t0015 | g0178 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0177 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0338 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0080 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0249 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02683 | hp1 | a0001 | c0001 | t0011 | g0076 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02717 | hp2 | a0001 | c0001 | t0023 | g0277 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0337 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02738 | hp1 | a0001 | c0001 | t0016 | g0332 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0276 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02895 | hp1 | a0001 | c0001 | t0046 | g0310 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02896 | hp1 | a0001 | c0001 | t0036 | g0060 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02896 | hp2 | a0001 | c0001 | t0030 | g0174 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02922 | hp2 | a0001 | c0001 | t0024 | g0015 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0175 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0333 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0312 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03017 | hp2 | a0001 | c0001 | t0035 | g0168 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03098 | hp1 | a0001 | c0001 | t0045 | g0295 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03098 | hp2 | a0001 | c0001 | t0013 | g0005 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0257 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0176 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03195 | hp1 | a0001 | c0001 | t0025 | g0013 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0256 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03209 | hp1 | a0001 | c0007 | t0052 | g0281 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0251 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03225 | hp1 | a0001 | c0006 | t0044 | g0294 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0183 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03453 | hp1 | a0001 | c0001 | t0059 | g0245 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0340 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0260 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0336 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0316 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0308 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0262 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03579 | hp2 | a0001 | c0001 | t0021 | g0081 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0330 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03831 | hp1 | a0001 | c0001 | t0012 | g0011 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03927 | hp2 | a0001 | c0001 | t0032 | g0163 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03942 | hp1 | a0001 | c0001 | t0018 | g0167 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0078 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0301 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04228 | hp1 | a0001 | c0001 | t0037 | g0293 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18522 | hp1 | a0001 | c0001 | t0042 | g0140 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CHB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18747 | hp1 | a0001 | c0001 | t0050 | g0046 | EAS | CHB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0264 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18949 | hp1 | a0001 | c0001 | t0022 | g0288 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0111 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18950 | hp1 | a0001 | c0001 | t0019 | g0306 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0084 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18957 | hp1 | a0001 | c0001 | t0039 | g0146 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18959 | hp2 | a0001 | c0001 | t0041 | g0232 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18973 | hp2 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18975 | hp1 | a0001 | c0001 | t0012 | g0265 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18978 | hp2 | a0001 | c0001 | t0012 | g0058 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18982 | hp2 | a0001 | c0001 | t0022 | g0158 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18985 | hp1 | a0001 | c0001 | t0027 | g0092 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18988 | hp2 | a0001 | c0001 | t0014 | g0101 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0209 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0104 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19005 | hp1 | a0001 | c0001 | t0063 | g0091 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19011 | hp1 | a0001 | c0001 | t0019 | g0215 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19012 | hp2 | a0001 | c0001 | t0016 | g0328 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19030 | hp2 | a0001 | c0001 | t0054 | g0282 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0261 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19054 | hp2 | a0001 | c0001 | t0027 | g0094 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0181 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19067 | hp1 | a0001 | c0001 | t0020 | g0024 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19067 | hp2 | a0001 | c0001 | t0012 | g0119 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19082 | hp2 | a0001 | c0001 | t0064 | g0283 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19086 | hp1 | a0001 | c0001 | t0062 | g0086 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19087 | hp2 | a0001 | c0001 | t0020 | g0116 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0115 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20129 | hp1 | a0001 | c0001 | t0048 | g0230 | AFR | ASW | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ASW | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0191 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20752 | hp2 | a0001 | c0001 | t0010 | g0027 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0274 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0009 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0342 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0218 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0079 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02559 | hp2 | a0001 | c0001 | t0051 | g0003 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0004 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0259 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0263 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0341 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0325 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA21309 | hp2 | a0001 | c0001 | t0055 | g0331 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0275 | REF | REF | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0061 | g0320 | REF | REF | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29671938
|
A | G | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1112A>G | p.Asn371Ser | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/16 | 1478/5950 | 1112/1788 | 371/595 | chr22 | 29671938 | ||
| chr22:29678254
|
G | A | 1 | a0002 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1505G>A | p.Gly502Asp | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/16 | 1871/5950 | 1505/1788 | 502/595 | chr22 | 29678254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29604010
|
C | T | 1 | a0001c0007 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.12C>T | p.Ala4Ala | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/16 | 378/5950 | 12/1788 | 4/595 | chr22 | 29604010 | ||
| chr22:29639167
|
A | G | 1 | a0001c0006 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.318A>G | p.Glu106Glu | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/16 | 684/5950 | 318/1788 | 106/595 | chr22 | 29639167 | ||
| chr22:29671939
|
C | T | 1 | a0001c0002 | 8 | NA18944.hp2 NA18968.hp1 NA18974.hp1 others(5): Show |
synonymous_variant | LOW | c.1113C>T | p.Asn371Asn | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/16 | 1479/5950 | 1113/1788 | 371/595 | chr22 | 29671939 | ||
| chr22:29674881
|
C | T | 1 | a0001c0004 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1386C>T | p.Arg462Arg | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/16 | 1752/5950 | 1386/1788 | 462/595 | chr22 | 29674881 | ||
| chr22:29674911
|
C | T | 1 | a0001c0004 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1416C>T | p.Leu472Leu | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/16 | 1782/5950 | 1416/1788 | 472/595 | chr22 | 29674911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29603753
|
C | G | 6 | a0001c0001t0009a0001c0001t0027a0001c0001t0062others(3): Show | 17 | HG00408.hp1 HG00558.hp1 HG01346.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-246C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/16 | 246 | chr22 | 29603753 | |||||
| chr22:29603795
|
C | A | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(14): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-204C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/16 | 204 | chr22 | 29603795 | |||||
| chr22:29603889
|
G | C | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
5_prime_UTR_variant | MODIFIER | c.-110G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/16 | 110 | chr22 | 29603889 | |||||
| chr22:29694806
|
G | A | 1 | a0001c0001t0036 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 4 | chr22 | 29694806 | |||||
| chr22:29695156
|
T | C | 23 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(20): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*354T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 354 | chr22 | 29695156 | |||||
| chr22:29695380
|
C | T | 1 | a0001c0001t0057 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 578 | chr22 | 29695380 | |||||
| chr22:29695518
|
A | G | 1 | a0001c0001t0060 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 716 | chr22 | 29695518 | |||||
| chr22:29695776
|
C | T | 2 | a0001c0001t0010a0001c0001t0056 | 11 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*974C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 974 | chr22 | 29695776 | |||||
| chr22:29695889
|
C | T | 1 | a0001c0001t0055 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1087 | chr22 | 29695889 | |||||
| chr22:29695944
|
G | A | 1 | a0001c0001t0037 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1142 | chr22 | 29695944 | |||||
| chr22:29695991
|
C | T | 1 | a0001c0001t0035 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1189 | chr22 | 29695991 | |||||
| chr22:29696010
|
C | T | 22 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(19): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1208C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1208 | chr22 | 29696010 | |||||
| chr22:29696066
|
C | CT | 14 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(11): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1287dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1288 | INFO_REALIGN_3_PRIME | chr22 | 29696066 | ||||
| chr22:29696066
|
CT | C | 6 | a0001c0001t0019a0001c0001t0024a0001c0001t0030others(3): Show | 9 | HG01099.hp2 HG02896.hp1 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1287delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1287 | INFO_REALIGN_3_PRIME | chr22 | 29696066 | ||||
| chr22:29696066
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0023 | 2 | HG02280.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1278_*1287delTTTT others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1278 | INFO_REALIGN_3_PRIME | chr22 | 29696066 | ||||
| chr22:29696072
|
T | C | 2 | a0001c0001t0029a0001c0001t0043 | 2 | HG01243.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1270 | chr22 | 29696072 | |||||
| chr22:29696118
|
GGTGGGA | G | 1 | a0001c0001t0016 | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1320_*1325delGGAG others(2): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1320 | INFO_REALIGN_3_PRIME | chr22 | 29696118 | ||||
| chr22:29696420
|
T | C | 3 | a0001c0001t0045a0001c0001t0046a0001c0006t0044 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1618T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1618 | chr22 | 29696420 | |||||
| chr22:29696442
|
A | C | 5 | a0001c0001t0015a0001c0001t0016a0001c0001t0030others(2): Show | 11 | HG00609.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1640A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1640 | chr22 | 29696442 | |||||
| chr22:29696594
|
G | A | 5 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(2): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1792G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1792 | chr22 | 29696594 | |||||
| chr22:29696706
|
A | G | 8 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(5): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1904A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 1904 | chr22 | 29696706 | |||||
| chr22:29696795
|
G | GT | 4 | a0001c0001t0020a0001c0001t0034a0001c0001t0041others(1): Show | 6 | HG00438.hp2 HG00558.hp2 NA18959.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2007dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2008 | INFO_REALIGN_3_PRIME | chr22 | 29696795 | ||||
| chr22:29696824
|
G | GT | 59 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(56): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*2032dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2033 | INFO_REALIGN_3_PRIME | chr22 | 29696824 | ||||
| chr22:29696851
|
C | G | 1 | a0001c0001t0024 | 2 | HG01099.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2049C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2049 | chr22 | 29696851 | |||||
| chr22:29696855
|
C | T | 1 | a0001c0001t0063 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2053 | chr22 | 29696855 | |||||
| chr22:29697026
|
A | G | 4 | a0001c0001t0011a0001c0001t0021a0001c0001t0050others(1): Show | 12 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2224A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2224 | chr22 | 29697026 | |||||
| chr22:29697037
|
G | A | 9 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(6): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2235G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2235 | chr22 | 29697037 | |||||
| chr22:29697171
|
T | C | 3 | a0001c0001t0045a0001c0001t0046a0001c0006t0044 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2369T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2369 | chr22 | 29697171 | |||||
| chr22:29697210
|
G | A | 1 | a0001c0001t0013 | 5 | HG03098.hp2 HG03209.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2408G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2408 | chr22 | 29697210 | |||||
| chr22:29697257
|
T | C | 1 | a0001c0001t0053 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2455T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2455 | chr22 | 29697257 | |||||
| chr22:29697266
|
G | A | 1 | a0001c0001t0032 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2464 | chr22 | 29697266 | |||||
| chr22:29697270
|
C | G | 18 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(15): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2468C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2468 | chr22 | 29697270 | |||||
| chr22:29697409
|
C | T | 1 | a0001c0001t0054 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2607C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2607 | chr22 | 29697409 | |||||
| chr22:29697445
|
GATGGAGA others(4): Show |
G | 1 | a0001c0001t0046 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644_*2654delATGG others(7): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2644 | chr22 | 29697445 | |||||
| chr22:29697561
|
G | A | 7 | a0001c0001t0003a0001c0001t0022a0001c0001t0025others(4): Show | 46 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2759G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2759 | chr22 | 29697561 | |||||
| chr22:29697643
|
C | T | 1 | a0001c0001t0049 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2841C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2841 | chr22 | 29697643 | |||||
| chr22:29697678
|
T | C | 19 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(16): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2876T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2876 | chr22 | 29697678 | |||||
| chr22:29697691
|
C | T | 1 | a0001c0001t0027 | 2 | NA18985.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2889C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 2889 | chr22 | 29697691 | |||||
| chr22:29698010
|
G | A | 1 | a0001c0001t0016 | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3208G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 3208 | chr22 | 29698010 | |||||
| chr22:29698076
|
G | A | 8 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(5): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*3274G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 3274 | chr22 | 29698076 | |||||
| chr22:29698377
|
G | A | 2 | a0001c0001t0026a0001c0001t0049 | 3 | HG01070.hp1 HG01071.hp1 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3575G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 16/16 | 3575 | chr22 | 29698377 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29604437
|
T | G | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.114+325T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29604437 | ||||||
| chr22:29604446
|
G | GT | 7 | a0001c0001t0003g0336a0001c0001t0003g0337a0001c0001t0003g0338others(4): Show | 7 | HG02486.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+335dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29604446 | |||||
| chr22:29604500
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.114+388A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29604500 | ||||||
| chr22:29604737
|
C | A | 2 | a0001c0001t0013g0004a0001c0001t0013g0005 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.114+625C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29604737 | ||||||
| chr22:29604844
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.114+732A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29604844 | ||||||
| chr22:29604874
|
A | G | 1 | a0001c0001t0019g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.114+762A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29604874 | ||||||
| chr22:29604993
|
C | G | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+881C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29604993 | ||||||
| chr22:29605151
|
AT | A | 220 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(217): Show | 220 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.114+1061delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29605151 | |||||
| chr22:29605151
|
ATT | A | 7 | a0001c0001t0002g0072a0001c0001t0003g0069a0001c0001t0004g0068others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+1060_114+1061d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29605151 | |||||
| chr22:29605151
|
ATTTT | A | 61 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.114+1058_114+1061d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29605151 | |||||
| chr22:29605402
|
A | T | 4 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326others(1): Show | 4 | HG01074.hp2 HG01168.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+1290A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29605402 | ||||||
| chr22:29605458
|
G | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+1346G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29605458 | ||||||
| chr22:29605792
|
C | T | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+1680C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29605792 | ||||||
| chr22:29606047
|
C | T | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.114+1935C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606047 | ||||||
| chr22:29606088
|
G | T | 6 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0273others(3): Show | 6 | HG00323.hp2 HG01168.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+1976G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606088 | ||||||
| chr22:29606141
|
G | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+2029G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606141 | ||||||
| chr22:29606193
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.114+2081A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606193 | ||||||
| chr22:29606451
|
T | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+2339T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606451 | ||||||
| chr22:29606495
|
G | A | 15 | a0001c0001t0004g0078a0001c0001t0008g0083a0001c0001t0011g0073others(12): Show | 15 | HG01070.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+2383G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606495 | ||||||
| chr22:29606613
|
AT | A | 14 | a0001c0001t0009g0084a0001c0001t0009g0085a0001c0001t0009g0087others(11): Show | 14 | HG00408.hp1 HG00558.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+2502delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606613 | ||||||
| chr22:29606614
|
T | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.114+2502T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606614 | ||||||
| chr22:29606766
|
C | T | 6 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268others(3): Show | 6 | HG00673.hp1 HG02074.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+2654C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606766 | ||||||
| chr22:29607247
|
A | G | 1 | a0001c0001t0007g0264 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.114+3135A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29607247 | ||||||
| chr22:29607259
|
T | C | 7 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(4): Show | 7 | HG01192.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+3147T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29607259 | ||||||
| chr22:29607303
|
T | TGAAAATA others(331): Show |
1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.114+3207_114+3208i others(340): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29607303 | |||||
| chr22:29607369
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114+3257T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29607369 | ||||||
| chr22:29607436
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.114+3324C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29607436 | ||||||
| chr22:29607756
|
T | C | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3644T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29607756 | ||||||
| chr22:29608172
|
C | CA | 179 | a0001c0001t0001g0100a0001c0001t0001g0120a0001c0001t0001g0123others(176): Show | 179 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.114+4085dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29608172 | |||||
| chr22:29608172
|
C | CAA | 25 | a0001c0001t0001g0103a0001c0001t0002g0107a0001c0001t0002g0109others(22): Show | 25 | HG01175.hp1 HG01496.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.114+4084_114+4085d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29608172 | |||||
| chr22:29608172
|
CA | C | 65 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+4085delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29608172 | |||||
| chr22:29608400
|
A | C | 10 | a0001c0001t0008g0113a0001c0001t0008g0114a0001c0001t0008g0115others(7): Show | 10 | HG01496.hp1 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4288A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29608400 | ||||||
| chr22:29608536
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114+4424G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29608536 | ||||||
| chr22:29608644
|
G | A | 6 | a0001c0001t0008g0083a0001c0001t0011g0079a0001c0001t0011g0080others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+4532G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29608644 | ||||||
| chr22:29608675
|
GA | G | 6 | a0001c0001t0001g0064a0001c0001t0024g0014a0001c0001t0024g0015others(3): Show | 6 | HG00558.hp2 HG01099.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+4577delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29608675 | |||||
| chr22:29608700
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.114+4588A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29608700 | ||||||
| chr22:29608940
|
C | T | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.114+4828C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29608940 | ||||||
| chr22:29609005
|
G | A | 6 | a0001c0001t0008g0256a0001c0001t0008g0257a0001c0001t0008g0258others(3): Show | 6 | HG02257.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4893G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29609005 | ||||||
| chr22:29609017
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0226a0001c0001t0003g0227 | 3 | HG00621.hp2 HG02523.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.114+4905A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29609017 | ||||||
| chr22:29609081
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.114+4969C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29609081 | ||||||
| chr22:29609420
|
G | A | 1 | a0001c0001t0025g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.114+5308G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29609420 | ||||||
| chr22:29609507
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114+5395C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29609507 | ||||||
| chr22:29609719
|
G | C | 1 | a0001c0001t0008g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.114+5607G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29609719 | ||||||
| chr22:29610033
|
T | TAG | 123 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.114+5943_114+5944d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29610033 | |||||
| chr22:29610033
|
T | TAGAG | 13 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0221others(10): Show | 13 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.114+5941_114+5944d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29610033 | |||||
| chr22:29610047
|
G | T | 1 | a0001c0001t0008g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114+5935G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610047 | ||||||
| chr22:29610206
|
C | T | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+6094C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610206 | ||||||
| chr22:29610337
|
C | A | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.114+6225C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610337 | ||||||
| chr22:29610499
|
C | T | 4 | a0001c0001t0008g0257a0001c0001t0008g0258a0001c0001t0008g0259others(1): Show | 4 | HG02257.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+6387C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610499 | ||||||
| chr22:29610567
|
C | T | 1 | a0001c0001t0012g0181 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.114+6455C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610567 | ||||||
| chr22:29610643
|
CA | C | 6 | a0001c0001t0002g0220a0001c0001t0003g0179a0001c0001t0004g0302others(3): Show | 6 | HG00280.hp2 HG01884.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+6546delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29610643 | |||||
| chr22:29610653
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.114+6541A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610653 | ||||||
| chr22:29610676
|
G | A | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+6564G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610676 | ||||||
| chr22:29610758
|
A | G | 118 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0002g0072others(115): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.114+6646A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29610758 | ||||||
| chr22:29611368
|
C | CA | 10 | a0001c0001t0008g0113a0001c0001t0008g0114a0001c0001t0008g0115others(7): Show | 10 | HG01496.hp1 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+7265dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29611368 | |||||
| chr22:29611466
|
G | A | 1 | a0001c0001t0014g0101 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.114+7354G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29611466 | ||||||
| chr22:29611474
|
C | T | 3 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0007g0218 | 3 | HG00642.hp1 HG01074.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.114+7362C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29611474 | ||||||
| chr22:29611518
|
A | AAAAC | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0014g0059 | 3 | HG00609.hp2 HG00621.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.114+7426_114+7429d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29611518 | |||||
| chr22:29611558
|
T | G | 2 | a0001c0001t0029g0151a0001c0001t0033g0152 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+7446T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29611558 | ||||||
| chr22:29611704
|
T | C | 1 | a0001c0001t0048g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.114+7592T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29611704 | ||||||
| chr22:29611774
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.114+7662A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29611774 | ||||||
| chr22:29611819
|
T | C | 165 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.114+7707T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29611819 | ||||||
| chr22:29611882
|
C | T | 1 | a0001c0001t0057g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.114+7770C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29611882 | ||||||
| chr22:29612171
|
C | G | 1 | a0001c0001t0019g0215 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.114+8059C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29612171 | ||||||
| chr22:29612472
|
G | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+8360G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29612472 | ||||||
| chr22:29612494
|
T | G | 219 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(216): Show | 219 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.114+8382T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29612494 | ||||||
| chr22:29612636
|
C | T | 1 | a0001c0001t0012g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.114+8524C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29612636 | ||||||
| chr22:29612754
|
A | G | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.114+8642A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29612754 | ||||||
| chr22:29612761
|
T | C | 317 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(314): Show | 317 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.114+8649T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29612761 | ||||||
| chr22:29612806
|
T | C | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+8694T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29612806 | ||||||
| chr22:29612842
|
TC | T | 3 | a0001c0001t0008g0113a0001c0001t0008g0114a0001c0001t0008g0115 | 3 | HG01496.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.114+8733delC | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29612842 | |||||
| chr22:29613044
|
A | C | 1 | a0001c0001t0003g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.114+8932A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29613044 | ||||||
| chr22:29613390
|
C | T | 1 | a0001c0001t0055g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.114+9278C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29613390 | ||||||
| chr22:29613517
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.114+9405C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29613517 | ||||||
| chr22:29613629
|
T | C | 1 | a0001c0001t0008g0257 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114+9517T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29613629 | ||||||
| chr22:29613712
|
T | G | 48 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(45): Show | 48 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.114+9600T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29613712 | ||||||
| chr22:29613766
|
C | CT | 77 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(74): Show | 77 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.114+9665dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29613766 | |||||
| chr22:29613790
|
C | T | 62 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.114+9678C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29613790 | ||||||
| chr22:29614103
|
A | G | 1 | a0001c0001t0016g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.114+9991A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29614103 | ||||||
| chr22:29614171
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.114+10059C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29614171 | ||||||
| chr22:29614345
|
G | A | 1 | a0001c0001t0005g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.114+10233G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29614345 | ||||||
| chr22:29614376
|
A | C | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.114+10264A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29614376 | ||||||
| chr22:29614395
|
G | A | 1 | a0001c0006t0044g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.114+10283G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29614395 | ||||||
| chr22:29614580
|
TA | T | 51 | a0001c0001t0002g0220a0001c0001t0003g0069a0001c0001t0003g0096others(48): Show | 51 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.114+10485delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29614580 | |||||
| chr22:29614786
|
C | T | 15 | a0001c0001t0004g0078a0001c0001t0008g0083a0001c0001t0011g0073others(12): Show | 15 | HG01070.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+10674C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29614786 | ||||||
| chr22:29614966
|
T | C | 1 | a0001c0001t0020g0116 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.114+10854T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29614966 | ||||||
| chr22:29615011
|
C | A | 4 | a0001c0001t0008g0257a0001c0001t0008g0258a0001c0001t0008g0259others(1): Show | 4 | HG02257.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+10899C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615011 | ||||||
| chr22:29615071
|
C | T | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+10959C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615071 | ||||||
| chr22:29615084
|
T | G | 1 | a0001c0001t0004g0117 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.114+10972T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615084 | ||||||
| chr22:29615108
|
C | A | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+10996C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615108 | ||||||
| chr22:29615211
|
A | C | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+11099A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615211 | ||||||
| chr22:29615416
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.114+11304T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615416 | ||||||
| chr22:29615434
|
G | A | 2 | a0001c0001t0005g0297a0001c0001t0005g0311 | 2 | NA18953.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.114+11322G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615434 | ||||||
| chr22:29615527
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.114+11415C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615527 | ||||||
| chr22:29615556
|
C | T | 1 | a0001c0001t0009g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.114+11444C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615556 | ||||||
| chr22:29615702
|
T | A | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.114+11590T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29615702 | ||||||
| chr22:29616069
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.114+11957C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616069 | ||||||
| chr22:29616148
|
G | T | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+12036G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616148 | ||||||
| chr22:29616203
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.114+12091G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616203 | ||||||
| chr22:29616294
|
T | G | 1 | a0001c0002t0003g0155 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.114+12182T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616294 | ||||||
| chr22:29616298
|
A | T | 1 | a0001c0002t0003g0155 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.114+12186A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616298 | ||||||
| chr22:29616299
|
T | G | 1 | a0001c0002t0003g0155 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.114+12187T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616299 | ||||||
| chr22:29616301
|
G | A | 1 | a0001c0002t0003g0155 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.114+12189G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616301 | ||||||
| chr22:29616341
|
A | T | 1 | a0001c0001t0004g0056 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.114+12229A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616341 | ||||||
| chr22:29616449
|
T | A | 1 | a0001c0002t0003g0156 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.114+12337T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616449 | ||||||
| chr22:29616510
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114+12398C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616510 | ||||||
| chr22:29616745
|
GA | G | 14 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0064others(11): Show | 14 | HG00280.hp1 HG02027.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+12650delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29616745 | |||||
| chr22:29616931
|
G | T | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+12819G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29616931 | ||||||
| chr22:29616935
|
G | GT | 6 | a0001c0001t0004g0068a0001c0001t0009g0284a0001c0001t0010g0053others(3): Show | 6 | HG01261.hp1 HG01515.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+12834dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29616935 | |||||
| chr22:29617089
|
C | T | 1 | a0001c0001t0045g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.114+12977C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617089 | ||||||
| chr22:29617390
|
T | G | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+13278T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617390 | ||||||
| chr22:29617700
|
G | A | 1 | a0001c0001t0016g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.114+13588G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617700 | ||||||
| chr22:29617702
|
A | G | 15 | a0001c0001t0004g0078a0001c0001t0008g0083a0001c0001t0011g0073others(12): Show | 15 | HG01070.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+13590A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617702 | ||||||
| chr22:29617740
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.114+13628G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617740 | ||||||
| chr22:29617758
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.114+13646G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617758 | ||||||
| chr22:29617802
|
C | A | 8 | a0001c0002t0003g0070a0001c0002t0003g0104a0001c0002t0003g0105others(5): Show | 8 | NA18944.hp2 NA18968.hp1 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+13690C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617802 | ||||||
| chr22:29617820
|
A | G | 164 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(161): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.114+13708A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617820 | ||||||
| chr22:29617845
|
A | G | 1 | a0001c0001t0019g0306 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.114+13733A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617845 | ||||||
| chr22:29617978
|
T | C | 5 | a0001c0001t0006g0235a0001c0001t0006g0236a0001c0001t0006g0237others(2): Show | 5 | HG01884.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+13866T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29617978 | ||||||
| chr22:29618003
|
A | T | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+13891A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618003 | ||||||
| chr22:29618226
|
T | C | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.114+14114T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618226 | ||||||
| chr22:29618392
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.114+14280C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618392 | ||||||
| chr22:29618415
|
A | G | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.114+14303A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618415 | ||||||
| chr22:29618466
|
TA | T | 110 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(107): Show | 110 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.114+14355delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618466 | ||||||
| chr22:29618592
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+14480A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618592 | ||||||
| chr22:29618826
|
C | T | 1 | a0001c0001t0048g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.114+14714C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618826 | ||||||
| chr22:29619326
|
C | T | 296 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(293): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.114+15214C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619326 | ||||||
| chr22:29619363
|
C | T | 4 | a0001c0001t0024g0014a0001c0001t0024g0015a0001c0001t0025g0013others(1): Show | 4 | HG01099.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+15251C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619363 | ||||||
| chr22:29619386
|
T | TTTTG | 92 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(89): Show | 92 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.114+15298_114+1530 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29619386 | |||||
| chr22:29619428
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG00140.hp2 HG01993.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.114+15316G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619428 | ||||||
| chr22:29619492
|
G | A | 1 | a0001c0001t0029g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.114+15380G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619492 | ||||||
| chr22:29619533
|
A | C | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+15421A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619533 | ||||||
| chr22:29619585
|
T | TG | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+15477dupG | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29619585 | |||||
| chr22:29619637
|
T | G | 1 | a0001c0001t0011g0073 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.114+15525T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619637 | ||||||
| chr22:29619646
|
C | T | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+15534C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619646 | ||||||
| chr22:29619690
|
C | T | 115 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.114+15578C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619690 | ||||||
| chr22:29619691
|
G | A | 5 | a0001c0001t0006g0235a0001c0001t0006g0236a0001c0001t0006g0237others(2): Show | 5 | HG01884.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+15579G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619691 | ||||||
| chr22:29619932
|
C | T | 1 | a0001c0001t0004g0117 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.114+15820C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29619932 | ||||||
| chr22:29620043
|
T | A | 48 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(45): Show | 48 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.114+15931T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620043 | ||||||
| chr22:29620120
|
G | A | 1 | a0001c0001t0003g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.114+16008G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620120 | ||||||
| chr22:29620131
|
C | T | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.114+16019C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620131 | ||||||
| chr22:29620175
|
C | G | 1 | a0001c0001t0016g0330 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.114+16063C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620175 | ||||||
| chr22:29620243
|
G | A | 5 | a0001c0001t0006g0235a0001c0001t0006g0236a0001c0001t0006g0237others(2): Show | 5 | HG01884.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+16131G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620243 | ||||||
| chr22:29620389
|
A | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.114+16277A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620389 | ||||||
| chr22:29620489
|
C | T | 1 | a0001c0001t0008g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115-16262C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620489 | ||||||
| chr22:29620524
|
AG | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.115-16225delG | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29620524 | |||||
| chr22:29620596
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0118a0001c0001t0004g0302 | 3 | NA18970.hp1 NA18974.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.115-16155G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620596 | ||||||
| chr22:29620639
|
T | C | 2 | a0001c0001t0003g0153a0001c0001t0003g0154 | 2 | NA18998.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.115-16112T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620639 | ||||||
| chr22:29620762
|
G | A | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-15989G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29620762 | ||||||
| chr22:29621011
|
G | C | 76 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(73): Show | 76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.115-15740G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29621011 | ||||||
| chr22:29621775
|
C | T | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-14976C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29621775 | ||||||
| chr22:29621923
|
C | A | 1 | a0001c0001t0009g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.115-14828C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29621923 | ||||||
| chr22:29622020
|
C | G | 4 | a0001c0001t0024g0014a0001c0001t0024g0015a0001c0001t0025g0013others(1): Show | 4 | HG01099.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-14731C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29622020 | ||||||
| chr22:29622211
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.115-14540A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29622211 | ||||||
| chr22:29622560
|
T | G | 1 | a0001c0001t0012g0119 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.115-14191T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29622560 | ||||||
| chr22:29622646
|
A | AT | 168 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-14078dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29622646 | |||||
| chr22:29622646
|
A | ATT | 30 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0051others(27): Show | 30 | HG00408.hp1 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.115-14079_115-1407 others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29622646 | |||||
| chr22:29622646
|
AT | A | 29 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0220others(26): Show | 29 | HG00323.hp1 HG00609.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.115-14078delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29622646 | |||||
| chr22:29622646
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0029g0151a0001c0001t0033g0152 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.115-14087_115-1407 others(14): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29622646 | |||||
| chr22:29622654
|
T | G | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-14097T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29622654 | ||||||
| chr22:29622686
|
C | T | 4 | a0001c0001t0024g0014a0001c0001t0024g0015a0001c0001t0025g0013others(1): Show | 4 | HG01099.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-14065C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29622686 | ||||||
| chr22:29622949
|
C | T | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG01192.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.115-13802C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29622949 | ||||||
| chr22:29622953
|
C | CT | 52 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0001g0052others(49): Show | 52 | HG01070.hp2 HG01106.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.115-13776dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29622953 | |||||
| chr22:29622953
|
CT | C | 18 | a0001c0001t0002g0190a0001c0001t0003g0096a0001c0001t0003g0097others(15): Show | 18 | HG01192.hp2 HG01256.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.115-13776delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29622953 | |||||
| chr22:29623290
|
C | T | 1 | a0001c0001t0042g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.115-13461C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623290 | ||||||
| chr22:29623309
|
A | C | 1 | a0001c0001t0011g0074 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.115-13442A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623309 | ||||||
| chr22:29623381
|
T | C | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-13370T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623381 | ||||||
| chr22:29623398
|
C | T | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.115-13353C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623398 | ||||||
| chr22:29623406
|
GT | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02071.hp2 NA18944.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-13342delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29623406 | |||||
| chr22:29623410
|
G | A | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-13341G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623410 | ||||||
| chr22:29623561
|
G | C | 1 | a0001c0001t0020g0116 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.115-13190G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623561 | ||||||
| chr22:29623631
|
C | A | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-13120C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623631 | ||||||
| chr22:29623737
|
C | T | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.115-13014C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623737 | ||||||
| chr22:29623760
|
A | C | 1 | a0001c0001t0006g0247 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.115-12991A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29623760 | ||||||
| chr22:29623959
|
ATATTTCC others(8): Show |
A | 1 | a0001c0001t0004g0302 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.115-12789_115-1277 others(19): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29623959 | |||||
| chr22:29624100
|
C | T | 1 | a0001c0001t0004g0269 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.115-12651C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624100 | ||||||
| chr22:29624209
|
TTTTG | T | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.115-12530_115-1252 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624209 | |||||
| chr22:29624231
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0150 | 3 | HG02083.hp2 HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.115-12520G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624231 | ||||||
| chr22:29624380
|
G | T | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-12371G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624380 | ||||||
| chr22:29624415
|
C | T | 1 | a0001c0001t0013g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.115-12336C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624415 | ||||||
| chr22:29624539
|
C | G | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.115-12212C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624539 | ||||||
| chr22:29624572
|
A | G | 11 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 11 | HG00438.hp2 HG01934.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-12179A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624572 | ||||||
| chr22:29624765
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.115-11986G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624765 | ||||||
| chr22:29624796
|
GTCCTCTT others(8): Show |
G | 1 | a0001c0001t0006g0246 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.115-11952_115-1193 others(19): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624796 | |||||
| chr22:29624797
|
TCCTCTTT others(5): Show |
T | 1 | a0001c0001t0025g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115-11953_115-1194 others(16): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624797 | ||||||
| chr22:29624797
|
TCCTCTTT others(9): Show |
T | 1 | a0001c0001t0025g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.115-11953_115-1193 others(20): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624797 | ||||||
| chr22:29624798
|
CCTCTTT | C | 3 | a0001c0001t0005g0313a0001c0001t0005g0322a0001c0001t0017g0323 | 3 | HG01256.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.115-11950_115-1194 others(10): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624798 | |||||
| chr22:29624798
|
CCTCTTTC others(3): Show |
C | 1 | a0001c0001t0006g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.115-11950_115-1194 others(14): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624798 | |||||
| chr22:29624798
|
CCTCTTTC others(11): Show |
C | 3 | a0001c0001t0006g0247a0001c0001t0006g0249a0001c0001t0006g0296 | 3 | HG02055.hp1 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.115-11950_115-1193 others(22): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624798 | |||||
| chr22:29624798
|
CCTCTTTC others(15): Show |
C | 1 | a0001c0001t0059g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.115-11950_115-1192 others(26): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624798 | |||||
| chr22:29624799
|
C | CTCTT | 19 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0139others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.115-11884_115-1188 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
C | CTCTTTCT others(1): Show |
5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0003g0166others(2): Show | 5 | NA18943.hp1 NA18957.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-11888_115-1188 others(12): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTT | C | 86 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.115-11884_115-1188 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(1): Show |
C | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(61): Show | 65 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.115-11888_115-1188 others(12): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(5): Show |
C | 43 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0120others(40): Show | 43 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.115-11892_115-1188 others(16): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(9): Show |
C | 14 | a0001c0001t0001g0018a0001c0001t0001g0184a0001c0001t0001g0228others(11): Show | 14 | HG00558.hp2 HG01074.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-11896_115-1188 others(20): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(13): Show |
C | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0003g0069others(2): Show | 5 | HG01175.hp2 HG01884.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-11900_115-1188 others(24): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(17): Show |
C | 6 | a0001c0001t0004g0012a0001c0001t0004g0023a0001c0001t0005g0314others(3): Show | 6 | HG02135.hp1 HG03209.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-11904_115-1188 others(28): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(21): Show |
C | 3 | a0001c0001t0001g0019a0001c0001t0010g0007a0001c0001t0033g0152 | 3 | HG01361.hp2 HG02451.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.115-11908_115-1188 others(32): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(25): Show |
C | 1 | a0001c0001t0029g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.115-11912_115-1188 others(36): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624799
|
CTCTTTCT others(29): Show |
C | 3 | a0001c0001t0005g0298a0001c0001t0017g0002a0003c0005t0017g0002 | 3 | HG00597.hp1 HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.115-11916_115-1188 others(40): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624799 | |||||
| chr22:29624807
|
T | C | 2 | a0001c0001t0024g0014a0001c0001t0024g0015 | 2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.115-11944T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624807 | ||||||
| chr22:29624811
|
T | C | 1 | a0001c0001t0025g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115-11940T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624811 | ||||||
| chr22:29624815
|
T | C | 2 | a0001c0001t0020g0116a0001c0001t0025g0013 | 2 | HG03195.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.115-11936T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624815 | ||||||
| chr22:29624855
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.115-11896T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624855 | ||||||
| chr22:29624857
|
CTTTCTTT others(8): Show |
C | 1 | a0001c0001t0003g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.115-11891_115-1187 others(19): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624857 | |||||
| chr22:29624866
|
T | TTTCTTTC others(4): Show |
1 | a0001c0001t0003g0339 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.115-11881_115-1188 others(15): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624866 | |||||
| chr22:29624871
|
CT | C | 3 | a0001c0001t0001g0103a0001c0001t0003g0153a0001c0007t0052g0281 | 3 | HG03209.hp1 NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.115-11877delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624871 | |||||
| chr22:29624901
|
T | TTCTC | 5 | a0001c0001t0002g0193a0001c0001t0002g0205a0001c0001t0007g0106others(2): Show | 5 | HG01934.hp2 HG01993.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-11832_115-1182 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624901 | |||||
| chr22:29624901
|
TTCTC | T | 14 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 14 | HG02071.hp1 HG03041.hp2 HG03491.hp2 others(11): Show |
intron_variant | MODIFIER | c.115-11832_115-1182 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624901 | |||||
| chr22:29624917
|
CTCTCTT | C | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.115-11830_115-1182 others(10): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624917 | |||||
| chr22:29624919
|
C | CTCTT | 3 | a0001c0001t0002g0206a0001c0002t0003g0156a0001c0002t0003g0157 | 3 | HG01361.hp1 NA18992.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.115-11810_115-1180 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624919 | |||||
| chr22:29624919
|
CTCTT | C | 6 | a0001c0001t0002g0273a0001c0001t0023g0231a0001c0001t0027g0092others(3): Show | 6 | HG00323.hp2 HG02280.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-11810_115-1180 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29624919 | |||||
| chr22:29624923
|
T | C | 5 | a0001c0001t0001g0123a0001c0001t0016g0328a0001c0001t0016g0329others(2): Show | 5 | HG00609.hp1 HG02071.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-11828T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624923 | ||||||
| chr22:29624957
|
C | T | 1 | a0001c0001t0012g0265 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.115-11794C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29624957 | ||||||
| chr22:29625096
|
T | C | 2 | a0001c0001t0017g0002a0003c0005t0017g0002 | 2 | HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.115-11655T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29625096 | ||||||
| chr22:29625215
|
T | C | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-11536T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29625215 | ||||||
| chr22:29625305
|
C | T | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.115-11446C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29625305 | ||||||
| chr22:29626014
|
A | G | 1 | a0001c0001t0019g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115-10737A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626014 | ||||||
| chr22:29626108
|
A | G | 1 | a0001c0001t0011g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115-10643A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626108 | ||||||
| chr22:29626153
|
C | CT | 82 | a0001c0001t0001g0026a0001c0001t0001g0100a0001c0001t0001g0103others(79): Show | 82 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.115-10579dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29626153 | |||||
| chr22:29626153
|
CT | C | 18 | a0001c0001t0001g0006a0001c0001t0004g0078a0001c0001t0008g0083others(15): Show | 18 | HG01070.hp2 HG01106.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.115-10579delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29626153 | |||||
| chr22:29626278
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(12): Show | 15 | HG00099.hp1 HG00140.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-10473C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626278 | ||||||
| chr22:29626394
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.115-10357C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626394 | ||||||
| chr22:29626666
|
C | T | 1 | a0001c0001t0007g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.115-10085C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626666 | ||||||
| chr22:29626679
|
A | G | 1 | a0001c0001t0003g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.115-10072A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626679 | ||||||
| chr22:29626934
|
G | A | 15 | a0001c0001t0004g0078a0001c0001t0008g0083a0001c0001t0011g0073others(12): Show | 15 | HG01070.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-9817G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626934 | ||||||
| chr22:29626947
|
A | G | 77 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(74): Show | 77 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.115-9804A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626947 | ||||||
| chr22:29626981
|
A | G | 1 | a0001c0001t0005g0312 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.115-9770A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29626981 | ||||||
| chr22:29627176
|
A | T | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-9575A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29627176 | ||||||
| chr22:29627221
|
A | G | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.115-9530A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29627221 | ||||||
| chr22:29627224
|
G | A | 3 | a0001c0001t0003g0159a0001c0001t0003g0166a0001c0001t0022g0158 | 3 | NA18971.hp2 NA18982.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.115-9527G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29627224 | ||||||
| chr22:29627600
|
T | C | 1 | a0001c0001t0057g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.115-9151T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29627600 | ||||||
| chr22:29627674
|
G | A | 3 | a0001c0001t0015g0175a0001c0001t0015g0177a0001c0001t0030g0174 | 3 | HG02630.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.115-9077G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29627674 | ||||||
| chr22:29627966
|
C | T | 1 | a0001c0001t0004g0122 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.115-8785C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29627966 | ||||||
| chr22:29627971
|
G | T | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.115-8780G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29627971 | ||||||
| chr22:29628041
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.115-8710C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628041 | ||||||
| chr22:29628140
|
C | CTG | 73 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(70): Show | 73 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.115-8567_115-8566d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
C | CTGTG | 38 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 38 | HG00323.hp2 HG01106.hp2 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.115-8569_115-8566d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
C | CTGTGTG | 22 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0103others(19): Show | 22 | HG01099.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.115-8571_115-8566d others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0042a0001c0001t0002g0206a0001c0001t0002g0210others(4): Show | 7 | HG01261.hp2 HG01361.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-8573_115-8566d others(10): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0002g0199a0001c0001t0042g0140 | 2 | HG01981.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.115-8575_115-8566d others(12): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
C | CTGTGTGT others(5): Show |
3 | a0001c0001t0002g0198a0001c0001t0011g0082a0001c0001t0019g0333 | 3 | HG02258.hp2 HG02976.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.115-8577_115-8566d others(14): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
CTG | C | 63 | a0001c0001t0001g0043a0001c0001t0002g0211a0001c0001t0002g0289others(60): Show | 63 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.115-8567_115-8566d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
CTGTG | C | 6 | a0001c0001t0003g0173a0001c0001t0011g0073a0001c0001t0021g0075others(3): Show | 6 | HG01515.hp1 HG02080.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-8569_115-8566d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
CTGTGTG | C | 31 | a0001c0001t0003g0097a0001c0001t0003g0179a0001c0001t0005g0001others(28): Show | 32 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8571_115-8566d others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
CTGTGTGT others(1): Show |
C | 15 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(12): Show | 15 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.115-8573_115-8566d others(10): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628140
|
CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0004g0147a0001c0001t0005g0318 | 2 | HG00099.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.115-8575_115-8566d others(12): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628140 | |||||
| chr22:29628185
|
T | C | 1 | a0001c0001t0004g0302 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.115-8566T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628185 | ||||||
| chr22:29628274
|
T | C | 165 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.115-8477T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628274 | ||||||
| chr22:29628324
|
G | A | 1 | a0001c0001t0004g0078 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.115-8427G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628324 | ||||||
| chr22:29628364
|
C | A | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-8387C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628364 | ||||||
| chr22:29628501
|
T | C | 1 | a0002c0003t0001g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.115-8250T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628501 | ||||||
| chr22:29628627
|
C | CT | 11 | a0001c0001t0006g0238a0001c0001t0006g0243a0001c0001t0006g0296others(8): Show | 11 | HG01496.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-8101dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628627 | |||||
| chr22:29628627
|
CT | C | 245 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.115-8101delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628627 | |||||
| chr22:29628627
|
CTT | C | 11 | a0001c0001t0001g0135a0001c0001t0002g0189a0001c0001t0003g0099others(8): Show | 11 | HG01069.hp2 HG01070.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-8102_115-8101d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29628627 | |||||
| chr22:29628692
|
G | A | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-8059G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628692 | ||||||
| chr22:29628787
|
C | T | 1 | a0001c0001t0008g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.115-7964C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628787 | ||||||
| chr22:29628788
|
G | A | 1 | a0001c0001t0021g0075 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.115-7963G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628788 | ||||||
| chr22:29628941
|
T | C | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-7810T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628941 | ||||||
| chr22:29628952
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.115-7799C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29628952 | ||||||
| chr22:29629359
|
A | G | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.115-7392A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29629359 | ||||||
| chr22:29629384
|
A | T | 1 | a0001c0001t0004g0302 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.115-7367A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29629384 | ||||||
| chr22:29629434
|
G | A | 5 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-7317G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29629434 | ||||||
| chr22:29629625
|
G | A | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.115-7126G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29629625 | ||||||
| chr22:29630116
|
T | C | 1 | a0001c0001t0006g0246 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.115-6635T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29630116 | ||||||
| chr22:29630290
|
A | G | 26 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(23): Show | 27 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.115-6461A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29630290 | ||||||
| chr22:29630530
|
G | A | 1 | a0001c0001t0048g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.115-6221G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29630530 | ||||||
| chr22:29630758
|
C | T | 5 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-5993C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29630758 | ||||||
| chr22:29630840
|
C | T | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-5911C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29630840 | ||||||
| chr22:29630926
|
T | TA | 5 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-5824dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29630926 | |||||
| chr22:29631085
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.115-5666G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29631085 | ||||||
| chr22:29631534
|
C | T | 5 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-5217C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29631534 | ||||||
| chr22:29631764
|
T | G | 1 | a0001c0001t0003g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.115-4987T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29631764 | ||||||
| chr22:29631811
|
C | T | 1 | a0002c0003t0001g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.115-4940C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29631811 | ||||||
| chr22:29631901
|
A | G | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.115-4850A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29631901 | ||||||
| chr22:29631905
|
A | G | 6 | a0001c0001t0003g0337a0001c0001t0003g0338a0001c0001t0003g0339others(3): Show | 6 | HG02486.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-4846A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29631905 | ||||||
| chr22:29632029
|
G | A | 1 | a0001c0001t0011g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.115-4722G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29632029 | ||||||
| chr22:29632111
|
A | G | 8 | a0001c0001t0004g0133a0001c0001t0004g0134a0001c0001t0004g0143others(5): Show | 8 | HG02027.hp1 HG02165.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-4640A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29632111 | ||||||
| chr22:29632628
|
CACTA | C | 4 | a0001c0001t0004g0269a0001c0001t0045g0295a0001c0001t0046g0310others(1): Show | 4 | HG00673.hp1 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-4118_115-4115d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29632628 | |||||
| chr22:29632891
|
A | G | 6 | a0001c0001t0003g0337a0001c0001t0003g0338a0001c0001t0003g0339others(3): Show | 6 | HG02486.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-3860A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29632891 | ||||||
| chr22:29632972
|
CCTCTTTT others(46): Show |
C | 1 | a0001c0002t0003g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115-3776_115-3724d others(55): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | 29632972 | |||||
| chr22:29633525
|
T | G | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-3226T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29633525 | ||||||
| chr22:29633628
|
T | C | 1 | a0001c0001t0009g0087 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.115-3123T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29633628 | ||||||
| chr22:29634090
|
A | G | 2 | a0001c0001t0013g0004a0001c0001t0013g0005 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.115-2661A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634090 | ||||||
| chr22:29634610
|
A | C | 1 | a0001c0002t0003g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115-2141A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634610 | ||||||
| chr22:29634611
|
A | C | 1 | a0001c0002t0003g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115-2140A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634611 | ||||||
| chr22:29634613
|
C | CTCCCCCC others(46): Show |
1 | a0001c0002t0003g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115-2138_115-2137i others(55): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634613 | ||||||
| chr22:29634615
|
T | C | 1 | a0001c0002t0003g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115-2136T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634615 | ||||||
| chr22:29634776
|
A | T | 5 | a0001c0001t0006g0235a0001c0001t0006g0236a0001c0001t0006g0237others(2): Show | 5 | HG01884.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-1975A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634776 | ||||||
| chr22:29634835
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.115-1916T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634835 | ||||||
| chr22:29634950
|
G | A | 48 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(45): Show | 48 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.115-1801G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634950 | ||||||
| chr22:29634954
|
T | A | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.115-1797T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29634954 | ||||||
| chr22:29635041
|
C | T | 1 | a0001c0001t0009g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.115-1710C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635041 | ||||||
| chr22:29635139
|
C | T | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.115-1612C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635139 | ||||||
| chr22:29635153
|
G | T | 8 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(5): Show | 8 | HG01496.hp2 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1598G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635153 | ||||||
| chr22:29635154
|
G | A | 8 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(5): Show | 8 | HG01496.hp2 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1597G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635154 | ||||||
| chr22:29635161
|
C | A | 1 | a0001c0001t0003g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.115-1590C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635161 | ||||||
| chr22:29635246
|
G | C | 1 | a0001c0001t0011g0074 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.115-1505G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635246 | ||||||
| chr22:29635409
|
A | G | 1 | a0001c0001t0004g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.115-1342A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635409 | ||||||
| chr22:29635427
|
C | A | 1 | a0001c0001t0031g0071 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.115-1324C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635427 | ||||||
| chr22:29635453
|
C | T | 1 | a0001c0001t0057g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.115-1298C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635453 | ||||||
| chr22:29635454
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.115-1297G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635454 | ||||||
| chr22:29635477
|
C | T | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-1274C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635477 | ||||||
| chr22:29635623
|
C | T | 2 | a0001c0001t0002g0110a0001c0001t0009g0093 | 2 | HG00408.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.115-1128C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635623 | ||||||
| chr22:29635664
|
A | C | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.115-1087A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635664 | ||||||
| chr22:29635666
|
C | T | 1 | a0001c0001t0055g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115-1085C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635666 | ||||||
| chr22:29635764
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0141 | 3 | NA18944.hp1 NA18986.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.115-987A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635764 | ||||||
| chr22:29635786
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.115-965C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635786 | ||||||
| chr22:29635824
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.115-927C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29635824 | ||||||
| chr22:29636246
|
A | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.115-505A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29636246 | ||||||
| chr22:29636290
|
CTT | C | 3 | a0001c0001t0008g0257a0001c0001t0008g0258a0001c0001t0008g0260 | 3 | HG02257.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.115-460_115-459del others(2): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29636290 | ||||||
| chr22:29636495
|
A | C | 77 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(74): Show | 77 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.115-256A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29636495 | ||||||
| chr22:29636519
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.115-232C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29636519 | ||||||
| chr22:29636638
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.115-113G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29636638 | ||||||
| chr22:29636640
|
TG | T | 7 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(4): Show | 7 | HG01192.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-110delG | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29636640 | ||||||
| chr22:29636686
|
C | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG02071.hp1 HG03491.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-65C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29636686 | ||||||
| chr22:29636891
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.240+15C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29636891 | ||||||
| chr22:29636967
|
T | C | 3 | a0001c0001t0002g0221a0001c0001t0007g0264a0001c0001t0019g0333 | 3 | HG01243.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.240+91T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29636967 | ||||||
| chr22:29637047
|
T | A | 232 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.240+171T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637047 | ||||||
| chr22:29637225
|
T | C | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0010g0030 | 3 | HG01256.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.240+349T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637225 | ||||||
| chr22:29637273
|
T | A | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.240+397T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637273 | ||||||
| chr22:29637651
|
A | G | 1 | a0001c0001t0005g0301 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.240+775A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637651 | ||||||
| chr22:29637690
|
AT | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(151): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.240+828delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr22 | 29637690 | |||||
| chr22:29637816
|
T | C | 4 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0147others(1): Show | 4 | HG02027.hp1 NA18951.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+940T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637816 | ||||||
| chr22:29637843
|
G | A | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.240+967G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637843 | ||||||
| chr22:29637912
|
G | A | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG01192.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.240+1036G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637912 | ||||||
| chr22:29637970
|
A | T | 3 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0021g0075 | 3 | HG01070.hp2 HG02080.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.240+1094A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29637970 | ||||||
| chr22:29638349
|
AT | A | 9 | a0001c0001t0001g0278a0001c0001t0001g0292a0001c0001t0002g0194others(6): Show | 9 | HG01069.hp1 HG01070.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.241-723delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr22 | 29638349 | |||||
| chr22:29638414
|
A | G | 1 | a0001c0006t0044g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.241-676A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29638414 | ||||||
| chr22:29638419
|
C | T | 4 | a0001c0001t0004g0102a0001c0001t0004g0117a0001c0001t0004g0118others(1): Show | 4 | NA18970.hp1 NA18974.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-671C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29638419 | ||||||
| chr22:29638420
|
G | A | 2 | a0001c0001t0002g0272a0001c0001t0007g0276 | 2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.241-670G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29638420 | ||||||
| chr22:29638643
|
C | T | 3 | a0001c0001t0008g0113a0001c0001t0008g0114a0001c0001t0008g0115 | 3 | HG01496.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-447C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29638643 | ||||||
| chr22:29638704
|
A | C | 1 | a0001c0001t0015g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.241-386A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29638704 | ||||||
| chr22:29639005
|
G | T | 110 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(107): Show | 110 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.241-85G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29639005 | ||||||
| chr22:29639032
|
G | A | 15 | a0001c0001t0004g0078a0001c0001t0008g0083a0001c0001t0011g0073others(12): Show | 15 | HG01070.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.241-58G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 2/15 | chr22 | 29639032 | ||||||
| chr22:29639236
|
C | A | 1 | a0001c0001t0016g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.363+24C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29639236 | ||||||
| chr22:29639316
|
A | C | 1 | a0001c0001t0001g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.363+104A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29639316 | ||||||
| chr22:29639571
|
A | G | 1 | a0001c0001t0045g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+359A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29639571 | ||||||
| chr22:29639738
|
C | T | 5 | a0001c0001t0006g0235a0001c0001t0006g0236a0001c0001t0006g0237others(2): Show | 5 | HG01884.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+526C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29639738 | ||||||
| chr22:29639769
|
C | A | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.363+557C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29639769 | ||||||
| chr22:29639838
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.363+626C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29639838 | ||||||
| chr22:29639881
|
C | CA | 52 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0061others(49): Show | 52 | HG00621.hp2 HG00642.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.363+695dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29639881 | |||||
| chr22:29639881
|
CA | C | 20 | a0001c0001t0003g0338a0001c0001t0003g0340a0001c0001t0004g0078others(17): Show | 20 | HG00140.hp1 HG01106.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.363+695delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29639881 | |||||
| chr22:29639881
|
CAA | C | 13 | a0001c0001t0008g0083a0001c0001t0008g0256a0001c0001t0011g0074others(10): Show | 13 | HG01070.hp2 HG01099.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+694_363+695del others(2): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29639881 | |||||
| chr22:29640194
|
T | TA | 30 | a0001c0001t0001g0280a0001c0001t0002g0072a0001c0001t0002g0110others(27): Show | 30 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.363+1007dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29640194 | |||||
| chr22:29640194
|
TA | T | 150 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.363+1007delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29640194 | |||||
| chr22:29640194
|
TAA | T | 31 | a0001c0001t0001g0065a0001c0001t0001g0120a0001c0001t0004g0012others(28): Show | 31 | HG01070.hp1 HG01070.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.363+1006_363+1007d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29640194 | |||||
| chr22:29640280
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1068G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640280 | ||||||
| chr22:29640282
|
GC | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0040others(14): Show | 17 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.363+1071delC | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640282 | ||||||
| chr22:29640326
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.363+1114A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640326 | ||||||
| chr22:29640444
|
C | T | 6 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+1232C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640444 | ||||||
| chr22:29640634
|
T | A | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.363+1422T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640634 | ||||||
| chr22:29640768
|
CGT | C | 311 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(308): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.364-1412_364-1411d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29640768 | |||||
| chr22:29640796
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.364-1406C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640796 | ||||||
| chr22:29640859
|
C | T | 1 | a0001c0001t0009g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.364-1343C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640859 | ||||||
| chr22:29640882
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0275 | 2 | HG00323.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.364-1320C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640882 | ||||||
| chr22:29641092
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.364-1110C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641092 | ||||||
| chr22:29641120
|
T | C | 297 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(294): Show | 297 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.364-1082T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641120 | ||||||
| chr22:29641163
|
C | G | 1 | a0001c0001t0050g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.364-1039C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641163 | ||||||
| chr22:29641179
|
T | C | 1 | a0001c0001t0007g0111 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.364-1023T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641179 | ||||||
| chr22:29641179
|
T | TC | 109 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(106): Show | 109 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.364-1017dupC | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr22 | 29641179 | |||||
| chr22:29641231
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.364-971A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641231 | ||||||
| chr22:29641310
|
G | A | 1 | a0001c0001t0021g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-892G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641310 | ||||||
| chr22:29641326
|
C | G | 62 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.364-876C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641326 | ||||||
| chr22:29641348
|
A | C | 1 | a0001c0001t0064g0283 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.364-854A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641348 | ||||||
| chr22:29641368
|
C | A | 2 | a0001c0001t0045g0295a0001c0001t0046g0310 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.364-834C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641368 | ||||||
| chr22:29641544
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.364-658G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641544 | ||||||
| chr22:29641575
|
T | G | 1 | a0001c0001t0005g0252 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.364-627T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641575 | ||||||
| chr22:29641726
|
C | T | 1 | a0001c0001t0032g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.364-476C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641726 | ||||||
| chr22:29641911
|
C | G | 76 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(73): Show | 76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.364-291C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641911 | ||||||
| chr22:29641945
|
G | A | 1 | a0001c0001t0008g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.364-257G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641945 | ||||||
| chr22:29641967
|
C | G | 2 | a0001c0001t0003g0166a0001c0001t0003g0179 | 2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.364-235C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29641967 | ||||||
| chr22:29642018
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0292 | 2 | NA18943.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.364-184T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29642018 | ||||||
| chr22:29642118
|
C | T | 1 | a0001c0001t0057g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.364-84C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29642118 | ||||||
| chr22:29642163
|
A | C | 76 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0120others(73): Show | 76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.364-39A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29642163 | ||||||
| chr22:29642474
|
A | G | 1 | a0001c0001t0005g0312 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.447+189A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29642474 | ||||||
| chr22:29642510
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.447+225G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29642510 | ||||||
| chr22:29642684
|
A | G | 1 | a0001c0001t0002g0201 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.447+399A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29642684 | ||||||
| chr22:29642742
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.447+457C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29642742 | ||||||
| chr22:29642778
|
A | G | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+493A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29642778 | ||||||
| chr22:29642840
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.447+555C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29642840 | ||||||
| chr22:29642960
|
C | CT | 51 | a0001c0001t0001g0065a0001c0001t0004g0078a0001c0001t0005g0001others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.447+689dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29642960 | |||||
| chr22:29643015
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.447+730C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643015 | ||||||
| chr22:29643151
|
T | A | 2 | a0001c0001t0004g0012a0001c0001t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.447+866T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643151 | ||||||
| chr22:29643292
|
A | AT | 16 | a0001c0001t0001g0280a0001c0001t0003g0159a0001c0001t0006g0238others(13): Show | 16 | HG01070.hp2 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.447+1024dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29643292 | |||||
| chr22:29643292
|
A | ATT | 13 | a0001c0001t0011g0073a0001c0001t0011g0076a0001c0001t0011g0077others(10): Show | 13 | HG01106.hp1 HG02056.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.447+1023_447+1024d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29643292 | |||||
| chr22:29643309
|
T | A | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0010g0030 | 3 | HG01256.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.447+1024T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643309 | ||||||
| chr22:29643344
|
C | A | 1 | a0001c0001t0002g0189 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.447+1059C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643344 | ||||||
| chr22:29643346
|
T | A | 1 | a0001c0001t0046g0310 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.447+1061T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643346 | ||||||
| chr22:29643436
|
G | A | 2 | a0001c0001t0002g0189a0001c0001t0002g0211 | 2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.447+1151G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643436 | ||||||
| chr22:29643438
|
A | C | 1 | a0001c0001t0002g0189 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.447+1153A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643438 | ||||||
| chr22:29643444
|
G | T | 1 | a0001c0001t0002g0189 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.447+1159G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643444 | ||||||
| chr22:29643448
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.447+1163C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643448 | ||||||
| chr22:29643463
|
G | T | 2 | a0001c0001t0005g0297a0001c0001t0005g0311 | 2 | NA18953.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.447+1178G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643463 | ||||||
| chr22:29643509
|
C | A | 33 | a0001c0001t0001g0043a0001c0001t0001g0100a0001c0001t0001g0103others(30): Show | 33 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.447+1224C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643509 | ||||||
| chr22:29643514
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.447+1229A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643514 | ||||||
| chr22:29643581
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02071.hp2 NA18944.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+1296A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643581 | ||||||
| chr22:29643680
|
G | A | 2 | a0001c0001t0029g0151a0001c0001t0033g0152 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.447+1395G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643680 | ||||||
| chr22:29643725
|
A | G | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1440A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643725 | ||||||
| chr22:29643775
|
C | T | 1 | a0001c0001t0004g0268 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.447+1490C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643775 | ||||||
| chr22:29643840
|
G | A | 2 | a0001c0001t0004g0068a0001c0001t0004g0127 | 2 | NA18948.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.447+1555G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643840 | ||||||
| chr22:29643864
|
C | T | 1 | a0001c0001t0011g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.447+1579C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643864 | ||||||
| chr22:29643887
|
C | T | 2 | a0001c0001t0013g0004a0001c0001t0013g0005 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.447+1602C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643887 | ||||||
| chr22:29643910
|
GGGCGGGG others(42): Show |
G | 1 | a0001c0001t0005g0312 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.447+1645_447+1693d others(51): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29643910 | |||||
| chr22:29643930
|
AACCTCCC others(42): Show |
A | 14 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.447+1678_447+1726d others(51): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29643930 | |||||
| chr22:29643962
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0335a0001c0001t0014g0101others(1): Show | 4 | HG00438.hp2 HG02015.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1677C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643962 | ||||||
| chr22:29643972
|
A | G | 2 | a0001c0001t0014g0022a0001c0001t0043g0047 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.447+1687A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643972 | ||||||
| chr22:29643995
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.447+1710G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29643995 | ||||||
| chr22:29644013
|
G | C | 43 | a0001c0001t0004g0068a0001c0001t0004g0102a0001c0001t0004g0117others(40): Show | 43 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.447+1728G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644013 | ||||||
| chr22:29644024
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.447+1739C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644024 | ||||||
| chr22:29644044
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.447+1759C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644044 | ||||||
| chr22:29644045
|
G | A | 1 | a0001c0001t0004g0127 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.447+1760G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644045 | ||||||
| chr22:29644073
|
C | T | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1788C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644073 | ||||||
| chr22:29644084
|
C | T | 14 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.447+1799C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644084 | ||||||
| chr22:29644124
|
T | C | 218 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.447+1839T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644124 | ||||||
| chr22:29644164
|
C | G | 1 | a0001c0001t0008g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.447+1879C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644164 | ||||||
| chr22:29644208
|
G | A | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.447+1923G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644208 | ||||||
| chr22:29644241
|
C | CG | 29 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0037others(26): Show | 29 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.447+1960dupG | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29644241 | |||||
| chr22:29644286
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.447+2001C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644286 | ||||||
| chr22:29644325
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0150 | 2 | HG02083.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.447+2040C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644325 | ||||||
| chr22:29644411
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.447+2126G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644411 | ||||||
| chr22:29644420
|
G | A | 1 | a0001c0001t0009g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.447+2135G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644420 | ||||||
| chr22:29644481
|
C | T | 1 | a0001c0001t0002g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.447+2196C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644481 | ||||||
| chr22:29644513
|
C | CG | 7 | a0001c0001t0001g0037a0001c0001t0002g0305a0001c0001t0004g0133others(4): Show | 7 | HG01496.hp2 HG03710.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.447+2232dupG | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29644513 | |||||
| chr22:29644521
|
C | T | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.447+2236C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644521 | ||||||
| chr22:29644525
|
C | T | 1 | a0001c0002t0003g0155 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.447+2240C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644525 | ||||||
| chr22:29644528
|
G | A | 14 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.447+2243G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644528 | ||||||
| chr22:29644544
|
C | T | 1 | a0001c0001t0006g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.447+2259C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644544 | ||||||
| chr22:29644640
|
T | G | 4 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(1): Show | 4 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+2355T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644640 | ||||||
| chr22:29644703
|
G | A | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.447+2418G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644703 | ||||||
| chr22:29644704
|
C | T | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.447+2419C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644704 | ||||||
| chr22:29644723
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.447+2438G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644723 | ||||||
| chr22:29644724
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.447+2439G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644724 | ||||||
| chr22:29644725
|
C | A | 1 | a0001c0001t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.447+2440C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644725 | ||||||
| chr22:29644748
|
G | A | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+2463G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644748 | ||||||
| chr22:29644786
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.447+2501T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644786 | ||||||
| chr22:29644814
|
G | A | 4 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263others(1): Show | 4 | HG01243.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+2529G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644814 | ||||||
| chr22:29644814
|
G | C | 2 | a0001c0001t0016g0330a0001c0001t0016g0332 | 2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.447+2529G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644814 | ||||||
| chr22:29644868
|
GCAGTA | G | 4 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(1): Show | 4 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+2584_447+2588d others(7): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644868 | ||||||
| chr22:29644885
|
T | C | 236 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(233): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.447+2600T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644885 | ||||||
| chr22:29644886
|
G | A | 112 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(109): Show | 112 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.447+2601G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644886 | ||||||
| chr22:29644895
|
TGAGAGGG others(18): Show |
T | 5 | a0001c0001t0009g0183a0001c0001t0009g0233a0001c0001t0024g0014others(2): Show | 5 | HG01099.hp2 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+2623_447+2647d others(27): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29644895 | |||||
| chr22:29644908
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.447+2623G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644908 | ||||||
| chr22:29644918
|
AGGGAGAG others(10): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.447+2663_447+2679d others(19): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29644918 | |||||
| chr22:29644963
|
G | A | 1 | a0001c0001t0031g0071 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.447+2678G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644963 | ||||||
| chr22:29644977
|
T | C | 1 | a0001c0001t0018g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.447+2692T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644977 | ||||||
| chr22:29645047
|
C | G | 1 | a0001c0001t0011g0074 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.447+2762C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645047 | ||||||
| chr22:29645082
|
A | G | 1 | a0001c0001t0011g0074 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.447+2797A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645082 | ||||||
| chr22:29645085
|
C | A | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+2800C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645085 | ||||||
| chr22:29645140
|
T | G | 1 | a0001c0001t0008g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.447+2855T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645140 | ||||||
| chr22:29645278
|
C | A | 7 | a0001c0001t0003g0336a0001c0001t0003g0337a0001c0001t0003g0338others(4): Show | 7 | HG02486.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.447+2993C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645278 | ||||||
| chr22:29645401
|
T | G | 1 | a0001c0001t0042g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.447+3116T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645401 | ||||||
| chr22:29645486
|
C | A | 48 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(45): Show | 48 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.447+3201C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645486 | ||||||
| chr22:29645550
|
C | T | 1 | a0001c0001t0048g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.447+3265C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645550 | ||||||
| chr22:29645604
|
C | T | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.447+3319C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645604 | ||||||
| chr22:29645628
|
G | A | 3 | a0001c0001t0002g0110a0001c0001t0002g0191a0001c0001t0007g0290 | 3 | HG01175.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.447+3343G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645628 | ||||||
| chr22:29645652
|
C | T | 7 | a0001c0001t0003g0336a0001c0001t0003g0337a0001c0001t0003g0338others(4): Show | 7 | HG02486.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.447+3367C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645652 | ||||||
| chr22:29645761
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.447+3476A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645761 | ||||||
| chr22:29645778
|
C | A | 2 | a0001c0001t0004g0133a0001c0001t0012g0181 | 2 | NA19062.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.447+3493C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29645778 | ||||||
| chr22:29646001
|
C | T | 1 | a0001c0001t0015g0176 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.447+3716C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29646001 | ||||||
| chr22:29646033
|
G | A | 1 | a0001c0001t0002g0274 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.447+3748G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29646033 | ||||||
| chr22:29646192
|
G | C | 3 | a0001c0001t0011g0076a0001c0001t0011g0077a0001c0001t0021g0066 | 3 | HG01106.hp1 HG02056.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.447+3907G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29646192 | ||||||
| chr22:29646201
|
G | A | 2 | a0001c0001t0024g0014a0001c0001t0024g0015 | 2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.447+3916G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29646201 | ||||||
| chr22:29646275
|
C | T | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.447+3990C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29646275 | ||||||
| chr22:29646905
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.447+4620G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29646905 | ||||||
| chr22:29647003
|
T | C | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.447+4718T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29647003 | ||||||
| chr22:29647035
|
C | CA | 34 | a0001c0001t0001g0038a0001c0001t0002g0206a0001c0001t0005g0301others(31): Show | 34 | HG00609.hp1 HG01070.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.447+4767dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29647035 | |||||
| chr22:29647035
|
C | CAA | 95 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.447+4766_447+4767d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29647035 | |||||
| chr22:29647253
|
A | T | 7 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(4): Show | 7 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+4968A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29647253 | ||||||
| chr22:29647264
|
G | A | 43 | a0001c0001t0004g0068a0001c0001t0004g0102a0001c0001t0004g0117others(40): Show | 43 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.447+4979G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29647264 | ||||||
| chr22:29647567
|
G | T | 3 | a0001c0001t0003g0285a0001c0001t0003g0286a0001c0001t0003g0287 | 3 | HG02572.hp1 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.447+5282G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29647567 | ||||||
| chr22:29647574
|
C | T | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.447+5289C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29647574 | ||||||
| chr22:29647713
|
T | A | 1 | a0001c0001t0012g0011 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.447+5428T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29647713 | ||||||
| chr22:29647950
|
AAAAT | A | 45 | a0001c0001t0001g0037a0001c0001t0001g0064a0001c0001t0004g0068others(42): Show | 45 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.447+5679_447+5682d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29647950 | |||||
| chr22:29647974
|
T | C | 2 | a0001c0001t0024g0014a0001c0001t0024g0015 | 2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.447+5689T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29647974 | ||||||
| chr22:29648020
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.447+5735A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29648020 | ||||||
| chr22:29648022
|
T | C | 6 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.447+5737T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29648022 | ||||||
| chr22:29648131
|
A | AAAAT | 73 | a0001c0001t0002g0110a0001c0001t0002g0191a0001c0001t0002g0195others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.447+5878_447+5881d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29648131 | |||||
| chr22:29648131
|
A | AAAATAAA others(1): Show |
58 | a0001c0001t0002g0072a0001c0001t0002g0197a0001c0001t0004g0068others(55): Show | 58 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.447+5874_447+5881d others(10): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29648131 | |||||
| chr22:29648131
|
A | AAAATAAA others(5): Show |
5 | a0001c0001t0004g0268a0001c0001t0016g0328a0001c0001t0016g0329others(2): Show | 5 | HG00609.hp1 HG03710.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+5870_447+5881d others(14): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29648131 | |||||
| chr22:29648131
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0016g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.447+5866_447+5881d others(18): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29648131 | |||||
| chr22:29648131
|
AAAAT | A | 102 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.447+5878_447+5881d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29648131 | |||||
| chr22:29648131
|
AAAATAAA others(5): Show |
A | 5 | a0001c0001t0001g0049a0001c0001t0003g0160a0001c0001t0003g0162others(2): Show | 5 | HG03195.hp2 HG03239.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+5870_447+5881d others(14): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29648131 | |||||
| chr22:29648162
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.447+5877A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29648162 | ||||||
| chr22:29648239
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.447+5954A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29648239 | ||||||
| chr22:29648680
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.448-5977A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29648680 | ||||||
| chr22:29648914
|
G | A | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.448-5743G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29648914 | ||||||
| chr22:29649103
|
G | T | 2 | a0001c0001t0003g0286a0001c0001t0003g0287 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.448-5554G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649103 | ||||||
| chr22:29649145
|
C | CA | 18 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(15): Show | 18 | HG01070.hp2 HG01106.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.448-5502dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29649145 | |||||
| chr22:29649295
|
T | C | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-5362T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649295 | ||||||
| chr22:29649300
|
G | A | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.448-5357G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649300 | ||||||
| chr22:29649326
|
A | C | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-5331A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649326 | ||||||
| chr22:29649423
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.448-5234G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649423 | ||||||
| chr22:29649432
|
G | C | 2 | a0001c0001t0038g0034a0001c0001t0040g0035 | 2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.448-5225G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649432 | ||||||
| chr22:29649438
|
C | T | 9 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(6): Show | 9 | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-5219C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649438 | ||||||
| chr22:29649455
|
C | A | 1 | a0001c0001t0037g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.448-5202C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649455 | ||||||
| chr22:29649633
|
T | G | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.448-5024T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649633 | ||||||
| chr22:29649738
|
G | T | 123 | a0001c0001t0002g0072a0001c0001t0002g0107a0001c0001t0002g0109others(120): Show | 123 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.448-4919G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649738 | ||||||
| chr22:29649774
|
T | C | 4 | a0001c0001t0008g0257a0001c0001t0008g0258a0001c0001t0008g0259others(1): Show | 4 | HG02257.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-4883T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649774 | ||||||
| chr22:29649779
|
C | CA | 19 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(16): Show | 19 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.448-4866dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29649779 | |||||
| chr22:29649956
|
C | T | 1 | a0001c0001t0037g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.448-4701C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29649956 | ||||||
| chr22:29650134
|
TTAGA | T | 13 | a0001c0001t0005g0312a0001c0001t0013g0251a0001c0001t0013g0262others(10): Show | 13 | HG01099.hp2 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.448-4519_448-4516d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29650134 | |||||
| chr22:29650155
|
A | C | 1 | a0001c0001t0007g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.448-4502A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650155 | ||||||
| chr22:29650299
|
A | G | 1 | a0001c0001t0005g0298 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.448-4358A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650299 | ||||||
| chr22:29650333
|
C | T | 1 | a0001c0001t0013g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.448-4324C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650333 | ||||||
| chr22:29650429
|
G | A | 1 | a0001c0001t0040g0035 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.448-4228G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650429 | ||||||
| chr22:29650530
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.448-4127C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650530 | ||||||
| chr22:29650531
|
T | C | 1 | a0001c0001t0002g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.448-4126T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650531 | ||||||
| chr22:29650544
|
CTCTT | C | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-4105_448-4102d others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29650544 | |||||
| chr22:29650546
|
C | CTT | 3 | a0001c0001t0004g0102a0001c0001t0004g0118a0001c0001t0004g0302 | 3 | NA18970.hp1 NA18974.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.448-4109_448-4108d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29650546 | |||||
| chr22:29650637
|
G | T | 1 | a0001c0001t0010g0028 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.448-4020G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650637 | ||||||
| chr22:29650715
|
G | A | 1 | a0001c0001t0002g0220 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.448-3942G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650715 | ||||||
| chr22:29650813
|
G | C | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.448-3844G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650813 | ||||||
| chr22:29650951
|
T | A | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.448-3706T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29650951 | ||||||
| chr22:29651266
|
C | T | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-3391C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651266 | ||||||
| chr22:29651309
|
T | G | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-3348T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651309 | ||||||
| chr22:29651432
|
A | G | 14 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.448-3225A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651432 | ||||||
| chr22:29651524
|
G | A | 3 | a0001c0001t0010g0021a0001c0001t0010g0032a0001c0004t0002g0208 | 3 | HG01069.hp2 HG01071.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.448-3133G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651524 | ||||||
| chr22:29651611
|
CTTG | C | 4 | a0001c0001t0002g0109a0001c0001t0002g0203a0001c0001t0002g0204others(1): Show | 4 | NA18612.hp1 NA18998.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-3040_448-3038d others(5): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29651611 | |||||
| chr22:29651698
|
C | A | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.448-2959C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651698 | ||||||
| chr22:29651734
|
A | G | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.448-2923A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651734 | ||||||
| chr22:29651743
|
T | C | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.448-2914T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651743 | ||||||
| chr22:29651805
|
C | T | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.448-2852C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651805 | ||||||
| chr22:29651810
|
G | A | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.448-2847G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651810 | ||||||
| chr22:29651902
|
C | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.448-2755C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651902 | ||||||
| chr22:29651931
|
C | T | 43 | a0001c0001t0004g0068a0001c0001t0004g0102a0001c0001t0004g0117others(40): Show | 43 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.448-2726C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29651931 | ||||||
| chr22:29652193
|
G | A | 230 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.448-2464G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29652193 | ||||||
| chr22:29652326
|
T | C | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.448-2331T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29652326 | ||||||
| chr22:29652408
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.448-2249G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29652408 | ||||||
| chr22:29652582
|
T | C | 293 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(290): Show | 293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.448-2075T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29652582 | ||||||
| chr22:29652829
|
G | A | 2 | a0001c0001t0024g0014a0001c0001t0024g0015 | 2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.448-1828G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29652829 | ||||||
| chr22:29652890
|
A | G | 1 | a0001c0001t0004g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.448-1767A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29652890 | ||||||
| chr22:29653097
|
T | C | 1 | a0001c0001t0003g0159 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.448-1560T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653097 | ||||||
| chr22:29653112
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.448-1545A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653112 | ||||||
| chr22:29653171
|
C | T | 1 | a0001c0001t0004g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.448-1486C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653171 | ||||||
| chr22:29653174
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0054 | 2 | HG00280.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.448-1483G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653174 | ||||||
| chr22:29653188
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0226a0001c0001t0003g0227 | 3 | HG00621.hp2 HG02523.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.448-1469G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653188 | ||||||
| chr22:29653301
|
C | T | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.448-1356C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653301 | ||||||
| chr22:29653443
|
C | CA | 13 | a0001c0001t0002g0212a0001c0001t0003g0069a0001c0001t0005g0252others(10): Show | 13 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.448-1194dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29653443 | |||||
| chr22:29653443
|
CA | C | 141 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.448-1194delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29653443 | |||||
| chr22:29653595
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.448-1062A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653595 | ||||||
| chr22:29653654
|
C | T | 49 | a0001c0001t0004g0078a0001c0001t0005g0001a0001c0001t0005g0252others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.448-1003C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653654 | ||||||
| chr22:29653831
|
G | C | 1 | a0001c0001t0008g0259 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.448-826G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29653831 | ||||||
| chr22:29653981
|
G | GGAAA | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.448-674_448-671dup others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | 29653981 | |||||
| chr22:29654303
|
T | C | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.448-354T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29654303 | ||||||
| chr22:29654959
|
G | A | 1 | a0001c0001t0008g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.516+234G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 5/15 | chr22 | 29654959 | ||||||
| chr22:29654984
|
A | C | 5 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+259A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 5/15 | chr22 | 29654984 | ||||||
| chr22:29655345
|
G | C | 2 | a0001c0001t0013g0004a0001c0001t0013g0005 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.517-249G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 5/15 | chr22 | 29655345 | ||||||
| chr22:29655444
|
C | T | 106 | a0001c0001t0004g0068a0001c0001t0004g0078a0001c0001t0004g0102others(103): Show | 107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.517-150C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 5/15 | chr22 | 29655444 | ||||||
| chr22:29655716
|
C | CT | 9 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0100others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.599+56dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr22 | 29655716 | |||||
| chr22:29655941
|
A | AT | 32 | a0001c0001t0001g0064a0001c0001t0003g0069a0001c0001t0003g0112others(29): Show | 32 | HG00558.hp2 HG00621.hp2 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.599+280dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr22 | 29655941 | |||||
| chr22:29655965
|
G | A | 1 | a0001c0001t0008g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.599+289G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29655965 | ||||||
| chr22:29656048
|
C | CCT | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.599+373_599+374dup others(2): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr22 | 29656048 | |||||
| chr22:29656105
|
G | A | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.599+429G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29656105 | ||||||
| chr22:29656358
|
A | C | 3 | a0001c0001t0003g0160a0001c0001t0003g0162a0001c0001t0032g0163 | 3 | HG03239.hp1 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.599+682A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29656358 | ||||||
| chr22:29656402
|
A | G | 1 | a0001c0001t0008g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.599+726A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29656402 | ||||||
| chr22:29656407
|
C | CT | 6 | a0001c0001t0002g0206a0001c0001t0005g0300a0001c0001t0006g0296others(3): Show | 6 | HG01361.hp1 HG02055.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+754dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr22 | 29656407 | |||||
| chr22:29656407
|
CT | C | 184 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0018others(181): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.599+754delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr22 | 29656407 | |||||
| chr22:29656541
|
A | G | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.599+865A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29656541 | ||||||
| chr22:29656855
|
C | T | 14 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.599+1179C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29656855 | ||||||
| chr22:29656906
|
C | G | 2 | a0001c0001t0010g0007a0001c0001t0056g0008 | 2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.599+1230C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29656906 | ||||||
| chr22:29657018
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600-1171A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657018 | ||||||
| chr22:29657019
|
CT | C | 6 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0249others(3): Show | 6 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.600-1160delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr22 | 29657019 | |||||
| chr22:29657102
|
T | G | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.600-1087T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657102 | ||||||
| chr22:29657129
|
G | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.600-1060G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657129 | ||||||
| chr22:29657198
|
G | A | 1 | a0001c0001t0040g0035 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.600-991G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657198 | ||||||
| chr22:29657212
|
A | G | 4 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(1): Show | 4 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.600-977A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657212 | ||||||
| chr22:29657821
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.600-368C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657821 | ||||||
| chr22:29657871
|
A | G | 1 | a0001c0001t0004g0127 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.600-318A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657871 | ||||||
| chr22:29657950
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG00140.hp2 HG01993.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.600-239C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657950 | ||||||
| chr22:29657974
|
A | G | 39 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(36): Show | 39 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.600-215A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657974 | ||||||
| chr22:29657995
|
A | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0121a0001c0001t0004g0122others(3): Show | 6 | NA18948.hp2 NA18959.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.600-194A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29657995 | ||||||
| chr22:29658035
|
G | A | 96 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.600-154G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29658035 | ||||||
| chr22:29658050
|
G | C | 2 | a0001c0001t0013g0004a0001c0001t0013g0005 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.600-139G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 6/15 | chr22 | 29658050 | ||||||
| chr22:29658313
|
T | C | 3 | a0001c0001t0009g0084a0001c0001t0009g0085a0001c0001t0009g0088 | 3 | HG02080.hp2 HG02523.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.675+49T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29658313 | ||||||
| chr22:29658612
|
A | G | 16 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(13): Show | 16 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.675+348A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29658612 | ||||||
| chr22:29658637
|
C | G | 1 | a0001c0001t0005g0324 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.675+373C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29658637 | ||||||
| chr22:29658637
|
C | T | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.675+373C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29658637 | ||||||
| chr22:29658704
|
A | G | 1 | a0001c0001t0002g0275 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.675+440A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29658704 | ||||||
| chr22:29658958
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.675+694T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29658958 | ||||||
| chr22:29658999
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.675+735T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29658999 | ||||||
| chr22:29659349
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.675+1085A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659349 | ||||||
| chr22:29659446
|
G | A | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+1182G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659446 | ||||||
| chr22:29659466
|
A | G | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.675+1202A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659466 | ||||||
| chr22:29659609
|
A | G | 2 | a0001c0001t0003g0153a0001c0001t0003g0154 | 2 | NA18998.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.675+1345A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659609 | ||||||
| chr22:29659644
|
G | T | 1 | a0001c0001t0014g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.675+1380G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659644 | ||||||
| chr22:29659685
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.675+1421A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659685 | ||||||
| chr22:29659691
|
G | C | 1 | a0001c0001t0012g0011 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.675+1427G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659691 | ||||||
| chr22:29659957
|
A | C | 1 | a0001c0001t0003g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.676-1248A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29659957 | ||||||
| chr22:29660113
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.676-1092C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660113 | ||||||
| chr22:29660191
|
G | A | 1 | a0001c0001t0031g0071 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.676-1014G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660191 | ||||||
| chr22:29660196
|
T | G | 95 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.676-1009T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660196 | ||||||
| chr22:29660211
|
G | A | 1 | a0001c0001t0009g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.676-994G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660211 | ||||||
| chr22:29660347
|
T | C | 12 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(9): Show | 12 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.676-858T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660347 | ||||||
| chr22:29660558
|
T | A | 1 | a0001c0001t0011g0074 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.676-647T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660558 | ||||||
| chr22:29660570
|
T | G | 1 | a0001c0001t0049g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.676-635T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660570 | ||||||
| chr22:29660709
|
C | T | 46 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(43): Show | 46 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.676-496C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660709 | ||||||
| chr22:29660710
|
G | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0135a0001c0001t0001g0137others(9): Show | 12 | HG00438.hp2 HG00597.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.676-495G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660710 | ||||||
| chr22:29660723
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.676-482C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660723 | ||||||
| chr22:29660729
|
AT | A | 29 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.676-469delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr22 | 29660729 | |||||
| chr22:29660956
|
G | A | 95 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.676-249G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29660956 | ||||||
| chr22:29661185
|
T | C | 1 | a0001c0001t0053g0128 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.676-20T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 7/15 | chr22 | 29661185 | ||||||
| chr22:29661434
|
T | A | 1 | a0001c0001t0010g0007 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.810+95T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29661434 | ||||||
| chr22:29661585
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.810+246A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29661585 | ||||||
| chr22:29661628
|
C | T | 1 | a0001c0001t0005g0309 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.810+289C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29661628 | ||||||
| chr22:29661686
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.810+347T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29661686 | ||||||
| chr22:29661831
|
C | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.810+492C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29661831 | ||||||
| chr22:29662278
|
G | A | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.810+939G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29662278 | ||||||
| chr22:29662495
|
G | T | 1 | a0001c0001t0001g0051 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.810+1156G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29662495 | ||||||
| chr22:29662765
|
A | G | 3 | a0001c0001t0009g0084a0001c0001t0009g0085a0001c0001t0009g0088 | 3 | HG02080.hp2 HG02523.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.810+1426A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29662765 | ||||||
| chr22:29662894
|
C | A | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.810+1555C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29662894 | ||||||
| chr22:29663005
|
C | T | 3 | a0001c0001t0002g0221a0001c0001t0007g0264a0001c0001t0019g0333 | 3 | HG01243.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.810+1666C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29663005 | ||||||
| chr22:29663094
|
GT | G | 4 | a0001c0001t0002g0188a0001c0001t0002g0193a0001c0001t0002g0205others(1): Show | 4 | HG01358.hp2 HG01934.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+1760delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr22 | 29663094 | |||||
| chr22:29663104
|
G | A | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.810+1765G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29663104 | ||||||
| chr22:29663332
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.811-1658C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29663332 | ||||||
| chr22:29663506
|
A | G | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.811-1484A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29663506 | ||||||
| chr22:29663763
|
A | T | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.811-1227A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29663763 | ||||||
| chr22:29664084
|
T | G | 210 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.811-906T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29664084 | ||||||
| chr22:29664147
|
G | A | 2 | a0001c0001t0002g0109a0001c0001t0007g0108 | 2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.811-843G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29664147 | ||||||
| chr22:29664248
|
C | T | 3 | a0001c0001t0013g0251a0001c0001t0013g0262a0001c0001t0013g0263 | 3 | HG03209.hp2 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.811-742C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29664248 | ||||||
| chr22:29664371
|
C | CCA | 31 | a0001c0001t0002g0187a0001c0001t0002g0196a0001c0001t0002g0211others(28): Show | 31 | HG01074.hp2 HG01168.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.811-584_811-583dup others(2): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr22 | 29664371 | |||||
| chr22:29664371
|
C | CCACA | 7 | a0001c0001t0002g0273a0001c0001t0003g0069a0001c0001t0003g0173others(4): Show | 7 | HG00323.hp2 HG02132.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.811-586_811-583dup others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr22 | 29664371 | |||||
| chr22:29664371
|
CCA | C | 26 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0055others(23): Show | 26 | HG00609.hp1 HG01099.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.811-584_811-583del others(2): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr22 | 29664371 | |||||
| chr22:29664371
|
CCACA | C | 100 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.811-586_811-583del others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr22 | 29664371 | |||||
| chr22:29664371
|
CCACACA | C | 14 | a0001c0001t0004g0267a0001c0001t0011g0073a0001c0001t0011g0074others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.811-588_811-583del others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr22 | 29664371 | |||||
| chr22:29664400
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0291a0001c0001t0053g0128 | 3 | HG00735.hp1 HG00738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.811-590C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 8/15 | chr22 | 29664400 | ||||||
| chr22:29665236
|
GT | G | 207 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.885+183delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr22 | 29665236 | |||||
| chr22:29665247
|
T | G | 1 | a0001c0001t0004g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.885+183T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29665247 | ||||||
| chr22:29665248
|
G | T | 1 | a0001c0001t0004g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.885+184G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29665248 | ||||||
| chr22:29665712
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.885+648C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29665712 | ||||||
| chr22:29665755
|
GA | G | 7 | a0001c0001t0004g0036a0001c0001t0016g0328a0001c0001t0016g0329others(4): Show | 7 | HG00609.hp1 HG02559.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.885+706delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr22 | 29665755 | |||||
| chr22:29665964
|
A | G | 98 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.885+900A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29665964 | ||||||
| chr22:29666026
|
C | T | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.885+962C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666026 | ||||||
| chr22:29666285
|
C | T | 13 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(10): Show | 13 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.885+1221C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666285 | ||||||
| chr22:29666386
|
A | G | 211 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.885+1322A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666386 | ||||||
| chr22:29666419
|
G | A | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.885+1355G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666419 | ||||||
| chr22:29666463
|
G | T | 6 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268others(3): Show | 6 | HG00673.hp1 HG02074.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.885+1399G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666463 | ||||||
| chr22:29666502
|
G | A | 3 | a0001c0001t0004g0036a0001c0001t0004g0044a0001c0001t0012g0058 | 3 | NA18978.hp2 NA18982.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.885+1438G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666502 | ||||||
| chr22:29666543
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.885+1479G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666543 | ||||||
| chr22:29666633
|
T | C | 4 | a0001c0001t0003g0159a0001c0001t0003g0166a0001c0001t0003g0179others(1): Show | 4 | NA18953.hp1 NA18971.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.885+1569T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666633 | ||||||
| chr22:29666793
|
A | T | 1 | a0001c0001t0004g0056 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.886-1540A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666793 | ||||||
| chr22:29666944
|
C | G | 1 | a0001c0001t0009g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.886-1389C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29666944 | ||||||
| chr22:29667015
|
G | A | 1 | a0001c0001t0016g0330 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.886-1318G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29667015 | ||||||
| chr22:29667257
|
A | C | 6 | a0001c0001t0008g0256a0001c0001t0008g0257a0001c0001t0008g0258others(3): Show | 6 | HG02257.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.886-1076A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29667257 | ||||||
| chr22:29667413
|
A | G | 1 | a0001c0001t0004g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.886-920A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29667413 | ||||||
| chr22:29667492
|
C | T | 1 | a0001c0001t0014g0186 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.886-841C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29667492 | ||||||
| chr22:29667561
|
G | T | 212 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.886-772G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29667561 | ||||||
| chr22:29667720
|
G | T | 1 | a0001c0001t0033g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.886-613G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29667720 | ||||||
| chr22:29667729
|
CTTT | C | 5 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(2): Show | 5 | HG00609.hp1 HG02559.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.886-599_886-597del others(3): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr22 | 29667729 | |||||
| chr22:29667884
|
C | CT | 14 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.886-447dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr22 | 29667884 | |||||
| chr22:29667935
|
A | G | 43 | a0001c0001t0004g0068a0001c0001t0004g0078a0001c0001t0004g0102others(40): Show | 43 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.886-398A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29667935 | ||||||
| chr22:29668084
|
A | AGT | 97 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.886-246_886-245dup others(2): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr22 | 29668084 | |||||
| chr22:29668128
|
C | T | 97 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.886-205C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29668128 | ||||||
| chr22:29668140
|
G | A | 1 | a0001c0001t0002g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.886-193G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29668140 | ||||||
| chr22:29668301
|
A | G | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.886-32A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 9/15 | chr22 | 29668301 | ||||||
| chr22:29668591
|
G | A | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+145G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29668591 | ||||||
| chr22:29668742
|
A | G | 97 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.999+296A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29668742 | ||||||
| chr22:29668854
|
C | T | 6 | a0001c0001t0008g0256a0001c0001t0008g0257a0001c0001t0008g0258others(3): Show | 6 | HG02257.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+408C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29668854 | ||||||
| chr22:29669062
|
G | C | 1 | a0001c0001t0031g0071 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.999+616G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29669062 | ||||||
| chr22:29669470
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.999+1024A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29669470 | ||||||
| chr22:29669604
|
G | A | 1 | a0001c0001t0004g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.999+1158G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29669604 | ||||||
| chr22:29669806
|
G | C | 15 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(12): Show | 15 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.999+1360G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29669806 | ||||||
| chr22:29669824
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.999+1378T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29669824 | ||||||
| chr22:29669978
|
G | T | 211 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.999+1532G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29669978 | ||||||
| chr22:29669984
|
G | A | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.999+1538G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29669984 | ||||||
| chr22:29670094
|
G | C | 11 | a0001c0001t0002g0107a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 11 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(8): Show |
intron_variant | MODIFIER | c.999+1648G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29670094 | ||||||
| chr22:29670312
|
TTTTC | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1000-1499_1000-149 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670312 | |||||
| chr22:29670345
|
T | A | 15 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(12): Show | 15 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1000-1481T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29670345 | ||||||
| chr22:29670355
|
G | A | 215 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1000-1471G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29670355 | ||||||
| chr22:29670503
|
T | TTG | 18 | a0001c0001t0002g0072a0001c0001t0002g0110a0001c0001t0002g0188others(15): Show | 18 | HG00609.hp1 HG00639.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1000-1289_1000-128 others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
T | TTGTG | 6 | a0001c0001t0002g0198a0001c0001t0003g0160a0001c0001t0003g0162others(3): Show | 6 | HG01517.hp2 HG02559.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000-1291_1000-128 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
T | TTGTGTG | 33 | a0001c0001t0003g0096a0001c0001t0003g0159a0001c0001t0003g0336others(30): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1000-1293_1000-128 others(10): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
T | TTGTGTGT others(1): Show |
55 | a0001c0001t0002g0194a0001c0001t0002g0214a0001c0001t0002g0216others(52): Show | 55 | HG00558.hp2 HG00642.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1000-1295_1000-128 others(12): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
T | TTGTGTGT others(3): Show |
13 | a0001c0001t0005g0297a0001c0001t0005g0300a0001c0001t0005g0311others(10): Show | 13 | HG00673.hp2 HG01891.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1000-1297_1000-128 others(14): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
T | TTGTGTGT others(5): Show |
15 | a0001c0001t0002g0305a0001c0001t0003g0112a0001c0001t0003g0226others(12): Show | 15 | HG00597.hp1 HG00621.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1000-1299_1000-128 others(16): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0008g0113a0001c0001t0050g0046 | 2 | HG01496.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1000-1301_1000-128 others(18): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
TTG | T | 7 | a0001c0001t0009g0089a0001c0001t0009g0233a0001c0001t0013g0004others(4): Show | 7 | HG00558.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-1289_1000-128 others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
TTGTG | T | 60 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1000-1291_1000-128 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670503
|
TTGTGTG | T | 83 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1000-1293_1000-128 others(10): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr22 | 29670503 | |||||
| chr22:29670579
|
C | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1000-1247C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29670579 | ||||||
| chr22:29670833
|
C | T | 1 | a0001c0001t0005g0309 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1000-993C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29670833 | ||||||
| chr22:29671139
|
C | A | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01192.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1000-687C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671139 | ||||||
| chr22:29671155
|
C | T | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-671C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671155 | ||||||
| chr22:29671219
|
C | T | 7 | a0001c0001t0002g0107a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | NA18951.hp2 NA18968.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-607C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671219 | ||||||
| chr22:29671257
|
G | A | 2 | a0001c0001t0002g0198a0001c0001t0031g0071 | 2 | HG01517.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1000-569G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671257 | ||||||
| chr22:29671261
|
C | T | 147 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1000-565C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671261 | ||||||
| chr22:29671398
|
G | A | 1 | a0001c0001t0016g0328 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1000-428G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671398 | ||||||
| chr22:29671562
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1000-264C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671562 | ||||||
| chr22:29671613
|
CTAG | C | 15 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(12): Show | 15 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1000-212_1000-210d others(5): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 10/15 | chr22 | 29671613 | ||||||
| chr22:29672077
|
A | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0291a0001c0001t0026g0067others(5): Show | 8 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1122+129A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672077 | ||||||
| chr22:29672117
|
A | C | 1 | a0001c0001t0008g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1122+169A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672117 | ||||||
| chr22:29672214
|
T | C | 9 | a0001c0001t0004g0133a0001c0001t0004g0134a0001c0001t0004g0143others(6): Show | 9 | HG02027.hp1 HG02165.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1122+266T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672214 | ||||||
| chr22:29672309
|
C | CT | 94 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1122+381dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr22 | 29672309 | |||||
| chr22:29672309
|
CT | C | 16 | a0001c0001t0002g0196a0001c0001t0002g0200a0001c0001t0002g0271others(13): Show | 16 | HG01168.hp1 HG01517.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1122+381delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr22 | 29672309 | |||||
| chr22:29672436
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1122+488C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672436 | ||||||
| chr22:29672533
|
C | T | 11 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(8): Show | 11 | HG00609.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1122+585C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672533 | ||||||
| chr22:29672558
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1122+610C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672558 | ||||||
| chr22:29672581
|
G | T | 7 | a0001c0001t0002g0194a0001c0001t0002g0198a0001c0001t0002g0214others(4): Show | 7 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+633G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672581 | ||||||
| chr22:29672626
|
T | C | 2 | a0001c0001t0015g0177a0001c0001t0030g0174 | 2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1123-643T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672626 | ||||||
| chr22:29672642
|
T | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1123-627T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672642 | ||||||
| chr22:29672740
|
C | T | 1 | a0001c0001t0004g0122 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1123-529C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672740 | ||||||
| chr22:29672762
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG03704.hp1 HG04204.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-507C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672762 | ||||||
| chr22:29672779
|
CT | C | 83 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1123-478delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr22 | 29672779 | |||||
| chr22:29672781
|
T | G | 50 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1123-488T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672781 | ||||||
| chr22:29672862
|
T | C | 283 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1123-407T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672862 | ||||||
| chr22:29672938
|
G | A | 6 | a0001c0001t0008g0256a0001c0001t0008g0257a0001c0001t0008g0258others(3): Show | 6 | HG02257.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1123-331G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29672938 | ||||||
| chr22:29673070
|
A | G | 1 | a0001c0001t0011g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1123-199A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29673070 | ||||||
| chr22:29673109
|
A | C | 2 | a0001c0001t0029g0151a0001c0001t0033g0152 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1123-160A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29673109 | ||||||
| chr22:29673218
|
C | T | 4 | a0001c0001t0002g0271a0001c0001t0002g0273a0001c0001t0002g0274others(1): Show | 4 | HG00323.hp2 HG01168.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.1123-51C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29673218 | ||||||
| chr22:29673705
|
G | A | 1 | a0001c0001t0009g0087 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1340+219G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29673705 | ||||||
| chr22:29673734
|
A | G | 9 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(6): Show | 9 | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1340+248A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29673734 | ||||||
| chr22:29673780
|
A | G | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1340+294A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29673780 | ||||||
| chr22:29674113
|
A | G | 1 | a0001c0001t0008g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1340+627A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29674113 | ||||||
| chr22:29674234
|
T | A | 278 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1341-602T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29674234 | ||||||
| chr22:29674235
|
C | T | 6 | a0001c0001t0005g0252a0001c0001t0005g0309a0001c0001t0005g0315others(3): Show | 6 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1341-601C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29674235 | ||||||
| chr22:29674291
|
A | T | 2 | a0001c0001t0002g0187a0001c0001t0002g0289 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1341-545A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29674291 | ||||||
| chr22:29674343
|
G | A | 1 | a0001c0001t0008g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1341-493G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29674343 | ||||||
| chr22:29674461
|
A | G | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1341-375A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 12/15 | chr22 | 29674461 | ||||||
| chr22:29674965
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1446+24G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29674965 | ||||||
| chr22:29675369
|
C | T | 103 | a0001c0001t0004g0012a0001c0001t0004g0023a0001c0001t0004g0036others(100): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1446+428C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29675369 | ||||||
| chr22:29675477
|
A | AT | 48 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0051others(45): Show | 48 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1446+549dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29675477 | |||||
| chr22:29675477
|
AT | A | 20 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(17): Show | 20 | HG01099.hp2 HG01496.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1446+549delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29675477 | |||||
| chr22:29675814
|
G | GAC | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1446+880_1446+881d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29675814 | |||||
| chr22:29675822
|
C | T | 3 | a0001c0001t0002g0221a0001c0001t0007g0264a0001c0001t0019g0333 | 3 | HG01243.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1446+881C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29675822 | ||||||
| chr22:29675946
|
C | T | 15 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(12): Show | 15 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+1005C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29675946 | ||||||
| chr22:29675955
|
C | T | 54 | a0001c0001t0004g0012a0001c0001t0004g0023a0001c0001t0004g0036others(51): Show | 54 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1446+1014C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29675955 | ||||||
| chr22:29676034
|
A | G | 2 | a0001c0001t0023g0231a0001c0001t0023g0277 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1446+1093A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676034 | ||||||
| chr22:29676159
|
T | A | 1 | a0001c0001t0003g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1446+1218T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676159 | ||||||
| chr22:29676173
|
A | T | 2 | a0001c0001t0002g0272a0001c0001t0007g0276 | 2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1446+1232A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676173 | ||||||
| chr22:29676430
|
C | G | 1 | a0001c0001t0005g0252 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1446+1489C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676430 | ||||||
| chr22:29676437
|
A | G | 3 | a0001c0001t0003g0285a0001c0001t0003g0286a0001c0001t0003g0287 | 3 | HG02572.hp1 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1446+1496A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676437 | ||||||
| chr22:29676461
|
C | T | 1 | a0001c0001t0005g0314 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1446+1520C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676461 | ||||||
| chr22:29676696
|
T | G | 12 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(9): Show | 12 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1447-1500T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676696 | ||||||
| chr22:29676770
|
T | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0019others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.1447-1426T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676770 | ||||||
| chr22:29676805
|
A | G | 2 | a0001c0001t0002g0271a0001c0001t0002g0274 | 2 | HG01168.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1447-1391A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676805 | ||||||
| chr22:29676827
|
G | T | 2 | a0001c0001t0023g0231a0001c0001t0023g0277 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1447-1369G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676827 | ||||||
| chr22:29676893
|
C | G | 8 | a0001c0001t0006g0149a0001c0001t0006g0239a0001c0001t0006g0240others(5): Show | 8 | HG01496.hp2 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1447-1303C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676893 | ||||||
| chr22:29676948
|
C | CCAGCACC others(45): Show |
30 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1447-1239_1447-118 others(56): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29676948 | |||||
| chr22:29676974
|
A | G | 3 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0007g0218 | 3 | HG00642.hp1 HG01074.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1447-1222A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29676974 | ||||||
| chr22:29677098
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1447-1098C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677098 | ||||||
| chr22:29677177
|
A | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0120a0001c0001t0001g0123others(8): Show | 11 | HG02071.hp2 HG02083.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1447-1019A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677177 | ||||||
| chr22:29677259
|
G | A | 1 | a0001c0001t0021g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1447-937G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677259 | ||||||
| chr22:29677298
|
C | T | 5 | a0001c0001t0005g0299a0001c0001t0005g0313a0001c0001t0005g0322others(2): Show | 5 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-898C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677298 | ||||||
| chr22:29677500
|
C | CA | 9 | a0001c0001t0002g0211a0001c0001t0004g0122a0001c0001t0006g0235others(6): Show | 9 | HG01884.hp2 HG01978.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1447-682dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29677500 | |||||
| chr22:29677500
|
CA | C | 30 | a0001c0001t0003g0069a0001c0001t0003g0112a0001c0001t0003g0153others(27): Show | 30 | HG00558.hp2 HG00621.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.1447-682delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29677500 | |||||
| chr22:29677572
|
C | T | 9 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(6): Show | 9 | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1447-624C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677572 | ||||||
| chr22:29677580
|
C | A | 279 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1447-616C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677580 | ||||||
| chr22:29677583
|
TGG | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1447-610_1447-609d others(4): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29677583 | |||||
| chr22:29677692
|
T | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1447-504T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677692 | ||||||
| chr22:29677796
|
A | T | 4 | a0001c0001t0016g0328a0001c0001t0016g0329a0001c0001t0016g0330others(1): Show | 4 | HG00609.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-400A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677796 | ||||||
| chr22:29677916
|
A | G | 4 | a0001c0001t0004g0102a0001c0001t0004g0117a0001c0001t0004g0118others(1): Show | 4 | NA18970.hp1 NA18974.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-280A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677916 | ||||||
| chr22:29677960
|
G | A | 1 | a0001c0001t0009g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1447-236G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | chr22 | 29677960 | ||||||
| chr22:29677970
|
T | TTGAGGGA | 85 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1447-222_1447-216d others(9): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr22 | 29677970 | |||||
| chr22:29678496
|
G | A | 12 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(9): Show | 12 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1574+173G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29678496 | ||||||
| chr22:29678749
|
A | G | 11 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1574+426A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29678749 | ||||||
| chr22:29678787
|
G | T | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1574+464G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29678787 | ||||||
| chr22:29678815
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1574+492A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29678815 | ||||||
| chr22:29678972
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1574+649G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29678972 | ||||||
| chr22:29679052
|
T | G | 1 | a0001c0001t0054g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1574+729T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29679052 | ||||||
| chr22:29679063
|
T | C | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1574+740T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29679063 | ||||||
| chr22:29679088
|
A | G | 1 | a0001c0001t0011g0074 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1574+765A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29679088 | ||||||
| chr22:29679098
|
A | C | 279 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1574+775A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29679098 | ||||||
| chr22:29679224
|
T | TCTG | 6 | a0001c0001t0005g0252a0001c0001t0005g0309a0001c0001t0005g0315others(3): Show | 6 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1574+903_1574+905d others(5): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr22 | 29679224 | |||||
| chr22:29679422
|
T | A | 1 | a0001c0001t0003g0338 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1574+1099T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29679422 | ||||||
| chr22:29679423
|
C | T | 1 | a0001c0001t0003g0338 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1574+1100C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29679423 | ||||||
| chr22:29679835
|
C | A | 1 | a0001c0001t0015g0176 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1574+1512C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29679835 | ||||||
| chr22:29679865
|
C | CA | 28 | a0001c0001t0002g0107a0001c0001t0002g0221a0001c0001t0002g0272others(25): Show | 28 | HG00099.hp1 HG01069.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1574+1556dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr22 | 29679865 | |||||
| chr22:29680116
|
C | CT | 16 | a0001c0001t0001g0043a0001c0001t0001g0135a0001c0001t0001g0137others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1575-1310dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr22 | 29680116 | |||||
| chr22:29680183
|
C | T | 2 | a0001c0001t0023g0231a0001c0001t0023g0277 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1575-1256C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29680183 | ||||||
| chr22:29680257
|
G | A | 39 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(36): Show | 39 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1575-1182G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29680257 | ||||||
| chr22:29680390
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1575-1049G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29680390 | ||||||
| chr22:29680409
|
C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1575-1030C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29680409 | ||||||
| chr22:29680731
|
G | A | 54 | a0001c0001t0004g0012a0001c0001t0004g0023a0001c0001t0004g0036others(51): Show | 54 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1575-708G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29680731 | ||||||
| chr22:29680853
|
T | TA | 50 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1575-574dupA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr22 | 29680853 | |||||
| chr22:29680853
|
TA | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1575-574delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr22 | 29680853 | |||||
| chr22:29680916
|
C | T | 2 | a0001c0001t0023g0231a0001c0001t0023g0277 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1575-523C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29680916 | ||||||
| chr22:29680946
|
GT | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1575-483delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr22 | 29680946 | |||||
| chr22:29681054
|
C | CT | 8 | a0001c0001t0002g0206a0001c0001t0011g0073a0001c0001t0011g0074others(5): Show | 8 | HG01070.hp2 HG01106.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1575-372dupT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr22 | 29681054 | |||||
| chr22:29681068
|
A | T | 50 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1575-371A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29681068 | ||||||
| chr22:29681069
|
A | T | 30 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1575-370A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29681069 | ||||||
| chr22:29681127
|
G | A | 2 | a0001c0001t0024g0014a0001c0001t0024g0015 | 2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1575-312G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29681127 | ||||||
| chr22:29681372
|
G | A | 342 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1575-67G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29681372 | ||||||
| chr22:29681736
|
T | C | 66 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(63): Show | 66 | HG00558.hp2 HG00621.hp2 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.1737+135T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29681736 | ||||||
| chr22:29681920
|
C | A | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1737+319C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29681920 | ||||||
| chr22:29681945
|
A | G | 1 | a0001c0001t0006g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1737+344A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29681945 | ||||||
| chr22:29682635
|
A | C | 1 | a0001c0001t0012g0265 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1737+1034A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29682635 | ||||||
| chr22:29682696
|
G | A | 1 | a0001c0001t0005g0298 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1737+1095G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29682696 | ||||||
| chr22:29683102
|
G | A | 1 | a0001c0001t0023g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1737+1501G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29683102 | ||||||
| chr22:29683165
|
G | A | 2 | a0001c0001t0003g0166a0001c0001t0003g0179 | 2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1737+1564G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29683165 | ||||||
| chr22:29683224
|
T | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1737+1623T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29683224 | ||||||
| chr22:29683486
|
G | A | 2 | a0001c0001t0004g0078a0001c0001t0036g0060 | 2 | HG02896.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1737+1885G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29683486 | ||||||
| chr22:29684124
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1737+2523C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29684124 | ||||||
| chr22:29684243
|
A | G | 3 | a0001c0001t0045g0295a0001c0001t0046g0310a0001c0006t0044g0294 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1737+2642A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29684243 | ||||||
| chr22:29684370
|
TTAC | T | 6 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(3): Show | 6 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+2771_1737+277 others(7): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29684370 | |||||
| chr22:29684374
|
T | C | 6 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(3): Show | 6 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+2773T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29684374 | ||||||
| chr22:29684528
|
G | A | 50 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1737+2927G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29684528 | ||||||
| chr22:29684925
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1737+3324G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29684925 | ||||||
| chr22:29685189
|
C | G | 3 | a0001c0001t0026g0067a0001c0001t0026g0132a0001c0001t0049g0131 | 3 | HG01070.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1737+3588C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29685189 | ||||||
| chr22:29685261
|
C | A | 53 | a0001c0001t0004g0012a0001c0001t0004g0023a0001c0001t0004g0036others(50): Show | 53 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1737+3660C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29685261 | ||||||
| chr22:29685521
|
C | T | 3 | a0001c0001t0005g0298a0001c0001t0017g0002a0003c0005t0017g0002 | 3 | HG00597.hp1 HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1737+3920C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29685521 | ||||||
| chr22:29685593
|
TG | T | 3 | a0001c0001t0011g0076a0001c0001t0011g0077a0001c0001t0021g0066 | 3 | HG01106.hp1 HG02056.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1737+3993delG | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29685593 | ||||||
| chr22:29685726
|
G | A | 103 | a0001c0001t0004g0012a0001c0001t0004g0023a0001c0001t0004g0036others(100): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1737+4125G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29685726 | ||||||
| chr22:29685955
|
CT | C | 64 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(61): Show | 64 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1737+4367delT | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29685955 | |||||
| chr22:29686003
|
C | T | 2 | a0001c0001t0002g0201a0001c0001t0002g0211 | 2 | NA18970.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1737+4402C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686003 | ||||||
| chr22:29686104
|
A | G | 1 | a0001c0001t0002g0196 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1737+4503A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686104 | ||||||
| chr22:29686193
|
A | G | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1737+4592A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686193 | ||||||
| chr22:29686236
|
G | A | 2 | a0001c0001t0002g0072a0001c0001t0007g0213 | 2 | HG00639.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1737+4635G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686236 | ||||||
| chr22:29686342
|
T | C | 30 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1737+4741T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686342 | ||||||
| chr22:29686377
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1737+4776T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686377 | ||||||
| chr22:29686580
|
A | G | 234 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(231): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1737+4979A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686580 | ||||||
| chr22:29686774
|
A | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG02071.hp1 HG03704.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+5173A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686774 | ||||||
| chr22:29686932
|
G | T | 66 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(63): Show | 66 | HG00558.hp2 HG00621.hp2 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.1737+5331G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686932 | ||||||
| chr22:29686995
|
T | C | 1 | a0001c0001t0042g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1737+5394T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29686995 | ||||||
| chr22:29687082
|
C | A | 6 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(3): Show | 6 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+5481C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687082 | ||||||
| chr22:29687158
|
A | C | 6 | a0001c0001t0008g0256a0001c0001t0008g0257a0001c0001t0008g0258others(3): Show | 6 | HG02257.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+5557A>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687158 | ||||||
| chr22:29687210
|
G | A | 4 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(1): Show | 4 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+5609G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687210 | ||||||
| chr22:29687292
|
T | G | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1737+5691T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687292 | ||||||
| chr22:29687401
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1737+5800G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687401 | ||||||
| chr22:29687428
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1737+5827C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687428 | ||||||
| chr22:29687437
|
T | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1737+5836T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687437 | ||||||
| chr22:29687464
|
G | A | 1 | a0001c0001t0024g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1737+5863G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687464 | ||||||
| chr22:29687491
|
T | C | 1 | a0001c0001t0018g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1737+5890T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687491 | ||||||
| chr22:29687530
|
G | A | 1 | a0001c0001t0008g0308 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1737+5929G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687530 | ||||||
| chr22:29687550
|
G | A | 51 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1737+5949G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687550 | ||||||
| chr22:29687776
|
G | A | 3 | a0001c0001t0011g0076a0001c0001t0011g0077a0001c0001t0021g0066 | 3 | HG01106.hp1 HG02056.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1737+6175G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687776 | ||||||
| chr22:29687971
|
G | A | 1 | a0001c0001t0023g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1737+6370G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29687971 | ||||||
| chr22:29688104
|
G | T | 11 | a0001c0001t0010g0007a0001c0001t0010g0021a0001c0001t0010g0027others(8): Show | 11 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1737+6503G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688104 | ||||||
| chr22:29688283
|
A | G | 1 | a0001c0001t0025g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1738-6469A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688283 | ||||||
| chr22:29688750
|
A | T | 87 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1738-6002A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688750 | ||||||
| chr22:29688887
|
A | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG02071.hp2 NA18944.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-5865A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688887 | ||||||
| chr22:29688900
|
G | A | 1 | a0001c0001t0019g0215 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1738-5852G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688900 | ||||||
| chr22:29688905
|
A | G | 2 | a0001c0001t0002g0072a0001c0001t0007g0213 | 2 | HG00639.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1738-5847A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688905 | ||||||
| chr22:29688947
|
G | A | 5 | a0001c0001t0013g0004a0001c0001t0013g0005a0001c0001t0013g0251others(2): Show | 5 | HG03098.hp2 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-5805G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688947 | ||||||
| chr22:29688987
|
T | C | 87 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1738-5765T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29688987 | ||||||
| chr22:29689061
|
TC | T | 5 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-5689delC | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29689061 | |||||
| chr22:29689172
|
C | T | 1 | a0001c0001t0035g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1738-5580C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29689172 | ||||||
| chr22:29689177
|
CA | C | 51 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0187others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1738-5552delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29689177 | |||||
| chr22:29689177
|
CAA | C | 116 | a0001c0001t0001g0052a0001c0001t0002g0200a0001c0001t0004g0012others(113): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1738-5553_1738-555 others(6): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29689177 | |||||
| chr22:29689177
|
CAAA | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1738-5554_1738-555 others(7): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29689177 | |||||
| chr22:29689177
|
CAAAA | C | 9 | a0001c0001t0001g0038a0001c0001t0001g0124a0001c0001t0003g0165others(6): Show | 9 | HG01070.hp1 HG01099.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-5555_1738-555 others(8): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29689177 | |||||
| chr22:29689208
|
T | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1738-5544T>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29689208 | ||||||
| chr22:29689230
|
A | T | 1 | a0001c0001t0007g0106 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1738-5522A>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29689230 | ||||||
| chr22:29689666
|
C | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1738-5086C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29689666 | ||||||
| chr22:29689987
|
G | A | 4 | a0001c0001t0005g0297a0001c0001t0005g0300a0001c0001t0005g0311others(1): Show | 4 | HG00673.hp2 HG02074.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-4765G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29689987 | ||||||
| chr22:29690040
|
G | A | 12 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0076others(9): Show | 12 | HG01070.hp2 HG01106.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-4712G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690040 | ||||||
| chr22:29690062
|
G | A | 46 | a0001c0001t0003g0069a0001c0001t0003g0096a0001c0001t0003g0097others(43): Show | 46 | HG00558.hp2 HG00621.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.1738-4690G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690062 | ||||||
| chr22:29690155
|
C | T | 279 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1738-4597C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690155 | ||||||
| chr22:29690308
|
G | A | 1 | a0001c0001t0012g0119 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1738-4444G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690308 | ||||||
| chr22:29690368
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0150 | 2 | HG02083.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1738-4384C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690368 | ||||||
| chr22:29690717
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1738-4035C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690717 | ||||||
| chr22:29690769
|
G | T | 4 | a0001c0001t0006g0235a0001c0001t0006g0237a0001c0001t0006g0238others(1): Show | 4 | HG01884.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-3983G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690769 | ||||||
| chr22:29690857
|
C | T | 30 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1738-3895C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690857 | ||||||
| chr22:29690963
|
C | T | 2 | a0001c0001t0023g0231a0001c0001t0023g0277 | 2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1738-3789C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29690963 | ||||||
| chr22:29691072
|
C | A | 3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG01192.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1738-3680C>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29691072 | ||||||
| chr22:29691170
|
G | A | 5 | a0001c0001t0013g0004a0001c0001t0013g0005a0001c0001t0013g0251others(2): Show | 5 | HG03098.hp2 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-3582G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29691170 | ||||||
| chr22:29691543
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1738-3209G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29691543 | ||||||
| chr22:29692050
|
T | G | 87 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1738-2702T>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692050 | ||||||
| chr22:29692194
|
C | T | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1738-2558C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692194 | ||||||
| chr22:29692240
|
C | T | 10 | a0001c0001t0015g0175a0001c0001t0015g0176a0001c0001t0015g0177others(7): Show | 10 | HG00609.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-2512C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692240 | ||||||
| chr22:29692268
|
C | T | 50 | a0001c0001t0005g0001a0001c0001t0005g0252a0001c0001t0005g0297others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1738-2484C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692268 | ||||||
| chr22:29692368
|
G | A | 1 | a0001c0001t0008g0259 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1738-2384G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692368 | ||||||
| chr22:29692453
|
T | C | 55 | a0001c0001t0004g0012a0001c0001t0004g0023a0001c0001t0004g0036others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1738-2299T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692453 | ||||||
| chr22:29692492
|
C | T | 1 | a0001c0001t0024g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1738-2260C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692492 | ||||||
| chr22:29692592
|
G | A | 1 | a0001c0001t0010g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1738-2160G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692592 | ||||||
| chr22:29692682
|
T | C | 40 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(37): Show | 40 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1738-2070T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692682 | ||||||
| chr22:29692935
|
AAGTGACC others(23): Show |
A | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1738-1812_1738-178 others(34): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | 29692935 | |||||
| chr22:29692965
|
C | G | 5 | a0001c0001t0008g0257a0001c0001t0008g0258a0001c0001t0008g0259others(2): Show | 5 | HG02257.hp2 HG03130.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-1787C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29692965 | ||||||
| chr22:29693211
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1738-1541G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693211 | ||||||
| chr22:29693397
|
C | G | 1 | a0001c0007t0052g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1738-1355C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693397 | ||||||
| chr22:29693514
|
G | A | 3 | a0001c0001t0002g0193a0001c0001t0002g0205a0001c0001t0007g0106 | 3 | HG01934.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1738-1238G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693514 | ||||||
| chr22:29693522
|
C | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1738-1230C>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693522 | ||||||
| chr22:29693666
|
G | A | 1 | a0001c0001t0008g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1738-1086G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693666 | ||||||
| chr22:29693680
|
G | C | 282 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1738-1072G>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693680 | ||||||
| chr22:29693681
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1738-1071G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693681 | ||||||
| chr22:29693746
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1738-1006G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693746 | ||||||
| chr22:29693888
|
C | T | 1 | a0001c0001t0055g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738-864C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693888 | ||||||
| chr22:29693966
|
G | A | 1 | a0001c0001t0021g0075 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1738-786G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693966 | ||||||
| chr22:29693997
|
C | T | 1 | a0001c0001t0051g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1738-755C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29693997 | ||||||
| chr22:29694125
|
C | T | 8 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(5): Show | 8 | HG01192.hp2 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-627C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29694125 | ||||||
| chr22:29694321
|
G | A | 2 | a0001c0001t0024g0014a0001c0001t0024g0015 | 2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1738-431G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29694321 | ||||||
| chr22:29694469
|
C | T | 4 | a0001c0001t0008g0083a0001c0001t0008g0113a0001c0001t0008g0114others(1): Show | 4 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-283C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29694469 | ||||||
| chr22:29694625
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0226a0001c0001t0003g0227 | 3 | HG00621.hp2 HG02523.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1738-127A>G | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | chr22 | 29694625 |