Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MAGAI others(590): Show |
chr22 | 29598633 | 29703598 |
| a0002 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | MAGAI others(590): Show |
chr22 | 29598633 | 29703598 |
| a0003 | 0/0 | 595 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | MAGAI others(590): Show |
chr22 | 29598633 | 29703598 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1785 | 331 | 87 | 62 | 129 | 16 | 35 | NF2_chr22_29598633_29703598 | NF2 | ATGGC others(1780): Show |
chr22 | 29598633 | 29703598 | ||
| a0001c0002 | 0/0 | 1785 | 8 | 0 | 0 | 8 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | ATGGC others(1780): Show |
chr22 | 29598633 | 29703598 | ||
| a0001c0004 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | ATGGC others(1780): Show |
chr22 | 29598633 | 29703598 | ||
| a0001c0006 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | ATGGC others(1780): Show |
chr22 | 29598633 | 29703598 | ||
| a0001c0007 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | ATGGC others(1780): Show |
chr22 | 29598633 | 29703598 | ||
| a0002c0005 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | ATGGC others(1780): Show |
chr22 | 29598633 | 29703598 | ||
| a0003c0003 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | ATGGC others(1780): Show |
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 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0002 | 0/1 | 5950 | 44 | 1 | 14 | 17 | 3 | 8 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0003 | 0/0 | 5951 | 31 | 13 | 1 | 12 | 0 | 5 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0004 | 0/0 | 5951 | 27 | 0 | 1 | 23 | 0 | 3 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0005 | 0/0 | 5952 | 23 | 1 | 8 | 5 | 4 | 5 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0006 | 0/0 | 5951 | 17 | 16 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0007 | 0/0 | 5951 | 11 | 2 | 5 | 3 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0008 | 0/0 | 5952 | 11 | 10 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0009 | 0/0 | 5951 | 11 | 0 | 3 | 7 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0010 | 0/0 | 5951 | 10 | 0 | 8 | 0 | 2 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0011 | 0/0 | 5951 | 7 | 3 | 2 | 1 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0012 | 0/0 | 5952 | 5 | 0 | 0 | 4 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0013 | 0/0 | 5951 | 5 | 5 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0014 | 0/0 | 5952 | 5 | 2 | 1 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0015 | 0/0 | 5951 | 4 | 4 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0016 | 0/0 | 5945 | 4 | 0 | 0 | 2 | 0 | 2 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5940): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0017 | 0/0 | 5951 | 3 | 0 | 1 | 1 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0018 | 0/0 | 5952 | 3 | 0 | 0 | 2 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0019 | 0/0 | 5949 | 3 | 1 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5944): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0020 | 0/0 | 5952 | 3 | 0 | 0 | 3 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0021 | 0/0 | 5952 | 3 | 1 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0022 | 0/0 | 5952 | 2 | 0 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0023 | 0/0 | 5941 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5936): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0024 | 0/0 | 5950 | 2 | 1 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0025 | 0/0 | 5951 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0026 | 0/0 | 5951 | 2 | 0 | 2 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0027 | 0/0 | 5952 | 2 | 0 | 0 | 2 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0028 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0029 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0030 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0031 | 0/0 | 5950 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0032 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0033 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0034 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0035 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0036 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0037 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0038 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0039 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0040 | 0/0 | 5950 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0041 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0042 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0043 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0045 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0046 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5935): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0047 | 0/0 | 5950 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0048 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0049 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0050 | 0/0 | 5951 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0051 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0053 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0054 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0055 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0056 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0057 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0058 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0059 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0060 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0061 | 1/0 | 5950 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0062 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0063 | 0/0 | 5951 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0064 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0001t0065 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5947): Show |
chr22 | 29598633 | 29703598 |
| a0001c0002t0003 | 0/0 | 5951 | 8 | 0 | 0 | 8 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0001c0004t0002 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0006t0044 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5945): Show |
chr22 | 29598633 | 29703598 |
| a0001c0007t0052 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0002c0005t0017 | 0/0 | 5951 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| a0003c0003t0001 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | GTGAC others(5946): Show |
chr22 | 29598633 | 29703598 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0036 | 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 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0058 | 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 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0121 | 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 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0136 | 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 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0181 | 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 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0215 | 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 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0152 | 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 |
| a0001c0001t0003g0158 | 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 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0225 | 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 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0003g0335 | 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 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0033 | 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 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0103 | 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 |
| a0001c0001t0004g0119 | 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 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0131 | 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 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0004g0264 | 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 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0005g0323 | 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 |
| a0001c0001t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 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 |
| 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 |
| a0001c0001t0006g0245 | 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 |
| a0001c0001t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0008g0255 | 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 |
| a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0009g0092 | 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 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0009g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0027 | 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 |
| a0001c0001t0010g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0010g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0011g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0011g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0012g0180 | 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 |
| a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0014g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0016g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0016g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0016g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0016g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0017g0006 | 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 |
| a0001c0001t0017g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0018g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0018g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0018g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0019g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0019g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0019g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0020g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0020g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0021g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0021g0076 | 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 |
| a0001c0001t0022g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0022g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0023g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0023g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0024g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0024g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0025g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0025g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0026g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0026g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0027g0093 | 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 |
| a0001c0001t0028g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0029g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0030g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0031g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0032g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0033g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0034g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0035g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0036g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0037g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0038g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0039g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0040g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0041g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0042g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0043g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0045g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0046g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0047g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0048g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0049g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0050g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0051g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0053g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0054g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0055g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0056g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0057g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0058g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0059g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0060g0247 | 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 |
| a0001c0001t0062g0087 | 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 |
| a0001c0001t0064g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0001t0065g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0071 | 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 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0002t0003g0154 | 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 |
| a0001c0002t0003g0169 | 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 |
| a0001c0004t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0006t0044g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0001c0007t0052g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0002c0005t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | g0001 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0311 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0319 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00280 | hp2 | a0001 | c0001 | t0028 | g0218 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0249 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0272 | EUR | FIN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0096 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00438 | hp2 | a0001 | c0001 | t0020 | g0139 | 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 | g0228 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0297 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00609 | hp1 | a0001 | c0001 | t0016 | g0326 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00621 | hp1 | a0001 | c0001 | t0014 | g0060 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00639 | hp2 | a0001 | c0001 | t0038 | g0031 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00673 | hp2 | a0001 | c0001 | t0018 | g0220 | EAS | CHS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00735 | hp1 | a0001 | c0001 | t0053 | g0132 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0300 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG00738 | hp2 | a0001 | c0001 | t0057 | g0147 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0313 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01070 | hp1 | a0001 | c0001 | t0026 | g0068 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01070 | hp2 | a0001 | c0001 | t0011 | g0075 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01071 | hp1 | a0001 | c0001 | t0026 | g0135 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0042 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0322 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01081 | hp1 | a0001 | c0001 | t0049 | g0134 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01099 | hp2 | a0001 | c0001 | t0024 | g0019 | 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 | g0312 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0324 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0287 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01175 | hp2 | a0001 | c0001 | t0056 | g0014 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01192 | hp1 | a0001 | c0001 | t0040 | g0029 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01243 | hp2 | a0001 | c0001 | t0029 | g0150 | AMR | PUR | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0045 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0309 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0043 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01257 | hp2 | a0001 | c0001 | t0017 | g0318 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0315 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0044 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0055 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0306 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01346 | hp2 | a0001 | c0001 | t0009 | g0232 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01358 | hp1 | a0001 | c0001 | t0065 | g0233 | 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 | g0205 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0015 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0114 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0148 | AMR | CLM | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01515 | hp1 | a0001 | c0001 | t0047 | g0143 | 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 | g0295 | EUR | IBS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01517 | hp2 | a0001 | c0001 | t0031 | g0072 | EUR | IBS | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0020 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01884 | hp2 | a0001 | c0001 | t0058 | g0251 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0210 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0323 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0196 | 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 | g0107 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01978 | hp1 | a0001 | c0001 | t0009 | g0281 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0206 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0088 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02015 | hp1 | a0002 | c0005 | t0017 | g0006 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0293 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0115 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02056 | hp1 | a0001 | c0001 | t0018 | g0166 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02056 | hp2 | a0001 | c0001 | t0021 | g0067 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0296 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02080 | hp1 | a0001 | c0001 | t0021 | g0076 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0086 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02083 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0149 | 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 | g0172 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02148 | hp1 | a0001 | c0001 | t0014 | g0183 | AMR | PEL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0211 | 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 | g0227 | EAS | CDX | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | CDX | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0256 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0192 | 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 | g0244 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02280 | hp2 | a0001 | c0001 | t0023 | g0230 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0202 | 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 | g0151 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02451 | hp2 | a0001 | c0001 | t0043 | g0034 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02523 | hp1 | a0001 | c0001 | t0009 | g0092 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02572 | hp2 | a0001 | c0001 | t0060 | g0247 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0128 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02622 | hp1 | a0001 | c0001 | t0015 | g0177 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0174 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0083 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02683 | hp1 | a0001 | c0001 | t0011 | g0078 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02717 | hp2 | a0001 | c0001 | t0023 | g0274 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0271 | 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 | g0329 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0273 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0013 | 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 | g0331 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02895 | hp1 | a0001 | c0001 | t0046 | g0307 | 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 | g0061 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02896 | hp2 | a0001 | c0001 | t0030 | g0173 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02922 | hp2 | a0001 | c0001 | t0024 | g0021 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0243 | 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 | g0330 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0310 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03017 | hp2 | a0001 | c0001 | t0035 | g0167 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03098 | hp1 | a0001 | c0001 | t0045 | g0292 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03098 | hp2 | a0001 | c0001 | t0013 | g0010 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0254 | 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 | g0018 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0253 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03209 | hp1 | a0001 | c0007 | t0052 | g0278 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0248 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03225 | hp1 | a0001 | c0006 | t0044 | g0291 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0182 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03453 | hp1 | a0001 | c0001 | t0059 | g0238 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0337 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0255 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0314 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0026 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0305 | AFR | ESN | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0259 | AFR | GWD | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0064 | 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 | g0111 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0049 | 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 | g0327 | SAS | PJL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03831 | hp1 | a0001 | c0001 | t0012 | g0016 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03927 | hp2 | a0001 | c0001 | t0032 | g0162 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03942 | hp1 | a0001 | c0001 | t0018 | g0168 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0079 | SAS | BEB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0298 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04228 | hp1 | a0001 | c0001 | t0037 | g0288 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18522 | hp1 | a0001 | c0001 | t0042 | g0141 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0335 | 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 | g0037 | EAS | CHB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0261 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0142 | 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 | g0262 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18949 | hp1 | a0001 | c0001 | t0022 | g0285 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0112 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18950 | hp1 | a0001 | c0001 | t0019 | g0303 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18957 | hp1 | a0001 | c0001 | t0039 | g0003 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18959 | hp2 | a0001 | c0001 | t0041 | g0231 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0058 | 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 | g0054 | 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 | g0154 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0299 | 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 | g0062 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18978 | hp2 | a0001 | c0001 | t0012 | g0059 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18982 | hp2 | a0001 | c0001 | t0022 | g0157 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0032 | 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 | g0048 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18985 | hp1 | a0001 | c0001 | t0027 | g0093 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0035 | 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 | g0187 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18988 | hp2 | a0001 | c0001 | t0014 | g0102 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0122 | 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 | g0152 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0121 | 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 | g0052 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19011 | hp1 | a0001 | c0001 | t0019 | g0214 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19012 | hp2 | a0001 | c0001 | t0016 | g0325 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19030 | hp2 | a0001 | c0001 | t0054 | g0279 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0258 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0252 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0137 | 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 | g0065 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0180 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19067 | hp1 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19067 | hp2 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19082 | hp2 | a0001 | c0001 | t0064 | g0280 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19086 | hp1 | a0001 | c0001 | t0062 | g0087 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19087 | hp2 | a0001 | c0001 | t0020 | g0117 | EAS | JPT | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0116 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0241 | AFR | YRI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20129 | hp1 | a0001 | c0001 | t0048 | g0229 | AFR | ASW | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ASW | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20752 | hp2 | a0001 | c0001 | t0010 | g0041 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0268 | EUR | TSI | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0217 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0080 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG02559 | hp2 | a0001 | c0001 | t0051 | g0008 | AFR | ACB | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | MSL | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0257 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0260 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0321 | AFR | USA | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| NA21309 | hp2 | a0001 | c0001 | t0055 | g0328 | AFR | LWK | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0270 | REF | REF | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0061 | g0320 | REF | REF | NF2_chr22_29598633_29703598 | NF2 | chr22 | 29598633 | 29703598 |
| view | 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 | a0002 | 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 | a0003 | 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 |
| view | 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 |
| view | 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 | a0001c0001t0009 a0001c0001t0027 a0001c0001t0062 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(14): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(292): 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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0010 a0001c0001t0056 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(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 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0030 others(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 | a0001c0001t0029 a0001c0001t0043 |
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 | a0001c0001t0045 a0001c0001t0046 a0001c0006t0044 |
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 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0030 others(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 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0018 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(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 | a0001c0001t0020 a0001c0001t0034 a0001c0001t0041 others(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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(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 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0050 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(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 | a0001c0001t0045 a0001c0001t0046 a0001c0006t0044 |
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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0014 others(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 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0025 others(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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0014 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(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 | a0001c0001t0026 a0001c0001t0049 |
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 |
| view | 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 | a0001c0001t0051g0008 | 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 | 6 | a0001c0001t0003g0007 a0001c0001t0003g0333 a0001c0001t0003g0334 others(3): 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 | a0001c0001t0001g0332 | 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 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
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 | a0001c0001t0001g0331 | 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 | a0001c0001t0019g0330 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | 217 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(214): Show |
219 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(216): 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 | a0001c0001t0002g0073 a0001c0001t0003g0070 a0001c0001t0004g0069 others(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 | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(57): 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 | a0001c0001t0005g0321 a0001c0001t0005g0322 a0001c0001t0005g0323 others(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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0007t0052g0278 | 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 | a0001c0001t0023g0274 | 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 | 5 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0001t0002g0271 others(2): Show |
5 | HG00323.hp2 HG01168.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+1976G>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29606088 | |||||||
| chr22:29606141 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0001g0066 | 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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0004g0079 a0001c0001t0008g0084 a0001c0001t0011g0074 others(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 | a0001c0001t0009g0085 a0001c0001t0009g0086 a0001c0001t0009g0088 others(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 | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(60): 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 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0264 others(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 | a0001c0001t0007g0261 | 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 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(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 | a0001c0001t0051g0008 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0003g0100 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | 177 | a0001c0001t0001g0101 a0001c0001t0001g0121 a0001c0001t0001g0124 others(174): Show |
178 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(175): 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 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0002g0110 others(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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(61): 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 | a0001c0001t0008g0114 a0001c0001t0008g0115 a0001c0001t0008g0116 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0008g0084 a0001c0001t0011g0080 a0001c0001t0011g0082 others(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 | a0001c0001t0001g0065 a0001c0001t0024g0019 a0001c0001t0024g0021 others(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 | a0001c0001t0001g0227 | 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 | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(60): 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 | a0001c0001t0008g0253 a0001c0001t0008g0254 a0001c0001t0008g0255 others(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 | a0001c0001t0003g0113 a0001c0001t0003g0225 a0001c0001t0003g0226 |
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 | a0001c0001t0008g0305 | 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 | a0001c0001t0025g0018 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0008g0114 | 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 | 121 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(118): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): 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 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0002g0221 others(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 | a0001c0001t0008g0258 | 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 | a0001c0007t0052g0278 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0008g0254 a0001c0001t0008g0255 a0001c0001t0008g0256 others(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 | a0001c0001t0012g0180 | 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 | a0001c0001t0002g0219 a0001c0001t0003g0178 a0001c0001t0004g0299 others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0023g0230 | 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 | 116 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0073 others(113): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): 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 | a0001c0001t0008g0114 a0001c0001t0008g0115 a0001c0001t0008g0116 others(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 | a0001c0001t0014g0102 | 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 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0007g0217 |
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 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0014g0060 |
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 | a0001c0001t0029g0150 a0001c0001t0033g0151 |
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 | a0001c0001t0048g0229 | 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 | a0001c0001t0001g0149 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(161): 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 | a0001c0001t0057g0147 | 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 | a0001c0001t0019g0214 | 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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | 217 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(214): Show |
218 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(215): 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 | a0001c0001t0012g0059 | 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 | a0001c0001t0051g0008 | 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 | 313 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(310): Show |
316 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(313): 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 | a0001c0007t0052g0278 | 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 | a0001c0001t0008g0114 a0001c0001t0008g0115 a0001c0001t0008g0116 |
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 | a0001c0001t0003g0172 | 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 | a0001c0001t0055g0328 | 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 | a0001c0001t0001g0332 | 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 | a0001c0001t0008g0254 | 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 | 47 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(44): 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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(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 | 61 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(58): Show |
61 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(58): 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 | a0001c0001t0016g0329 | 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0005g0005 | 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 | a0001c0001t0023g0274 | 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 | a0001c0006t0044g0291 | 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 | 50 | a0001c0001t0002g0219 a0001c0001t0003g0007 a0001c0001t0003g0070 others(47): 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 | a0001c0001t0004g0079 a0001c0001t0008g0084 a0001c0001t0011g0074 others(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 | a0001c0001t0020g0117 | 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 | a0001c0001t0008g0254 a0001c0001t0008g0255 a0001c0001t0008g0256 others(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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0004g0118 | 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 | a0001c0007t0052g0278 | 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 | a0001c0007t0052g0278 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0005g0294 a0001c0001t0005g0308 |
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 | a0001c0001t0001g0058 | 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 | a0001c0001t0009g0182 | 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 | a0001c0001t0051g0008 | 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 | a0001c0001t0003g0171 | 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 | a0001c0001t0023g0230 | 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 | a0001c0001t0002g0186 | 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 | a0001c0002t0003g0154 | 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 | a0001c0002t0003g0154 | 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 | a0001c0002t0003g0154 | 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 | a0001c0002t0003g0154 | 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 | a0001c0001t0004g0046 | 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 | a0001c0002t0003g0155 | 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 | a0001c0001t0003g0097 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0065 others(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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0004g0069 a0001c0001t0009g0281 a0001c0001t0010g0055 others(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 | a0001c0001t0045g0292 | 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 | a0001c0001t0023g0230 | 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 | a0001c0001t0016g0329 | 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 | a0001c0001t0004g0079 a0001c0001t0008g0084 a0001c0001t0011g0074 others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0003g0113 | 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 | a0001c0002t0003g0071 a0001c0002t0003g0105 a0001c0002t0003g0106 others(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 | 163 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(160): 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 | a0001c0001t0019g0303 | 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 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0236 others(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 | a0001c0007t0052g0278 | 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 | a0001c0001t0051g0008 | 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0051g0008 | 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 | 108 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(105): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.114+14355delA | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | chr22 | 29618466 | |||||||
| chr22:29618592 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0048g0229 | 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 | 293 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(290): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(292): 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 | a0001c0001t0024g0019 a0001c0001t0024g0021 a0001c0001t0025g0018 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0001t0029g0150 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0011g0074 | 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 | a0001c0001t0023g0230 | 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 | 113 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(110): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): 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 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0236 others(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 | a0001c0001t0004g0118 | 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 | 47 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(44): 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 | a0001c0001t0003g0334 | 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 | a0001c0001t0023g0274 | 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 | a0001c0001t0016g0327 | 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 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0236 others(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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0008g0084 | 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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0004g0103 a0001c0001t0004g0119 a0001c0001t0004g0299 |
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 | a0001c0001t0003g0152 a0001c0001t0003g0153 |
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 | a0001c0001t0023g0274 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(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 | a0001c0007t0052g0278 | 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 | a0001c0001t0009g0281 | 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 | a0001c0001t0024g0019 a0001c0001t0024g0021 a0001c0001t0025g0018 others(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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(61): 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 | a0001c0001t0012g0120 | 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 | 166 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(163): 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 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0219 others(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 | a0001c0001t0029g0150 a0001c0001t0033g0151 |
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 | a0001c0001t0023g0274 | 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 | a0001c0001t0024g0019 a0001c0001t0024g0021 a0001c0001t0025g0018 others(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 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0100 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0054 others(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 | a0001c0001t0002g0189 a0001c0001t0003g0097 a0001c0001t0003g0098 others(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 | a0001c0001t0042g0141 | 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 | a0001c0001t0011g0075 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0020g0117 | 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 | a0001c0001t0023g0274 | 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 | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(60): 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 | a0001c0001t0006g0244 | 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 | a0001c0001t0004g0299 | 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 | a0001c0001t0004g0266 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0149 |
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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0013g0260 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0003g0225 | 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 | a0001c0001t0006g0243 | 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 | a0001c0001t0025g0020 | 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 | a0001c0001t0025g0018 | 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 | a0001c0001t0005g0309 a0001c0001t0005g0315 a0001c0001t0017g0318 |
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 | a0001c0001t0006g0246 | 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 | a0001c0001t0006g0244 a0001c0001t0006g0245 a0001c0001t0006g0293 |
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 | a0001c0001t0059g0238 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0137 others(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 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0003g0158 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0227 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0003g0070 others(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 | a0001c0001t0004g0017 a0001c0001t0004g0047 a0001c0001t0005g0316 others(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 | a0001c0001t0001g0024 a0001c0001t0010g0015 a0001c0001t0033g0151 |
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 | a0001c0001t0029g0150 | 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 | a0001c0001t0005g0297 a0001c0001t0017g0006 a0002c0005t0017g0006 |
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 | a0001c0001t0024g0019 a0001c0001t0024g0021 |
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 | a0001c0001t0025g0020 | 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 | a0001c0001t0020g0117 a0001c0001t0025g0018 |
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 | a0001c0001t0003g0172 | 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 | a0001c0001t0003g0172 | 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 | a0001c0001t0003g0335 | 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 | a0001c0001t0001g0104 a0001c0001t0003g0152 a0001c0007t0052g0278 |
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 | a0001c0001t0002g0190 a0001c0001t0002g0202 a0001c0001t0007g0107 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0048 others(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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0002g0205 a0001c0002t0003g0155 a0001c0002t0003g0156 |
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 | a0001c0001t0002g0272 a0001c0001t0023g0230 a0001c0001t0027g0093 others(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 | a0001c0001t0001g0125 a0001c0001t0016g0325 a0001c0001t0016g0326 others(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 | a0001c0001t0017g0006 a0002c0005t0017g0006 |
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 | a0001c0007t0052g0278 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | a0001c0001t0019g0330 | 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 | a0001c0001t0011g0083 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0011 a0001c0001t0004g0079 a0001c0001t0008g0084 others(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 | 14 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0007g0206 | 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 | a0001c0001t0003g0171 | 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 | a0001c0001t0004g0079 a0001c0001t0008g0084 a0001c0001t0011g0074 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(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 | a0001c0001t0005g0310 | 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 | a0001c0007t0052g0278 | 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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0003g0158 a0001c0001t0003g0159 a0001c0001t0022g0157 |
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 | a0001c0001t0057g0147 | 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0030g0173 |
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 | a0001c0001t0004g0123 | 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 | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(60): 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 | a0001c0001t0001g0057 | 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 | 72 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(69): Show |
72 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(69): 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 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0048 a0001c0001t0002g0205 a0001c0001t0002g0212 others(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 | a0001c0001t0002g0197 a0001c0001t0042g0141 |
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 | a0001c0001t0002g0198 a0001c0001t0011g0082 a0001c0001t0019g0330 |
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 | a0001c0001t0001g0028 a0001c0001t0002g0207 a0001c0001t0002g0286 others(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 | a0001c0001t0003g0172 a0001c0001t0011g0074 a0001c0001t0021g0076 others(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 | a0001c0001t0003g0098 a0001c0001t0003g0178 a0001c0001t0005g0005 others(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 | 14 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(11): 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 | a0001c0001t0004g0146 a0001c0001t0005g0311 |
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 | a0001c0001t0004g0299 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(161): 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 | a0001c0001t0004g0079 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0003c0003t0001g0128 | 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 | a0001c0001t0006g0237 a0001c0001t0006g0241 a0001c0001t0006g0293 others(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 | 242 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(239): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): 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 | a0001c0001t0001g0136 a0001c0001t0002g0187 a0001c0001t0003g0100 others(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 | a0001c0007t0052g0278 | 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 | a0001c0001t0008g0258 | 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 | a0001c0001t0021g0076 | 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 | a0001c0001t0023g0274 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | a0001c0001t0004g0299 | 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | a0001c0001t0006g0243 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(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 | a0001c0001t0048g0229 | 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0003g0171 | 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 | a0003c0003t0001g0128 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0334 a0001c0001t0003g0335 others(2): 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 | a0001c0001t0004g0003 a0001c0001t0004g0130 a0001c0001t0004g0131 others(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 | a0001c0001t0004g0266 a0001c0001t0045g0292 a0001c0001t0046g0307 others(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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0334 a0001c0001t0003g0335 others(2): 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 | a0001c0002t0003g0105 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0009g0088 | 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 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
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 | a0001c0002t0003g0105 | 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 | a0001c0002t0003g0105 | 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 | a0001c0002t0003g0105 | 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 | a0001c0002t0003g0105 | 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 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0236 others(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 | a0001c0001t0001g0149 | 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 | 47 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(44): 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | a0001c0001t0009g0092 | 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 | a0001c0001t0051g0008 | 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 | 7 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(4): 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 | 7 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(4): 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 | a0001c0001t0011g0075 | 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 | a0001c0001t0004g0131 | 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 | a0001c0001t0031g0072 | 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 | a0001c0001t0057g0147 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0023g0274 | 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 | a0001c0001t0002g0111 a0001c0001t0009g0096 |
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 | a0001c0001t0008g0305 | 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 | a0001c0001t0055g0328 | 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 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0290 | 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 | a0001c0001t0002g0212 | 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 | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(60): 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 | a0001c0001t0008g0254 a0001c0001t0008g0255 a0001c0001t0008g0256 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(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 | a0001c0001t0006g0239 | 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 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0002g0224 a0001c0001t0007g0261 a0001c0001t0019g0330 |
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 | 230 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(227): 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 | a0001c0001t0010g0043 a0001c0001t0010g0044 a0001c0001t0010g0045 |
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 | a0001c0007t0052g0278 | 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 | a0001c0001t0005g0298 | 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 | 153 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(150): 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 | a0001c0001t0004g0003 a0001c0001t0004g0144 a0001c0001t0004g0146 others(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 | a0001c0001t0051g0008 | 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 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0100 |
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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0021g0076 |
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 | a0001c0001t0001g0276 a0001c0001t0001g0289 a0001c0001t0002g0191 others(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 | a0001c0006t0044g0291 | 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 | a0001c0001t0004g0103 a0001c0001t0004g0118 a0001c0001t0004g0119 others(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 | a0001c0001t0002g0271 a0001c0001t0007g0273 |
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 | a0001c0001t0008g0114 a0001c0001t0008g0115 a0001c0001t0008g0116 |
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 | a0001c0001t0015g0177 | 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 | 108 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(105): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(106): 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 | a0001c0001t0004g0079 a0001c0001t0008g0084 a0001c0001t0011g0074 others(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 | a0001c0001t0016g0329 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0045g0292 | 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 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0236 others(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 | a0001c0001t0023g0274 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0062 others(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 | a0001c0001t0003g0336 a0001c0001t0003g0337 a0001c0001t0004g0079 others(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 | a0001c0001t0008g0084 a0001c0001t0008g0253 a0001c0001t0011g0075 others(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 | 29 | a0001c0001t0001g0275 a0001c0001t0002g0073 a0001c0001t0002g0111 others(26): Show |
29 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(26): 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 | 149 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(146): 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 | a0001c0001t0001g0066 a0001c0001t0001g0121 a0001c0001t0004g0017 others(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 | 15 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): 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 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0001g0137 | 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 | 307 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(304): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0001g0136 | 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 | 1 | a0001c0001t0002g0272 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.364-1320C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 3/15 | chr22 | 29640882 | |||||||
| chr22:29641092 | C | T | 1 | a0001c0001t0008g0305 | 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 | 294 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(291): Show |
296 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(293): 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 | a0001c0001t0050g0037 | 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 | a0001c0001t0007g0112 | 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 | 107 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(104): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): 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 | a0001c0001t0001g0023 | 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 | 61 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(58): Show |
61 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(58): 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 | a0001c0001t0064g0280 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 |
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 | a0001c0001t0005g0249 | 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 | a0001c0001t0032g0162 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(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 | a0001c0001t0008g0258 | 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 | a0001c0001t0003g0158 a0001c0001t0003g0178 |
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 | a0001c0001t0001g0181 a0001c0001t0001g0289 |
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 | a0001c0001t0057g0147 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0121 others(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 | a0001c0001t0005g0310 | 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 | a0001c0001t0002g0192 | 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 | a0001c0001t0002g0200 | 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0008g0305 | 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 | 50 | a0001c0001t0001g0066 a0001c0001t0004g0079 a0001c0001t0005g0005 others(47): 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0004g0017 a0001c0001t0004g0047 |
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 | a0001c0001t0001g0275 a0001c0001t0003g0159 a0001c0001t0006g0237 others(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 | a0001c0001t0011g0074 a0001c0001t0011g0077 a0001c0001t0011g0078 others(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 | a0001c0001t0010g0043 a0001c0001t0010g0044 a0001c0001t0010g0045 |
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 | a0001c0001t0002g0187 | 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 | a0001c0001t0046g0307 | 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 | a0001c0001t0002g0187 a0001c0001t0002g0207 |
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 | a0001c0001t0002g0187 | 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 | a0001c0001t0002g0187 | 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 | a0001c0001t0002g0187 | 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 | a0001c0001t0005g0294 a0001c0001t0005g0308 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0029g0150 a0001c0001t0033g0151 |
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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0004g0264 | 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 | a0001c0001t0004g0069 a0001c0001t0004g0129 |
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 | a0001c0001t0011g0083 | 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 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
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 | a0001c0001t0005g0310 | 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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0332 a0001c0001t0014g0102 others(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 | a0001c0001t0014g0026 a0001c0001t0043g0034 |
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 | a0001c0001t0001g0179 | 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 | a0001c0001t0004g0003 a0001c0001t0004g0069 a0001c0001t0004g0103 others(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 | a0001c0001t0003g0070 | 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 | a0001c0001t0004g0129 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | 216 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(213): 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 | a0001c0001t0008g0253 | 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0276 | 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 | a0001c0001t0009g0281 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0035 a0001c0001t0002g0301 a0001c0001t0004g0130 others(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 | a0001c0001t0023g0230 | 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 | a0001c0002t0003g0154 | 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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | a0001c0001t0051g0008 | 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 | a0001c0001t0051g0008 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 others(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 | a0001c0001t0016g0327 a0001c0001t0016g0329 |
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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | 233 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(230): Show |
235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.447+2600T>C | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | chr22 | 29644885 | |||||||
| chr22:29644886 | G | A | 110 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(107): Show |
111 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(108): 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 | a0001c0001t0009g0182 a0001c0001t0009g0232 a0001c0001t0024g0019 others(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 | a0001c0001t0002g0200 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0031g0072 | 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 | a0001c0001t0018g0166 | 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 | a0001c0001t0011g0075 | 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 | a0001c0001t0011g0075 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0008g0253 | 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 | 6 | a0001c0001t0003g0007 a0001c0001t0003g0333 a0001c0001t0003g0334 others(3): 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 | a0001c0001t0042g0141 | 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 | 47 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(44): 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 | a0001c0001t0048g0229 | 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 | a0001c0001t0023g0230 | 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 | a0001c0001t0002g0111 a0001c0001t0002g0193 a0001c0001t0007g0287 |
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 | 6 | a0001c0001t0003g0007 a0001c0001t0003g0333 a0001c0001t0003g0334 others(3): 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 | a0001c0001t0002g0193 | 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 | a0001c0001t0004g0130 a0001c0001t0012g0180 |
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 | a0001c0001t0002g0268 | 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 | a0001c0001t0011g0077 a0001c0001t0011g0078 a0001c0001t0021g0067 |
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 | a0001c0001t0024g0019 a0001c0001t0024g0021 |
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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0001g0275 | 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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0001g0038 a0001c0001t0002g0205 a0001c0001t0005g0298 others(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 | 94 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(91): 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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0004g0003 a0001c0001t0004g0069 a0001c0001t0004g0103 others(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 | a0001c0001t0003g0282 a0001c0001t0003g0283 a0001c0001t0003g0284 |
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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | a0001c0001t0012g0016 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0004g0003 others(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 | a0001c0001t0024g0019 a0001c0001t0024g0021 |
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 | a0001c0001t0003g0113 | 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | 72 | a0001c0001t0002g0111 a0001c0001t0002g0192 a0001c0001t0002g0193 others(69): 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 | a0001c0001t0002g0073 a0001c0001t0002g0196 a0001c0001t0004g0003 others(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 | a0001c0001t0004g0264 a0001c0001t0016g0325 a0001c0001t0016g0326 others(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 | a0001c0001t0016g0329 | 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 | 101 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(98): 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 | a0001c0001t0001g0051 a0001c0001t0003g0160 a0001c0001t0003g0161 others(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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0003g0283 a0001c0001t0003g0284 |
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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0023g0230 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0038g0031 a0001c0001t0040g0029 |
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 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(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 | a0001c0001t0037g0288 | 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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | 121 | a0001c0001t0002g0073 a0001c0001t0002g0108 a0001c0001t0002g0110 others(118): Show |
122 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(119): 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 | a0001c0001t0008g0254 a0001c0001t0008g0255 a0001c0001t0008g0256 others(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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | a0001c0001t0037g0288 | 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 | a0001c0001t0005g0310 a0001c0001t0013g0248 a0001c0001t0013g0259 others(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 | a0001c0001t0007g0208 | 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 | a0001c0001t0005g0297 | 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 | a0001c0001t0013g0260 | 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 | a0001c0001t0040g0029 | 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 | a0001c0001t0002g0110 | 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 | a0001c0001t0002g0110 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0004g0103 a0001c0001t0004g0119 a0001c0001t0004g0299 |
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 | a0001c0001t0010g0043 | 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 | a0001c0001t0002g0219 | 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 | a0001c0001t0023g0230 | 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0010g0027 a0001c0001t0010g0042 a0001c0004t0002g0210 |
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 | a0001c0001t0002g0110 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0051g0008 | 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | a0001c0001t0023g0274 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | a0001c0001t0004g0003 a0001c0001t0004g0069 a0001c0001t0004g0103 others(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 | 228 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(225): 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 | a0001c0001t0023g0274 | 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 | a0001c0001t0001g0101 | 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 | 290 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(287): Show |
292 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(289): 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 | a0001c0001t0024g0019 a0001c0001t0024g0021 |
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 | a0001c0001t0004g0131 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0004g0053 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0056 |
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 | a0001c0001t0003g0113 a0001c0001t0003g0225 a0001c0001t0003g0226 |
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 | a0001c0001t0023g0274 | 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 | a0001c0001t0002g0209 a0001c0001t0003g0070 a0001c0001t0005g0249 others(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 | 140 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(137): 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | 48 | a0001c0001t0004g0079 a0001c0001t0005g0005 a0001c0001t0005g0249 others(45): 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 | a0001c0001t0008g0257 | 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | a0001c0001t0008g0258 | 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
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 | 105 | a0001c0001t0004g0003 a0001c0001t0004g0069 a0001c0001t0004g0079 others(102): 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 | a0001c0001t0001g0013 a0001c0001t0001g0064 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0065 a0001c0001t0003g0070 a0001c0001t0003g0113 others(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 | a0001c0001t0008g0253 | 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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0032g0162 |
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 | a0001c0001t0008g0253 | 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 | a0001c0001t0002g0205 a0001c0001t0005g0296 a0001c0001t0006g0293 others(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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(179): 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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0010g0015 a0001c0001t0056g0014 |
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 | a0001c0001t0002g0224 | 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 | a0001c0001t0006g0243 a0001c0001t0006g0244 a0001c0001t0006g0245 others(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 | a0001c0001t0008g0305 | 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 | 224 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(221): 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 | a0001c0001t0040g0029 | 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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | a0001c0001t0001g0136 | 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 | a0001c0001t0004g0129 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0001t0003g0070 a0001c0001t0003g0097 a0001c0001t0003g0098 others(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 | a0001c0001t0004g0069 a0001c0001t0004g0122 a0001c0001t0004g0123 others(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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): 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 | a0001c0001t0013g0009 a0001c0001t0013g0010 |
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 | a0001c0001t0009g0085 a0001c0001t0009g0086 a0001c0001t0009g0092 |
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 | 15 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(12): 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 | a0001c0001t0005g0322 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | |||||||
| chr22:29658958 | T | C | 1 | a0001c0001t0002g0193 | 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 | a0001c0001t0004g0046 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0051g0008 | 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 | a0001c0001t0003g0152 a0001c0001t0003g0153 |
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 | a0001c0001t0014g0026 | 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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): 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 | a0001c0001t0012g0016 | 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 | a0001c0001t0003g0172 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0031g0072 | 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 | 94 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(91): 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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | a0001c0001t0011g0075 | 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 | a0001c0001t0049g0134 | 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 | 45 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(42): 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 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(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 | 94 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(91): 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 | a0001c0001t0053g0132 | 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 | a0001c0001t0010g0015 | 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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): 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 | a0001c0001t0005g0306 | 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 | a0001c0001t0001g0227 | 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 | 94 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(91): 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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0009g0085 a0001c0001t0009g0086 a0001c0001t0009g0092 |
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 | a0001c0001t0051g0008 | 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 | a0001c0001t0002g0224 a0001c0001t0007g0261 a0001c0001t0019g0330 |
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 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0202 others(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 | a0001c0001t0023g0274 | 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | 208 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(205): 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 | a0001c0001t0002g0110 a0001c0001t0007g0109 |
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 | a0001c0001t0013g0248 a0001c0001t0013g0259 a0001c0001t0013g0260 |
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 | a0001c0001t0002g0186 a0001c0001t0002g0195 a0001c0001t0002g0207 others(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 | a0001c0001t0002g0272 a0001c0001t0003g0070 a0001c0001t0003g0172 others(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 | 25 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0057 others(22): 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(95): 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 | a0001c0001t0004g0263 a0001c0001t0011g0074 a0001c0001t0011g0075 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0290 a0001c0001t0053g0132 |
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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(202): 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 | a0001c0001t0004g0053 | 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 | a0001c0001t0004g0053 | 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 | a0001c0001t0002g0209 | 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 | a0001c0001t0004g0033 a0001c0001t0016g0325 a0001c0001t0016g0326 others(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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(94): 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 | a0001c0001t0023g0274 | 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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | 209 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(206): 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0264 others(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 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0012g0059 |
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 | a0001c0001t0002g0205 | 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 | a0001c0001t0003g0158 a0001c0001t0003g0159 a0001c0001t0003g0178 others(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 | a0001c0001t0004g0046 | 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 | a0001c0001t0009g0182 | 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 | a0001c0001t0016g0327 | 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 | a0001c0001t0008g0253 a0001c0001t0008g0254 a0001c0001t0008g0255 others(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 | a0001c0001t0014g0183 | 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 | 210 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(207): 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 | a0001c0001t0033g0151 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0004g0003 a0001c0001t0004g0069 a0001c0001t0004g0079 others(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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): 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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): 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 | a0001c0001t0008g0253 a0001c0001t0008g0254 a0001c0001t0008g0255 others(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 | a0001c0001t0031g0072 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0004g0131 | 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 | 14 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(11): 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(95): 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 | 209 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(206): 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 | a0001c0007t0052g0278 | 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 | a0001c0001t0002g0108 a0001c0001t0002g0187 a0001c0001t0002g0189 others(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 | 92 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(89): 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 | 14 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(11): 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 | 213 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(210): 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 | a0001c0001t0002g0073 a0001c0001t0002g0111 a0001c0001t0002g0188 others(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 | a0001c0001t0002g0198 a0001c0001t0003g0160 a0001c0001t0003g0161 others(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 | 32 | a0001c0001t0003g0007 a0001c0001t0003g0097 a0001c0001t0003g0159 others(29): 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 | a0001c0001t0002g0191 a0001c0001t0002g0213 a0001c0001t0002g0215 others(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 |
12 | a0001c0001t0005g0294 a0001c0001t0005g0296 a0001c0001t0005g0308 others(9): 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 | a0001c0001t0002g0301 a0001c0001t0003g0113 a0001c0001t0003g0225 others(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 | a0001c0001t0008g0114 a0001c0001t0050g0037 |
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 | a0001c0001t0009g0089 a0001c0001t0009g0232 a0001c0001t0013g0009 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0048 others(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 | 82 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0022 others(79): 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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): 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 | a0001c0001t0005g0306 | 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 | a0001c0001t0003g0098 a0001c0001t0003g0099 |
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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0002g0108 a0001c0001t0002g0187 a0001c0001t0002g0189 others(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 | a0001c0001t0002g0198 a0001c0001t0031g0072 |
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 | 145 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(142): 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 | a0001c0001t0016g0325 | 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 | a0001c0001t0002g0205 | 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 | 14 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(11): 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 | a0001c0001t0001g0133 a0001c0001t0001g0290 a0001c0001t0026g0068 others(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 | a0001c0001t0008g0258 | 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 | a0001c0001t0004g0003 a0001c0001t0004g0130 a0001c0001t0004g0131 others(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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): 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 | 15 | a0001c0001t0002g0195 a0001c0001t0002g0199 a0001c0001t0002g0269 others(12): Show |
15 | HG01168.hp1 HG01517.hp1 HG01517.hp2 others(12): 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 | a0001c0001t0003g0097 | 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0003g0097 | 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 | a0001c0001t0002g0191 a0001c0001t0002g0198 a0001c0001t0002g0213 others(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 | a0001c0001t0015g0174 a0001c0001t0030g0173 |
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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(80): 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 | a0001c0001t0004g0123 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0048 others(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 | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(79): 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 | 49 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(46): 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 | 280 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(277): 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 | a0001c0001t0008g0253 a0001c0001t0008g0254 a0001c0001t0008g0255 others(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 | a0001c0001t0011g0080 | 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 | a0001c0001t0029g0150 a0001c0001t0033g0151 |
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 | 3 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0001t0002g0272 |
3 | HG00323.hp2 HG01168.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1123-51C>T | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 11/15 | chr22 | 29673218 | |||||||
| chr22:29673705 | G | A | 1 | a0001c0001t0009g0088 | 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 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(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 | a0001c0001t0008g0305 | 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 | a0001c0001t0008g0258 | 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 | 275 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(272): 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 | a0001c0001t0005g0249 a0001c0001t0005g0306 a0001c0001t0005g0311 others(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 | a0001c0001t0002g0186 a0001c0001t0002g0286 |
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 | a0001c0001t0008g0258 | 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 | a0001c0001t0023g0274 | 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 | a0001c0001t0006g0239 | 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 | 102 | a0001c0001t0004g0003 a0001c0001t0004g0017 a0001c0001t0004g0032 others(99): 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 | 47 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0052 others(44): 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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | a0001c0001t0002g0224 a0001c0001t0007g0261 a0001c0001t0019g0330 |
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 | 14 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(11): 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 | a0001c0001t0004g0003 a0001c0001t0004g0017 a0001c0001t0004g0032 others(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 | a0001c0001t0023g0230 a0001c0001t0023g0274 |
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 | a0001c0001t0003g0333 | 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 | a0001c0001t0002g0271 a0001c0001t0007g0273 |
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 | a0001c0001t0005g0249 | 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 | a0001c0001t0003g0282 a0001c0001t0003g0283 a0001c0001t0003g0284 |
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 | a0001c0001t0005g0316 | 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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | 42 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0024 others(39): 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 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
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 | a0001c0001t0023g0230 a0001c0001t0023g0274 |
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 | 7 | a0001c0001t0006g0004 a0001c0001t0006g0148 a0001c0001t0006g0239 others(4): 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 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(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 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0007g0217 |
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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0124 others(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 | a0001c0001t0021g0067 | 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 | a0001c0001t0005g0295 a0001c0001t0005g0309 a0001c0001t0005g0315 others(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 | a0001c0001t0002g0207 a0001c0001t0004g0123 a0001c0001t0006g0234 others(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 | a0001c0001t0003g0070 a0001c0001t0003g0113 a0001c0001t0003g0152 others(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 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(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 | 276 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(273): 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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(80): 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 | 84 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(81): 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 | a0001c0001t0016g0325 a0001c0001t0016g0326 a0001c0001t0016g0327 others(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 | a0001c0001t0004g0103 a0001c0001t0004g0118 a0001c0001t0004g0119 others(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 | a0001c0001t0009g0182 | 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 | 84 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(81): 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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | a0001c0001t0054g0279 | 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | a0001c0001t0011g0075 | 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 | 276 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(273): 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 | a0001c0001t0005g0249 a0001c0001t0005g0306 a0001c0001t0005g0311 others(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 | a0001c0001t0003g0336 | 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 | a0001c0001t0003g0336 | 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 | 27 | a0001c0001t0002g0108 a0001c0001t0002g0224 a0001c0001t0002g0271 others(24): 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 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0001c0001t0023g0230 a0001c0001t0023g0274 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(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 | a0001c0001t0003g0225 | 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 | 84 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(81): 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 | a0001c0001t0004g0003 a0001c0001t0004g0017 a0001c0001t0004g0032 others(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 | 49 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(46): 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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(80): 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 | a0001c0001t0023g0230 a0001c0001t0023g0274 |
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 | 84 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(81): 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 | a0001c0001t0002g0205 a0001c0001t0011g0074 a0001c0001t0011g0075 others(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 | 49 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(46): 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 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(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 | a0001c0001t0024g0019 a0001c0001t0024g0021 |
2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1575-312G>A | NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 14/15 | chr22 | 29681127 | |||||||
| chr22:29681736 | T | C | 65 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(62): 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 | a0001c0001t0051g0008 | 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 | a0001c0001t0006g0252 | 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 | a0001c0001t0005g0297 | 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 | a0001c0001t0023g0230 | 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 | a0001c0001t0003g0158 a0001c0001t0003g0178 |
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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(84): 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 | a0001c0001t0004g0079 a0001c0001t0036g0061 |
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 | a0001c0001t0008g0305 | 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 | a0001c0001t0045g0292 a0001c0001t0046g0307 a0001c0006t0044g0291 |
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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | 49 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(46): 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0026g0068 a0001c0001t0026g0135 a0001c0001t0049g0134 |
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 | a0001c0001t0004g0003 a0001c0001t0004g0017 a0001c0001t0004g0032 others(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 | a0001c0001t0005g0297 a0001c0001t0017g0006 a0002c0005t0017g0006 |
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 | a0001c0001t0011g0077 a0001c0001t0011g0078 a0001c0001t0021g0067 |
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 | 102 | a0001c0001t0004g0003 a0001c0001t0004g0017 a0001c0001t0004g0032 others(99): 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 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(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 | a0001c0001t0002g0200 a0001c0001t0002g0207 |
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 | a0001c0001t0002g0195 | 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 | a0001c0001t0008g0305 | 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 | a0001c0001t0002g0073 a0001c0001t0007g0211 |
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 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(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 | a0001c0001t0001g0065 | 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 | 232 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(229): 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 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0048 others(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 | 65 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(62): 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 | a0001c0001t0042g0141 | 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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | a0001c0001t0008g0253 a0001c0001t0008g0254 a0001c0001t0008g0255 others(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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0003g0070 | 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 | a0001c0001t0002g0268 | 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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(84): 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 | a0001c0001t0024g0021 | 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 | a0001c0001t0018g0166 | 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 | a0001c0001t0008g0305 | 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 | 50 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(47): 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 | a0001c0001t0011g0077 a0001c0001t0011g0078 a0001c0001t0021g0067 |
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 | a0001c0001t0023g0274 | 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 | 10 | a0001c0001t0010g0001 a0001c0001t0010g0015 a0001c0001t0010g0027 others(7): 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 | a0001c0001t0025g0018 | 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(83): 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 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0019g0214 | 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 | a0001c0001t0002g0073 a0001c0001t0007g0211 |
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 | a0001c0001t0013g0009 a0001c0001t0013g0010 a0001c0001t0013g0248 others(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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(83): 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0035g0167 | 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 | a0001c0001t0002g0108 a0001c0001t0002g0110 a0001c0001t0002g0186 others(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 | 115 | a0001c0001t0001g0054 a0001c0001t0002g0199 a0001c0001t0004g0003 others(112): 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 | 138 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(135): 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 | a0001c0001t0001g0038 a0001c0001t0001g0124 a0001c0001t0003g0165 others(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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | a0001c0001t0007g0107 | 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | a0001c0001t0005g0294 a0001c0001t0005g0296 a0001c0001t0005g0308 others(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 | a0001c0001t0011g0074 a0001c0001t0011g0075 a0001c0001t0011g0077 others(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 | 45 | a0001c0001t0003g0007 a0001c0001t0003g0070 a0001c0001t0003g0097 others(42): 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 | 276 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(273): 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 | a0001c0001t0012g0120 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0140 | 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 | a0001c0001t0006g0234 a0001c0001t0006g0236 a0001c0001t0006g0237 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(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 | a0001c0001t0023g0230 a0001c0001t0023g0274 |
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 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0100 |
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 | a0001c0001t0013g0009 a0001c0001t0013g0010 a0001c0001t0013g0248 others(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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(83): 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | a0001c0001t0015g0174 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | 49 | a0001c0001t0005g0005 a0001c0001t0005g0249 a0001c0001t0005g0294 others(46): 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 | a0001c0001t0008g0257 | 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 | a0001c0001t0004g0003 a0001c0001t0004g0017 a0001c0001t0004g0032 others(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 | a0001c0001t0024g0021 | 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 | a0001c0001t0010g0041 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0003g0097 | 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 | a0001c0001t0008g0254 a0001c0001t0008g0255 a0001c0001t0008g0256 others(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 | a0001c0001t0001g0227 | 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 | a0001c0007t0052g0278 | 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 | a0001c0001t0002g0190 a0001c0001t0002g0202 a0001c0001t0007g0107 |
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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): 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 | a0001c0001t0008g0084 | 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 | 279 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(276): 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0055g0328 | 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 | a0001c0001t0021g0076 | 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 | a0001c0001t0051g0008 | 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 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0100 others(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 | a0001c0001t0024g0019 a0001c0001t0024g0021 |
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 | a0001c0001t0008g0084 a0001c0001t0008g0114 a0001c0001t0008g0115 others(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 | a0001c0001t0003g0113 a0001c0001t0003g0225 a0001c0001t0003g0226 |
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 |