| geneid | 2675 |
|---|---|
| ensemblid | ENSG00000168546.11 |
| hgncid | 4244 |
| symbol | GFRA2 |
| name | GDNF family receptor alpha 2 |
| refseq_nuc | NM_001495.5 |
| refseq_prot | NP_001486.4 |
| ensembl_nuc | ENST00000524240.6 |
| ensembl_prot | ENSP00000428518.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 21690398 |
| end | 21788875 |
| strand | - |
| ver | v1.2 |
| region | chr8:21690398-21788875 |
| region5000 | chr8:21685398-21793875 |
| regionname0 | GFRA2_chr8_21690398_21788875 |
| regionname5000 | GFRA2_chr8_21685398_21793875 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 464 | 185 | 51 | 28 | 66 | 10 | 29 | 41 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002 | 0/1 | 464 | 111 | 29 | 16 | 49 | 4 | 12 | 41 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0003 | 0/0 | 464 | 9 | 0 | 0 | 9 | 0 | 0 | 8 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004 | 0/0 | 464 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005 | 0/0 | 464 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0006 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0007 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0008 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1395 | 126 | 31 | 18 | 42 | 10 | 24 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0002 | 0/1 | 1395 | 84 | 24 | 14 | 31 | 4 | 10 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0003 | 0/0 | 1395 | 24 | 1 | 7 | 13 | 0 | 3 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0004 | 0/0 | 1395 | 14 | 3 | 3 | 7 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0005 | 0/0 | 1395 | 14 | 0 | 2 | 11 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0006 | 0/0 | 1395 | 12 | 12 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0007 | 0/0 | 1395 | 8 | 3 | 0 | 5 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0008 | 0/0 | 1395 | 8 | 0 | 0 | 8 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0009 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0010 | 0/0 | 1395 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0011 | 0/0 | 1395 | 2 | 1 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0012 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0013 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0014 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0015 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0016 | 0/0 | 1395 | 2 | 1 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0017 | 0/0 | 1395 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0018 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0019 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0020 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0021 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0022 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0023 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0024 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0025 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0026 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0027 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0028 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| c0029 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3597 | 62 | 3 | 16 | 27 | 5 | 10 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0002 | 0/1 | 3597 | 55 | 11 | 10 | 23 | 4 | 6 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0003 | 0/0 | 3597 | 34 | 10 | 5 | 13 | 0 | 6 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0004 | 0/0 | 3597 | 31 | 1 | 5 | 21 | 1 | 3 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0005 | 0/0 | 3597 | 16 | 9 | 1 | 4 | 0 | 2 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0006 | 0/0 | 3597 | 15 | 8 | 1 | 4 | 2 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0007 | 0/0 | 3597 | 13 | 7 | 0 | 1 | 0 | 5 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0008 | 0/0 | 3597 | 8 | 5 | 0 | 1 | 0 | 2 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0009 | 0/0 | 3597 | 8 | 6 | 2 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0010 | 0/0 | 3597 | 6 | 6 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0011 | 0/0 | 3597 | 6 | 0 | 3 | 0 | 2 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0012 | 0/0 | 3597 | 5 | 0 | 0 | 5 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0013 | 0/0 | 3597 | 5 | 5 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0014 | 0/0 | 3597 | 4 | 0 | 0 | 4 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0015 | 0/0 | 3597 | 4 | 4 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0016 | 0/0 | 3597 | 4 | 4 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0017 | 0/0 | 3597 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0018 | 0/0 | 3597 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0019 | 0/0 | 3597 | 3 | 3 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0020 | 0/0 | 3597 | 3 | 3 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0021 | 0/0 | 3597 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0022 | 0/0 | 3597 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0023 | 0/0 | 3597 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0024 | 0/0 | 3597 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0025 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0026 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0027 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0028 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0029 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0030 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0031 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0032 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0033 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0034 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0035 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0036 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0037 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0038 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0039 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0040 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0041 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0042 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0043 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0044 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0045 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0046 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0047 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0048 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0049 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| t0050 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1395 | 126 | 31 | 18 | 42 | 10 | 24 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003 | 0/0 | 1395 | 24 | 1 | 7 | 13 | 0 | 3 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004 | 0/0 | 1395 | 14 | 3 | 3 | 7 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0006 | 0/0 | 1395 | 12 | 12 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0010 | 0/0 | 1395 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0019 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0020 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0022 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0023 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0025 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0028 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002 | 0/1 | 1395 | 84 | 24 | 14 | 31 | 4 | 10 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0005 | 0/0 | 1395 | 14 | 0 | 2 | 11 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0007 | 0/0 | 1395 | 8 | 3 | 0 | 5 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0016 | 0/0 | 1395 | 2 | 1 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0017 | 0/0 | 1395 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0021 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0003c0008 | 0/0 | 1395 | 8 | 0 | 0 | 8 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0003c0027 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0009 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0011 | 0/0 | 1395 | 2 | 1 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0015 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0018 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0012 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0013 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0014 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0006c0029 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0007c0024 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0008c0026 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4991 | 46 | 2 | 9 | 21 | 5 | 8 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0003 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0004 | 0/0 | 4991 | 22 | 1 | 5 | 12 | 1 | 3 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0005 | 0/0 | 4991 | 10 | 5 | 0 | 3 | 0 | 2 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0006 | 0/0 | 4991 | 9 | 5 | 0 | 2 | 2 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0007 | 0/0 | 4991 | 9 | 5 | 0 | 0 | 0 | 4 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0008 | 0/0 | 4991 | 4 | 3 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0009 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0011 | 0/0 | 4991 | 6 | 0 | 3 | 0 | 2 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0013 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0019 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0020 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0024 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0025 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0030 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0031 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0033 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0034 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0035 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0036 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0041 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0042 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0001t0049 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0001 | 0/0 | 4991 | 14 | 1 | 6 | 5 | 0 | 2 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0004 | 0/0 | 4991 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0005 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0006 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0007 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0021 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0032 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0003t0043 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0001 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0004 | 0/0 | 4991 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0005 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0006 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0007 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0008 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0009 | 0/0 | 4991 | 2 | 1 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0013 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0004t0018 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0006t0002 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0006t0007 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0006t0009 | 0/0 | 4991 | 4 | 4 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0006t0016 | 0/0 | 4991 | 4 | 4 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0006t0023 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0010t0004 | 0/0 | 4991 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0019t0020 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0020t0005 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0022t0007 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0023t0018 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0025t0029 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0001c0028t0048 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0002 | 0/1 | 4991 | 41 | 7 | 9 | 15 | 4 | 5 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0003 | 0/0 | 4991 | 25 | 7 | 4 | 10 | 0 | 4 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0005 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0006 | 0/0 | 4991 | 2 | 1 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0008 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0010 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0015 | 0/0 | 4991 | 4 | 4 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0017 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0027 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0028 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0037 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0038 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0044 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0046 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0002t0050 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0005t0002 | 0/0 | 4991 | 7 | 0 | 1 | 5 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0005t0003 | 0/0 | 4991 | 2 | 0 | 1 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0005t0017 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0005t0026 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0005t0045 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0005t0047 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0007t0002 | 0/0 | 4991 | 4 | 3 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0007t0003 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0007t0022 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0016t0003 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0016t0006 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0017t0002 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0002c0021t0010 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0003c0008t0012 | 0/0 | 4991 | 5 | 0 | 0 | 5 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0003c0008t0014 | 0/0 | 4991 | 3 | 0 | 0 | 3 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0003c0027t0014 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0009t0005 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0009t0013 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0009t0039 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0011t0005 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0011t0009 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0015t0008 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0004c0018t0040 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0012t0010 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0013t0003 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0013t0010 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0014t0003 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0005c0014t0006 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0006c0029t0001 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0007c0024t0019 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| a0008c0026t0003 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | copy fasta | chr8 | 21685398 | 21793875 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0008g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0011g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0011g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0011g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0011g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0011g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0011g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0019g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0020g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0020g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0024g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0024g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0025g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0031g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0033g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0034g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0035g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0036g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0041g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0042g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0001t0049g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0021g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0021g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0032g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0003t0043g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0008g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0009g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0013g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0018g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0004t0018g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0016g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0016g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0016g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0023g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0006t0023g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0010t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0010t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0010t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0019t0020g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0020t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0022t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0023t0018g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0025t0029g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0001c0028t0048g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0027g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0028g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0037g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0038g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0044g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0046g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0002t0050g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0017g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0017g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0026g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0045g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0005t0047g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0022g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0007t0022g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0016t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0016t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0017t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0017t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0002c0021t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0012g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0012g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0012g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0012g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0014g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0014g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0008t0014g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0003c0027t0014g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0009t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0009t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0009t0039g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0011t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0011t0009g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0015t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0015t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0004c0018t0040g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0005c0012t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0005c0012t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0005c0013t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0005c0013t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0005c0014t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0005c0014t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0006c0029t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0007c0024t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| a0008c0026t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0133 | EUR | GBR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0296 | EUR | FIN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0094 | EUR | FIN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00408 | hp1 | a0001 | c0001 | t0024 | g0291 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00408 | hp2 | a0003 | c0008 | t0012 | g0248 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00438 | hp1 | a0002 | c0002 | t0008 | g0220 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00597 | hp1 | a0001 | c0004 | t0004 | g0257 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00597 | hp2 | a0001 | c0003 | t0021 | g0044 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00621 | hp1 | a0001 | c0004 | t0018 | g0120 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00621 | hp2 | a0001 | c0003 | t0006 | g0049 | EAS | CHS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0177 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00639 | hp2 | a0001 | c0004 | t0009 | g0235 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0319 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0128 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00733 | hp1 | a0001 | c0004 | t0006 | g0010 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00733 | hp2 | a0002 | c0002 | t0050 | g0317 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0320 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00735 | hp2 | a0002 | c0002 | t0003 | g0262 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0316 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0106 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01169 | hp2 | a0001 | c0003 | t0032 | g0148 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01175 | hp1 | a0001 | c0001 | t0049 | g0315 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01243 | hp2 | a0004 | c0011 | t0009 | g0195 | AMR | PUR | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01255 | hp1 | a0001 | c0004 | t0005 | g0276 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0295 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0278 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01358 | hp2 | a0006 | c0029 | t0001 | g0059 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0172 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0260 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0300 | AMR | CLM | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0100 | EUR | IBS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0142 | EUR | IBS | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01884 | hp1 | a0002 | c0007 | t0002 | g0165 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01891 | hp1 | a0001 | c0006 | t0016 | g0069 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01891 | hp2 | a0002 | c0007 | t0002 | g0022 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0277 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0271 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0171 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0050 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0125 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0299 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0282 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02055 | hp1 | a0002 | c0016 | t0006 | g0017 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0203 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02056 | hp2 | a0001 | c0004 | t0018 | g0116 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02129 | hp1 | a0001 | c0023 | t0018 | g0150 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02129 | hp2 | a0002 | c0005 | t0002 | g0045 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02132 | hp2 | a0001 | c0001 | t0042 | g0268 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | CDX | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02165 | hp2 | a0002 | c0005 | t0047 | g0313 | EAS | CDX | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0181 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02258 | hp2 | a0002 | c0002 | t0010 | g0191 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02280 | hp1 | a0001 | c0006 | t0002 | g0028 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0025 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0170 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02293 | hp2 | a0002 | c0005 | t0002 | g0048 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02300 | hp2 | a0002 | c0005 | t0003 | g0183 | AMR | PEL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02523 | hp1 | a0001 | c0001 | t0041 | g0239 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02572 | hp1 | a0001 | c0006 | t0016 | g0031 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0302 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0119 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0193 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02615 | hp2 | a0001 | c0004 | t0013 | g0230 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02622 | hp1 | a0001 | c0001 | t0020 | g0309 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02647 | hp1 | a0002 | c0002 | t0010 | g0185 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02647 | hp2 | a0005 | c0012 | t0010 | g0198 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02698 | hp2 | a0001 | c0001 | t0011 | g0322 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02717 | hp1 | a0001 | c0006 | t0023 | g0208 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02717 | hp2 | a0002 | c0007 | t0002 | g0021 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02735 | hp1 | a0001 | c0001 | t0008 | g0285 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0112 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02809 | hp1 | a0007 | c0024 | t0019 | g0062 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02818 | hp2 | a0002 | c0002 | t0015 | g0006 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02886 | hp1 | a0001 | c0006 | t0016 | g0026 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02886 | hp2 | a0001 | c0019 | t0020 | g0310 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02895 | hp1 | a0004 | c0015 | t0008 | g0196 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02895 | hp2 | a0001 | c0022 | t0007 | g0020 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02896 | hp1 | a0005 | c0014 | t0003 | g0199 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02922 | hp1 | a0001 | c0020 | t0005 | g0186 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02965 | hp2 | a0001 | c0006 | t0009 | g0305 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02970 | hp1 | a0001 | c0006 | t0023 | g0234 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02976 | hp2 | a0005 | c0014 | t0006 | g0083 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0087 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03017 | hp2 | a0002 | c0016 | t0003 | g0272 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03041 | hp1 | a0005 | c0012 | t0010 | g0194 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03041 | hp2 | a0001 | c0001 | t0019 | g0070 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03098 | hp1 | a0002 | c0021 | t0010 | g0225 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03098 | hp2 | a0004 | c0015 | t0008 | g0189 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0205 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0202 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03139 | hp1 | a0005 | c0013 | t0010 | g0229 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03139 | hp2 | a0002 | c0002 | t0037 | g0204 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0207 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0303 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03209 | hp2 | a0001 | c0001 | t0020 | g0307 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03225 | hp1 | a0001 | c0004 | t0009 | g0228 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0284 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03453 | hp1 | a0001 | c0001 | t0025 | g0001 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03486 | hp1 | a0002 | c0002 | t0015 | g0004 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03486 | hp2 | a0002 | c0002 | t0044 | g0308 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0162 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0053 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03491 | hp2 | a0002 | c0002 | t0003 | g0279 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0054 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0245 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03516 | hp1 | a0001 | c0006 | t0009 | g0233 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03516 | hp2 | a0002 | c0002 | t0005 | g0242 | AFR | ESN | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03540 | hp1 | a0001 | c0004 | t0013 | g0232 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03540 | hp2 | a0001 | c0006 | t0016 | g0072 | AFR | GWD | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03579 | hp1 | a0001 | c0006 | t0009 | g0243 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0236 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03669 | hp2 | a0008 | c0026 | t0003 | g0274 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03688 | hp1 | a0001 | c0001 | t0034 | g0104 | SAS | STU | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0264 | SAS | STU | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03704 | hp1 | a0001 | c0001 | t0031 | g0121 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03710 | hp1 | a0001 | c0028 | t0048 | g0314 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0266 | SAS | PJL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03831 | hp1 | a0001 | c0001 | t0036 | g0155 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03831 | hp2 | a0002 | c0002 | t0027 | g0015 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03834 | hp1 | a0001 | c0001 | t0033 | g0122 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0180 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03927 | hp1 | a0002 | c0005 | t0002 | g0052 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03927 | hp2 | a0001 | c0001 | t0035 | g0113 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0283 | SAS | BEB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG04199 | hp1 | a0001 | c0004 | t0008 | g0224 | SAS | STU | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0164 | SAS | STU | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0261 | SAS | STU | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | YRI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | YRI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | CHB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18747 | hp2 | a0001 | c0004 | t0007 | g0179 | EAS | CHB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18906 | hp1 | a0001 | c0006 | t0007 | g0033 | AFR | YRI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18906 | hp2 | a0004 | c0011 | t0005 | g0197 | AFR | YRI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18942 | hp2 | a0001 | c0003 | t0043 | g0287 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18943 | hp1 | a0002 | c0002 | t0028 | g0105 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18944 | hp1 | a0002 | c0002 | t0003 | g0275 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18944 | hp2 | a0002 | c0017 | t0002 | g0047 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0159 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18947 | hp2 | a0001 | c0010 | t0004 | g0292 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18948 | hp1 | a0001 | c0001 | t0024 | g0294 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18948 | hp2 | a0002 | c0005 | t0002 | g0174 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18949 | hp2 | a0002 | c0007 | t0022 | g0227 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0259 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18952 | hp2 | a0001 | c0004 | t0004 | g0258 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18954 | hp2 | a0002 | c0005 | t0002 | g0057 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18957 | hp1 | a0001 | c0010 | t0004 | g0298 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18961 | hp1 | a0003 | c0027 | t0014 | g0042 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18962 | hp1 | a0002 | c0017 | t0002 | g0058 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18963 | hp1 | a0003 | c0008 | t0012 | g0281 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18966 | hp1 | a0002 | c0005 | t0045 | g0311 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18966 | hp2 | a0002 | c0007 | t0003 | g0237 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18971 | hp1 | a0002 | c0002 | t0003 | g0286 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18971 | hp2 | a0003 | c0008 | t0014 | g0137 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18974 | hp1 | a0003 | c0008 | t0014 | g0101 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18974 | hp2 | a0002 | c0005 | t0026 | g0175 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18979 | hp2 | a0001 | c0004 | t0004 | g0249 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18980 | hp2 | a0002 | c0005 | t0017 | g0009 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18983 | hp1 | a0002 | c0005 | t0002 | g0055 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18983 | hp2 | a0001 | c0003 | t0004 | g0212 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0288 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18995 | hp2 | a0003 | c0008 | t0012 | g0289 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18998 | hp1 | a0002 | c0007 | t0022 | g0211 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19000 | hp2 | a0001 | c0003 | t0004 | g0209 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19004 | hp1 | a0001 | c0003 | t0021 | g0178 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19004 | hp2 | a0002 | c0007 | t0002 | g0157 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19007 | hp1 | a0001 | c0003 | t0005 | g0253 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19009 | hp2 | a0002 | c0005 | t0003 | g0247 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19010 | hp2 | a0002 | c0002 | t0017 | g0107 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19011 | hp1 | a0002 | c0007 | t0003 | g0301 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0240 | AFR | LWK | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0252 | AFR | LWK | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19058 | hp2 | a0003 | c0008 | t0012 | g0216 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19060 | hp1 | a0002 | c0002 | t0006 | g0110 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19060 | hp2 | a0002 | c0002 | t0003 | g0280 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19066 | hp1 | a0003 | c0008 | t0014 | g0135 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19068 | hp1 | a0002 | c0005 | t0017 | g0167 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0255 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19070 | hp2 | a0002 | c0002 | t0003 | g0297 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19084 | hp2 | a0001 | c0003 | t0004 | g0210 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19085 | hp1 | a0001 | c0010 | t0004 | g0293 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19085 | hp2 | a0002 | c0005 | t0002 | g0046 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19090 | hp1 | a0003 | c0008 | t0012 | g0256 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19091 | hp1 | a0002 | c0002 | t0046 | g0312 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | YRI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA19240 | hp2 | a0001 | c0001 | t0030 | g0077 | AFR | YRI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | ASW | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20129 | hp2 | a0004 | c0009 | t0013 | g0190 | AFR | ASW | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0111 | EUR | TSI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20752 | hp2 | a0001 | c0001 | t0011 | g0321 | EUR | TSI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20805 | hp1 | a0001 | c0001 | t0011 | g0318 | EUR | TSI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0089 | EUR | TSI | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20905 | hp1 | a0002 | c0002 | t0003 | g0250 | SAS | GIH | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20905 | hp2 | a0001 | c0003 | t0007 | g0051 | SAS | GIH | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02109 | hp1 | a0001 | c0006 | t0009 | g0304 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02109 | hp2 | a0005 | c0013 | t0003 | g0201 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0206 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02486 | hp2 | a0002 | c0002 | t0006 | g0065 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG02559 | hp2 | a0002 | c0002 | t0015 | g0029 | AFR | ACB | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03471 | hp1 | a0004 | c0018 | t0040 | g0187 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG03471 | hp2 | a0004 | c0009 | t0039 | g0188 | AFR | MSL | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG06807 | hp1 | a0004 | c0009 | t0005 | g0200 | AFR | USA | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0182 | AFR | USA | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA18955 | hp2 | a0002 | c0002 | t0038 | g0265 | EAS | JPT | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20300 | hp1 | a0002 | c0002 | t0015 | g0007 | AFR | USA | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA20300 | hp2 | a0001 | c0025 | t0029 | g0071 | AFR | USA | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | LWK | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0076 | REF | REF | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0088 | REF | REF | GFRA2_chr8_21685398_21793875 | GFRA2 | chr8 | 21685398 | 21793875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:21693288
|
A | T | 4 | a0002a0003a0005others(1): Show | 127 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(124): Show |
missense_variant | MODERATE | c.1385T>A | p.Leu462Gln | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2101/4991 | 1385/1395 | 462/464 | chr8 | 21693288 | ||
| chr8:21693346
|
G | A | 1 | a0003 | 9 | HG00408.hp2 NA18961.hp1 NA18963.hp1 others(6): Show |
missense_variant | MODERATE | c.1327C>T | p.Pro443Ser | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2043/4991 | 1327/1395 | 443/464 | chr8 | 21693346 | ||
| chr8:21702845
|
C | T | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1178G>A | p.Ser393Asn | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/9 | 1894/4991 | 1178/1395 | 393/464 | chr8 | 21702845 | ||
| chr8:21705970
|
T | C | 1 | a0008 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.866A>G | p.Asn289Ser | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/9 | 1582/4991 | 866/1395 | 289/464 | chr8 | 21705970 | ||
| chr8:21782891
|
G | A | 1 | a0006 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.49C>T | p.Leu17Phe | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/9 | 765/4991 | 49/1395 | 17/464 | chr8 | 21782891 | ||
| chr8:21782895
|
C | G | 2 | a0004a0005 | 14 | HG01243.hp2 HG02109.hp2 HG02647.hp2 others(11): Show |
missense_variant | MODERATE | c.45G>C | p.Glu15Asp | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/9 | 761/4991 | 45/1395 | 15/464 | chr8 | 21782895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:21693326
|
C | T | 2 | a0001c0025a0004c0018 | 2 | HG03471.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.1347G>A | p.Ser449Ser | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2063/4991 | 1347/1395 | 449/464 | chr8 | 21693326 | ||
| chr8:21693365
|
C | T | 1 | a0001c0020 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1308G>A | p.Val436Val | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2024/4991 | 1308/1395 | 436/464 | chr8 | 21693365 | ||
| chr8:21702943
|
G | A | 8 | a0001c0006a0001c0022a0001c0028others(5): Show | 23 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
synonymous_variant | LOW | c.1080C>T | p.Asp360Asp | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/9 | 1796/4991 | 1080/1395 | 360/464 | chr8 | 21702943 | ||
| chr8:21705960
|
C | T | 1 | a0001c0023 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.876G>A | p.Ala292Ala | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/9 | 1592/4991 | 876/1395 | 292/464 | chr8 | 21705960 | ||
| chr8:21750593
|
C | G | 11 | a0001c0004a0001c0010a0001c0019others(8): Show | 36 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(33): Show |
synonymous_variant | LOW | c.789G>C | p.Leu263Leu | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/9 | 1505/4991 | 789/1395 | 263/464 | chr8 | 21750593 | ||
| chr8:21750680
|
C | T | 1 | a0001c0019 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.702G>A | p.Arg234Arg | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/9 | 1418/4991 | 702/1395 | 234/464 | chr8 | 21750680 | ||
| chr8:21782862
|
C | A | 7 | a0001c0003a0001c0010a0001c0028others(4): Show | 46 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(43): Show |
synonymous_variant | LOW | c.78G>T | p.Leu26Leu | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/9 | 794/4991 | 78/1395 | 26/464 | chr8 | 21782862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:21690433
|
C | A | 1 | a0001c0001t0035 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2845G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2845 | chr8 | 21690433 | |||||
| chr8:21690673
|
T | C | 1 | a0002c0002t0027 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2605A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2605 | chr8 | 21690673 | |||||
| chr8:21690801
|
C | T | 64 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(61): Show | 188 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*2477G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2477 | chr8 | 21690801 | |||||
| chr8:21690832
|
C | T | 22 | a0001c0001t0003a0001c0006t0002a0002c0002t0002others(19): Show | 100 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2446G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2446 | chr8 | 21690832 | |||||
| chr8:21690841
|
C | A | 1 | a0001c0001t0041 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2437G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2437 | chr8 | 21690841 | |||||
| chr8:21690964
|
T | C | 2 | a0001c0004t0018a0001c0023t0018 | 3 | HG00621.hp1 HG02056.hp2 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2314A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2314 | chr8 | 21690964 | |||||
| chr8:21691153
|
G | A | 22 | a0001c0001t0003a0001c0006t0002a0002c0002t0002others(19): Show | 100 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2125C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2125 | chr8 | 21691153 | |||||
| chr8:21691185
|
A | G | 11 | a0001c0001t0007a0001c0001t0008a0001c0001t0030others(8): Show | 23 | HG00438.hp1 HG02559.hp1 HG02572.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2093T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2093 | chr8 | 21691185 | |||||
| chr8:21691202
|
G | A | 1 | a0002c0002t0028 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2076C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2076 | chr8 | 21691202 | |||||
| chr8:21691226
|
C | A | 1 | a0001c0001t0042 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2052G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2052 | chr8 | 21691226 | |||||
| chr8:21691242
|
A | G | 1 | a0001c0001t0034 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2036T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 2036 | chr8 | 21691242 | |||||
| chr8:21691280
|
G | A | 1 | a0004c0009t0039 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1998C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1998 | chr8 | 21691280 | |||||
| chr8:21691418
|
A | T | 1 | a0001c0001t0033 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1860 | chr8 | 21691418 | |||||
| chr8:21691506
|
G | C | 74 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(71): Show | 205 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1772C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1772 | chr8 | 21691506 | |||||
| chr8:21691553
|
A | T | 1 | a0001c0006t0023 | 2 | HG02717.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1725T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1725 | chr8 | 21691553 | |||||
| chr8:21691725
|
C | G | 1 | a0001c0003t0032 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1553G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1553 | chr8 | 21691725 | |||||
| chr8:21691743
|
C | T | 1 | a0002c0007t0022 | 2 | NA18949.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1535 | chr8 | 21691743 | |||||
| chr8:21691795
|
G | T | 1 | a0001c0001t0031 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1483C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1483 | chr8 | 21691795 | |||||
| chr8:21691957
|
G | A | 1 | a0001c0006t0023 | 2 | HG02717.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1321C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1321 | chr8 | 21691957 | |||||
| chr8:21692062
|
C | T | 2 | a0001c0025t0029a0004c0018t0040 | 2 | HG03471.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1216 | chr8 | 21692062 | |||||
| chr8:21692269
|
T | C | 2 | a0001c0025t0029a0004c0018t0040 | 2 | HG03471.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1009A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 1009 | chr8 | 21692269 | |||||
| chr8:21692295
|
G | A | 1 | a0001c0001t0030 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*983C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 983 | chr8 | 21692295 | |||||
| chr8:21692330
|
C | T | 5 | a0002c0002t0010a0002c0002t0015a0002c0021t0010others(2): Show | 10 | HG02258.hp2 HG02559.hp2 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*948G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 948 | chr8 | 21692330 | |||||
| chr8:21692437
|
C | T | 3 | a0003c0008t0012a0003c0008t0014a0003c0027t0014 | 9 | HG00408.hp2 NA18961.hp1 NA18963.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*841G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 841 | chr8 | 21692437 | |||||
| chr8:21692457
|
G | C | 1 | a0001c0001t0025 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*821C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 821 | chr8 | 21692457 | |||||
| chr8:21692477
|
C | T | 1 | a0002c0002t0037 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 801 | chr8 | 21692477 | |||||
| chr8:21692739
|
G | A | 5 | a0002c0002t0010a0002c0002t0015a0002c0021t0010others(2): Show | 10 | HG02258.hp2 HG02559.hp2 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*539C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 539 | chr8 | 21692739 | |||||
| chr8:21692823
|
C | T | 2 | a0001c0001t0024a0001c0003t0021 | 4 | HG00408.hp1 HG00597.hp2 NA18948.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 455 | chr8 | 21692823 | |||||
| chr8:21692854
|
G | A | 5 | a0002c0002t0010a0002c0002t0015a0002c0021t0010others(2): Show | 10 | HG02258.hp2 HG02559.hp2 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*424C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 424 | chr8 | 21692854 | |||||
| chr8:21693009
|
T | C | 1 | a0001c0003t0043 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 269 | chr8 | 21693009 | |||||
| chr8:21693229
|
G | A | 1 | a0001c0001t0030 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 49 | chr8 | 21693229 | |||||
| chr8:21693240
|
C | G | 3 | a0002c0002t0017a0002c0002t0046a0002c0005t0017 | 4 | NA18980.hp2 NA19010.hp2 NA19068.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 38 | chr8 | 21693240 | |||||
| chr8:21693256
|
A | C | 62 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(59): Show | 182 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*22T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 9/9 | 22 | chr8 | 21693256 | |||||
| chr8:21788241
|
G | C | 49 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(46): Show | 135 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
5_prime_UTR_variant | MODIFIER | c.-82C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 82 | chr8 | 21788241 | |||||
| chr8:21788338
|
G | C | 3 | a0001c0001t0020a0001c0019t0020a0002c0002t0044 | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-179C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 179 | chr8 | 21788338 | |||||
| chr8:21788379
|
C | T | 1 | a0001c0001t0049 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-220G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 220 | chr8 | 21788379 | |||||
| chr8:21788516
|
G | C | 1 | a0002c0005t0045 | 1 | NA18966.hp1 | 5_prime_UTR_variant | MODIFIER | c.-357C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 357 | chr8 | 21788516 | |||||
| chr8:21788527
|
G | A | 2 | a0002c0002t0046a0002c0005t0047 | 2 | HG02165.hp2 NA19091.hp1 |
5_prime_UTR_variant | MODIFIER | c.-368C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 368 | chr8 | 21788527 | |||||
| chr8:21788592
|
G | A | 1 | a0001c0028t0048 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-433C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 433 | chr8 | 21788592 | |||||
| chr8:21788667
|
C | G | 1 | a0001c0001t0025 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-508G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 508 | chr8 | 21788667 | |||||
| chr8:21788735
|
T | G | 3 | a0001c0001t0011a0001c0001t0049a0002c0002t0050 | 8 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-576A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/9 | 576 | chr8 | 21788735 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:21693471
|
G | A | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1273-71C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693471 | ||||||
| chr8:21693475
|
C | A | 55 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(52): Show | 55 | HG00621.hp2 HG00733.hp1 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.1273-75G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693475 | ||||||
| chr8:21693505
|
C | A | 1 | a0005c0012t0010g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1273-105G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693505 | ||||||
| chr8:21693538
|
G | A | 1 | a0001c0003t0006g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1273-138C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693538 | ||||||
| chr8:21693539
|
A | C | 1 | a0001c0003t0006g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1273-139T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693539 | ||||||
| chr8:21693565
|
G | A | 1 | a0002c0002t0003g0286 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1273-165C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693565 | ||||||
| chr8:21693568
|
G | A | 1 | a0002c0002t0006g0110 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1273-168C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693568 | ||||||
| chr8:21693607
|
T | C | 9 | a0003c0008t0012g0216a0003c0008t0012g0248a0003c0008t0012g0256others(6): Show | 9 | HG00408.hp2 NA18961.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1273-207A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693607 | ||||||
| chr8:21693782
|
A | AGAGGAAG others(71): Show |
1 | a0002c0002t0003g0280 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1273-383_1273-382i others(80): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693782 | ||||||
| chr8:21693782
|
A | AGAGGGGA others(76): Show |
317 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.1273-383_1273-382i others(85): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693782 | ||||||
| chr8:21693782
|
A | AGAGGGGA others(77): Show |
1 | a0003c0027t0014g0042 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1273-383_1273-382i others(86): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693782 | ||||||
| chr8:21693784
|
A | AGGGGAAG others(78): Show |
1 | a0001c0003t0006g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1273-385_1273-384i others(87): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693784 | ||||||
| chr8:21693802
|
G | A | 1 | a0002c0002t0003g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1273-402C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693802 | ||||||
| chr8:21693811
|
A | AAGGAGAG others(77): Show |
1 | a0002c0002t0003g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1273-412_1273-411i others(86): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693811 | ||||||
| chr8:21693840
|
C | T | 10 | a0002c0002t0010g0185a0002c0002t0010g0191a0002c0002t0015g0004others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1273-440G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693840 | ||||||
| chr8:21693864
|
A | G | 1 | a0001c0003t0005g0253 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1273-464T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693864 | ||||||
| chr8:21693995
|
G | A | 2 | a0002c0002t0002g0076a0002c0002t0002g0128 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1272+469C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21693995 | ||||||
| chr8:21694004
|
A | C | 9 | a0003c0008t0012g0216a0003c0008t0012g0248a0003c0008t0012g0256others(6): Show | 9 | HG00408.hp2 NA18961.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1272+460T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694004 | ||||||
| chr8:21694024
|
T | C | 1 | a0001c0001t0041g0239 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1272+440A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694024 | ||||||
| chr8:21694029
|
G | A | 1 | a0002c0002t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1272+435C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694029 | ||||||
| chr8:21694042
|
G | GAT | 101 | a0001c0001t0005g0254a0001c0006t0023g0208a0001c0006t0023g0234others(98): Show | 101 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1272+420_1272+421d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694042 | ||||||
| chr8:21694042
|
G | GATAT | 11 | a0001c0001t0013g0182a0001c0001t0013g0240a0001c0001t0019g0025others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1272+418_1272+421d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694042 | ||||||
| chr8:21694042
|
G | GATATATA others(31): Show |
1 | a0002c0002t0002g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1272+421_1272+422i others(40): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694042 | ||||||
| chr8:21694055
|
T | A | 2 | a0002c0002t0002g0035a0002c0017t0002g0047 | 2 | HG03195.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1272+409A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694055 | ||||||
| chr8:21694055
|
TTA | T | 7 | a0002c0002t0010g0185a0002c0002t0010g0191a0002c0002t0015g0004others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+407_1272+408d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694055 | ||||||
| chr8:21694066
|
T | TTTAC | 5 | a0001c0001t0007g0005a0001c0001t0007g0073a0001c0001t0008g0252others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+397_1272+398i others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694066 | ||||||
| chr8:21694067
|
T | A | 1 | a0002c0002t0002g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1272+397A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694067 | ||||||
| chr8:21694071
|
T | A | 2 | a0002c0002t0002g0035a0002c0002t0005g0242 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1272+393A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TATTATAT others(33): Show |
1 | a0002c0017t0002g0047 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1272+392_1272+393i others(42): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0007g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1272+392_1272+393i others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(11): Show |
2 | a0002c0002t0006g0065a0005c0014t0006g0083 | 2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1272+392_1272+393i others(20): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(13): Show |
1 | a0002c0016t0006g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1272+392_1272+393i others(22): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(15): Show |
1 | a0002c0002t0003g0275 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1272+392_1272+393i others(24): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(17): Show |
1 | a0002c0002t0003g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1272+392_1272+393i others(26): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(23): Show |
3 | a0002c0002t0002g0163a0002c0002t0050g0317a0005c0014t0003g0199 | 3 | HG00733.hp2 HG02896.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1272+392_1272+393i others(32): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(25): Show |
1 | a0002c0002t0044g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1272+392_1272+393i others(34): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(27): Show |
1 | a0002c0002t0002g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1272+392_1272+393i others(36): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694071
|
T | TTATATAT others(29): Show |
1 | a0002c0002t0002g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1272+392_1272+393i others(38): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694071 | ||||||
| chr8:21694075
|
T | A | 21 | a0001c0001t0007g0005a0001c0001t0007g0063a0001c0001t0007g0073others(18): Show | 21 | HG00733.hp2 HG02055.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.1272+389A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TATATATA others(28): Show |
1 | a0002c0002t0002g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1272+388_1272+389i others(37): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATA | 33 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(30): Show | 33 | HG00733.hp1 HG01255.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATAATA others(26): Show |
1 | a0002c0002t0003g0280 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1272+388_1272+389i others(35): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATA | 23 | a0001c0001t0005g0231a0001c0001t0007g0075a0001c0001t0007g0119others(20): Show | 23 | HG00621.hp2 HG02280.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(5): Show |
4 | a0002c0002t0003g0193a0002c0002t0003g0203a0002c0002t0003g0205others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(9): Show |
3 | a0002c0002t0002g0086a0002c0002t0002g0129a0002c0002t0002g0130 | 3 | HG01168.hp1 HG01169.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1272+388_1272+389i others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(11): Show |
1 | a0002c0002t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1272+388_1272+389i others(20): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(13): Show |
6 | a0002c0002t0002g0079a0002c0002t0002g0082a0002c0002t0002g0109others(3): Show | 6 | HG02155.hp2 NA18959.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(22): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(15): Show |
4 | a0002c0002t0002g0098a0002c0002t0002g0147a0002c0002t0003g0246others(1): Show | 4 | NA18962.hp1 NA19000.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(24): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(17): Show |
5 | a0002c0002t0002g0089a0002c0002t0003g0297a0002c0007t0002g0021others(2): Show | 5 | HG02717.hp2 NA18949.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(26): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(19): Show |
5 | a0001c0001t0005g0254a0002c0002t0002g0095a0002c0002t0002g0139others(2): Show | 5 | NA18994.hp1 NA18994.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(28): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(21): Show |
2 | a0002c0002t0003g0262a0002c0005t0003g0247 | 2 | HG00735.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1272+388_1272+389i others(30): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(23): Show |
4 | a0002c0002t0002g0038a0002c0002t0002g0128a0002c0002t0003g0266others(1): Show | 4 | HG00642.hp2 HG03453.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(32): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(25): Show |
10 | a0002c0002t0002g0019a0002c0002t0002g0076a0002c0002t0002g0094others(7): Show | 10 | HG00323.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(34): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(27): Show |
21 | a0002c0002t0002g0030a0002c0002t0002g0032a0002c0002t0002g0066others(18): Show | 21 | HG00738.hp2 HG01081.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(36): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(29): Show |
16 | a0002c0002t0002g0037a0002c0002t0002g0078a0002c0002t0002g0081others(13): Show | 16 | HG00099.hp1 HG00438.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1272+388_1272+389i others(38): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(31): Show |
3 | a0002c0002t0002g0169a0002c0002t0003g0259a0005c0013t0003g0201 | 3 | HG02083.hp1 HG02109.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1272+388_1272+389i others(40): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(37): Show |
1 | a0002c0002t0027g0015 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1272+388_1272+389i others(46): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATATAT others(39): Show |
1 | a0002c0002t0003g0271 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1272+388_1272+389i others(48): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATTTAT others(23): Show |
1 | a0002c0002t0002g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1272+388_1272+389i others(32): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATTTAT others(27): Show |
1 | a0002c0002t0003g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1272+388_1272+389i others(36): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694075
|
T | TTATTTAT others(29): Show |
2 | a0002c0002t0002g0034a0002c0002t0002g0106 | 2 | HG01081.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1272+388_1272+389i others(38): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694075 | ||||||
| chr8:21694077
|
T | A | 182 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(179): Show | 182 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1272+387A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694077 | ||||||
| chr8:21694092
|
T | TATATATA others(24): Show |
1 | a0002c0016t0003g0272 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1272+371_1272+372i others(33): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694092 | ||||||
| chr8:21694165
|
C | G | 1 | a0002c0002t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1272+299G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694165 | ||||||
| chr8:21694194
|
C | G | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1272+270G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694194 | ||||||
| chr8:21694302
|
C | T | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1272+162G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694302 | ||||||
| chr8:21694310
|
C | G | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1272+154G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694310 | ||||||
| chr8:21694422
|
G | C | 1 | a0001c0003t0006g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1272+42C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694422 | ||||||
| chr8:21694423
|
C | G | 1 | a0001c0003t0006g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1272+41G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 8/8 | chr8 | 21694423 | ||||||
| chr8:21694621
|
T | C | 11 | a0001c0001t0013g0182a0001c0001t0013g0240a0001c0001t0019g0025others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-104A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21694621 | ||||||
| chr8:21694649
|
G | A | 8 | a0001c0001t0001g0127a0001c0001t0001g0176a0001c0001t0004g0213others(5): Show | 8 | NA18942.hp2 NA18943.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219-132C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21694649 | ||||||
| chr8:21694677
|
G | T | 78 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(75): Show | 78 | HG00621.hp2 HG00733.hp1 HG01255.hp1 others(75): Show |
intron_variant | MODIFIER | c.1219-160C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21694677 | ||||||
| chr8:21694767
|
G | A | 8 | a0001c0001t0005g0238a0001c0001t0005g0251a0001c0001t0006g0013others(5): Show | 8 | HG00733.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-250C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21694767 | ||||||
| chr8:21694915
|
T | C | 9 | a0003c0008t0012g0216a0003c0008t0012g0248a0003c0008t0012g0256others(6): Show | 9 | HG00408.hp2 NA18961.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-398A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21694915 | ||||||
| chr8:21694980
|
A | T | 1 | a0001c0025t0029g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1219-463T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21694980 | ||||||
| chr8:21694997
|
C | G | 1 | a0002c0002t0010g0191 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1219-480G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21694997 | ||||||
| chr8:21695042
|
G | C | 1 | a0005c0012t0010g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1219-525C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695042 | ||||||
| chr8:21695057
|
A | C | 10 | a0002c0002t0037g0204a0003c0008t0012g0216a0003c0008t0012g0248others(7): Show | 10 | HG00408.hp2 HG03139.hp2 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-540T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695057 | ||||||
| chr8:21695120
|
T | G | 2 | a0002c0002t0002g0123a0002c0002t0050g0317 | 2 | HG00733.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1219-603A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695120 | ||||||
| chr8:21695168
|
GAAGGGCT others(9): Show |
G | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-667_1219-652d others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695168 | ||||||
| chr8:21695198
|
T | A | 105 | a0001c0001t0004g0222a0002c0002t0002g0002a0002c0002t0002g0019others(102): Show | 105 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1219-681A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695198 | ||||||
| chr8:21695228
|
G | A | 62 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(59): Show | 62 | HG00621.hp2 HG00733.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1219-711C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695228 | ||||||
| chr8:21695299
|
G | T | 25 | a0001c0001t0004g0221a0001c0001t0005g0192a0001c0001t0005g0223others(22): Show | 25 | HG00733.hp1 HG01255.hp1 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.1219-782C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695299 | ||||||
| chr8:21695310
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1219-793C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695310 | ||||||
| chr8:21695380
|
T | G | 1 | a0001c0003t0004g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1219-863A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695380 | ||||||
| chr8:21695417
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0145others(2): Show | 5 | HG00642.hp1 HG01169.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-900G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695417 | ||||||
| chr8:21695477
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1219-960C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695477 | ||||||
| chr8:21695513
|
G | C | 206 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0004g0222others(203): Show | 206 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.1219-996C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695513 | ||||||
| chr8:21695573
|
A | C | 13 | a0001c0001t0013g0182a0001c0001t0013g0240a0001c0001t0019g0025others(10): Show | 13 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1219-1056T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695573 | ||||||
| chr8:21695600
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1219-1083T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695600 | ||||||
| chr8:21695657
|
G | A | 1 | a0002c0002t0002g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1219-1140C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695657 | ||||||
| chr8:21695672
|
T | C | 4 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0001g0141others(1): Show | 4 | NA18977.hp2 NA18979.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-1155A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695672 | ||||||
| chr8:21695819
|
C | G | 9 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0176others(6): Show | 9 | NA18942.hp2 NA18943.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1219-1302G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695819 | ||||||
| chr8:21695927
|
A | G | 11 | a0001c0001t0013g0182a0001c0001t0013g0240a0001c0001t0019g0025others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1219-1410T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21695927 | ||||||
| chr8:21696029
|
C | T | 2 | a0001c0006t0023g0208a0001c0006t0023g0234 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1219-1512G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696029 | ||||||
| chr8:21696045
|
C | T | 62 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(59): Show | 62 | HG00621.hp2 HG00733.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1219-1528G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696045 | ||||||
| chr8:21696076
|
T | TC | 16 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0004g0263others(13): Show | 16 | HG00597.hp1 HG00621.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-1560dupG | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696076 | ||||||
| chr8:21696077
|
C | T | 9 | a0003c0008t0012g0216a0003c0008t0012g0248a0003c0008t0012g0256others(6): Show | 9 | HG00408.hp2 NA18961.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-1560G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696077 | ||||||
| chr8:21696127
|
CTCCCCTC others(8): Show |
C | 320 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(317): Show | 320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1219-1625_1219-161 others(19): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696127 | ||||||
| chr8:21696131
|
C | T | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-1614G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696131 | ||||||
| chr8:21696133
|
T | C | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-1616A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696133 | ||||||
| chr8:21696134
|
C | T | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-1617G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696134 | ||||||
| chr8:21696136
|
C | T | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-1619G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696136 | ||||||
| chr8:21696141
|
T | C | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-1624A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696141 | ||||||
| chr8:21696142
|
G | C | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1219-1625C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696142 | ||||||
| chr8:21696171
|
T | C | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1219-1654A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696171 | ||||||
| chr8:21696331
|
T | TTGTTTTG others(17): Show |
4 | a0002c0002t0002g0163a0002c0002t0003g0286a0002c0002t0028g0105others(1): Show | 4 | HG02293.hp2 NA18943.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-1838_1219-181 others(28): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696331 | ||||||
| chr8:21696405
|
A | G | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1219-1888T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696405 | ||||||
| chr8:21696461
|
G | A | 1 | a0001c0001t0030g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1219-1944C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696461 | ||||||
| chr8:21696477
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-1960C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696477 | ||||||
| chr8:21696673
|
C | T | 4 | a0001c0001t0009g0202a0001c0004t0009g0228a0001c0004t0009g0235others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-2156G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696673 | ||||||
| chr8:21696676
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-2159C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696676 | ||||||
| chr8:21696712
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1219-2195G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696712 | ||||||
| chr8:21696713
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-2196C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696713 | ||||||
| chr8:21696799
|
A | T | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1219-2282T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696799 | ||||||
| chr8:21696826
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-2309C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696826 | ||||||
| chr8:21696891
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-2374C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696891 | ||||||
| chr8:21696909
|
GA | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0001t0001g0132others(5): Show | 8 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-2393delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696909 | ||||||
| chr8:21696924
|
AGGGAAGG others(12): Show |
A | 1 | a0001c0001t0042g0268 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1219-2426_1219-240 others(23): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696924 | ||||||
| chr8:21696937
|
G | A | 1 | a0005c0014t0003g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1219-2420C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696937 | ||||||
| chr8:21696943
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-2426C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21696943 | ||||||
| chr8:21697056
|
G | A | 1 | a0001c0003t0001g0173 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1219-2539C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697056 | ||||||
| chr8:21697067
|
C | A | 117 | a0001c0001t0001g0108a0001c0001t0004g0222a0001c0001t0005g0231others(114): Show | 117 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1219-2550G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697067 | ||||||
| chr8:21697075
|
G | T | 104 | a0001c0001t0001g0108a0001c0001t0004g0222a0002c0002t0002g0002others(101): Show | 104 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.1219-2558C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697075 | ||||||
| chr8:21697084
|
A | ACAGAGGA others(232): Show |
1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1219-2568_1219-256 others(243): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697084 | ||||||
| chr8:21697084
|
A | ACAGAGGA others(287): Show |
1 | a0002c0005t0002g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1219-2568_1219-256 others(298): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697084 | ||||||
| chr8:21697084
|
A | ACAGAGGA others(287): Show |
300 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1219-2568_1219-256 others(298): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697084 | ||||||
| chr8:21697084
|
A | ACAGAGGA others(288): Show |
1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1219-2568_1219-256 others(299): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697084 | ||||||
| chr8:21697084
|
A | ACAGAGGA others(287): Show |
2 | a0001c0006t0023g0208a0001c0006t0023g0234 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1219-2568_1219-256 others(298): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697084 | ||||||
| chr8:21697084
|
A | ACAGAGGA others(288): Show |
1 | a0001c0001t0004g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1219-2568_1219-256 others(299): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697084 | ||||||
| chr8:21697084
|
A | ACAGAGGA others(287): Show |
9 | a0003c0008t0012g0216a0003c0008t0012g0248a0003c0008t0012g0256others(6): Show | 9 | HG00408.hp2 NA18961.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219-2568_1219-256 others(298): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697084 | ||||||
| chr8:21697099
|
A | AGGGACAG others(290): Show |
1 | a0002c0002t0003g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1219-2583_1219-258 others(301): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697099 | ||||||
| chr8:21697113
|
G | A | 5 | a0001c0001t0001g0080a0001c0001t0001g0127a0001c0003t0001g0173others(2): Show | 5 | HG00438.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-2596C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697113 | ||||||
| chr8:21697124
|
A | AGAAGGGG others(302): Show |
2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1219-2608_1219-260 others(313): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697124 | ||||||
| chr8:21697127
|
A | AGGGGAAG others(288): Show |
2 | a0001c0001t0001g0080a0001c0003t0001g0173 | 2 | HG00438.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1219-2611_1219-261 others(299): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697127 | ||||||
| chr8:21697132
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-2615C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697132 | ||||||
| chr8:21697133
|
A | AGGGGACA others(290): Show |
1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1219-2617_1219-261 others(301): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697133 | ||||||
| chr8:21697143
|
G | T | 2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1219-2626C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697143 | ||||||
| chr8:21697159
|
C | A | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1219-2642G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697159 | ||||||
| chr8:21697253
|
T | C | 1 | a0002c0002t0003g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1219-2736A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697253 | ||||||
| chr8:21697272
|
A | G | 1 | a0001c0001t0005g0192 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1219-2755T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697272 | ||||||
| chr8:21697339
|
G | T | 16 | a0001c0001t0004g0273a0001c0001t0009g0202a0001c0001t0030g0077others(13): Show | 16 | HG00408.hp2 HG00639.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-2822C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697339 | ||||||
| chr8:21697386
|
G | A | 1 | a0001c0001t0005g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1219-2869C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697386 | ||||||
| chr8:21697389
|
G | C | 2 | a0001c0001t0004g0277a0001c0003t0001g0171 | 2 | HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1219-2872C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697389 | ||||||
| chr8:21697394
|
T | G | 1 | a0001c0001t0031g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1219-2877A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697394 | ||||||
| chr8:21697535
|
G | A | 1 | a0001c0001t0007g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1219-3018C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697535 | ||||||
| chr8:21697554
|
A | T | 12 | a0001c0001t0004g0273a0001c0025t0029g0071a0003c0008t0012g0216others(9): Show | 12 | HG00408.hp2 HG03471.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.1219-3037T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697554 | ||||||
| chr8:21697644
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1219-3127C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697644 | ||||||
| chr8:21697812
|
T | G | 1 | a0003c0008t0012g0281 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1219-3295A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697812 | ||||||
| chr8:21697850
|
T | A | 28 | a0001c0001t0004g0221a0001c0001t0005g0223a0001c0001t0005g0238others(25): Show | 28 | HG00733.hp1 HG02027.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.1219-3333A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21697850 | ||||||
| chr8:21698147
|
C | G | 1 | a0001c0001t0006g0146 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1219-3630G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698147 | ||||||
| chr8:21698337
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1219-3820C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698337 | ||||||
| chr8:21698414
|
A | G | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1219-3897T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698414 | ||||||
| chr8:21698459
|
C | T | 2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1219-3942G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698459 | ||||||
| chr8:21698569
|
T | C | 13 | a0001c0006t0007g0033a0001c0006t0009g0233a0001c0006t0009g0243others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1219-4052A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698569 | ||||||
| chr8:21698575
|
C | T | 1 | a0001c0025t0029g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1219-4058G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698575 | ||||||
| chr8:21698691
|
A | G | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1218+4114T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698691 | ||||||
| chr8:21698706
|
G | A | 109 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0001g0143others(106): Show | 109 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1218+4099C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698706 | ||||||
| chr8:21698706
|
G | C | 2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1218+4099C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698706 | ||||||
| chr8:21698742
|
G | GGCACAGC others(53): Show |
2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1218+4003_1218+406 others(64): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21698742 | ||||||
| chr8:21699111
|
C | T | 3 | a0001c0006t0002g0028a0004c0015t0008g0189a0004c0015t0008g0196 | 3 | HG02280.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1218+3694G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699111 | ||||||
| chr8:21699118
|
T | C | 1 | a0002c0002t0002g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1218+3687A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699118 | ||||||
| chr8:21699146
|
T | C | 1 | a0003c0008t0012g0281 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1218+3659A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699146 | ||||||
| chr8:21699148
|
T | C | 2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1218+3657A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699148 | ||||||
| chr8:21699202
|
T | C | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1218+3603A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699202 | ||||||
| chr8:21699220
|
T | C | 210 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0134others(207): Show | 210 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1218+3585A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699220 | ||||||
| chr8:21699296
|
C | T | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1218+3509G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699296 | ||||||
| chr8:21699422
|
G | C | 4 | a0001c0001t0006g0036a0001c0001t0007g0063a0001c0025t0029g0071others(1): Show | 4 | HG02451.hp1 HG02486.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+3383C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699422 | ||||||
| chr8:21699445
|
G | A | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1218+3360C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699445 | ||||||
| chr8:21699704
|
C | T | 4 | a0001c0001t0006g0036a0001c0001t0007g0063a0001c0025t0029g0071others(1): Show | 4 | HG02451.hp1 HG02486.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+3101G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699704 | ||||||
| chr8:21699713
|
G | A | 2 | a0001c0028t0048g0314a0002c0016t0003g0272 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1218+3092C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699713 | ||||||
| chr8:21699721
|
G | A | 40 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(37): Show | 40 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1218+3084C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699721 | ||||||
| chr8:21699747
|
C | A | 1 | a0001c0001t0005g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1218+3058G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699747 | ||||||
| chr8:21699773
|
C | T | 129 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0134others(126): Show | 129 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1218+3032G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699773 | ||||||
| chr8:21699860
|
T | C | 2 | a0002c0002t0002g0169a0002c0005t0047g0313 | 2 | HG02083.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1218+2945A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699860 | ||||||
| chr8:21699912
|
C | T | 2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1218+2893G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699912 | ||||||
| chr8:21699926
|
G | A | 1 | a0001c0003t0032g0148 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1218+2879C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699926 | ||||||
| chr8:21699931
|
C | A | 41 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(38): Show | 41 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1218+2874G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699931 | ||||||
| chr8:21699952
|
A | G | 2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1218+2853T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699952 | ||||||
| chr8:21699958
|
C | T | 1 | a0001c0001t0005g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1218+2847G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21699958 | ||||||
| chr8:21700016
|
T | C | 1 | a0005c0014t0003g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1218+2789A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700016 | ||||||
| chr8:21700056
|
C | T | 1 | a0001c0001t0041g0239 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1218+2749G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700056 | ||||||
| chr8:21700057
|
A | T | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1218+2748T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700057 | ||||||
| chr8:21700100
|
G | C | 1 | a0001c0003t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1218+2705C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700100 | ||||||
| chr8:21700119
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0035g0113a0002c0002t0003g0181 | 3 | HG01433.hp2 HG02258.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1218+2686G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700119 | ||||||
| chr8:21700213
|
G | A | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1218+2592C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700213 | ||||||
| chr8:21700257
|
A | ACATGGGC others(4): Show |
190 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0134others(187): Show | 190 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1218+2547_1218+254 others(15): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700257 | ||||||
| chr8:21700556
|
G | C | 192 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0134others(189): Show | 192 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1218+2249C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700556 | ||||||
| chr8:21700563
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1218+2242G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700563 | ||||||
| chr8:21700620
|
T | A | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1218+2185A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700620 | ||||||
| chr8:21700620
|
T | C | 44 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1218+2185A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700620 | ||||||
| chr8:21700684
|
G | A | 1 | a0002c0002t0002g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1218+2121C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700684 | ||||||
| chr8:21700704
|
C | T | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1218+2101G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700704 | ||||||
| chr8:21700705
|
A | T | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1218+2100T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700705 | ||||||
| chr8:21700727
|
T | C | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1218+2078A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21700727 | ||||||
| chr8:21701047
|
G | T | 1 | a0002c0002t0006g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1218+1758C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701047 | ||||||
| chr8:21701072
|
A | G | 13 | a0001c0001t0001g0126a0001c0001t0004g0184a0001c0001t0004g0278others(10): Show | 13 | HG00639.hp1 HG01258.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1218+1733T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701072 | ||||||
| chr8:21701123
|
G | A | 2 | a0002c0002t0002g0019a0002c0002t0002g0066 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1218+1682C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701123 | ||||||
| chr8:21701220
|
C | A | 1 | a0001c0006t0009g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1218+1585G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701220 | ||||||
| chr8:21701316
|
C | T | 3 | a0001c0006t0007g0033a0001c0006t0009g0304a0001c0006t0023g0208 | 3 | HG02109.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1218+1489G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701316 | ||||||
| chr8:21701321
|
G | C | 1 | a0001c0006t0016g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1218+1484C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701321 | ||||||
| chr8:21701389
|
G | A | 1 | a0001c0001t0011g0319 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1218+1416C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701389 | ||||||
| chr8:21701654
|
A | G | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+1151T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701654 | ||||||
| chr8:21701664
|
C | T | 10 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+1141G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701664 | ||||||
| chr8:21701775
|
C | T | 1 | a0002c0002t0002g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1218+1030G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701775 | ||||||
| chr8:21701797
|
C | A | 1 | a0005c0012t0010g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1218+1008G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701797 | ||||||
| chr8:21701854
|
G | T | 1 | a0001c0006t0023g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1218+951C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701854 | ||||||
| chr8:21701915
|
C | T | 2 | a0002c0002t0002g0076a0002c0002t0002g0128 | 2 | HG00642.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1218+890G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701915 | ||||||
| chr8:21701978
|
C | T | 10 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+827G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21701978 | ||||||
| chr8:21702114
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1218+691T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702114 | ||||||
| chr8:21702213
|
T | C | 1 | a0005c0013t0010g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1218+592A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702213 | ||||||
| chr8:21702225
|
G | A | 4 | a0001c0006t0002g0028a0001c0006t0023g0208a0004c0015t0008g0189others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+580C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702225 | ||||||
| chr8:21702448
|
G | T | 16 | a0001c0006t0007g0033a0001c0006t0009g0233a0001c0006t0009g0243others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1218+357C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702448 | ||||||
| chr8:21702640
|
C | A | 10 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+165G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702640 | ||||||
| chr8:21702670
|
C | T | 1 | a0001c0001t0004g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1218+135G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702670 | ||||||
| chr8:21702702
|
G | A | 4 | a0001c0006t0002g0028a0001c0006t0023g0208a0004c0015t0008g0189others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+103C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702702 | ||||||
| chr8:21702714
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1218+91C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702714 | ||||||
| chr8:21702781
|
C | G | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1218+24G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 7/8 | chr8 | 21702781 | ||||||
| chr8:21703024
|
C | T | 2 | a0002c0002t0002g0038a0002c0002t0003g0206 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1046-47G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703024 | ||||||
| chr8:21703041
|
C | T | 2 | a0002c0016t0006g0017a0005c0014t0006g0083 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1046-64G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703041 | ||||||
| chr8:21703164
|
G | A | 4 | a0001c0001t0009g0202a0001c0004t0009g0228a0001c0004t0009g0235others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046-187C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703164 | ||||||
| chr8:21703228
|
G | A | 1 | a0002c0002t0002g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1046-251C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703228 | ||||||
| chr8:21703241
|
G | T | 4 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046-264C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703241 | ||||||
| chr8:21703394
|
G | A | 10 | a0001c0006t0002g0028a0001c0006t0007g0033a0001c0006t0023g0208others(7): Show | 10 | HG02055.hp1 HG02280.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1046-417C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703394 | ||||||
| chr8:21703394
|
G | C | 11 | a0001c0001t0001g0008a0002c0002t0002g0094a0002c0002t0002g0111others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046-417C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703394 | ||||||
| chr8:21703438
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0004g0300 | 2 | HG01496.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1046-461G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703438 | ||||||
| chr8:21703533
|
C | G | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1046-556G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703533 | ||||||
| chr8:21703601
|
C | T | 10 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1046-624G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703601 | ||||||
| chr8:21703726
|
G | A | 10 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1046-749C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21703726 | ||||||
| chr8:21704037
|
G | A | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1045+948C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704037 | ||||||
| chr8:21704194
|
C | A | 1 | a0002c0002t0002g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1045+791G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704194 | ||||||
| chr8:21704396
|
T | G | 5 | a0001c0001t0006g0036a0001c0001t0007g0063a0001c0025t0029g0071others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045+589A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704396 | ||||||
| chr8:21704581
|
C | T | 1 | a0005c0013t0003g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1045+404G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704581 | ||||||
| chr8:21704607
|
T | C | 39 | a0001c0001t0003g0226a0001c0001t0004g0221a0001c0001t0005g0192others(36): Show | 39 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1045+378A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704607 | ||||||
| chr8:21704643
|
A | G | 133 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0134others(130): Show | 133 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1045+342T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704643 | ||||||
| chr8:21704738
|
A | G | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1045+247T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704738 | ||||||
| chr8:21704881
|
C | T | 2 | a0001c0028t0048g0314a0002c0016t0003g0272 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1045+104G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704881 | ||||||
| chr8:21704912
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1045+73A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 6/8 | chr8 | 21704912 | ||||||
| chr8:21705350
|
C | T | 4 | a0002c0002t0002g0094a0002c0002t0002g0111a0002c0002t0002g0125others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-225G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705350 | ||||||
| chr8:21705480
|
A | G | 211 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0134others(208): Show | 211 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.905-355T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705480 | ||||||
| chr8:21705501
|
T | C | 18 | a0001c0001t0003g0226a0001c0001t0007g0005a0001c0001t0007g0073others(15): Show | 18 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-376A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705501 | ||||||
| chr8:21705502
|
G | A | 1 | a0001c0003t0007g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.905-377C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705502 | ||||||
| chr8:21705556
|
A | G | 5 | a0001c0001t0006g0036a0001c0001t0007g0063a0001c0025t0029g0071others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+376T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705556 | ||||||
| chr8:21705624
|
G | A | 206 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0134others(203): Show | 206 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.904+308C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705624 | ||||||
| chr8:21705710
|
C | T | 207 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0134others(204): Show | 207 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.904+222G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705710 | ||||||
| chr8:21705736
|
T | C | 1 | a0002c0002t0003g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.904+196A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705736 | ||||||
| chr8:21705842
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.904+90G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705842 | ||||||
| chr8:21705852
|
T | G | 2 | a0001c0028t0048g0314a0002c0016t0003g0272 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.904+80A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705852 | ||||||
| chr8:21705853
|
G | A | 2 | a0002c0002t0003g0288a0002c0002t0003g0297 | 2 | NA18994.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.904+79C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 5/8 | chr8 | 21705853 | ||||||
| chr8:21706151
|
A | C | 1 | a0001c0001t0006g0158 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.795-110T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706151 | ||||||
| chr8:21706277
|
C | A | 1 | a0002c0002t0003g0299 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.795-236G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706277 | ||||||
| chr8:21706291
|
A | C | 7 | a0002c0002t0010g0185a0002c0002t0010g0191a0002c0002t0015g0004others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.795-250T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706291 | ||||||
| chr8:21706298
|
G | T | 2 | a0001c0001t0006g0100a0001c0001t0006g0142 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.795-257C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706298 | ||||||
| chr8:21706394
|
G | C | 1 | a0002c0002t0002g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.795-353C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706394 | ||||||
| chr8:21706480
|
C | T | 2 | a0001c0004t0018g0116a0001c0004t0018g0120 | 2 | HG00621.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.795-439G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706480 | ||||||
| chr8:21706525
|
G | A | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.795-484C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706525 | ||||||
| chr8:21706557
|
A | G | 30 | a0001c0001t0006g0036a0001c0001t0007g0063a0001c0001t0009g0202others(27): Show | 30 | HG00639.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.795-516T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706557 | ||||||
| chr8:21706678
|
C | T | 1 | a0002c0007t0002g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.795-637G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706678 | ||||||
| chr8:21706689
|
C | A | 11 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.795-648G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706689 | ||||||
| chr8:21706754
|
T | G | 1 | a0001c0001t0005g0254 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.795-713A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706754 | ||||||
| chr8:21706772
|
T | C | 12 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.795-731A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706772 | ||||||
| chr8:21706780
|
A | T | 66 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0145others(63): Show | 66 | HG00438.hp1 HG00597.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.795-739T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706780 | ||||||
| chr8:21706810
|
G | A | 5 | a0001c0001t0019g0025a0001c0006t0002g0028a0001c0006t0023g0208others(2): Show | 5 | HG02280.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.795-769C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706810 | ||||||
| chr8:21706818
|
G | A | 1 | a0002c0002t0002g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795-777C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706818 | ||||||
| chr8:21706876
|
T | C | 1 | a0005c0012t0010g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.795-835A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706876 | ||||||
| chr8:21706915
|
C | T | 1 | a0001c0003t0001g0043 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.795-874G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706915 | ||||||
| chr8:21706975
|
G | A | 13 | a0001c0001t0005g0231a0001c0001t0006g0036a0001c0001t0009g0202others(10): Show | 13 | HG00639.hp2 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.795-934C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21706975 | ||||||
| chr8:21707093
|
T | C | 1 | a0001c0001t0019g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.795-1052A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707093 | ||||||
| chr8:21707116
|
C | T | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-1075G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707116 | ||||||
| chr8:21707426
|
G | A | 7 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-1385C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707426 | ||||||
| chr8:21707427
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.795-1386C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707427 | ||||||
| chr8:21707503
|
G | A | 23 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0145others(20): Show | 23 | HG00642.hp1 HG01515.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.795-1462C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707503 | ||||||
| chr8:21707503
|
G | T | 3 | a0001c0006t0023g0208a0002c0002t0002g0019a0002c0002t0002g0066 | 3 | HG02145.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.795-1462C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707503 | ||||||
| chr8:21707522
|
C | G | 23 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0145others(20): Show | 23 | HG00642.hp1 HG01175.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.795-1481G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707522 | ||||||
| chr8:21707576
|
A | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.795-1535T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707576 | ||||||
| chr8:21707653
|
T | C | 68 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0145others(65): Show | 68 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.795-1612A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707653 | ||||||
| chr8:21707657
|
C | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0004g0244others(2): Show | 5 | HG00733.hp2 HG01255.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-1616G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707657 | ||||||
| chr8:21707735
|
G | A | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-1694C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707735 | ||||||
| chr8:21707770
|
G | C | 3 | a0001c0001t0006g0100a0001c0001t0006g0142a0002c0002t0002g0162 | 3 | HG01516.hp2 HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.795-1729C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707770 | ||||||
| chr8:21707882
|
A | G | 1 | a0001c0004t0004g0257 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.795-1841T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707882 | ||||||
| chr8:21707890
|
C | A | 39 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(36): Show | 39 | HG00597.hp2 HG00733.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.795-1849G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21707890 | ||||||
| chr8:21708036
|
T | C | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-1995A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708036 | ||||||
| chr8:21708048
|
G | A | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-2007C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708048 | ||||||
| chr8:21708079
|
A | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.795-2038T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708079 | ||||||
| chr8:21708111
|
T | G | 70 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0145others(67): Show | 70 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.795-2070A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708111 | ||||||
| chr8:21708234
|
A | G | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-2193T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708234 | ||||||
| chr8:21708357
|
C | A | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-2316G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708357 | ||||||
| chr8:21708506
|
C | T | 229 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.795-2465G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708506 | ||||||
| chr8:21708535
|
A | T | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-2494T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708535 | ||||||
| chr8:21708540
|
C | T | 32 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0009g0202others(29): Show | 32 | HG00621.hp1 HG00639.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.795-2499G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708540 | ||||||
| chr8:21708576
|
T | C | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-2535A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708576 | ||||||
| chr8:21708614
|
G | A | 1 | a0001c0001t0005g0192 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.795-2573C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708614 | ||||||
| chr8:21708711
|
T | C | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-2670A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708711 | ||||||
| chr8:21708871
|
A | G | 32 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0009g0202others(29): Show | 32 | HG00621.hp1 HG02056.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.795-2830T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708871 | ||||||
| chr8:21708899
|
C | T | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-2858G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708899 | ||||||
| chr8:21708923
|
G | C | 1 | a0001c0001t0033g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.795-2882C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21708923 | ||||||
| chr8:21709005
|
GA | G | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-2965delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709005 | ||||||
| chr8:21709194
|
G | A | 3 | a0001c0001t0031g0121a0002c0002t0002g0089a0002c0002t0002g0106 | 3 | HG01081.hp2 HG03704.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.795-3153C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709194 | ||||||
| chr8:21709201
|
C | T | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-3160G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709201 | ||||||
| chr8:21709285
|
G | A | 7 | a0001c0001t0019g0025a0001c0006t0002g0028a0001c0006t0016g0026others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.795-3244C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709285 | ||||||
| chr8:21709299
|
G | C | 6 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(3): Show | 6 | HG02615.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-3258C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709299 | ||||||
| chr8:21709300
|
C | A | 1 | a0001c0020t0005g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.795-3259G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709300 | ||||||
| chr8:21709344
|
A | G | 2 | a0001c0006t0023g0234a0002c0002t0003g0236 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.795-3303T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709344 | ||||||
| chr8:21709549
|
G | A | 4 | a0001c0001t0011g0322a0001c0003t0001g0053a0001c0003t0001g0054others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-3508C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709549 | ||||||
| chr8:21709619
|
G | A | 5 | a0001c0001t0006g0036a0001c0001t0009g0202a0001c0001t0013g0182others(2): Show | 5 | HG02451.hp1 HG03130.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.795-3578C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709619 | ||||||
| chr8:21709628
|
T | C | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-3587A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21709628 | ||||||
| chr8:21710065
|
G | A | 2 | a0002c0002t0002g0019a0002c0002t0002g0066 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.795-4024C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710065 | ||||||
| chr8:21710181
|
T | A | 2 | a0001c0001t0035g0113a0002c0002t0002g0111 | 2 | HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.795-4140A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710181 | ||||||
| chr8:21710264
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.795-4223C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710264 | ||||||
| chr8:21710271
|
C | T | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-4230G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710271 | ||||||
| chr8:21710287
|
C | T | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-4246G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710287 | ||||||
| chr8:21710383
|
C | T | 3 | a0001c0006t0023g0208a0002c0002t0002g0019a0002c0002t0002g0066 | 3 | HG02145.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.795-4342G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710383 | ||||||
| chr8:21710398
|
G | A | 12 | a0001c0003t0007g0051a0002c0002t0002g0078a0002c0002t0002g0079others(9): Show | 12 | HG02040.hp1 NA18959.hp2 NA18961.hp2 others(9): Show |
intron_variant | MODIFIER | c.795-4357C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710398 | ||||||
| chr8:21710539
|
C | T | 4 | a0001c0001t0007g0063a0002c0002t0006g0065a0002c0002t0010g0185others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-4498G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710539 | ||||||
| chr8:21710565
|
C | T | 18 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0009g0202others(15): Show | 18 | HG00621.hp1 HG02056.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.795-4524G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710565 | ||||||
| chr8:21710651
|
C | T | 31 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0009g0202others(28): Show | 31 | HG00621.hp1 HG02056.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.795-4610G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710651 | ||||||
| chr8:21710667
|
A | C | 1 | a0002c0002t0003g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.795-4626T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710667 | ||||||
| chr8:21710745
|
G | C | 5 | a0001c0001t0007g0063a0002c0002t0002g0129a0002c0002t0002g0130others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-4704C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710745 | ||||||
| chr8:21710765
|
C | A | 6 | a0001c0001t0001g0117a0002c0002t0003g0275a0002c0002t0003g0286others(3): Show | 6 | NA18942.hp1 NA18944.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.795-4724G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710765 | ||||||
| chr8:21710786
|
C | A | 1 | a0001c0001t0004g0217 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.795-4745G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710786 | ||||||
| chr8:21710811
|
G | A | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-4770C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710811 | ||||||
| chr8:21710843
|
G | A | 1 | a0004c0009t0039g0188 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.795-4802C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710843 | ||||||
| chr8:21710921
|
G | C | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.795-4880C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710921 | ||||||
| chr8:21710958
|
G | A | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-4917C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21710958 | ||||||
| chr8:21711025
|
G | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.795-4984C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711025 | ||||||
| chr8:21711047
|
T | G | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-5006A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711047 | ||||||
| chr8:21711048
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.795-5007G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711048 | ||||||
| chr8:21711085
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.795-5044A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711085 | ||||||
| chr8:21711529
|
A | G | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.795-5488T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711529 | ||||||
| chr8:21711592
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.795-5551C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711592 | ||||||
| chr8:21711673
|
C | T | 242 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.795-5632G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711673 | ||||||
| chr8:21711682
|
G | GTTTTTCT others(7): Show |
1 | a0002c0002t0006g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.795-5655_795-5642d others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711682 | ||||||
| chr8:21711682
|
G | GTTTTTCT others(8): Show |
2 | a0001c0001t0006g0036a0001c0001t0007g0063 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.795-5656_795-5642d others(17): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711682 | ||||||
| chr8:21711688
|
C | CT | 12 | a0001c0001t0020g0307a0002c0002t0002g0078a0002c0002t0002g0079others(9): Show | 12 | HG02559.hp2 HG02647.hp1 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.795-5648dupA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711688 | ||||||
| chr8:21711689
|
T | TTTTTTTT others(6): Show |
1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.795-5649_795-5648i others(15): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711689 | ||||||
| chr8:21711689
|
T | TTTTTTTT others(7): Show |
21 | a0001c0001t0009g0202a0001c0001t0013g0182a0001c0001t0013g0240others(18): Show | 21 | HG01168.hp1 HG01169.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.795-5649_795-5648i others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711689 | ||||||
| chr8:21711689
|
T | TTTTTTTT others(8): Show |
11 | a0001c0001t0004g0218a0001c0004t0004g0258a0001c0004t0018g0116others(8): Show | 11 | HG00621.hp1 HG02056.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.795-5649_795-5648i others(17): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711689 | ||||||
| chr8:21711726
|
C | A | 3 | a0002c0021t0010g0225a0005c0012t0010g0198a0007c0024t0019g0062 | 3 | HG02647.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.795-5685G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711726 | ||||||
| chr8:21711751
|
A | G | 37 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0007g0063others(34): Show | 37 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.795-5710T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711751 | ||||||
| chr8:21711826
|
C | A | 1 | a0001c0001t0007g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.795-5785G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711826 | ||||||
| chr8:21711907
|
C | T | 18 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0124others(15): Show | 18 | HG00438.hp2 HG00639.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.795-5866G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21711907 | ||||||
| chr8:21712172
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.795-6131C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712172 | ||||||
| chr8:21712223
|
G | A | 1 | a0004c0009t0013g0190 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.795-6182C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712223 | ||||||
| chr8:21712233
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.795-6192C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712233 | ||||||
| chr8:21712256
|
G | T | 1 | a0002c0002t0044g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.795-6215C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712256 | ||||||
| chr8:21712291
|
A | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.795-6250T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712291 | ||||||
| chr8:21712292
|
G | A | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-6251C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712292 | ||||||
| chr8:21712293
|
GGCGGCCG others(33): Show |
G | 3 | a0002c0021t0010g0225a0005c0012t0010g0198a0007c0024t0019g0062 | 3 | HG02647.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.795-6292_795-6253d others(42): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712293 | ||||||
| chr8:21712295
|
C | T | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-6254G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712295 | ||||||
| chr8:21712300
|
G | A | 4 | a0001c0001t0006g0036a0001c0001t0009g0202a0001c0001t0013g0182others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-6259C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712300 | ||||||
| chr8:21712375
|
C | T | 1 | a0001c0001t0005g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.795-6334G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712375 | ||||||
| chr8:21712376
|
G | A | 2 | a0001c0006t0023g0234a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.795-6335C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712376 | ||||||
| chr8:21712405
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0004g0217 | 2 | HG00544.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.795-6364C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712405 | ||||||
| chr8:21712412
|
G | A | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-6371C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712412 | ||||||
| chr8:21712456
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.795-6415C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712456 | ||||||
| chr8:21712560
|
C | T | 14 | a0001c0001t0007g0063a0001c0003t0007g0051a0002c0002t0002g0078others(11): Show | 14 | HG02040.hp1 HG02486.hp2 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.795-6519G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712560 | ||||||
| chr8:21712572
|
AGGCAGAG others(33): Show |
A | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-6571_795-6532d others(42): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712572 | ||||||
| chr8:21712599
|
C | CG | 4 | a0001c0006t0009g0304a0001c0010t0004g0293a0002c0002t0017g0107others(1): Show | 4 | HG02109.hp1 NA18949.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-6559dupC | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712599 | ||||||
| chr8:21712630
|
T | C | 88 | a0001c0001t0004g0218a0001c0001t0005g0192a0001c0001t0005g0238others(85): Show | 88 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.795-6589A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712630 | ||||||
| chr8:21712684
|
G | A | 2 | a0001c0006t0016g0026a0001c0006t0016g0072 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.795-6643C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712684 | ||||||
| chr8:21712742
|
C | T | 1 | a0001c0001t0030g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.795-6701G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712742 | ||||||
| chr8:21712779
|
C | T | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-6738G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712779 | ||||||
| chr8:21712789
|
G | A | 1 | a0002c0002t0015g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.795-6748C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712789 | ||||||
| chr8:21712803
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.795-6762C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712803 | ||||||
| chr8:21712872
|
C | T | 40 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0007g0063others(37): Show | 40 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.795-6831G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712872 | ||||||
| chr8:21712875
|
T | C | 205 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.795-6834A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712875 | ||||||
| chr8:21712982
|
C | CAGAGGGA others(16): Show |
1 | a0002c0002t0002g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.795-6964_795-6942d others(25): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712982 | ||||||
| chr8:21712994
|
G | A | 2 | a0001c0001t0006g0100a0001c0001t0006g0142 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.795-6953C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712994 | ||||||
| chr8:21712999
|
A | AAGAGGGA others(14): Show |
4 | a0002c0002t0017g0107a0002c0002t0046g0312a0002c0005t0017g0009others(1): Show | 4 | NA18980.hp2 NA19010.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-6979_795-6959d others(23): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21712999 | ||||||
| chr8:21713022
|
GAGGGAGA others(35): Show |
G | 1 | a0001c0001t0006g0158 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.795-7023_795-6982d others(44): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713022 | ||||||
| chr8:21713050
|
AGGGAGAC others(17): Show |
A | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-7033_795-7010d others(26): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713050 | ||||||
| chr8:21713051
|
G | C | 35 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0007g0063others(32): Show | 35 | HG00621.hp1 HG02056.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.795-7010C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713051 | ||||||
| chr8:21713052
|
GGAGACGA others(5): Show |
G | 35 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0007g0063others(32): Show | 35 | HG00621.hp1 HG02056.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.795-7023_795-7012d others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713052 | ||||||
| chr8:21713057
|
C | G | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.795-7016G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713057 | ||||||
| chr8:21713058
|
G | A | 45 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(42): Show | 45 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.795-7017C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713058 | ||||||
| chr8:21713058
|
G | C | 22 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0124others(19): Show | 22 | HG00438.hp2 HG00639.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.795-7017C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713058 | ||||||
| chr8:21713059
|
A | G | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.795-7018T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713059 | ||||||
| chr8:21713060
|
G | A | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.795-7019C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713060 | ||||||
| chr8:21713062
|
G | A | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.795-7021C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713062 | ||||||
| chr8:21713063
|
A | C | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.795-7022T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713063 | ||||||
| chr8:21713064
|
A | G | 2 | a0001c0022t0007g0020a0005c0012t0010g0194 | 2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.795-7023T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713064 | ||||||
| chr8:21713075
|
A | C | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-7034T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713075 | ||||||
| chr8:21713086
|
C | G | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-7045G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713086 | ||||||
| chr8:21713113
|
T | C | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-7072A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713113 | ||||||
| chr8:21713167
|
T | C | 37 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0007g0063others(34): Show | 37 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.795-7126A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713167 | ||||||
| chr8:21713187
|
C | CTGTTT | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-7151_795-7147d others(7): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713187 | ||||||
| chr8:21713215
|
G | T | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-7174C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713215 | ||||||
| chr8:21713295
|
G | A | 1 | a0002c0002t0015g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.795-7254C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713295 | ||||||
| chr8:21713345
|
G | A | 45 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(42): Show | 45 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.795-7304C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713345 | ||||||
| chr8:21713364
|
T | G | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-7323A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713364 | ||||||
| chr8:21713622
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0004g0217 | 2 | HG00544.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.795-7581A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713622 | ||||||
| chr8:21713649
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.795-7608G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713649 | ||||||
| chr8:21713650
|
G | A | 1 | a0001c0001t0007g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.795-7609C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713650 | ||||||
| chr8:21713673
|
C | G | 1 | a0001c0001t0001g0024 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.795-7632G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713673 | ||||||
| chr8:21713948
|
G | A | 21 | a0001c0001t0001g0154a0001c0001t0004g0218a0001c0001t0006g0036others(18): Show | 21 | HG00621.hp1 HG02056.hp2 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.795-7907C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713948 | ||||||
| chr8:21713957
|
A | G | 243 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.795-7916T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713957 | ||||||
| chr8:21713975
|
C | G | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-7934G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713975 | ||||||
| chr8:21713992
|
G | A | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.795-7951C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21713992 | ||||||
| chr8:21714028
|
G | A | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.795-7987C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714028 | ||||||
| chr8:21714057
|
CTTCCCAG others(4): Show |
C | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-8027_795-8017d others(13): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714057 | ||||||
| chr8:21714133
|
C | G | 4 | a0001c0001t0006g0036a0001c0001t0009g0202a0001c0001t0013g0182others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-8092G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714133 | ||||||
| chr8:21714183
|
T | TAGAATA | 44 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.795-8148_795-8143d others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714183 | ||||||
| chr8:21714236
|
G | A | 18 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0009g0202others(15): Show | 18 | HG00621.hp1 HG02056.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.795-8195C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714236 | ||||||
| chr8:21714246
|
C | CTTTTT | 35 | a0001c0001t0005g0238a0001c0001t0005g0251a0001c0001t0006g0013others(32): Show | 35 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.795-8210_795-8206d others(7): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTT | 42 | a0001c0001t0001g0061a0001c0001t0001g0099a0001c0001t0001g0168others(39): Show | 42 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.795-8211_795-8206d others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTTT | 100 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(97): Show | 100 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.795-8212_795-8206d others(9): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTTT others(1): Show |
50 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0090others(47): Show | 50 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.795-8213_795-8206d others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0064others(4): Show | 7 | HG01255.hp2 HG01258.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-8214_795-8206d others(11): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTTT others(9): Show |
1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.795-8221_795-8206d others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0019g0025a0001c0006t0002g0028 | 2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.795-8227_795-8206d others(24): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTTT others(17): Show |
1 | a0004c0015t0008g0189 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.795-8206_795-8205i others(26): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714246
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0007g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.795-8206_795-8205i others(28): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714246 | ||||||
| chr8:21714372
|
C | T | 2 | a0001c0001t0001g0080a0001c0003t0001g0056 | 2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.795-8331G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714372 | ||||||
| chr8:21714448
|
C | T | 16 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(13): Show | 16 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.795-8407G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714448 | ||||||
| chr8:21714464
|
G | C | 23 | a0001c0001t0005g0238a0001c0001t0005g0251a0001c0001t0006g0013others(20): Show | 23 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.795-8423C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714464 | ||||||
| chr8:21714496
|
C | A | 1 | a0001c0004t0008g0224 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.795-8455G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714496 | ||||||
| chr8:21714554
|
G | C | 11 | a0001c0001t0004g0218a0001c0004t0004g0258a0001c0004t0018g0116others(8): Show | 11 | HG00621.hp1 HG02056.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.795-8513C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714554 | ||||||
| chr8:21714573
|
C | T | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-8532G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714573 | ||||||
| chr8:21714668
|
C | T | 44 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(41): Show | 44 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.795-8627G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714668 | ||||||
| chr8:21714703
|
C | T | 1 | a0001c0010t0004g0292 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.795-8662G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714703 | ||||||
| chr8:21714720
|
C | T | 240 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.795-8679G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714720 | ||||||
| chr8:21714796
|
G | A | 12 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(9): Show | 12 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.795-8755C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714796 | ||||||
| chr8:21714880
|
G | A | 5 | a0001c0001t0004g0218a0001c0004t0004g0258a0002c0002t0003g0288others(2): Show | 5 | NA18952.hp2 NA18994.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.795-8839C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714880 | ||||||
| chr8:21714882
|
G | A | 1 | a0002c0002t0015g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.795-8841C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714882 | ||||||
| chr8:21714891
|
A | T | 4 | a0002c0002t0017g0107a0002c0002t0046g0312a0002c0005t0017g0009others(1): Show | 4 | NA18980.hp2 NA19010.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-8850T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21714891 | ||||||
| chr8:21715245
|
G | T | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.795-9204C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715245 | ||||||
| chr8:21715267
|
G | A | 14 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.795-9226C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715267 | ||||||
| chr8:21715295
|
T | C | 1 | a0004c0011t0009g0195 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.795-9254A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715295 | ||||||
| chr8:21715365
|
A | G | 2 | a0002c0002t0010g0185a0002c0002t0015g0029 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.795-9324T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715365 | ||||||
| chr8:21715395
|
G | A | 1 | a0002c0005t0002g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.795-9354C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715395 | ||||||
| chr8:21715417
|
T | A | 3 | a0001c0006t0023g0208a0002c0002t0002g0019a0002c0002t0002g0066 | 3 | HG02145.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.795-9376A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715417 | ||||||
| chr8:21715529
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0004g0277a0001c0001t0033g0122others(2): Show | 5 | HG01358.hp2 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.795-9488A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715529 | ||||||
| chr8:21715583
|
T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.795-9542A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715583 | ||||||
| chr8:21715620
|
A | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.795-9579T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715620 | ||||||
| chr8:21715626
|
GACCTGGG others(15): Show |
G | 1 | a0001c0020t0005g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.795-9607_795-9586d others(24): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715626 | ||||||
| chr8:21715627
|
A | T | 1 | a0001c0006t0023g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.795-9586T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715627 | ||||||
| chr8:21715646
|
G | A | 3 | a0001c0001t0019g0025a0001c0006t0002g0028a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.795-9605C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715646 | ||||||
| chr8:21715657
|
C | T | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.795-9616G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715657 | ||||||
| chr8:21715674
|
C | A | 10 | a0001c0006t0009g0233a0001c0006t0009g0243a0001c0006t0009g0305others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.795-9633G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715674 | ||||||
| chr8:21715880
|
GGAGAGAG others(7): Show |
G | 1 | a0002c0002t0002g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.795-9853_795-9840d others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715880 | ||||||
| chr8:21715939
|
A | T | 1 | a0001c0020t0005g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.795-9898T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21715939 | ||||||
| chr8:21716040
|
C | T | 43 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(40): Show | 43 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.795-9999G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716040 | ||||||
| chr8:21716051
|
G | A | 6 | a0001c0001t0003g0226a0001c0001t0007g0005a0001c0001t0007g0073others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-10010C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716051 | ||||||
| chr8:21716099
|
G | A | 6 | a0001c0001t0004g0278a0001c0003t0001g0043a0001c0003t0001g0050others(3): Show | 6 | HG00639.hp1 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-10058C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716099 | ||||||
| chr8:21716136
|
A | G | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.795-10095T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716136 | ||||||
| chr8:21716287
|
C | T | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.795-10246G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716287 | ||||||
| chr8:21716308
|
G | GA | 221 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.795-10268dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716308 | ||||||
| chr8:21716308
|
G | GGA | 19 | a0001c0001t0004g0218a0001c0001t0005g0231a0001c0001t0006g0036others(16): Show | 19 | HG00621.hp1 HG02056.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.795-10268_795-1026 others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716308 | ||||||
| chr8:21716366
|
G | C | 1 | a0002c0002t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.795-10325C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716366 | ||||||
| chr8:21716425
|
C | T | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.795-10384G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716425 | ||||||
| chr8:21716426
|
G | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.795-10385C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716426 | ||||||
| chr8:21716447
|
C | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.795-10406G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716447 | ||||||
| chr8:21716484
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.795-10443A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716484 | ||||||
| chr8:21716651
|
T | C | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-10610A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716651 | ||||||
| chr8:21716673
|
C | T | 13 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(10): Show | 13 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.795-10632G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716673 | ||||||
| chr8:21716963
|
G | A | 12 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(9): Show | 12 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.795-10922C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21716963 | ||||||
| chr8:21717266
|
G | A | 2 | a0001c0001t0005g0238a0001c0004t0006g0010 | 2 | HG00733.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.795-11225C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21717266 | ||||||
| chr8:21717334
|
A | G | 3 | a0002c0002t0002g0129a0002c0002t0002g0130a0002c0016t0003g0272 | 3 | HG01168.hp1 HG01169.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.795-11293T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21717334 | ||||||
| chr8:21717511
|
T | G | 48 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(45): Show | 48 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.795-11470A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21717511 | ||||||
| chr8:21717632
|
C | T | 4 | a0001c0001t0006g0036a0001c0001t0009g0202a0001c0001t0013g0182others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-11591G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21717632 | ||||||
| chr8:21717633
|
G | A | 12 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0145others(9): Show | 12 | HG00642.hp1 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.795-11592C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21717633 | ||||||
| chr8:21717907
|
C | A | 1 | a0001c0006t0023g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.795-11866G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21717907 | ||||||
| chr8:21717929
|
A | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.795-11888T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21717929 | ||||||
| chr8:21718065
|
T | C | 3 | a0002c0021t0010g0225a0005c0012t0010g0198a0007c0024t0019g0062 | 3 | HG02647.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.795-12024A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718065 | ||||||
| chr8:21718114
|
A | G | 20 | a0001c0001t0004g0218a0001c0001t0005g0231a0001c0001t0006g0036others(17): Show | 20 | HG00621.hp1 HG02056.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-12073T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718114 | ||||||
| chr8:21718177
|
G | T | 34 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0009g0202others(31): Show | 34 | HG00621.hp1 HG02056.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.795-12136C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718177 | ||||||
| chr8:21718178
|
G | T | 34 | a0001c0001t0004g0218a0001c0001t0006g0036a0001c0001t0009g0202others(31): Show | 34 | HG00621.hp1 HG02056.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.795-12137C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718178 | ||||||
| chr8:21718217
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.795-12176A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718217 | ||||||
| chr8:21718310
|
C | T | 1 | a0001c0001t0011g0319 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.795-12269G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718310 | ||||||
| chr8:21718324
|
G | A | 1 | a0005c0012t0010g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.795-12283C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718324 | ||||||
| chr8:21718360
|
G | A | 45 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(42): Show | 45 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.795-12319C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718360 | ||||||
| chr8:21718399
|
G | A | 6 | a0001c0006t0023g0208a0002c0002t0003g0193a0002c0002t0003g0203others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.795-12358C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718399 | ||||||
| chr8:21718444
|
C | T | 321 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.795-12403G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718444 | ||||||
| chr8:21718611
|
A | C | 1 | a0002c0002t0010g0191 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.795-12570T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718611 | ||||||
| chr8:21718611
|
A | G | 2 | a0001c0001t0007g0063a0002c0002t0006g0065 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.795-12570T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718611 | ||||||
| chr8:21718637
|
C | T | 46 | a0001c0001t0005g0192a0001c0001t0005g0238a0001c0001t0005g0251others(43): Show | 46 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.795-12596G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718637 | ||||||
| chr8:21718688
|
C | A | 1 | a0001c0001t0005g0241 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.795-12647G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718688 | ||||||
| chr8:21718897
|
C | G | 33 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0001g0127others(30): Show | 33 | HG00621.hp1 HG00642.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.795-12856G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718897 | ||||||
| chr8:21718968
|
T | C | 13 | a0001c0001t0001g0117a0001c0004t0004g0258a0001c0004t0018g0116others(10): Show | 13 | HG00735.hp2 HG01433.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.795-12927A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21718968 | ||||||
| chr8:21719010
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0090others(7): Show | 10 | HG00733.hp2 HG01081.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.795-12969G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719010 | ||||||
| chr8:21719022
|
C | A | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.795-12981G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719022 | ||||||
| chr8:21719057
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.795-13016G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719057 | ||||||
| chr8:21719214
|
C | T | 1 | a0002c0002t0044g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.795-13173G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719214 | ||||||
| chr8:21719267
|
C | T | 37 | a0001c0001t0003g0226a0001c0001t0005g0192a0001c0001t0005g0238others(34): Show | 37 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.795-13226G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719267 | ||||||
| chr8:21719456
|
A | AAT | 63 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0099others(60): Show | 63 | HG00597.hp2 HG00642.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.795-13417_795-1341 others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719456 | ||||||
| chr8:21719467
|
T | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0114a0001c0001t0031g0121others(11): Show | 14 | HG00597.hp2 HG01081.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.795-13426A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719467 | ||||||
| chr8:21719479
|
T | C | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-13438A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719479 | ||||||
| chr8:21719531
|
G | A | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-13490C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719531 | ||||||
| chr8:21719671
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.795-13630C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719671 | ||||||
| chr8:21719673
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.795-13632A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719673 | ||||||
| chr8:21719894
|
G | A | 2 | a0001c0025t0029g0071a0005c0012t0010g0194 | 2 | HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.795-13853C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21719894 | ||||||
| chr8:21720009
|
A | T | 19 | a0001c0001t0004g0218a0001c0001t0034g0104a0001c0004t0004g0257others(16): Show | 19 | HG00597.hp1 HG00621.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.795-13968T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720009 | ||||||
| chr8:21720061
|
C | T | 11 | a0001c0001t0004g0218a0001c0004t0004g0257a0001c0004t0004g0258others(8): Show | 11 | HG00597.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.795-14020G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720061 | ||||||
| chr8:21720114
|
T | C | 2 | a0001c0006t0009g0304a0002c0002t0010g0191 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.795-14073A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720114 | ||||||
| chr8:21720118
|
G | T | 1 | a0007c0024t0019g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.795-14077C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720118 | ||||||
| chr8:21720137
|
A | T | 11 | a0001c0001t0004g0218a0001c0004t0004g0257a0001c0004t0004g0258others(8): Show | 11 | HG00597.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.795-14096T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720137 | ||||||
| chr8:21720155
|
A | AT | 258 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.795-14115dupA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720155 | ||||||
| chr8:21720260
|
G | C | 5 | a0001c0006t0009g0304a0002c0002t0002g0019a0002c0002t0002g0066others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-14219C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720260 | ||||||
| chr8:21720277
|
C | T | 17 | a0001c0001t0006g0036a0001c0001t0007g0063a0001c0001t0008g0252others(14): Show | 17 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.795-14236G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720277 | ||||||
| chr8:21720330
|
G | C | 1 | a0002c0002t0044g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.795-14289C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720330 | ||||||
| chr8:21720550
|
C | T | 18 | a0001c0001t0006g0036a0001c0001t0007g0063a0001c0001t0008g0252others(15): Show | 18 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.795-14509G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720550 | ||||||
| chr8:21720642
|
G | C | 1 | a0002c0002t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.795-14601C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720642 | ||||||
| chr8:21720684
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.795-14643C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720684 | ||||||
| chr8:21720745
|
C | G | 12 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(9): Show | 12 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.795-14704G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720745 | ||||||
| chr8:21720749
|
T | A | 1 | a0001c0001t0030g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.795-14708A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720749 | ||||||
| chr8:21720771
|
A | T | 1 | a0005c0014t0003g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.795-14730T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720771 | ||||||
| chr8:21720826
|
C | G | 2 | a0002c0002t0002g0019a0002c0002t0002g0066 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.795-14785G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720826 | ||||||
| chr8:21720846
|
T | G | 1 | a0001c0004t0013g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.795-14805A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720846 | ||||||
| chr8:21720875
|
T | C | 258 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.795-14834A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720875 | ||||||
| chr8:21720886
|
A | G | 57 | a0001c0001t0003g0226a0001c0001t0005g0238a0001c0001t0005g0251others(54): Show | 57 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.795-14845T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720886 | ||||||
| chr8:21720892
|
G | C | 1 | a0002c0005t0045g0311 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.795-14851C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720892 | ||||||
| chr8:21720983
|
G | A | 2 | a0001c0001t0008g0252a0001c0020t0005g0186 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.795-14942C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21720983 | ||||||
| chr8:21721001
|
A | G | 55 | a0001c0001t0003g0226a0001c0001t0005g0238a0001c0001t0005g0251others(52): Show | 55 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.795-14960T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721001 | ||||||
| chr8:21721037
|
G | A | 1 | a0001c0001t0007g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.795-14996C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721037 | ||||||
| chr8:21721105
|
C | T | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.795-15064G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721105 | ||||||
| chr8:21721150
|
A | G | 3 | a0001c0006t0023g0234a0002c0021t0010g0225a0005c0012t0010g0198 | 3 | HG02647.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.795-15109T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721150 | ||||||
| chr8:21721181
|
C | T | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.795-15140G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721181 | ||||||
| chr8:21721255
|
C | T | 1 | a0001c0003t0001g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.795-15214G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721255 | ||||||
| chr8:21721264
|
C | T | 2 | a0001c0025t0029g0071a0005c0012t0010g0194 | 2 | HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.795-15223G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721264 | ||||||
| chr8:21721282
|
C | T | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-15241G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721282 | ||||||
| chr8:21721413
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.795-15372A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721413 | ||||||
| chr8:21721443
|
C | T | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-15402G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721443 | ||||||
| chr8:21721519
|
G | A | 2 | a0002c0002t0002g0019a0002c0002t0002g0066 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.795-15478C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721519 | ||||||
| chr8:21721652
|
C | T | 35 | a0001c0001t0003g0226a0001c0001t0005g0238a0001c0001t0005g0251others(32): Show | 35 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.795-15611G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721652 | ||||||
| chr8:21721711
|
A | G | 3 | a0001c0006t0023g0234a0002c0021t0010g0225a0005c0012t0010g0198 | 3 | HG02647.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.795-15670T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21721711 | ||||||
| chr8:21722006
|
T | C | 1 | a0002c0016t0006g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.795-15965A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722006 | ||||||
| chr8:21722498
|
G | A | 222 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.795-16457C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722498 | ||||||
| chr8:21722661
|
C | T | 19 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0127others(16): Show | 19 | HG00642.hp1 HG01175.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.795-16620G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722661 | ||||||
| chr8:21722664
|
T | A | 35 | a0001c0001t0003g0226a0001c0001t0005g0238a0001c0001t0005g0251others(32): Show | 35 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.795-16623A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722664 | ||||||
| chr8:21722668
|
C | T | 1 | a0002c0005t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.795-16627G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722668 | ||||||
| chr8:21722670
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.795-16629G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722670 | ||||||
| chr8:21722770
|
A | G | 2 | a0002c0021t0010g0225a0005c0012t0010g0198 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.795-16729T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722770 | ||||||
| chr8:21722953
|
T | C | 6 | a0001c0001t0001g0117a0002c0002t0003g0275a0002c0002t0003g0286others(3): Show | 6 | NA18942.hp1 NA18944.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.795-16912A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21722953 | ||||||
| chr8:21723057
|
G | T | 1 | a0001c0006t0002g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.795-17016C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723057 | ||||||
| chr8:21723103
|
G | T | 3 | a0001c0004t0009g0228a0001c0004t0009g0235a0004c0011t0009g0195 | 3 | HG00639.hp2 HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.795-17062C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723103 | ||||||
| chr8:21723118
|
C | T | 4 | a0002c0002t0015g0004a0002c0002t0015g0006a0002c0002t0015g0007others(1): Show | 4 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-17077G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723118 | ||||||
| chr8:21723152
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0004g0217 | 2 | HG00544.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.795-17111G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723152 | ||||||
| chr8:21723303
|
T | C | 5 | a0001c0006t0009g0304a0002c0002t0002g0019a0002c0002t0002g0066others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-17262A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723303 | ||||||
| chr8:21723580
|
G | C | 273 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.795-17539C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723580 | ||||||
| chr8:21723610
|
C | T | 5 | a0001c0006t0009g0304a0002c0002t0002g0019a0002c0002t0002g0066others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-17569G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723610 | ||||||
| chr8:21723639
|
G | A | 21 | a0001c0001t0004g0296a0001c0001t0005g0192a0001c0001t0005g0306others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.795-17598C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723639 | ||||||
| chr8:21723666
|
G | C | 273 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.795-17625C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723666 | ||||||
| chr8:21723669
|
G | A | 34 | a0001c0001t0003g0226a0001c0001t0005g0238a0001c0001t0005g0251others(31): Show | 34 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.795-17628C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723669 | ||||||
| chr8:21723708
|
T | C | 104 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0127others(101): Show | 104 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.795-17667A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723708 | ||||||
| chr8:21723741
|
C | T | 10 | a0001c0001t0004g0218a0001c0004t0004g0257a0001c0004t0004g0258others(7): Show | 10 | HG00597.hp1 HG00621.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.795-17700G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723741 | ||||||
| chr8:21723744
|
G | C | 1 | a0007c0024t0019g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.795-17703C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723744 | ||||||
| chr8:21723846
|
C | T | 1 | a0001c0001t0006g0158 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.795-17805G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723846 | ||||||
| chr8:21723901
|
C | A | 24 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0127others(21): Show | 24 | HG00642.hp1 HG01175.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.795-17860G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723901 | ||||||
| chr8:21723960
|
A | G | 6 | a0001c0001t0008g0252a0001c0006t0009g0304a0002c0002t0002g0019others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-17919T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723960 | ||||||
| chr8:21723962
|
C | A | 1 | a0002c0002t0003g0280 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.795-17921G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21723962 | ||||||
| chr8:21724076
|
C | T | 1 | a0001c0003t0001g0014 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.795-18035G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724076 | ||||||
| chr8:21724229
|
T | G | 65 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0127others(62): Show | 65 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.795-18188A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724229 | ||||||
| chr8:21724341
|
C | T | 19 | a0001c0001t0004g0296a0001c0001t0005g0192a0001c0001t0005g0306others(16): Show | 19 | HG00323.hp1 HG00642.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.795-18300G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724341 | ||||||
| chr8:21724464
|
G | A | 21 | a0001c0001t0004g0296a0001c0001t0005g0192a0001c0001t0005g0306others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.795-18423C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724464 | ||||||
| chr8:21724564
|
C | T | 1 | a0007c0024t0019g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.795-18523G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724564 | ||||||
| chr8:21724614
|
G | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.795-18573C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724614 | ||||||
| chr8:21724714
|
C | T | 14 | a0001c0006t0009g0304a0001c0006t0023g0208a0002c0002t0002g0030others(11): Show | 14 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.795-18673G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724714 | ||||||
| chr8:21724743
|
C | T | 12 | a0001c0006t0023g0208a0002c0002t0002g0030a0002c0002t0002g0032others(9): Show | 12 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.795-18702G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724743 | ||||||
| chr8:21724779
|
T | C | 110 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0114others(107): Show | 110 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.795-18738A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21724779 | ||||||
| chr8:21725130
|
A | T | 1 | a0001c0001t0007g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.795-19089T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725130 | ||||||
| chr8:21725190
|
A | T | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.795-19149T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725190 | ||||||
| chr8:21725286
|
A | T | 1 | a0001c0010t0004g0292 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.795-19245T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725286 | ||||||
| chr8:21725304
|
C | T | 2 | a0002c0016t0006g0017a0005c0014t0006g0083 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.795-19263G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725304 | ||||||
| chr8:21725365
|
C | G | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.795-19324G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725365 | ||||||
| chr8:21725409
|
G | A | 19 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0127others(16): Show | 19 | HG00642.hp1 HG01169.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.795-19368C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725409 | ||||||
| chr8:21725414
|
G | C | 2 | a0001c0006t0009g0304a0002c0002t0010g0191 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.795-19373C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725414 | ||||||
| chr8:21725435
|
C | T | 23 | a0001c0001t0004g0296a0001c0001t0005g0192a0001c0001t0005g0306others(20): Show | 23 | HG00323.hp1 HG00642.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.795-19394G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725435 | ||||||
| chr8:21725538
|
T | A | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.795-19497A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725538 | ||||||
| chr8:21725587
|
T | C | 8 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-19546A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725587 | ||||||
| chr8:21725666
|
G | A | 1 | a0001c0006t0023g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.795-19625C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725666 | ||||||
| chr8:21725905
|
C | T | 1 | a0001c0001t0007g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.795-19864G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725905 | ||||||
| chr8:21725967
|
C | G | 9 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(6): Show | 9 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-19926G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725967 | ||||||
| chr8:21725975
|
T | C | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-19934A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21725975 | ||||||
| chr8:21726289
|
T | C | 1 | a0001c0006t0023g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.795-20248A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726289 | ||||||
| chr8:21726415
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.795-20374C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726415 | ||||||
| chr8:21726514
|
G | T | 65 | a0001c0001t0001g0114a0001c0001t0003g0226a0001c0001t0004g0296others(62): Show | 65 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.795-20473C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726514 | ||||||
| chr8:21726581
|
G | A | 258 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.795-20540C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726581 | ||||||
| chr8:21726735
|
A | G | 2 | a0001c0001t0020g0307a0002c0002t0010g0185 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.795-20694T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726735 | ||||||
| chr8:21726750
|
A | AT | 8 | a0001c0001t0001g0080a0001c0001t0001g0143a0001c0001t0007g0063others(5): Show | 8 | HG00544.hp2 HG02559.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.795-20710dupA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726750 | ||||||
| chr8:21726750
|
AT | A | 80 | a0001c0001t0004g0218a0001c0001t0004g0296a0001c0001t0005g0238others(77): Show | 80 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.795-20710delA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726750 | ||||||
| chr8:21726750
|
ATT | A | 6 | a0001c0001t0001g0114a0001c0001t0003g0226a0001c0001t0007g0005others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-20711_795-2071 others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726750 | ||||||
| chr8:21726794
|
C | T | 1 | a0002c0002t0044g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.795-20753G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726794 | ||||||
| chr8:21726898
|
G | A | 2 | a0002c0016t0006g0017a0005c0014t0006g0083 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.795-20857C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726898 | ||||||
| chr8:21726900
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0025g0001 | 2 | HG01433.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.795-20859C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21726900 | ||||||
| chr8:21727111
|
G | A | 25 | a0001c0001t0004g0296a0001c0001t0005g0192a0001c0001t0005g0306others(22): Show | 25 | HG00323.hp1 HG00642.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.795-21070C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727111 | ||||||
| chr8:21727291
|
T | C | 11 | a0001c0001t0004g0218a0001c0004t0004g0257a0001c0004t0004g0258others(8): Show | 11 | HG00597.hp1 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.795-21250A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727291 | ||||||
| chr8:21727465
|
C | T | 3 | a0001c0001t0006g0036a0001c0001t0009g0202a0001c0025t0029g0071 | 3 | HG02451.hp1 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.795-21424G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727465 | ||||||
| chr8:21727512
|
C | T | 1 | a0002c0007t0002g0022 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.795-21471G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727512 | ||||||
| chr8:21727536
|
C | T | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795-21495G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727536 | ||||||
| chr8:21727548
|
G | A | 42 | a0001c0001t0001g0114a0001c0001t0003g0226a0001c0001t0005g0238others(39): Show | 42 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.795-21507C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727548 | ||||||
| chr8:21727549
|
G | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.795-21508C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727549 | ||||||
| chr8:21727552
|
A | G | 321 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.795-21511T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727552 | ||||||
| chr8:21727621
|
T | C | 1 | a0002c0002t0002g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.795-21580A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727621 | ||||||
| chr8:21727628
|
G | A | 1 | a0001c0006t0023g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.795-21587C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727628 | ||||||
| chr8:21727769
|
C | A | 2 | a0001c0006t0009g0304a0002c0002t0010g0191 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.795-21728G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727769 | ||||||
| chr8:21727805
|
A | G | 1 | a0001c0001t0004g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.795-21764T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727805 | ||||||
| chr8:21727806
|
C | T | 23 | a0001c0001t0004g0296a0001c0001t0005g0192a0001c0001t0005g0306others(20): Show | 23 | HG00323.hp1 HG00642.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.795-21765G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727806 | ||||||
| chr8:21727872
|
T | A | 23 | a0001c0001t0004g0296a0001c0001t0005g0192a0001c0001t0005g0306others(20): Show | 23 | HG00323.hp1 HG00642.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.795-21831A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727872 | ||||||
| chr8:21727893
|
A | T | 1 | a0002c0007t0002g0022 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.795-21852T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21727893 | ||||||
| chr8:21728002
|
G | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.795-21961C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728002 | ||||||
| chr8:21728124
|
G | C | 3 | a0001c0001t0008g0285a0002c0002t0002g0144a0002c0002t0003g0259 | 3 | HG02155.hp2 HG02735.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.795-22083C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728124 | ||||||
| chr8:21728209
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0149a0001c0001t0035g0113others(2): Show | 5 | HG01175.hp2 HG01433.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.795-22168G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728209 | ||||||
| chr8:21728265
|
G | GT | 146 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.795-22225dupA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728265 | ||||||
| chr8:21728265
|
G | GTT | 53 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0080others(50): Show | 53 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.795-22226_795-2222 others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728265 | ||||||
| chr8:21728265
|
G | GTTT | 9 | a0001c0001t0005g0264a0001c0001t0006g0027a0001c0001t0020g0307others(6): Show | 9 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.795-22227_795-2222 others(7): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728265 | ||||||
| chr8:21728265
|
GT | G | 32 | a0001c0001t0001g0176a0001c0001t0004g0214a0001c0001t0004g0222others(29): Show | 32 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.795-22225delA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728265 | ||||||
| chr8:21728343
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.794+22245A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728343 | ||||||
| chr8:21728350
|
C | T | 12 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(9): Show | 12 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+22238G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728350 | ||||||
| chr8:21728415
|
C | T | 1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.794+22173G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728415 | ||||||
| chr8:21728436
|
G | A | 2 | a0001c0006t0009g0304a0002c0002t0010g0191 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.794+22152C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728436 | ||||||
| chr8:21728662
|
C | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.794+21926G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728662 | ||||||
| chr8:21728706
|
C | T | 1 | a0001c0001t0036g0155 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.794+21882G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728706 | ||||||
| chr8:21728862
|
C | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.794+21726G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728862 | ||||||
| chr8:21728915
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.794+21673C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728915 | ||||||
| chr8:21728967
|
G | T | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.794+21621C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21728967 | ||||||
| chr8:21729014
|
C | T | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.794+21574G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729014 | ||||||
| chr8:21729046
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.794+21542C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729046 | ||||||
| chr8:21729222
|
C | T | 1 | a0002c0002t0044g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.794+21366G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729222 | ||||||
| chr8:21729278
|
C | G | 1 | a0001c0020t0005g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.794+21310G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729278 | ||||||
| chr8:21729466
|
G | T | 2 | a0002c0002t0002g0129a0002c0002t0002g0130 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.794+21122C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729466 | ||||||
| chr8:21729516
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.794+21072C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729516 | ||||||
| chr8:21729595
|
C | T | 6 | a0001c0001t0004g0296a0001c0001t0007g0063a0001c0001t0036g0155others(3): Show | 6 | HG00323.hp1 HG02486.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.794+20993G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729595 | ||||||
| chr8:21729649
|
G | A | 1 | a0002c0002t0003g0266 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.794+20939C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729649 | ||||||
| chr8:21729687
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0136 | 2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.794+20901G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729687 | ||||||
| chr8:21729761
|
C | A | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.794+20827G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729761 | ||||||
| chr8:21729851
|
C | T | 1 | a0007c0024t0019g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.794+20737G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21729851 | ||||||
| chr8:21730027
|
G | C | 78 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0091others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.794+20561C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730027 | ||||||
| chr8:21730054
|
C | G | 2 | a0001c0006t0009g0304a0002c0002t0010g0191 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.794+20534G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730054 | ||||||
| chr8:21730082
|
G | C | 1 | a0005c0013t0010g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.794+20506C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730082 | ||||||
| chr8:21730236
|
C | G | 5 | a0001c0004t0013g0232a0002c0002t0003g0236a0002c0002t0015g0004others(2): Show | 5 | HG02818.hp2 HG03486.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.794+20352G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730236 | ||||||
| chr8:21730242
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.794+20346A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730242 | ||||||
| chr8:21730250
|
C | A | 2 | a0002c0016t0006g0017a0005c0014t0006g0083 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.794+20338G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730250 | ||||||
| chr8:21730251
|
G | A | 4 | a0001c0006t0009g0304a0001c0025t0029g0071a0002c0002t0010g0191others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+20337C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730251 | ||||||
| chr8:21730328
|
G | A | 10 | a0001c0001t0004g0300a0001c0001t0013g0240a0001c0001t0019g0070others(7): Show | 10 | HG01496.hp2 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.794+20260C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730328 | ||||||
| chr8:21730403
|
CA | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.794+20184delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730403 | ||||||
| chr8:21730485
|
A | C | 200 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(197): Show | 200 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.794+20103T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730485 | ||||||
| chr8:21730492
|
G | A | 1 | a0001c0010t0004g0292 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.794+20096C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730492 | ||||||
| chr8:21730519
|
G | A | 1 | a0001c0001t0004g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.794+20069C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730519 | ||||||
| chr8:21730669
|
A | C | 1 | a0002c0002t0003g0282 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.794+19919T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730669 | ||||||
| chr8:21730820
|
T | G | 3 | a0002c0002t0003g0181a0002c0016t0006g0017a0005c0014t0006g0083 | 3 | HG02055.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.794+19768A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730820 | ||||||
| chr8:21730970
|
A | G | 4 | a0001c0001t0007g0067a0001c0006t0002g0028a0001c0006t0023g0208others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+19618T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21730970 | ||||||
| chr8:21731013
|
C | G | 3 | a0001c0006t0009g0304a0002c0002t0010g0191a0002c0002t0037g0204 | 3 | HG02109.hp1 HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.794+19575G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731013 | ||||||
| chr8:21731027
|
A | G | 1 | a0001c0001t0036g0155 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.794+19561T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731027 | ||||||
| chr8:21731040
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794+19548C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731040 | ||||||
| chr8:21731042
|
G | A | 192 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(189): Show | 192 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(189): Show |
intron_variant | MODIFIER | c.794+19546C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731042 | ||||||
| chr8:21731069
|
C | T | 3 | a0002c0002t0003g0181a0002c0016t0006g0017a0005c0014t0006g0083 | 3 | HG02055.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.794+19519G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731069 | ||||||
| chr8:21731107
|
C | T | 4 | a0001c0001t0007g0067a0001c0006t0002g0028a0001c0006t0023g0208others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+19481G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731107 | ||||||
| chr8:21731140
|
C | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(36): Show | 39 | HG00323.hp1 HG00735.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.794+19448G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731140 | ||||||
| chr8:21731162
|
G | A | 29 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0126others(26): Show | 29 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.794+19426C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731162 | ||||||
| chr8:21731163
|
T | C | 67 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(64): Show | 67 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.794+19425A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731163 | ||||||
| chr8:21731191
|
C | G | 195 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(192): Show | 195 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(192): Show |
intron_variant | MODIFIER | c.794+19397G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731191 | ||||||
| chr8:21731198
|
G | C | 7 | a0001c0001t0005g0238a0001c0001t0009g0202a0001c0001t0020g0307others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+19390C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731198 | ||||||
| chr8:21731355
|
G | A | 29 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0126others(26): Show | 29 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.794+19233C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731355 | ||||||
| chr8:21731450
|
T | C | 74 | a0001c0001t0001g0090a0001c0001t0001g0097a0001c0001t0001g0114others(71): Show | 74 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.794+19138A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731450 | ||||||
| chr8:21731548
|
C | A | 1 | a0002c0002t0003g0282 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.794+19040G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731548 | ||||||
| chr8:21731609
|
A | T | 2 | a0001c0001t0007g0075a0001c0006t0007g0033 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.794+18979T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731609 | ||||||
| chr8:21731664
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.794+18924A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731664 | ||||||
| chr8:21731666
|
C | T | 1 | a0002c0005t0047g0313 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.794+18922G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731666 | ||||||
| chr8:21731862
|
T | C | 3 | a0001c0006t0009g0304a0002c0002t0010g0191a0002c0002t0037g0204 | 3 | HG02109.hp1 HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.794+18726A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731862 | ||||||
| chr8:21731867
|
G | T | 15 | a0001c0001t0005g0306a0001c0001t0006g0018a0001c0001t0006g0027others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.794+18721C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731867 | ||||||
| chr8:21731897
|
T | C | 3 | a0002c0002t0003g0181a0002c0016t0006g0017a0005c0014t0006g0083 | 3 | HG02055.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.794+18691A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21731897 | ||||||
| chr8:21732035
|
T | C | 9 | a0001c0001t0001g0108a0001c0001t0001g0154a0001c0001t0005g0254others(6): Show | 9 | HG00438.hp1 HG00438.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+18553A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732035 | ||||||
| chr8:21732045
|
G | A | 110 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0090others(107): Show | 110 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.794+18543C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732045 | ||||||
| chr8:21732047
|
C | T | 1 | a0001c0001t0005g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.794+18541G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732047 | ||||||
| chr8:21732063
|
C | T | 1 | a0001c0003t0001g0043 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.794+18525G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732063 | ||||||
| chr8:21732070
|
C | T | 9 | a0001c0001t0013g0240a0001c0001t0019g0070a0001c0001t0020g0309others(6): Show | 9 | HG01891.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.794+18518G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732070 | ||||||
| chr8:21732216
|
G | T | 1 | a0001c0001t0042g0268 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.794+18372C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732216 | ||||||
| chr8:21732700
|
C | T | 1 | a0001c0001t0005g0192 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.794+17888G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732700 | ||||||
| chr8:21732837
|
G | A | 1 | a0001c0023t0018g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.794+17751C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21732837 | ||||||
| chr8:21733178
|
A | G | 7 | a0001c0001t0006g0074a0002c0002t0002g0128a0002c0002t0003g0181others(4): Show | 7 | HG00642.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+17410T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733178 | ||||||
| chr8:21733194
|
C | T | 37 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(34): Show | 37 | HG00323.hp1 HG00735.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.794+17394G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733194 | ||||||
| chr8:21733398
|
A | G | 1 | a0001c0001t0007g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.794+17190T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733398 | ||||||
| chr8:21733417
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.794+17171G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733417 | ||||||
| chr8:21733463
|
C | A | 2 | a0001c0001t0007g0075a0001c0006t0007g0033 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.794+17125G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733463 | ||||||
| chr8:21733558
|
G | T | 3 | a0002c0002t0003g0181a0002c0016t0006g0017a0005c0014t0006g0083 | 3 | HG02055.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.794+17030C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733558 | ||||||
| chr8:21733611
|
C | T | 1 | a0001c0001t0007g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.794+16977G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733611 | ||||||
| chr8:21733790
|
G | A | 2 | a0002c0002t0002g0037a0002c0007t0002g0165 | 2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.794+16798C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733790 | ||||||
| chr8:21733839
|
C | G | 3 | a0001c0001t0004g0267a0002c0002t0002g0125a0002c0002t0002g0133 | 3 | HG00099.hp1 HG02004.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.794+16749G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733839 | ||||||
| chr8:21733951
|
C | T | 242 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.794+16637G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21733951 | ||||||
| chr8:21734013
|
C | A | 4 | a0001c0001t0006g0036a0001c0006t0016g0069a0002c0002t0002g0019others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+16575G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734013 | ||||||
| chr8:21734203
|
G | A | 1 | a0002c0002t0003g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.794+16385C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734203 | ||||||
| chr8:21734500
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0154others(9): Show | 12 | HG00099.hp1 HG00438.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+16088A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734500 | ||||||
| chr8:21734533
|
AT | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(36): Show | 39 | HG00323.hp1 HG00735.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.794+16054delA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734533 | ||||||
| chr8:21734554
|
T | A | 1 | a0001c0001t0004g0221 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.794+16034A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734554 | ||||||
| chr8:21734655
|
G | A | 8 | a0001c0001t0005g0238a0001c0001t0009g0202a0001c0001t0020g0307others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.794+15933C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734655 | ||||||
| chr8:21734683
|
G | A | 49 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(46): Show | 49 | HG00323.hp1 HG00735.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.794+15905C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734683 | ||||||
| chr8:21734774
|
C | A | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.794+15814G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21734774 | ||||||
| chr8:21735009
|
C | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.794+15579G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735009 | ||||||
| chr8:21735080
|
A | G | 36 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(33): Show | 36 | HG00323.hp1 HG00735.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.794+15508T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735080 | ||||||
| chr8:21735144
|
C | A | 1 | a0002c0002t0002g0147 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.794+15444G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735144 | ||||||
| chr8:21735153
|
G | A | 1 | a0002c0005t0002g0046 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.794+15435C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735153 | ||||||
| chr8:21735199
|
G | A | 24 | a0001c0001t0005g0192a0001c0001t0005g0306a0001c0001t0006g0018others(21): Show | 24 | HG00738.hp2 HG01099.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.794+15389C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735199 | ||||||
| chr8:21735221
|
G | C | 1 | a0001c0004t0009g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.794+15367C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735221 | ||||||
| chr8:21735249
|
A | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.794+15339T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735249 | ||||||
| chr8:21735307
|
C | T | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.794+15281G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735307 | ||||||
| chr8:21735325
|
T | C | 30 | a0001c0001t0005g0192a0001c0001t0005g0306a0001c0001t0006g0018others(27): Show | 30 | HG00738.hp2 HG01099.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.794+15263A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735325 | ||||||
| chr8:21735374
|
C | G | 2 | a0001c0006t0009g0304a0002c0002t0010g0191 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.794+15214G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735374 | ||||||
| chr8:21735377
|
C | A | 1 | a0001c0001t0006g0018 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.794+15211G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735377 | ||||||
| chr8:21735406
|
T | C | 1 | a0001c0003t0001g0166 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.794+15182A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735406 | ||||||
| chr8:21735517
|
G | A | 1 | a0001c0001t0006g0146 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.794+15071C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735517 | ||||||
| chr8:21735560
|
G | GTC | 35 | a0001c0001t0005g0238a0001c0001t0005g0251a0001c0001t0007g0075others(32): Show | 35 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.794+15027_794+1502 others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735560 | ||||||
| chr8:21735563
|
GTCTC | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0002c0002t0028g0105 | 3 | HG02132.hp1 HG02165.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.794+15021_794+1502 others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735563 | ||||||
| chr8:21735636
|
C | G | 42 | a0001c0001t0001g0003a0001c0001t0005g0192a0001c0001t0005g0306others(39): Show | 42 | HG00738.hp2 HG01099.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.794+14952G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735636 | ||||||
| chr8:21735645
|
C | G | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.794+14943G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735645 | ||||||
| chr8:21735687
|
G | A | 1 | a0001c0001t0004g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.794+14901C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735687 | ||||||
| chr8:21735724
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0023others(67): Show | 70 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.794+14864C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735724 | ||||||
| chr8:21735830
|
A | C | 33 | a0001c0001t0005g0192a0001c0001t0005g0306a0001c0001t0006g0018others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.794+14758T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735830 | ||||||
| chr8:21735835
|
T | TA | 41 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(38): Show | 41 | HG00323.hp1 HG00735.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.794+14752dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735835 | ||||||
| chr8:21735835
|
TA | T | 12 | a0001c0001t0004g0263a0001c0001t0006g0074a0001c0001t0007g0075others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+14752delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735835 | ||||||
| chr8:21735858
|
G | A | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.794+14730C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735858 | ||||||
| chr8:21735887
|
G | T | 1 | a0002c0002t0003g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794+14701C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735887 | ||||||
| chr8:21735949
|
G | A | 3 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.794+14639C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21735949 | ||||||
| chr8:21736050
|
C | G | 40 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(37): Show | 40 | HG00323.hp1 HG00735.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.794+14538G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736050 | ||||||
| chr8:21736159
|
G | A | 1 | a0002c0005t0002g0057 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.794+14429C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736159 | ||||||
| chr8:21736355
|
A | T | 1 | a0001c0001t0005g0223 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.794+14233T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736355 | ||||||
| chr8:21736482
|
T | C | 6 | a0001c0004t0013g0230a0001c0004t0013g0232a0001c0022t0007g0020others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+14106A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736482 | ||||||
| chr8:21736608
|
A | G | 27 | a0001c0001t0005g0192a0001c0001t0005g0306a0001c0001t0006g0018others(24): Show | 27 | HG00738.hp2 HG01099.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.794+13980T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736608 | ||||||
| chr8:21736639
|
G | C | 69 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0097others(66): Show | 69 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.794+13949C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736639 | ||||||
| chr8:21736901
|
A | G | 1 | a0002c0002t0038g0265 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.794+13687T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736901 | ||||||
| chr8:21736904
|
A | G | 1 | a0002c0002t0038g0265 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.794+13684T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736904 | ||||||
| chr8:21736907
|
T | TGAGGGGA others(3): Show |
1 | a0002c0002t0002g0130 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794+13671_794+1368 others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736907 | ||||||
| chr8:21736909
|
A | AGGGGAGG others(4): Show |
1 | a0002c0002t0002g0129 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.794+13668_794+1367 others(15): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736909 | ||||||
| chr8:21736912
|
G | GGAGGGGA others(10): Show |
1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.794+13675_794+1367 others(21): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736912 | ||||||
| chr8:21736912
|
G | GGAGGGGA others(13): Show |
1 | a0002c0002t0003g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.794+13656_794+1367 others(24): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21736912 | ||||||
| chr8:21737051
|
A | C | 1 | a0002c0005t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.794+13537T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737051 | ||||||
| chr8:21737143
|
C | T | 5 | a0001c0001t0003g0226a0001c0001t0007g0005a0001c0001t0007g0073others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+13445G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737143 | ||||||
| chr8:21737173
|
A | G | 199 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(196): Show | 199 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.794+13415T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737173 | ||||||
| chr8:21737246
|
A | G | 89 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(86): Show | 89 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.794+13342T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737246 | ||||||
| chr8:21737368
|
C | CA | 51 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(48): Show | 51 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.794+13219dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737368 | ||||||
| chr8:21737368
|
CA | C | 8 | a0001c0001t0020g0309a0001c0006t0016g0026a0001c0006t0016g0031others(5): Show | 8 | HG02572.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.794+13219delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737368 | ||||||
| chr8:21737382
|
G | C | 3 | a0001c0006t0002g0028a0001c0006t0023g0208a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.794+13206C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737382 | ||||||
| chr8:21737541
|
T | A | 1 | a0002c0002t0050g0317 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.794+13047A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21737541 | ||||||
| chr8:21738017
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.794+12571G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738017 | ||||||
| chr8:21738054
|
CA | C | 15 | a0001c0001t0001g0011a0001c0001t0003g0226a0001c0001t0004g0217others(12): Show | 15 | HG00642.hp2 HG02004.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.794+12533delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738054 | ||||||
| chr8:21738169
|
C | A | 1 | a0002c0002t0003g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.794+12419G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738169 | ||||||
| chr8:21738178
|
CCGTTCCT others(6): Show |
C | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.794+12397_794+1240 others(17): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738178 | ||||||
| chr8:21738179
|
C | CT | 148 | a0001c0001t0001g0011a0001c0001t0001g0090a0001c0001t0001g0096others(145): Show | 148 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.794+12408_794+1240 others(5): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738179 | ||||||
| chr8:21738180
|
G | T | 45 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(42): Show | 45 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+12408C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738180 | ||||||
| chr8:21738181
|
T | G | 45 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(42): Show | 45 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+12407A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738181 | ||||||
| chr8:21738181
|
TTCCTCCT others(8): Show |
T | 1 | a0001c0003t0001g0170 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.794+12392_794+1240 others(19): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738181 | ||||||
| chr8:21738182
|
TCCTCCTC others(7): Show |
T | 45 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(42): Show | 45 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+12392_794+1240 others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738182 | ||||||
| chr8:21738194
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.794+12394G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738194 | ||||||
| chr8:21738195
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.794+12393G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738195 | ||||||
| chr8:21738196
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.794+12392G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738196 | ||||||
| chr8:21738205
|
C | T | 2 | a0002c0016t0006g0017a0005c0014t0006g0083 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.794+12383G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738205 | ||||||
| chr8:21738223
|
C | T | 46 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.794+12365G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738223 | ||||||
| chr8:21738312
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.794+12276G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738312 | ||||||
| chr8:21738329
|
C | G | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.794+12259G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738329 | ||||||
| chr8:21738368
|
C | T | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.794+12220G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738368 | ||||||
| chr8:21738369
|
A | C | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794+12219T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738369 | ||||||
| chr8:21738698
|
T | C | 4 | a0001c0001t0008g0252a0002c0016t0006g0017a0004c0009t0039g0188others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+11890A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738698 | ||||||
| chr8:21738778
|
G | A | 24 | a0001c0001t0005g0192a0001c0001t0005g0306a0001c0001t0006g0018others(21): Show | 24 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.794+11810C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738778 | ||||||
| chr8:21738788
|
G | A | 1 | a0001c0001t0006g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.794+11800C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738788 | ||||||
| chr8:21738806
|
A | G | 24 | a0001c0001t0005g0192a0001c0001t0005g0306a0001c0001t0006g0018others(21): Show | 24 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.794+11782T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738806 | ||||||
| chr8:21738846
|
A | C | 1 | a0001c0001t0001g0080 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.794+11742T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738846 | ||||||
| chr8:21738917
|
A | G | 46 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.794+11671T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738917 | ||||||
| chr8:21738955
|
G | A | 1 | a0001c0001t0006g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.794+11633C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738955 | ||||||
| chr8:21738980
|
C | T | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794+11608G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738980 | ||||||
| chr8:21738985
|
C | T | 4 | a0001c0001t0008g0252a0002c0016t0006g0017a0004c0009t0039g0188others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+11603G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21738985 | ||||||
| chr8:21739048
|
C | T | 1 | a0002c0002t0002g0156 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.794+11540G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739048 | ||||||
| chr8:21739076
|
G | A | 7 | a0001c0004t0013g0230a0001c0004t0013g0232a0001c0006t0009g0304others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+11512C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739076 | ||||||
| chr8:21739263
|
A | C | 3 | a0002c0002t0002g0128a0002c0002t0003g0279a0002c0002t0003g0299 | 3 | HG00642.hp2 HG02004.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.794+11325T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739263 | ||||||
| chr8:21739594
|
G | C | 35 | a0001c0001t0005g0231a0001c0001t0005g0238a0001c0001t0005g0251others(32): Show | 35 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.794+10994C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739594 | ||||||
| chr8:21739656
|
TC | T | 6 | a0001c0001t0005g0192a0001c0001t0006g0036a0002c0002t0015g0004others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+10931delG | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739656 | ||||||
| chr8:21739660
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.794+10928G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739660 | ||||||
| chr8:21739661
|
C | A | 39 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0097others(36): Show | 39 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.794+10927G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739661 | ||||||
| chr8:21739746
|
T | TC | 34 | a0001c0001t0005g0231a0001c0001t0005g0238a0001c0001t0005g0251others(31): Show | 34 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.794+10841dupG | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21739746 | ||||||
| chr8:21740006
|
A | G | 6 | a0001c0001t0005g0192a0001c0001t0006g0036a0002c0002t0015g0004others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+10582T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740006 | ||||||
| chr8:21740365
|
C | A | 8 | a0001c0001t0020g0309a0001c0006t0016g0026a0001c0006t0016g0031others(5): Show | 8 | HG02572.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.794+10223G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740365 | ||||||
| chr8:21740503
|
C | T | 5 | a0002c0007t0022g0211a0002c0007t0022g0227a0002c0017t0002g0047others(2): Show | 5 | NA18944.hp2 NA18949.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.794+10085G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740503 | ||||||
| chr8:21740512
|
C | T | 85 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0097others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.794+10076G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740512 | ||||||
| chr8:21740565
|
A | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(194): Show | 197 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.794+10023T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740565 | ||||||
| chr8:21740735
|
T | C | 6 | a0001c0001t0005g0192a0001c0001t0006g0036a0002c0002t0015g0004others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+9853A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740735 | ||||||
| chr8:21740858
|
C | A | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+9730G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740858 | ||||||
| chr8:21740868
|
T | C | 1 | a0001c0001t0005g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.794+9720A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21740868 | ||||||
| chr8:21741005
|
T | G | 7 | a0001c0001t0005g0192a0001c0001t0006g0036a0001c0006t0007g0033others(4): Show | 7 | HG02451.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+9583A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741005 | ||||||
| chr8:21741084
|
T | A | 16 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(13): Show | 16 | HG00438.hp1 HG01361.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+9504A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741084 | ||||||
| chr8:21741219
|
C | G | 8 | a0001c0001t0020g0309a0001c0006t0016g0026a0001c0006t0016g0031others(5): Show | 8 | HG02572.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.794+9369G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741219 | ||||||
| chr8:21741244
|
C | A | 2 | a0002c0002t0002g0030a0002c0002t0002g0032 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.794+9344G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741244 | ||||||
| chr8:21741307
|
C | T | 16 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(13): Show | 16 | HG00438.hp1 HG01361.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+9281G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741307 | ||||||
| chr8:21741334
|
T | C | 1 | a0002c0002t0010g0191 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.794+9254A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741334 | ||||||
| chr8:21741344
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0008g0285 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.794+9244G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741344 | ||||||
| chr8:21741389
|
G | C | 1 | a0001c0006t0009g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.794+9199C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741389 | ||||||
| chr8:21741414
|
T | C | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+9174A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741414 | ||||||
| chr8:21741530
|
C | T | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.794+9058G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741530 | ||||||
| chr8:21741653
|
C | T | 124 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0118others(121): Show | 124 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.794+8935G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741653 | ||||||
| chr8:21741666
|
G | C | 3 | a0001c0006t0016g0069a0002c0002t0002g0019a0002c0002t0002g0066 | 3 | HG01891.hp1 HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.794+8922C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741666 | ||||||
| chr8:21741725
|
C | T | 45 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(42): Show | 45 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+8863G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741725 | ||||||
| chr8:21741914
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.794+8674G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741914 | ||||||
| chr8:21741920
|
C | CA | 6 | a0001c0001t0001g0124a0001c0001t0006g0158a0001c0006t0007g0033others(3): Show | 6 | HG00323.hp2 HG02027.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+8667dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741920 | ||||||
| chr8:21741920
|
CA | C | 49 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0118others(46): Show | 49 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.794+8667delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741920 | ||||||
| chr8:21741928
|
A | AAAAG | 30 | a0001c0001t0005g0231a0001c0001t0005g0238a0001c0001t0005g0306others(27): Show | 30 | HG00738.hp2 HG01099.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.794+8659_794+8660i others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741928 | ||||||
| chr8:21741928
|
A | AAAAGAAA others(1): Show |
7 | a0001c0001t0005g0192a0001c0001t0036g0155a0002c0002t0003g0203others(4): Show | 7 | HG02055.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+8659_794+8660i others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741928 | ||||||
| chr8:21741932
|
A | G | 37 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(34): Show | 37 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.794+8656T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21741932 | ||||||
| chr8:21742035
|
G | A | 1 | a0001c0001t0005g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.794+8553C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742035 | ||||||
| chr8:21742160
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0004g0295a0002c0002t0003g0271 | 3 | HG01258.hp1 HG01496.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.794+8428A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742160 | ||||||
| chr8:21742265
|
C | T | 1 | a0001c0003t0001g0172 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.794+8323G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742265 | ||||||
| chr8:21742325
|
A | G | 1 | a0001c0001t0004g0277 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.794+8263T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742325 | ||||||
| chr8:21742489
|
A | T | 39 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(36): Show | 39 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.794+8099T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742489 | ||||||
| chr8:21742571
|
T | C | 1 | a0002c0002t0010g0191 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.794+8017A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742571 | ||||||
| chr8:21742691
|
C | T | 1 | a0002c0002t0002g0082 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.794+7897G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742691 | ||||||
| chr8:21742855
|
C | T | 1 | a0001c0003t0001g0014 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.794+7733G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742855 | ||||||
| chr8:21742957
|
T | C | 197 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(194): Show | 197 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.794+7631A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21742957 | ||||||
| chr8:21743036
|
A | G | 3 | a0001c0001t0006g0074a0004c0009t0005g0200a0004c0009t0013g0190 | 3 | HG02922.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794+7552T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743036 | ||||||
| chr8:21743143
|
C | T | 1 | a0001c0001t0007g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.794+7445G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743143 | ||||||
| chr8:21743187
|
T | C | 10 | a0001c0001t0007g0087a0001c0001t0019g0025a0001c0001t0036g0155others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.794+7401A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743187 | ||||||
| chr8:21743229
|
A | C | 1 | a0001c0001t0008g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.794+7359T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743229 | ||||||
| chr8:21743301
|
C | A | 1 | a0002c0005t0017g0167 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.794+7287G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743301 | ||||||
| chr8:21743335
|
C | T | 1 | a0001c0003t0001g0014 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.794+7253G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743335 | ||||||
| chr8:21743549
|
G | A | 54 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.794+7039C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743549 | ||||||
| chr8:21743588
|
C | T | 18 | a0001c0001t0005g0306a0001c0001t0006g0018a0001c0001t0006g0027others(15): Show | 18 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.794+7000G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743588 | ||||||
| chr8:21743660
|
C | T | 4 | a0002c0002t0015g0004a0002c0002t0015g0006a0002c0002t0015g0007others(1): Show | 4 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+6928G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743660 | ||||||
| chr8:21743761
|
G | A | 44 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(41): Show | 44 | HG00738.hp2 HG01099.hp1 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.794+6827C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743761 | ||||||
| chr8:21743800
|
C | A | 4 | a0001c0001t0008g0252a0002c0016t0006g0017a0004c0009t0039g0188others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+6788G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743800 | ||||||
| chr8:21743822
|
G | A | 2 | a0001c0001t0007g0063a0001c0001t0007g0067 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.794+6766C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743822 | ||||||
| chr8:21743945
|
T | C | 1 | a0001c0022t0007g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.794+6643A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743945 | ||||||
| chr8:21743969
|
G | T | 4 | a0001c0001t0007g0075a0001c0006t0016g0069a0002c0002t0002g0019others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+6619C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21743969 | ||||||
| chr8:21744016
|
C | T | 3 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.794+6572G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744016 | ||||||
| chr8:21744325
|
T | C | 29 | a0001c0004t0001g0159a0001c0004t0004g0249a0001c0004t0004g0257others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.794+6263A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744325 | ||||||
| chr8:21744360
|
C | T | 1 | a0002c0002t0015g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.794+6228G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744360 | ||||||
| chr8:21744397
|
G | T | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+6191C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744397 | ||||||
| chr8:21744486
|
G | C | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+6102C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744486 | ||||||
| chr8:21744550
|
A | AAC | 34 | a0001c0001t0001g0097a0001c0001t0001g0118a0001c0001t0005g0223others(31): Show | 34 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.794+6036_794+6037d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACAC | 13 | a0001c0001t0001g0011a0001c0001t0003g0226a0001c0001t0007g0005others(10): Show | 13 | HG02004.hp2 HG02083.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.794+6034_794+6037d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACAC | 29 | a0001c0001t0005g0251a0001c0004t0004g0257a0001c0004t0004g0258others(26): Show | 29 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.794+6032_794+6037d others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(1): Show |
16 | a0001c0001t0004g0217a0001c0001t0008g0252a0001c0004t0001g0159others(13): Show | 16 | HG01255.hp1 HG02055.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.794+6030_794+6037d others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(3): Show |
1 | a0001c0001t0006g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.794+6028_794+6037d others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(5): Show |
6 | a0001c0001t0005g0306a0001c0001t0006g0018a0002c0002t0002g0030others(3): Show | 6 | HG01099.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.794+6026_794+6037d others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(7): Show |
12 | a0001c0001t0006g0027a0001c0001t0006g0074a0001c0001t0019g0025others(9): Show | 12 | HG00621.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.794+6024_794+6037d others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(9): Show |
6 | a0001c0001t0006g0013a0001c0001t0036g0155a0001c0006t0002g0028others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.794+6022_794+6037d others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(11): Show |
8 | a0001c0001t0005g0231a0001c0001t0013g0240a0001c0001t0020g0307others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.794+6020_794+6037d others(20): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(13): Show |
5 | a0001c0001t0009g0202a0001c0001t0019g0070a0002c0002t0015g0004others(2): Show | 5 | HG02818.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+6018_794+6037d others(22): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(17): Show |
1 | a0001c0001t0005g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.794+6014_794+6037d others(26): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
A | AACACACA others(19): Show |
1 | a0001c0001t0005g0192 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.794+6012_794+6037d others(28): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
AAC | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0012others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.794+6036_794+6037d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
AACAC | A | 45 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(42): Show | 45 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+6034_794+6037d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744550
|
AACACACA others(11): Show |
A | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+6020_794+6037d others(20): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744550 | ||||||
| chr8:21744680
|
C | T | 58 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(55): Show | 58 | HG00438.hp1 HG00738.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.794+5908G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744680 | ||||||
| chr8:21744770
|
G | A | 4 | a0001c0001t0008g0252a0002c0016t0006g0017a0004c0009t0039g0188others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+5818C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744770 | ||||||
| chr8:21744817
|
C | A | 1 | a0001c0001t0006g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.794+5771G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21744817 | ||||||
| chr8:21745024
|
A | T | 2 | a0001c0001t0005g0251a0001c0006t0009g0304 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.794+5564T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745024 | ||||||
| chr8:21745152
|
G | A | 1 | a0001c0001t0007g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.794+5436C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745152 | ||||||
| chr8:21745166
|
A | G | 5 | a0001c0001t0007g0075a0001c0006t0007g0033a0001c0006t0016g0069others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+5422T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745166 | ||||||
| chr8:21745167
|
C | T | 3 | a0001c0001t0006g0074a0004c0009t0005g0200a0004c0009t0013g0190 | 3 | HG02922.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794+5421G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745167 | ||||||
| chr8:21745327
|
G | A | 40 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(37): Show | 40 | HG00738.hp2 HG01099.hp1 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.794+5261C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745327 | ||||||
| chr8:21745557
|
A | C | 1 | a0002c0002t0017g0107 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.794+5031T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745557 | ||||||
| chr8:21745577
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0008g0285 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.794+5011G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745577 | ||||||
| chr8:21745663
|
CTGCTCTC others(12): Show |
C | 1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.794+4906_794+4924d others(21): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745663 | ||||||
| chr8:21745731
|
C | A | 4 | a0001c0001t0008g0252a0002c0016t0006g0017a0004c0009t0039g0188others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+4857G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745731 | ||||||
| chr8:21745868
|
C | G | 1 | a0001c0003t0001g0171 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.794+4720G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745868 | ||||||
| chr8:21745882
|
T | A | 1 | a0002c0005t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.794+4706A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21745882 | ||||||
| chr8:21746026
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.794+4562C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746026 | ||||||
| chr8:21746178
|
G | A | 2 | a0001c0001t0008g0252a0004c0009t0039g0188 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.794+4410C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746178 | ||||||
| chr8:21746286
|
C | T | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+4302G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746286 | ||||||
| chr8:21746327
|
G | A | 1 | a0001c0020t0005g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.794+4261C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746327 | ||||||
| chr8:21746539
|
A | C | 1 | a0004c0015t0008g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.794+4049T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746539 | ||||||
| chr8:21746719
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.794+3869T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746719 | ||||||
| chr8:21746724
|
G | A | 1 | a0002c0002t0002g0089 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.794+3864C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746724 | ||||||
| chr8:21746782
|
C | G | 2 | a0001c0001t0041g0239a0002c0002t0002g0169 | 2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.794+3806G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746782 | ||||||
| chr8:21746796
|
C | CA | 15 | a0001c0001t0004g0213a0001c0001t0005g0251a0001c0001t0005g0284others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.794+3791dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746796 | ||||||
| chr8:21746857
|
G | A | 13 | a0001c0001t0005g0238a0001c0001t0006g0074a0001c0001t0009g0202others(10): Show | 13 | HG02280.hp1 HG02559.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.794+3731C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746857 | ||||||
| chr8:21746870
|
CA | C | 3 | a0001c0006t0002g0028a0001c0006t0023g0208a0004c0015t0008g0189 | 3 | HG02280.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.794+3717delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746870 | ||||||
| chr8:21746892
|
C | T | 4 | a0001c0004t0006g0010a0001c0020t0005g0186a0004c0011t0005g0197others(1): Show | 4 | HG00733.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+3696G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21746892 | ||||||
| chr8:21747063
|
C | G | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.794+3525G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747063 | ||||||
| chr8:21747104
|
T | C | 1 | a0002c0002t0002g0139 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.794+3484A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747104 | ||||||
| chr8:21747168
|
T | C | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.794+3420A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747168 | ||||||
| chr8:21747224
|
A | C | 52 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0097others(49): Show | 52 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.794+3364T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747224 | ||||||
| chr8:21747246
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+3342C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747246 | ||||||
| chr8:21747269
|
G | A | 3 | a0001c0001t0006g0074a0004c0009t0005g0200a0004c0009t0013g0190 | 3 | HG02922.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794+3319C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747269 | ||||||
| chr8:21747319
|
C | T | 1 | a0001c0001t0006g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.794+3269G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747319 | ||||||
| chr8:21747580
|
C | T | 10 | a0001c0001t0020g0309a0001c0006t0016g0026a0001c0006t0016g0031others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.794+3008G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747580 | ||||||
| chr8:21747642
|
A | G | 4 | a0001c0001t0008g0252a0002c0016t0006g0017a0004c0009t0039g0188others(1): Show | 4 | HG02055.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+2946T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747642 | ||||||
| chr8:21747697
|
A | G | 189 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(186): Show | 189 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(186): Show |
intron_variant | MODIFIER | c.794+2891T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747697 | ||||||
| chr8:21747754
|
CACCACAC others(3): Show |
C | 1 | a0002c0007t0022g0211 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.794+2824_794+2833d others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747754 | ||||||
| chr8:21747756
|
C | CCA | 63 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(60): Show | 63 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.794+2830_794+2831d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
C | CCACA | 19 | a0001c0001t0001g0108a0001c0001t0005g0238a0001c0001t0007g0112others(16): Show | 19 | HG00735.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.794+2828_794+2831d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
C | CCACACA | 10 | a0001c0001t0004g0270a0001c0001t0005g0306a0001c0001t0006g0018others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.794+2826_794+2831d others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
CCA | C | 92 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0024others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.794+2830_794+2831d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
CCACA | C | 4 | a0001c0001t0001g0060a0001c0001t0005g0251a0001c0003t0001g0053others(1): Show | 4 | HG01168.hp2 HG02622.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+2828_794+2831d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
CCACACA | C | 5 | a0001c0001t0001g0011a0001c0001t0013g0182a0001c0006t0023g0234others(2): Show | 5 | HG02683.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794+2826_794+2831d others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
CCACACAC others(1): Show |
C | 11 | a0001c0001t0001g0097a0001c0001t0007g0063a0001c0001t0007g0067others(8): Show | 11 | HG00639.hp2 HG02109.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.794+2824_794+2831d others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
CCACACAC others(3): Show |
C | 76 | a0001c0001t0001g0118a0001c0001t0003g0226a0001c0001t0004g0217others(73): Show | 76 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.794+2822_794+2831d others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747756
|
CCACACAC others(9): Show |
C | 4 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305others(1): Show | 4 | HG02965.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+2816_794+2831d others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747756 | ||||||
| chr8:21747801
|
C | T | 49 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0118others(46): Show | 49 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.794+2787G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747801 | ||||||
| chr8:21747958
|
C | T | 2 | a0001c0001t0005g0231a0001c0001t0006g0013 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.794+2630G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21747958 | ||||||
| chr8:21748007
|
C | T | 21 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(18): Show | 21 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.794+2581G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21748007 | ||||||
| chr8:21748196
|
A | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0004g0218others(1): Show | 4 | HG02056.hp1 HG02074.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+2392T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21748196 | ||||||
| chr8:21748426
|
CAG | C | 78 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(75): Show | 78 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.794+2160_794+2161d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21748426 | ||||||
| chr8:21748520
|
A | G | 1 | a0001c0001t0007g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.794+2068T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21748520 | ||||||
| chr8:21748822
|
G | A | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.794+1766C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21748822 | ||||||
| chr8:21748839
|
G | A | 1 | a0001c0001t0007g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.794+1749C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21748839 | ||||||
| chr8:21749000
|
A | T | 37 | a0001c0004t0001g0159a0001c0004t0004g0249a0001c0004t0004g0257others(34): Show | 37 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.794+1588T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749000 | ||||||
| chr8:21749049
|
C | T | 2 | a0001c0006t0007g0033a0002c0002t0010g0191 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.794+1539G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749049 | ||||||
| chr8:21749108
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.794+1480G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749108 | ||||||
| chr8:21749171
|
T | C | 95 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(92): Show | 95 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.794+1417A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749171 | ||||||
| chr8:21749204
|
G | A | 3 | a0001c0001t0005g0238a0001c0001t0013g0240a0001c0001t0019g0070 | 3 | HG02965.hp1 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.794+1384C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749204 | ||||||
| chr8:21749239
|
C | CA | 49 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0108others(46): Show | 49 | HG00438.hp1 HG00735.hp1 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.794+1348dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749239 | ||||||
| chr8:21749313
|
G | A | 4 | a0001c0001t0005g0238a0001c0001t0009g0202a0001c0001t0013g0240others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+1275C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749313 | ||||||
| chr8:21749331
|
G | A | 5 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0304others(2): Show | 5 | HG02109.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+1257C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749331 | ||||||
| chr8:21749403
|
G | A | 1 | a0002c0002t0006g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.794+1185C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749403 | ||||||
| chr8:21749494
|
GGACCCAT others(10): Show |
G | 2 | a0001c0001t0001g0016a0001c0001t0008g0285 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.794+1077_794+1093d others(19): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749494 | ||||||
| chr8:21749511
|
T | A | 1 | a0002c0002t0017g0107 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.794+1077A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749511 | ||||||
| chr8:21749655
|
G | C | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.794+933C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749655 | ||||||
| chr8:21749679
|
T | TTA | 44 | a0001c0001t0007g0075a0001c0001t0025g0001a0001c0004t0001g0159others(41): Show | 44 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.794+907_794+908dup others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749679 | ||||||
| chr8:21749716
|
T | A | 1 | a0001c0003t0001g0171 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.794+872A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749716 | ||||||
| chr8:21749719
|
G | A | 78 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(75): Show | 78 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.794+869C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749719 | ||||||
| chr8:21749757
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+831C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749757 | ||||||
| chr8:21749807
|
A | T | 6 | a0001c0001t0005g0192a0001c0001t0006g0036a0002c0002t0015g0004others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+781T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749807 | ||||||
| chr8:21749819
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+769C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749819 | ||||||
| chr8:21749844
|
A | G | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.794+744T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749844 | ||||||
| chr8:21749881
|
G | A | 6 | a0001c0001t0005g0192a0001c0001t0006g0036a0002c0002t0015g0004others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+707C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749881 | ||||||
| chr8:21749943
|
A | G | 1 | a0002c0002t0003g0282 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.794+645T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749943 | ||||||
| chr8:21749947
|
CA | C | 4 | a0001c0004t0004g0249a0001c0010t0004g0293a0001c0010t0004g0298others(1): Show | 4 | NA18957.hp1 NA18966.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+640delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749947 | ||||||
| chr8:21749967
|
A | G | 8 | a0001c0004t0013g0230a0001c0004t0013g0232a0001c0019t0020g0310others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.794+621T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21749967 | ||||||
| chr8:21750002
|
G | A | 2 | a0004c0009t0005g0200a0004c0009t0013g0190 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794+586C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750002 | ||||||
| chr8:21750071
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.794+517T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750071 | ||||||
| chr8:21750085
|
G | A | 119 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(116): Show | 119 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.794+503C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750085 | ||||||
| chr8:21750088
|
T | C | 120 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(117): Show | 120 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.794+500A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750088 | ||||||
| chr8:21750088
|
T | TAC | 14 | a0001c0001t0001g0118a0001c0001t0008g0252a0001c0004t0013g0230others(11): Show | 14 | HG01099.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.794+498_794+499dup others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750088 | ||||||
| chr8:21750107
|
A | ACACACAC others(15): Show |
12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.794+480_794+481ins others(22): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750107 | ||||||
| chr8:21750107
|
A | ACACACAC others(5): Show |
5 | a0001c0001t0005g0238a0001c0001t0006g0074a0001c0001t0009g0202others(2): Show | 5 | HG02922.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+480_794+481ins others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750107 | ||||||
| chr8:21750107
|
A | ACACACAC others(3): Show |
16 | a0001c0001t0001g0023a0001c0001t0005g0192a0001c0001t0006g0100others(13): Show | 16 | HG01258.hp2 HG01516.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+480_794+481ins others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750107 | ||||||
| chr8:21750107
|
A | ACACACAC others(1): Show |
55 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0099others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.794+480_794+481ins others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750107 | ||||||
| chr8:21750303
|
A | G | 2 | a0002c0016t0006g0017a0005c0014t0006g0083 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.794+285T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750303 | ||||||
| chr8:21750339
|
T | A | 85 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(82): Show | 85 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.794+249A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750339 | ||||||
| chr8:21750401
|
T | C | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794+187A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750401 | ||||||
| chr8:21750554
|
C | T | 1 | a0002c0005t0002g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.794+34G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 4/8 | chr8 | 21750554 | ||||||
| chr8:21751215
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.440-273C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21751215 | ||||||
| chr8:21751252
|
C | T | 2 | a0001c0001t0001g0097a0001c0003t0001g0056 | 2 | NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.440-310G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21751252 | ||||||
| chr8:21751533
|
C | CA | 15 | a0001c0001t0005g0306a0001c0001t0006g0018a0001c0001t0006g0027others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.440-592dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21751533 | ||||||
| chr8:21751586
|
T | C | 36 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(33): Show | 36 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-644A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21751586 | ||||||
| chr8:21751714
|
G | A | 4 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305others(1): Show | 4 | HG02965.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-772C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21751714 | ||||||
| chr8:21751722
|
G | A | 3 | a0002c0002t0003g0260a0002c0002t0003g0261a0002c0002t0003g0262 | 3 | HG00735.hp2 HG01433.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.440-780C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21751722 | ||||||
| chr8:21752065
|
A | G | 4 | a0001c0001t0005g0251a0001c0001t0007g0075a0002c0002t0003g0181others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-1123T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752065 | ||||||
| chr8:21752163
|
A | T | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.440-1221T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752163 | ||||||
| chr8:21752180
|
A | T | 2 | a0001c0001t0007g0075a0002c0002t0037g0204 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.440-1238T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752180 | ||||||
| chr8:21752181
|
A | T | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.440-1239T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752181 | ||||||
| chr8:21752187
|
G | T | 15 | a0001c0001t0005g0306a0001c0001t0006g0018a0001c0001t0006g0027others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.440-1245C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752187 | ||||||
| chr8:21752340
|
A | G | 43 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(40): Show | 43 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.440-1398T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752340 | ||||||
| chr8:21752369
|
A | G | 43 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(40): Show | 43 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.440-1427T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752369 | ||||||
| chr8:21752519
|
A | G | 1 | a0002c0002t0002g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.440-1577T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752519 | ||||||
| chr8:21752539
|
C | T | 36 | a0001c0004t0001g0159a0001c0004t0004g0249a0001c0004t0004g0257others(33): Show | 36 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.440-1597G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752539 | ||||||
| chr8:21752725
|
C | T | 37 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(34): Show | 37 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(34): Show |
intron_variant | MODIFIER | c.440-1783G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752725 | ||||||
| chr8:21752830
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00438.hp1 HG01361.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.440-1888C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21752830 | ||||||
| chr8:21753048
|
A | G | 4 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305others(1): Show | 4 | HG02965.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-2106T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753048 | ||||||
| chr8:21753052
|
C | A | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.440-2110G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753052 | ||||||
| chr8:21753123
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.440-2181G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753123 | ||||||
| chr8:21753212
|
G | A | 44 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0118others(41): Show | 44 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.440-2270C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753212 | ||||||
| chr8:21753416
|
T | A | 4 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305others(1): Show | 4 | HG02965.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-2474A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753416 | ||||||
| chr8:21753479
|
G | A | 4 | a0002c0002t0002g0078a0002c0002t0002g0079a0002c0002t0002g0082others(1): Show | 4 | HG02074.hp1 NA18961.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-2537C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753479 | ||||||
| chr8:21753509
|
C | T | 2 | a0001c0001t0007g0075a0002c0002t0037g0204 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.440-2567G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753509 | ||||||
| chr8:21753513
|
G | A | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440-2571C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753513 | ||||||
| chr8:21753618
|
C | CA | 13 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(10): Show | 13 | HG00438.hp1 HG01361.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.440-2677dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753618 | ||||||
| chr8:21753885
|
C | T | 36 | a0001c0004t0001g0159a0001c0004t0004g0249a0001c0004t0004g0257others(33): Show | 36 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.440-2943G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753885 | ||||||
| chr8:21753895
|
C | T | 8 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0304others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-2953G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753895 | ||||||
| chr8:21753925
|
C | T | 36 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(33): Show | 36 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-2983G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753925 | ||||||
| chr8:21753926
|
G | A | 1 | a0002c0002t0003g0266 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.440-2984C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21753926 | ||||||
| chr8:21754070
|
C | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(85): Show | 88 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.440-3128G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754070 | ||||||
| chr8:21754108
|
C | T | 4 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305others(1): Show | 4 | HG02965.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-3166G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754108 | ||||||
| chr8:21754214
|
G | A | 3 | a0001c0006t0016g0069a0002c0002t0002g0019a0002c0002t0002g0066 | 3 | HG01891.hp1 HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.440-3272C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754214 | ||||||
| chr8:21754338
|
A | C | 36 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(33): Show | 36 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-3396T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754338 | ||||||
| chr8:21754448
|
A | G | 10 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0176others(7): Show | 10 | HG00438.hp1 NA18942.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-3506T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754448 | ||||||
| chr8:21754505
|
C | CT | 63 | a0001c0001t0001g0011a0001c0001t0001g0118a0001c0001t0001g0149others(60): Show | 63 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.440-3564dupA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754505 | ||||||
| chr8:21754505
|
C | CTT | 28 | a0001c0001t0001g0097a0001c0001t0005g0223a0001c0001t0005g0241others(25): Show | 28 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.440-3565_440-3564d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754505 | ||||||
| chr8:21754509
|
T | A | 4 | a0001c0001t0005g0306a0001c0001t0006g0027a0001c0006t0009g0243others(1): Show | 4 | HG02630.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-3567A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754509 | ||||||
| chr8:21754510
|
T | A | 1 | a0001c0001t0006g0018 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.440-3568A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754510 | ||||||
| chr8:21754510
|
T | C | 1 | a0001c0001t0007g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.440-3568A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754510 | ||||||
| chr8:21754516
|
T | TC | 37 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0099others(34): Show | 37 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.440-3575_440-3574i others(3): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754516 | ||||||
| chr8:21754637
|
T | C | 36 | a0001c0004t0001g0159a0001c0004t0004g0249a0001c0004t0004g0257others(33): Show | 36 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.440-3695A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754637 | ||||||
| chr8:21754737
|
G | C | 1 | a0001c0001t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.440-3795C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754737 | ||||||
| chr8:21754739
|
C | A | 1 | a0001c0001t0011g0316 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.440-3797G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754739 | ||||||
| chr8:21754756
|
G | A | 89 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(86): Show | 89 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.440-3814C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754756 | ||||||
| chr8:21754761
|
G | A | 1 | a0001c0001t0006g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.440-3819C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754761 | ||||||
| chr8:21754843
|
G | A | 4 | a0001c0001t0025g0001a0001c0006t0009g0233a0001c0006t0009g0305others(1): Show | 4 | HG02965.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-3901C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754843 | ||||||
| chr8:21754873
|
G | T | 1 | a0002c0002t0003g0266 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.440-3931C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754873 | ||||||
| chr8:21754875
|
G | A | 1 | a0001c0003t0006g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.440-3933C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754875 | ||||||
| chr8:21754876
|
G | T | 4 | a0001c0003t0032g0148a0002c0002t0002g0089a0002c0002t0003g0266others(1): Show | 4 | HG01169.hp2 HG03017.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-3934C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754876 | ||||||
| chr8:21754885
|
T | G | 1 | a0002c0007t0022g0211 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.440-3943A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21754885 | ||||||
| chr8:21755071
|
G | A | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.440-4129C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755071 | ||||||
| chr8:21755112
|
T | C | 1 | a0002c0002t0002g0106 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.440-4170A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755112 | ||||||
| chr8:21755207
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.440-4265G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755207 | ||||||
| chr8:21755320
|
C | T | 1 | a0001c0003t0043g0287 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.440-4378G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755320 | ||||||
| chr8:21755393
|
C | G | 1 | a0002c0002t0037g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.440-4451G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755393 | ||||||
| chr8:21755602
|
G | A | 89 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(86): Show | 89 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.440-4660C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755602 | ||||||
| chr8:21755709
|
A | C | 1 | a0001c0001t0005g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.440-4767T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755709 | ||||||
| chr8:21755801
|
C | A | 2 | a0001c0001t0007g0063a0001c0001t0007g0067 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.440-4859G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755801 | ||||||
| chr8:21755960
|
G | T | 37 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(34): Show | 37 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(34): Show |
intron_variant | MODIFIER | c.440-5018C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755960 | ||||||
| chr8:21755973
|
C | T | 37 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(34): Show | 37 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(34): Show |
intron_variant | MODIFIER | c.440-5031G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755973 | ||||||
| chr8:21755990
|
C | T | 2 | a0001c0001t0007g0075a0002c0002t0037g0204 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.440-5048G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21755990 | ||||||
| chr8:21756035
|
G | A | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440-5093C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756035 | ||||||
| chr8:21756198
|
T | C | 2 | a0001c0001t0007g0063a0001c0001t0007g0067 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.440-5256A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756198 | ||||||
| chr8:21756356
|
G | A | 36 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(33): Show | 36 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-5414C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756356 | ||||||
| chr8:21756373
|
C | G | 1 | a0002c0002t0003g0299 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.440-5431G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756373 | ||||||
| chr8:21756375
|
G | A | 1 | a0001c0001t0007g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440-5433C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756375 | ||||||
| chr8:21756396
|
C | A | 2 | a0002c0002t0002g0115a0002c0002t0003g0250 | 2 | HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.440-5454G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756396 | ||||||
| chr8:21756397
|
G | A | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.440-5455C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756397 | ||||||
| chr8:21756425
|
G | A | 10 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0176others(7): Show | 10 | HG00438.hp1 NA18942.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-5483C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756425 | ||||||
| chr8:21756464
|
C | A | 36 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(33): Show | 36 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.440-5522G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756464 | ||||||
| chr8:21756516
|
T | G | 189 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(186): Show | 189 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(186): Show |
intron_variant | MODIFIER | c.440-5574A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756516 | ||||||
| chr8:21756558
|
T | C | 59 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(56): Show | 59 | HG00438.hp1 HG01361.hp1 HG01891.hp1 others(56): Show |
intron_variant | MODIFIER | c.440-5616A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756558 | ||||||
| chr8:21756644
|
A | G | 59 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(56): Show | 59 | HG00438.hp1 HG01361.hp1 HG01891.hp1 others(56): Show |
intron_variant | MODIFIER | c.440-5702T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21756644 | ||||||
| chr8:21757026
|
G | T | 44 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(41): Show | 44 | HG00438.hp1 HG01361.hp1 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.440-6084C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757026 | ||||||
| chr8:21757052
|
A | G | 321 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.440-6110T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757052 | ||||||
| chr8:21757096
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0006g0100a0002c0002t0002g0162 | 3 | HG01516.hp2 HG01517.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.440-6154G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757096 | ||||||
| chr8:21757132
|
G | A | 46 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(43): Show | 46 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.440-6190C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757132 | ||||||
| chr8:21757227
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.440-6285G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757227 | ||||||
| chr8:21757228
|
G | C | 188 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(185): Show | 188 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.440-6286C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757228 | ||||||
| chr8:21757356
|
G | A | 2 | a0001c0001t0005g0251a0002c0002t0003g0181 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.440-6414C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757356 | ||||||
| chr8:21757472
|
T | C | 44 | a0001c0001t0001g0060a0001c0001t0001g0141a0001c0001t0004g0221others(41): Show | 44 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.440-6530A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757472 | ||||||
| chr8:21757506
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0005g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.440-6565_440-6564i others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757506 | ||||||
| chr8:21757506
|
C | CTTTTTTT others(6): Show |
6 | a0001c0001t0007g0075a0001c0001t0019g0025a0001c0001t0025g0001others(3): Show | 6 | HG02280.hp2 HG02965.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-6565_440-6564i others(15): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757506 | ||||||
| chr8:21757506
|
C | CTTTTTTT others(7): Show |
14 | a0001c0001t0005g0306a0001c0001t0006g0018a0001c0001t0006g0027others(11): Show | 14 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.440-6565_440-6564i others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757506 | ||||||
| chr8:21757506
|
C | CTTTTTTT others(8): Show |
8 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0006g0036others(5): Show | 8 | HG02451.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-6565_440-6564i others(17): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757506 | ||||||
| chr8:21757506
|
C | CTTTTTTT others(9): Show |
16 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0176others(13): Show | 16 | HG00438.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.440-6565_440-6564i others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757506 | ||||||
| chr8:21757506
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0090a0002c0002t0027g0015 | 2 | HG01361.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.440-6565_440-6564i others(19): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757506 | ||||||
| chr8:21757538
|
C | T | 2 | a0001c0001t0005g0231a0001c0001t0005g0251 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.440-6596G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757538 | ||||||
| chr8:21757563
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0132a0001c0001t0007g0164 | 3 | HG01515.hp1 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.440-6621C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757563 | ||||||
| chr8:21757620
|
A | G | 28 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0127others(25): Show | 28 | HG00438.hp1 HG01361.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.440-6678T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757620 | ||||||
| chr8:21757642
|
C | T | 5 | a0001c0001t0005g0192a0002c0002t0015g0004a0002c0002t0015g0006others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-6700G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757642 | ||||||
| chr8:21757654
|
C | G | 5 | a0001c0001t0006g0013a0001c0001t0008g0252a0002c0016t0006g0017others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-6712G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757654 | ||||||
| chr8:21757674
|
A | T | 1 | a0001c0001t0006g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.440-6732T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757674 | ||||||
| chr8:21757837
|
A | T | 58 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0090others(55): Show | 58 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.440-6895T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757837 | ||||||
| chr8:21757962
|
C | T | 1 | a0005c0013t0010g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.440-7020G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757962 | ||||||
| chr8:21757966
|
G | A | 1 | a0002c0002t0027g0015 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.440-7024C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21757966 | ||||||
| chr8:21758027
|
A | G | 1 | a0002c0002t0002g0079 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.440-7085T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758027 | ||||||
| chr8:21758075
|
C | T | 1 | a0001c0001t0005g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.440-7133G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758075 | ||||||
| chr8:21758136
|
C | A | 35 | a0001c0001t0006g0013a0001c0001t0006g0036a0001c0001t0008g0252others(32): Show | 35 | HG00738.hp2 HG01099.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.440-7194G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758136 | ||||||
| chr8:21758203
|
C | G | 1 | a0001c0003t0006g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.440-7261G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758203 | ||||||
| chr8:21758205
|
CCA | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(192): Show | 195 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.440-7265_440-7264d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758205 | ||||||
| chr8:21758209
|
A | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0004g0295others(3): Show | 6 | HG00733.hp2 HG01258.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-7267T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758209 | ||||||
| chr8:21758227
|
A | C | 166 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0061others(163): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.440-7285T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758227 | ||||||
| chr8:21758270
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.440-7328C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758270 | ||||||
| chr8:21758281
|
G | T | 1 | a0002c0007t0003g0237 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.440-7339C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758281 | ||||||
| chr8:21758305
|
C | T | 60 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0085others(57): Show | 60 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.440-7363G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758305 | ||||||
| chr8:21758417
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.440-7475T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758417 | ||||||
| chr8:21758484
|
T | C | 5 | a0001c0001t0013g0182a0001c0006t0009g0304a0001c0006t0016g0072others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-7542A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758484 | ||||||
| chr8:21758504
|
G | T | 5 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0218others(2): Show | 5 | HG02056.hp1 HG02074.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-7562C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758504 | ||||||
| chr8:21758551
|
T | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.440-7609A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758551 | ||||||
| chr8:21758565
|
C | T | 8 | a0001c0001t0009g0202a0001c0001t0013g0182a0001c0001t0020g0309others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-7623G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758565 | ||||||
| chr8:21758623
|
C | T | 2 | a0001c0001t0006g0146a0002c0002t0002g0147 | 2 | NA18957.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.440-7681G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758623 | ||||||
| chr8:21758676
|
C | T | 1 | a0001c0004t0008g0224 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.440-7734G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758676 | ||||||
| chr8:21758888
|
G | GCA | 29 | a0001c0001t0001g0118a0001c0001t0001g0168a0001c0001t0004g0222others(26): Show | 29 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.440-7948_440-7947d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758888 | ||||||
| chr8:21758906
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.440-7964C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758906 | ||||||
| chr8:21758928
|
C | T | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.440-7986G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758928 | ||||||
| chr8:21758942
|
A | G | 155 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(152): Show | 155 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.440-8000T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758942 | ||||||
| chr8:21758946
|
G | A | 1 | a0002c0002t0002g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.440-8004C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758946 | ||||||
| chr8:21758946
|
G | C | 22 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0013g0182others(19): Show | 22 | HG00738.hp2 HG01099.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.440-8004C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758946 | ||||||
| chr8:21758951
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.440-8009G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21758951 | ||||||
| chr8:21759023
|
T | G | 7 | a0001c0001t0025g0001a0001c0006t0016g0026a0001c0006t0016g0031others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-8081A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759023 | ||||||
| chr8:21759032
|
G | T | 36 | a0001c0001t0001g0039a0001c0001t0001g0168a0001c0001t0004g0213others(33): Show | 36 | HG00099.hp2 HG00597.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.440-8090C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759032 | ||||||
| chr8:21759205
|
G | A | 15 | a0001c0001t0013g0182a0001c0001t0025g0001a0001c0006t0016g0026others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.440-8263C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759205 | ||||||
| chr8:21759211
|
C | A | 2 | a0001c0001t0005g0231a0001c0004t0013g0232 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.440-8269G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759211 | ||||||
| chr8:21759268
|
C | T | 44 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0141others(41): Show | 44 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.440-8326G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759268 | ||||||
| chr8:21759321
|
G | T | 128 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(125): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.440-8379C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759321 | ||||||
| chr8:21759341
|
G | A | 128 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(125): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.440-8399C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759341 | ||||||
| chr8:21759364
|
C | T | 84 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0061others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.440-8422G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759364 | ||||||
| chr8:21759375
|
G | A | 7 | a0001c0001t0009g0202a0001c0006t0002g0028a0001c0006t0023g0208others(4): Show | 7 | HG02280.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-8433C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759375 | ||||||
| chr8:21759398
|
AAGGAAGA others(1): Show |
A | 4 | a0001c0004t0009g0228a0002c0002t0003g0193a0002c0021t0010g0225others(1): Show | 4 | HG02615.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-8464_440-8457d others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759398 | ||||||
| chr8:21759401
|
G | A | 122 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(119): Show | 122 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.440-8459C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759401 | ||||||
| chr8:21759408
|
GAGAGGGA others(1): Show |
G | 120 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(117): Show | 120 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.440-8474_440-8467d others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759408 | ||||||
| chr8:21759412
|
GGGAA | G | 4 | a0001c0004t0009g0228a0002c0002t0003g0193a0002c0021t0010g0225others(1): Show | 4 | HG02615.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-8474_440-8471d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759412 | ||||||
| chr8:21759429
|
GGAAAGAG others(9): Show |
G | 1 | a0002c0002t0050g0317 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.440-8503_440-8488d others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759429 | ||||||
| chr8:21759432
|
A | G | 3 | a0001c0001t0005g0192a0001c0001t0008g0285a0002c0002t0010g0191 | 3 | HG02258.hp2 HG02735.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.440-8490T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759432 | ||||||
| chr8:21759433
|
A | G | 3 | a0001c0001t0005g0192a0001c0001t0008g0285a0002c0002t0010g0191 | 3 | HG02258.hp2 HG02735.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.440-8491T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759433 | ||||||
| chr8:21759437
|
G | A | 3 | a0001c0001t0005g0192a0001c0001t0008g0285a0002c0002t0010g0191 | 3 | HG02258.hp2 HG02735.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.440-8495C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759437 | ||||||
| chr8:21759453
|
A | G | 3 | a0001c0001t0005g0192a0001c0001t0008g0285a0002c0002t0010g0191 | 3 | HG02258.hp2 HG02735.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.440-8511T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759453 | ||||||
| chr8:21759453
|
AGAGG | A | 12 | a0001c0001t0001g0118a0001c0001t0005g0231a0001c0003t0001g0014others(9): Show | 12 | HG01099.hp2 HG02293.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.440-8515_440-8512d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759453 | ||||||
| chr8:21759453
|
AGAGGGAG others(1): Show |
A | 6 | a0001c0001t0005g0264a0001c0001t0009g0202a0001c0004t0007g0179others(3): Show | 6 | HG03130.hp2 HG03669.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-8519_440-8512d others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759453 | ||||||
| chr8:21759460
|
G | A | 3 | a0001c0001t0005g0192a0001c0001t0008g0285a0002c0002t0010g0191 | 3 | HG02258.hp2 HG02735.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.440-8518C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759460 | ||||||
| chr8:21759461
|
G | A | 4 | a0001c0001t0005g0192a0001c0001t0008g0285a0002c0002t0010g0191others(1): Show | 4 | HG00733.hp2 HG02258.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-8519C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759461 | ||||||
| chr8:21759464
|
G | A | 3 | a0001c0001t0005g0192a0001c0001t0008g0285a0002c0002t0010g0191 | 3 | HG02258.hp2 HG02735.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.440-8522C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759464 | ||||||
| chr8:21759468
|
G | A | 121 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.440-8526C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759468 | ||||||
| chr8:21759468
|
G | GGGAAAGA others(13): Show |
1 | a0001c0001t0004g0278 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.440-8527_440-8526i others(22): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759468 | ||||||
| chr8:21759469
|
G | A | 121 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.440-8527C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759469 | ||||||
| chr8:21759469
|
G | GGAAA | 8 | a0001c0003t0001g0041a0001c0003t0001g0056a0001c0003t0021g0178others(5): Show | 8 | HG00597.hp1 NA18948.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.440-8528_440-8527i others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759469 | ||||||
| chr8:21759469
|
G | GGAAAGAA others(5): Show |
2 | a0001c0003t0001g0172a0001c0003t0006g0049 | 2 | HG00621.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.440-8528_440-8527i others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759469 | ||||||
| chr8:21759470
|
G | GAAAGA | 10 | a0001c0001t0001g0141a0001c0003t0001g0043a0001c0003t0001g0171others(7): Show | 10 | HG00438.hp2 HG00639.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-8529_440-8528i others(7): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759470 | ||||||
| chr8:21759472
|
G | A | 141 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0039others(138): Show | 141 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.440-8530C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759472 | ||||||
| chr8:21759473
|
G | A | 9 | a0001c0001t0001g0012a0001c0003t0001g0040a0001c0004t0004g0258others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.440-8531C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759473 | ||||||
| chr8:21759473
|
G | GAAA | 10 | a0001c0001t0001g0141a0001c0003t0001g0043a0001c0003t0001g0171others(7): Show | 10 | HG00438.hp2 HG00639.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-8532_440-8531i others(5): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759473 | ||||||
| chr8:21759477
|
A | G | 22 | a0001c0001t0001g0012a0001c0001t0001g0141a0001c0001t0004g0278others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.440-8535T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759477 | ||||||
| chr8:21759481
|
G | A | 8 | a0001c0003t0001g0040a0001c0004t0004g0258a0001c0020t0005g0186others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.440-8539C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759481 | ||||||
| chr8:21759485
|
A | AGAAG | 62 | a0001c0001t0001g0061a0001c0001t0001g0096a0001c0001t0001g0097others(59): Show | 62 | HG00544.hp2 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.440-8547_440-8544d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
A | AGAAGGAA others(5): Show |
5 | a0001c0006t0016g0031a0002c0002t0002g0030a0002c0002t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-8544_440-8543i others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
A | AGAAGGAA others(1): Show |
34 | a0001c0001t0001g0003a0001c0001t0001g0099a0001c0001t0001g0114others(31): Show | 34 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.440-8551_440-8544d others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
A | AGAAGGAA others(5): Show |
9 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0011g0316others(6): Show | 9 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.440-8555_440-8544d others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
A | AGAAGGAA others(9): Show |
2 | a0001c0001t0005g0306a0001c0025t0029g0071 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.440-8559_440-8544d others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
A | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0141others(34): Show | 37 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.440-8543T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
AGAAG | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0068others(38): Show | 41 | HG00544.hp1 HG01168.hp2 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.440-8547_440-8544d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
AGAAGGAA others(5): Show |
A | 1 | a0001c0004t0013g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.440-8555_440-8544d others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759485
|
AGAAGGAA others(9): Show |
A | 4 | a0001c0001t0005g0231a0001c0001t0005g0241a0002c0002t0002g0086others(1): Show | 4 | HG02040.hp2 HG03834.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-8559_440-8544d others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759485 | ||||||
| chr8:21759493
|
G | A | 6 | a0001c0001t0005g0264a0001c0001t0009g0202a0001c0004t0007g0179others(3): Show | 6 | HG00733.hp2 HG03130.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-8551C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759493 | ||||||
| chr8:21759497
|
G | A | 1 | a0008c0026t0003g0274 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.440-8555C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759497 | ||||||
| chr8:21759528
|
A | AGGAAGGA others(21): Show |
1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440-8587_440-8586i others(30): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759528 | ||||||
| chr8:21759528
|
A | AGGAAGGA others(5): Show |
5 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(2): Show | 5 | HG02615.hp1 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-8587_440-8586i others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759528 | ||||||
| chr8:21759543
|
A | AAGGAAGG others(5): Show |
2 | a0001c0001t0004g0213a0007c0024t0019g0062 | 2 | HG02809.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.440-8602_440-8601i others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759543 | ||||||
| chr8:21759543
|
A | AAGGAAGG others(1): Show |
12 | a0001c0001t0004g0218a0001c0001t0004g0219a0001c0001t0005g0223others(9): Show | 12 | HG02074.hp2 HG02280.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.440-8602_440-8601i others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759543 | ||||||
| chr8:21759543
|
A | AAGGG | 12 | a0001c0001t0004g0222a0001c0003t0001g0050a0001c0004t0004g0249others(9): Show | 12 | HG01358.hp2 HG01993.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.440-8602_440-8601i others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759543 | ||||||
| chr8:21759543
|
A | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0168a0001c0001t0004g0214others(8): Show | 11 | HG00099.hp2 HG00597.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.440-8601T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759543 | ||||||
| chr8:21759562
|
G | A | 42 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0141others(39): Show | 42 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.440-8620C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759562 | ||||||
| chr8:21759593
|
A | T | 6 | a0001c0006t0002g0028a0001c0006t0023g0208a0002c0002t0015g0004others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-8651T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759593 | ||||||
| chr8:21759765
|
T | A | 27 | a0001c0001t0001g0168a0001c0001t0004g0222a0001c0001t0005g0251others(24): Show | 27 | HG00099.hp2 HG00597.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.440-8823A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759765 | ||||||
| chr8:21759844
|
G | A | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.440-8902C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759844 | ||||||
| chr8:21759884
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.440-8942C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759884 | ||||||
| chr8:21759888
|
C | CA | 58 | a0001c0001t0001g0060a0001c0001t0001g0124a0001c0001t0001g0126others(55): Show | 58 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.440-8947dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759888 | ||||||
| chr8:21759888
|
C | CAA | 43 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(40): Show | 43 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.440-8948_440-8947d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759888 | ||||||
| chr8:21759888
|
CA | C | 86 | a0001c0001t0001g0012a0001c0001t0001g0108a0001c0001t0001g0118others(83): Show | 86 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.440-8947delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759888 | ||||||
| chr8:21759888
|
CAAAA | C | 9 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(6): Show | 9 | HG02056.hp1 HG02074.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.440-8950_440-8947d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759888 | ||||||
| chr8:21759954
|
A | G | 84 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0061others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.440-9012T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759954 | ||||||
| chr8:21759959
|
A | T | 1 | a0002c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.440-9017T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21759959 | ||||||
| chr8:21760038
|
G | A | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440-9096C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760038 | ||||||
| chr8:21760065
|
C | G | 6 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-9123G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760065 | ||||||
| chr8:21760128
|
G | A | 6 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-9186C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760128 | ||||||
| chr8:21760177
|
C | T | 1 | a0002c0002t0015g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.440-9235G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760177 | ||||||
| chr8:21760181
|
C | T | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.440-9239G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760181 | ||||||
| chr8:21760223
|
C | T | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440-9281G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760223 | ||||||
| chr8:21760227
|
G | A | 2 | a0001c0001t0005g0231a0001c0004t0013g0232 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.440-9285C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760227 | ||||||
| chr8:21760243
|
G | A | 1 | a0002c0002t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.440-9301C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760243 | ||||||
| chr8:21760272
|
T | G | 88 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0141others(85): Show | 88 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.440-9330A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760272 | ||||||
| chr8:21760325
|
G | T | 5 | a0001c0001t0006g0074a0001c0001t0007g0063a0001c0001t0007g0067others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-9383C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760325 | ||||||
| chr8:21760405
|
A | T | 1 | a0002c0002t0002g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.440-9463T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760405 | ||||||
| chr8:21760486
|
T | C | 1 | a0002c0002t0002g0086 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.440-9544A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760486 | ||||||
| chr8:21760549
|
G | A | 6 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-9607C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760549 | ||||||
| chr8:21760608
|
A | T | 1 | a0002c0002t0010g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.440-9666T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760608 | ||||||
| chr8:21760615
|
G | A | 2 | a0001c0006t0009g0304a0005c0013t0010g0229 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.440-9673C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760615 | ||||||
| chr8:21760747
|
G | A | 2 | a0001c0001t0004g0213a0001c0001t0005g0223 | 2 | NA19070.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.440-9805C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760747 | ||||||
| chr8:21760751
|
C | T | 218 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0039others(215): Show | 218 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.440-9809G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760751 | ||||||
| chr8:21760805
|
C | T | 127 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(124): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.440-9863G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760805 | ||||||
| chr8:21760817
|
A | C | 18 | a0001c0001t0005g0306a0001c0001t0006g0018a0001c0001t0006g0027others(15): Show | 18 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.440-9875T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760817 | ||||||
| chr8:21760865
|
G | A | 13 | a0001c0001t0005g0231a0001c0004t0013g0230a0001c0004t0013g0232others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.440-9923C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760865 | ||||||
| chr8:21760902
|
A | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0141others(35): Show | 38 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.440-9960T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21760902 | ||||||
| chr8:21761241
|
T | C | 1 | a0001c0006t0016g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.440-10299A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761241 | ||||||
| chr8:21761347
|
C | T | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.440-10405G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761347 | ||||||
| chr8:21761448
|
C | T | 306 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.440-10506G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761448 | ||||||
| chr8:21761455
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.440-10513G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761455 | ||||||
| chr8:21761629
|
T | C | 1 | a0002c0002t0002g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.440-10687A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761629 | ||||||
| chr8:21761634
|
A | C | 1 | a0001c0001t0008g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.440-10692T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761634 | ||||||
| chr8:21761745
|
T | A | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.440-10803A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761745 | ||||||
| chr8:21761752
|
C | T | 1 | a0001c0001t0004g0273 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.440-10810G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761752 | ||||||
| chr8:21761766
|
A | G | 7 | a0001c0001t0009g0202a0001c0006t0002g0028a0001c0006t0009g0304others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-10824T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761766 | ||||||
| chr8:21761802
|
T | A | 1 | a0002c0002t0002g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.440-10860A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761802 | ||||||
| chr8:21761803
|
A | C | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.440-10861T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761803 | ||||||
| chr8:21761821
|
G | T | 8 | a0001c0004t0013g0230a0001c0006t0009g0243a0001c0022t0007g0020others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-10879C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761821 | ||||||
| chr8:21761857
|
C | T | 1 | a0002c0002t0003g0266 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.440-10915G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761857 | ||||||
| chr8:21761880
|
G | A | 4 | a0001c0001t0004g0267a0001c0004t0005g0276a0002c0002t0003g0266others(1): Show | 4 | HG01255.hp1 HG02145.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-10938C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761880 | ||||||
| chr8:21761959
|
T | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(99): Show | 102 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.440-11017A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761959 | ||||||
| chr8:21761968
|
T | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(99): Show | 102 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.440-11026A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761968 | ||||||
| chr8:21761981
|
C | G | 1 | a0002c0002t0003g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.440-11039G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21761981 | ||||||
| chr8:21762079
|
C | T | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-11137G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762079 | ||||||
| chr8:21762375
|
C | T | 10 | a0001c0001t0004g0222a0001c0003t0001g0050a0001c0003t0021g0044others(7): Show | 10 | HG00597.hp2 HG01358.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-11433G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762375 | ||||||
| chr8:21762490
|
A | G | 3 | a0001c0003t0001g0171a0002c0005t0026g0175a0002c0005t0045g0311 | 3 | HG01993.hp1 NA18966.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.440-11548T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762490 | ||||||
| chr8:21762570
|
G | A | 1 | a0001c0028t0048g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.440-11628C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762570 | ||||||
| chr8:21762573
|
G | A | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.440-11631C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762573 | ||||||
| chr8:21762749
|
T | A | 112 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(109): Show | 112 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.440-11807A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762749 | ||||||
| chr8:21762770
|
A | G | 4 | a0004c0011t0005g0197a0004c0011t0009g0195a0004c0015t0008g0196others(1): Show | 4 | HG01243.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-11828T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762770 | ||||||
| chr8:21762816
|
G | C | 16 | a0001c0001t0009g0202a0001c0006t0002g0028a0001c0006t0009g0304others(13): Show | 16 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.440-11874C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762816 | ||||||
| chr8:21762837
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.440-11895C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762837 | ||||||
| chr8:21762856
|
C | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.440-11914G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21762856 | ||||||
| chr8:21763123
|
T | C | 112 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(109): Show | 112 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.439+11849A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763123 | ||||||
| chr8:21763246
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.439+11726T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763246 | ||||||
| chr8:21763301
|
A | G | 1 | a0002c0002t0002g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.439+11671T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763301 | ||||||
| chr8:21763312
|
G | A | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+11660C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763312 | ||||||
| chr8:21763315
|
G | A | 112 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(109): Show | 112 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.439+11657C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763315 | ||||||
| chr8:21763383
|
A | G | 1 | a0001c0003t0001g0041 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.439+11589T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763383 | ||||||
| chr8:21763459
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0007g0119a0001c0001t0034g0104 | 3 | HG02602.hp2 HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.439+11513A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763459 | ||||||
| chr8:21763534
|
A | G | 1 | a0002c0002t0002g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.439+11438T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763534 | ||||||
| chr8:21763696
|
C | T | 1 | a0002c0002t0002g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.439+11276G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763696 | ||||||
| chr8:21763735
|
C | A | 207 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(204): Show | 207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.439+11237G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763735 | ||||||
| chr8:21763752
|
C | A | 40 | a0001c0001t0001g0141a0001c0001t0004g0278a0001c0003t0001g0040others(37): Show | 40 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.439+11220G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763752 | ||||||
| chr8:21763869
|
A | G | 1 | a0002c0002t0006g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.439+11103T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763869 | ||||||
| chr8:21763943
|
A | C | 1 | a0001c0003t0032g0148 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.439+11029T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763943 | ||||||
| chr8:21763950
|
AACAC | A | 16 | a0001c0001t0004g0218a0001c0001t0004g0295a0001c0003t0001g0053others(13): Show | 16 | HG00438.hp1 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.439+11018_439+1102 others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACAC | A | 13 | a0001c0001t0004g0277a0001c0001t0013g0182a0001c0001t0025g0001others(10): Show | 13 | HG01952.hp2 HG02976.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.439+11016_439+1102 others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(1): Show |
A | 40 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0149others(37): Show | 40 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.439+11014_439+1102 others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(3): Show |
A | 46 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0092others(43): Show | 46 | HG00639.hp1 HG00642.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.439+11012_439+1102 others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(5): Show |
A | 46 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0080others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.439+11010_439+1102 others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(7): Show |
A | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0090others(19): Show | 22 | HG00597.hp2 HG01361.hp1 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.439+11008_439+1102 others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(9): Show |
A | 22 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0152others(19): Show | 22 | HG00099.hp1 HG00408.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.439+11006_439+1102 others(20): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(11): Show |
A | 18 | a0001c0001t0004g0273a0001c0001t0004g0296a0001c0001t0006g0013others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.439+11004_439+1102 others(22): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(13): Show |
A | 45 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(42): Show | 45 | HG00408.hp1 HG00544.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.439+11002_439+1102 others(24): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(15): Show |
A | 12 | a0001c0004t0007g0179a0001c0004t0009g0228a0001c0006t0009g0304others(9): Show | 12 | HG02083.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.439+11000_439+1102 others(26): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(17): Show |
A | 15 | a0001c0001t0005g0192a0001c0001t0007g0075a0001c0001t0009g0202others(12): Show | 15 | HG01243.hp2 HG02040.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.439+10998_439+1102 others(28): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(19): Show |
A | 1 | a0001c0001t0004g0221 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.439+10996_439+1102 others(30): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763950
|
AACACACA others(21): Show |
A | 17 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0005g0238others(14): Show | 17 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.439+10994_439+1102 others(32): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763950 | ||||||
| chr8:21763991
|
ACACACAC others(12): Show |
A | 1 | a0008c0026t0003g0274 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.439+10962_439+1098 others(23): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763991 | ||||||
| chr8:21763995
|
ACACACAC others(8): Show |
A | 1 | a0001c0006t0023g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.439+10962_439+1097 others(19): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763995 | ||||||
| chr8:21763999
|
ACACACAC others(4): Show |
A | 1 | a0002c0005t0002g0048 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.439+10962_439+1097 others(15): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21763999 | ||||||
| chr8:21764121
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+10851C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764121 | ||||||
| chr8:21764226
|
G | C | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+10746C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764226 | ||||||
| chr8:21764357
|
G | C | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+10615C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764357 | ||||||
| chr8:21764408
|
C | G | 52 | a0001c0001t0001g0085a0001c0001t0001g0141a0001c0001t0004g0278others(49): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.439+10564G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764408 | ||||||
| chr8:21764452
|
C | G | 5 | a0001c0006t0002g0028a0002c0002t0015g0004a0002c0002t0015g0006others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+10520G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764452 | ||||||
| chr8:21764479
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0134a0002c0002t0002g0095 | 3 | NA19002.hp2 NA19007.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.439+10493G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764479 | ||||||
| chr8:21764530
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+10442C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764530 | ||||||
| chr8:21764543
|
C | A | 1 | a0001c0004t0001g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.439+10429G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764543 | ||||||
| chr8:21764630
|
T | C | 6 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+10342A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764630 | ||||||
| chr8:21764679
|
T | C | 9 | a0001c0001t0004g0273a0001c0001t0005g0264a0001c0001t0024g0294others(6): Show | 9 | HG02083.hp1 HG03669.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+10293A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764679 | ||||||
| chr8:21764735
|
T | C | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+10237A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764735 | ||||||
| chr8:21764761
|
C | A | 80 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(77): Show | 80 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.439+10211G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764761 | ||||||
| chr8:21764830
|
T | C | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+10142A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764830 | ||||||
| chr8:21764880
|
T | C | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+10092A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764880 | ||||||
| chr8:21764926
|
T | C | 1 | a0001c0006t0016g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.439+10046A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764926 | ||||||
| chr8:21764990
|
G | C | 9 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.439+9982C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764990 | ||||||
| chr8:21764997
|
T | A | 9 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0006t0009g0305others(6): Show | 9 | HG00438.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+9975A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21764997 | ||||||
| chr8:21765121
|
AT | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+9850delA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765121 | ||||||
| chr8:21765125
|
T | A | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+9847A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765125 | ||||||
| chr8:21765157
|
A | G | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+9815T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765157 | ||||||
| chr8:21765205
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+9767C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765205 | ||||||
| chr8:21765255
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+9717C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765255 | ||||||
| chr8:21765272
|
T | C | 79 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(76): Show | 79 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.439+9700A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765272 | ||||||
| chr8:21765293
|
T | C | 1 | a0002c0002t0002g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.439+9679A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765293 | ||||||
| chr8:21765302
|
G | C | 2 | a0002c0002t0002g0019a0002c0007t0002g0165 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.439+9670C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765302 | ||||||
| chr8:21765311
|
A | G | 7 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0006t0009g0305others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+9661T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765311 | ||||||
| chr8:21765358
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+9614C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765358 | ||||||
| chr8:21765487
|
C | A | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.439+9485G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765487 | ||||||
| chr8:21765532
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+9440C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765532 | ||||||
| chr8:21765560
|
T | C | 15 | a0001c0001t0009g0202a0001c0006t0002g0028a0002c0002t0015g0004others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.439+9412A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765560 | ||||||
| chr8:21765570
|
C | T | 6 | a0001c0001t0001g0080a0002c0002t0002g0078a0002c0002t0002g0079others(3): Show | 6 | NA18961.hp2 NA18971.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+9402G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765570 | ||||||
| chr8:21765608
|
T | C | 80 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(77): Show | 80 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.439+9364A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765608 | ||||||
| chr8:21765613
|
T | G | 1 | a0001c0001t0005g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.439+9359A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765613 | ||||||
| chr8:21765782
|
C | T | 16 | a0001c0001t0009g0202a0001c0006t0002g0028a0001c0006t0009g0304others(13): Show | 16 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.439+9190G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765782 | ||||||
| chr8:21765791
|
TCTC | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(98): Show | 101 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.439+9178_439+9180d others(5): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765791 | ||||||
| chr8:21765882
|
C | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.439+9090G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765882 | ||||||
| chr8:21765910
|
T | C | 113 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.439+9062A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21765910 | ||||||
| chr8:21766052
|
C | G | 1 | a0001c0001t0005g0241 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.439+8920G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766052 | ||||||
| chr8:21766061
|
C | T | 218 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(215): Show | 218 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.439+8911G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766061 | ||||||
| chr8:21766066
|
C | T | 111 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0061others(108): Show | 111 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.439+8906G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766066 | ||||||
| chr8:21766077
|
G | C | 1 | a0002c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.439+8895C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766077 | ||||||
| chr8:21766121
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+8851C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766121 | ||||||
| chr8:21766319
|
T | C | 3 | a0001c0001t0004g0290a0001c0001t0024g0291a0001c0001t0042g0268 | 3 | HG00408.hp1 HG02132.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.439+8653A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766319 | ||||||
| chr8:21766349
|
T | C | 1 | a0002c0002t0002g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.439+8623A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766349 | ||||||
| chr8:21766472
|
G | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0090a0001c0001t0001g0132others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+8500C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766472 | ||||||
| chr8:21766679
|
G | T | 1 | a0001c0001t0005g0254 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.439+8293C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766679 | ||||||
| chr8:21766680
|
G | T | 1 | a0001c0001t0005g0254 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.439+8292C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766680 | ||||||
| chr8:21766746
|
C | T | 6 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+8226G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766746 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2292): Show |
8 | a0001c0004t0013g0230a0001c0006t0009g0243a0001c0022t0007g0020others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2301): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2292): Show |
2 | a0001c0001t0005g0231a0001c0004t0013g0232 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2301): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2290): Show |
1 | a0002c0002t0044g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2299): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2292): Show |
2 | a0001c0001t0020g0307a0001c0001t0020g0309 | 2 | HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2301): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2292): Show |
1 | a0001c0019t0020g0310 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2301): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2288): Show |
8 | a0001c0001t0005g0241a0001c0001t0006g0036a0001c0006t0009g0305others(5): Show | 8 | HG00438.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2297): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2286): Show |
1 | a0005c0013t0010g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2295): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2288): Show |
1 | a0001c0001t0019g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2297): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2290): Show |
7 | a0001c0001t0001g0168a0001c0001t0011g0316a0001c0001t0011g0319others(4): Show | 7 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2299): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2290): Show |
4 | a0001c0001t0001g0149a0001c0001t0011g0318a0001c0001t0011g0321others(1): Show | 4 | HG01175.hp2 NA19240.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2299): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2290): Show |
1 | a0001c0001t0001g0096 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2299): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2286): Show |
39 | a0001c0001t0001g0085a0001c0001t0001g0141a0001c0001t0004g0278others(36): Show | 39 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2295): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2284): Show |
1 | a0001c0003t0001g0166 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2293): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2286): Show |
1 | a0001c0003t0001g0014 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2295): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2268): Show |
1 | a0001c0001t0004g0277 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2277): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2271): Show |
1 | a0001c0001t0001g0160 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2280): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2272): Show |
1 | a0001c0001t0008g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2281): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2273): Show |
81 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(78): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2282): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2273): Show |
13 | a0001c0001t0004g0222a0001c0001t0005g0251a0001c0001t0006g0013others(10): Show | 13 | HG00597.hp2 HG01358.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2282): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2271): Show |
1 | a0002c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2280): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2273): Show |
1 | a0001c0001t0007g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2282): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2285): Show |
9 | a0001c0001t0025g0001a0001c0006t0007g0033a0001c0006t0016g0031others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2294): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2283): Show |
1 | a0001c0020t0005g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2292): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2281): Show |
1 | a0002c0005t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2290): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2284): Show |
18 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0004g0221others(15): Show | 18 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2293): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2273): Show |
1 | a0001c0006t0023g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2282): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2293): Show |
1 | a0002c0002t0003g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2302): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2273): Show |
1 | a0001c0001t0001g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2282): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2274): Show |
1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2283): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2279): Show |
2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2288): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2269): Show |
1 | a0002c0002t0002g0082 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2278): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2266): Show |
1 | a0003c0008t0012g0281 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2275): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2268): Show |
1 | a0002c0002t0003g0282 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2277): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2268): Show |
67 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(64): Show | 67 | HG00323.hp1 HG00408.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2277): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2252): Show |
1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2261): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2268): Show |
1 | a0001c0001t0007g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2277): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2268): Show |
1 | a0002c0002t0002g0079 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2277): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2264): Show |
1 | a0002c0002t0002g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2273): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2268): Show |
2 | a0001c0006t0016g0069a0002c0002t0006g0065 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2277): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2265): Show |
1 | a0001c0001t0005g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2274): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2268): Show |
1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2277): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2266): Show |
8 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0217others(5): Show | 8 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2275): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2266): Show |
1 | a0001c0001t0004g0214 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2275): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2266): Show |
2 | a0001c0001t0006g0146a0002c0002t0002g0147 | 2 | NA18957.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2275): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2293): Show |
3 | a0001c0004t0009g0228a0002c0021t0010g0225a0005c0012t0010g0198 | 3 | HG02647.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2302): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2293): Show |
2 | a0001c0001t0005g0192a0002c0002t0010g0191 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2302): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2270): Show |
1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.439+8177_439+8178i others(2279): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2264): Show |
11 | a0001c0001t0009g0202a0001c0006t0002g0028a0002c0002t0015g0004others(8): Show | 11 | HG02280.hp1 HG02818.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2273): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766794
|
C | CACAGCCA others(2264): Show |
4 | a0004c0011t0005g0197a0004c0011t0009g0195a0004c0015t0008g0196others(1): Show | 4 | HG01243.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+8177_439+8178i others(2273): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766794 | ||||||
| chr8:21766819
|
C | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(80): Show | 83 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.439+8153G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766819 | ||||||
| chr8:21766857
|
CCT | C | 6 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+8113_439+8114d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766857 | ||||||
| chr8:21766906
|
C | T | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+8066G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766906 | ||||||
| chr8:21766920
|
TACAC | T | 79 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0068others(76): Show | 79 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.439+8048_439+8051d others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766920 | ||||||
| chr8:21766942
|
CA | C | 15 | a0001c0001t0009g0202a0001c0006t0002g0028a0002c0002t0015g0004others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.439+8029delT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21766942 | ||||||
| chr8:21767034
|
C | G | 15 | a0001c0001t0009g0202a0001c0006t0002g0028a0002c0002t0015g0004others(12): Show | 15 | HG01243.hp2 HG02280.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.439+7938G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767034 | ||||||
| chr8:21767084
|
ACACACAC others(2): Show |
A | 8 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0006t0009g0305others(5): Show | 8 | HG00438.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+7879_439+7887d others(11): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767084 | ||||||
| chr8:21767113
|
C | T | 10 | a0001c0001t0005g0231a0001c0004t0013g0230a0001c0004t0013g0232others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.439+7859G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767113 | ||||||
| chr8:21767135
|
C | G | 1 | a0001c0006t0007g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.439+7837G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767135 | ||||||
| chr8:21767174
|
C | T | 1 | a0001c0001t0011g0322 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.439+7798G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767174 | ||||||
| chr8:21767175
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.439+7797T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767175 | ||||||
| chr8:21767215
|
CAA | C | 55 | a0001c0001t0001g0085a0001c0001t0001g0141a0001c0001t0004g0278others(52): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.439+7755_439+7756d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767215 | ||||||
| chr8:21767217
|
A | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0060others(164): Show | 167 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.439+7755T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767217 | ||||||
| chr8:21767334
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.439+7638G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767334 | ||||||
| chr8:21767359
|
T | G | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+7613A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767359 | ||||||
| chr8:21767419
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.439+7553G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767419 | ||||||
| chr8:21767615
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.439+7357G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767615 | ||||||
| chr8:21767639
|
A | T | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+7333T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767639 | ||||||
| chr8:21767716
|
AC | A | 321 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.439+7255delG | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767716 | ||||||
| chr8:21767958
|
CAG | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.439+7012_439+7013d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767958 | ||||||
| chr8:21767960
|
G | C | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+7012C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21767960 | ||||||
| chr8:21768195
|
G | C | 1 | a0002c0002t0006g0110 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.439+6777C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768195 | ||||||
| chr8:21768211
|
G | C | 1 | a0005c0014t0006g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439+6761C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768211 | ||||||
| chr8:21768416
|
C | T | 3 | a0001c0001t0004g0273a0001c0001t0024g0294a0002c0002t0038g0265 | 3 | NA18948.hp1 NA18949.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.439+6556G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768416 | ||||||
| chr8:21768504
|
C | T | 7 | a0001c0001t0004g0273a0001c0001t0005g0264a0001c0001t0008g0285others(4): Show | 7 | HG02735.hp1 HG03669.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+6468G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768504 | ||||||
| chr8:21768505
|
G | A | 77 | a0001c0001t0001g0085a0001c0001t0001g0141a0001c0001t0004g0278others(74): Show | 77 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.439+6467C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768505 | ||||||
| chr8:21768598
|
C | G | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.439+6374G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768598 | ||||||
| chr8:21768637
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.439+6335G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768637 | ||||||
| chr8:21768729
|
C | G | 7 | a0001c0001t0006g0036a0001c0001t0019g0025a0002c0002t0002g0037others(4): Show | 7 | HG00438.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+6243G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768729 | ||||||
| chr8:21768987
|
C | T | 2 | a0001c0006t0009g0243a0002c0002t0005g0242 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.439+5985G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21768987 | ||||||
| chr8:21769009
|
A | G | 1 | a0001c0001t0005g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.439+5963T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769009 | ||||||
| chr8:21769060
|
C | G | 1 | a0002c0002t0010g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.439+5912G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769060 | ||||||
| chr8:21769117
|
A | G | 168 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(165): Show | 168 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.439+5855T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769117 | ||||||
| chr8:21769162
|
G | C | 19 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0004g0221others(16): Show | 19 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.439+5810C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769162 | ||||||
| chr8:21769221
|
C | T | 216 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(213): Show | 216 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.439+5751G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769221 | ||||||
| chr8:21769227
|
C | T | 1 | a0001c0028t0048g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.439+5745G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769227 | ||||||
| chr8:21769255
|
C | CCCGCCCC others(4): Show |
81 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.439+5716_439+5717i others(13): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769255 | ||||||
| chr8:21769265
|
C | A | 40 | a0001c0001t0001g0085a0001c0003t0001g0014a0001c0003t0001g0040others(37): Show | 40 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.439+5707G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769265 | ||||||
| chr8:21769284
|
G | A | 81 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.439+5688C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769284 | ||||||
| chr8:21769300
|
G | A | 81 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.439+5672C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769300 | ||||||
| chr8:21769327
|
C | T | 5 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+5645G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769327 | ||||||
| chr8:21769459
|
G | A | 2 | a0001c0001t0004g0221a0002c0007t0022g0211 | 2 | NA18998.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.439+5513C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769459 | ||||||
| chr8:21769571
|
G | T | 51 | a0001c0001t0001g0085a0001c0001t0006g0036a0001c0001t0019g0025others(48): Show | 51 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.439+5401C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769571 | ||||||
| chr8:21769588
|
T | C | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.439+5384A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769588 | ||||||
| chr8:21769662
|
G | A | 2 | a0002c0002t0002g0133a0002c0002t0002g0162 | 2 | HG00099.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.439+5310C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769662 | ||||||
| chr8:21769665
|
TCA | T | 81 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.439+5305_439+5306d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769665 | ||||||
| chr8:21769724
|
G | A | 2 | a0001c0001t0013g0182a0001c0020t0005g0186 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.439+5248C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769724 | ||||||
| chr8:21769736
|
T | C | 224 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(221): Show | 224 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.439+5236A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769736 | ||||||
| chr8:21769740
|
T | C | 236 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(233): Show | 236 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.439+5232A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769740 | ||||||
| chr8:21769742
|
C | T | 49 | a0001c0001t0001g0085a0001c0001t0006g0036a0001c0001t0019g0025others(46): Show | 49 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.439+5230G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769742 | ||||||
| chr8:21769792
|
C | G | 1 | a0002c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.439+5180G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769792 | ||||||
| chr8:21769792
|
C | T | 31 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0008g0302others(28): Show | 31 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.439+5180G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769792 | ||||||
| chr8:21769817
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.439+5155C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769817 | ||||||
| chr8:21769850
|
G | C | 1 | a0002c0002t0008g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.439+5122C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769850 | ||||||
| chr8:21769858
|
T | G | 165 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(162): Show | 165 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.439+5114A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769858 | ||||||
| chr8:21769941
|
A | G | 49 | a0001c0001t0001g0085a0001c0001t0006g0036a0001c0001t0019g0025others(46): Show | 49 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.439+5031T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769941 | ||||||
| chr8:21769984
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.439+4988C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21769984 | ||||||
| chr8:21770127
|
A | G | 170 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(167): Show | 170 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.439+4845T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770127 | ||||||
| chr8:21770178
|
A | G | 170 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(167): Show | 170 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.439+4794T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770178 | ||||||
| chr8:21770389
|
C | T | 13 | a0001c0006t0002g0028a0004c0009t0005g0200a0004c0009t0013g0190others(10): Show | 13 | HG01243.hp2 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.439+4583G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770389 | ||||||
| chr8:21770404
|
C | A | 5 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+4568G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770404 | ||||||
| chr8:21770452
|
A | T | 1 | a0002c0002t0002g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.439+4520T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770452 | ||||||
| chr8:21770472
|
A | G | 170 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(167): Show | 170 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.439+4500T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770472 | ||||||
| chr8:21770709
|
T | C | 171 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(168): Show | 171 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.439+4263A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770709 | ||||||
| chr8:21770725
|
C | T | 22 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0008g0302others(19): Show | 22 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.439+4247G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770725 | ||||||
| chr8:21770729
|
GGCCCAGT | G | 13 | a0001c0006t0002g0028a0004c0009t0005g0200a0004c0009t0013g0190others(10): Show | 13 | HG01243.hp2 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.439+4236_439+4242d others(9): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770729 | ||||||
| chr8:21770740
|
G | A | 1 | a0002c0016t0003g0272 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.439+4232C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770740 | ||||||
| chr8:21770773
|
T | C | 53 | a0001c0001t0001g0085a0001c0001t0006g0036a0001c0001t0019g0025others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.439+4199A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21770773 | ||||||
| chr8:21771001
|
G | A | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+3971C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771001 | ||||||
| chr8:21771008
|
A | C | 177 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.439+3964T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771008 | ||||||
| chr8:21771009
|
C | T | 4 | a0001c0006t0009g0304a0002c0002t0015g0004a0002c0002t0015g0006others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+3963G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771009 | ||||||
| chr8:21771066
|
G | A | 52 | a0001c0001t0001g0085a0001c0001t0006g0036a0001c0001t0019g0025others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.439+3906C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771066 | ||||||
| chr8:21771264
|
T | C | 177 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(174): Show | 177 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.439+3708A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771264 | ||||||
| chr8:21771291
|
T | C | 86 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(83): Show | 86 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.439+3681A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771291 | ||||||
| chr8:21771359
|
T | C | 1 | a0002c0002t0003g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.439+3613A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771359 | ||||||
| chr8:21771382
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+3590C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771382 | ||||||
| chr8:21771473
|
T | C | 53 | a0001c0001t0001g0085a0001c0001t0006g0036a0001c0001t0019g0025others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.439+3499A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771473 | ||||||
| chr8:21771800
|
C | G | 47 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0003g0226others(44): Show | 47 | HG00639.hp2 HG01168.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.439+3172G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771800 | ||||||
| chr8:21771869
|
T | G | 3 | a0001c0001t0004g0222a0001c0004t0004g0249a0002c0002t0003g0259 | 3 | HG02135.hp1 NA18950.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.439+3103A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771869 | ||||||
| chr8:21771949
|
G | A | 4 | a0001c0001t0004g0184a0001c0001t0005g0254a0002c0002t0003g0255others(1): Show | 4 | HG00408.hp2 HG01952.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+3023C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21771949 | ||||||
| chr8:21772151
|
A | G | 1 | a0002c0005t0003g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.439+2821T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772151 | ||||||
| chr8:21772165
|
T | A | 2 | a0001c0006t0016g0069a0002c0002t0006g0065 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.439+2807A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772165 | ||||||
| chr8:21772196
|
C | T | 18 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0004g0221others(15): Show | 18 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.439+2776G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772196 | ||||||
| chr8:21772341
|
T | C | 54 | a0001c0001t0001g0085a0001c0001t0006g0036a0001c0001t0009g0202others(51): Show | 54 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.439+2631A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772341 | ||||||
| chr8:21772499
|
C | T | 3 | a0001c0001t0001g0141a0002c0002t0002g0139a0002c0002t0002g0140 | 3 | NA18994.hp1 NA19002.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.439+2473G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772499 | ||||||
| chr8:21772532
|
T | C | 1 | a0001c0001t0036g0155 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.439+2440A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772532 | ||||||
| chr8:21772613
|
C | A | 4 | a0001c0006t0009g0304a0002c0002t0015g0004a0002c0002t0015g0006others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2359G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772613 | ||||||
| chr8:21772834
|
C | A | 5 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+2138G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772834 | ||||||
| chr8:21772835
|
A | G | 1 | a0002c0016t0003g0272 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.439+2137T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772835 | ||||||
| chr8:21772876
|
T | A | 114 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(111): Show | 114 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.439+2096A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772876 | ||||||
| chr8:21772879
|
C | T | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2093G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772879 | ||||||
| chr8:21772882
|
C | T | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2090G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772882 | ||||||
| chr8:21772987
|
G | A | 1 | a0004c0009t0039g0188 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.439+1985C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21772987 | ||||||
| chr8:21773182
|
A | G | 1 | a0002c0005t0047g0313 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.439+1790T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773182 | ||||||
| chr8:21773224
|
G | A | 46 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0003t0001g0014others(43): Show | 46 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.439+1748C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773224 | ||||||
| chr8:21773339
|
G | A | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+1633C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773339 | ||||||
| chr8:21773346
|
G | A | 4 | a0001c0001t0004g0184a0001c0001t0005g0254a0002c0002t0003g0255others(1): Show | 4 | HG00408.hp2 HG01952.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+1626C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773346 | ||||||
| chr8:21773368
|
C | T | 1 | a0002c0007t0002g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.439+1604G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773368 | ||||||
| chr8:21773384
|
A | G | 1 | a0001c0001t0009g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.439+1588T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773384 | ||||||
| chr8:21773418
|
C | T | 7 | a0001c0001t0004g0273a0001c0001t0024g0294a0001c0004t0007g0179others(4): Show | 7 | HG02083.hp1 HG03669.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+1554G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773418 | ||||||
| chr8:21773428
|
T | A | 2 | a0001c0001t0013g0182a0001c0020t0005g0186 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.439+1544A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773428 | ||||||
| chr8:21773446
|
C | T | 4 | a0001c0001t0006g0036a0001c0001t0019g0025a0002c0002t0002g0037others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+1526G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773446 | ||||||
| chr8:21773451
|
T | C | 1 | a0001c0001t0041g0239 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.439+1521A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773451 | ||||||
| chr8:21773459
|
C | T | 10 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.439+1513G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773459 | ||||||
| chr8:21773555
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.439+1417T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773555 | ||||||
| chr8:21773618
|
G | C | 2 | a0001c0001t0005g0231a0001c0004t0013g0232 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.439+1354C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773618 | ||||||
| chr8:21773672
|
T | G | 9 | a0001c0001t0025g0001a0001c0006t0007g0033a0001c0006t0016g0031others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+1300A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773672 | ||||||
| chr8:21773755
|
T | G | 226 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(223): Show | 226 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.439+1217A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773755 | ||||||
| chr8:21773849
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439+1123C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773849 | ||||||
| chr8:21773951
|
A | G | 1 | a0002c0005t0003g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.439+1021T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773951 | ||||||
| chr8:21773999
|
C | A | 3 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0021t0010g0225 | 3 | HG02896.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439+973G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21773999 | ||||||
| chr8:21774049
|
C | A | 4 | a0004c0011t0005g0197a0004c0011t0009g0195a0004c0015t0008g0196others(1): Show | 4 | HG01243.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+923G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774049 | ||||||
| chr8:21774057
|
C | T | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+915G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774057 | ||||||
| chr8:21774330
|
G | C | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+642C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774330 | ||||||
| chr8:21774344
|
T | C | 236 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(233): Show | 236 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.439+628A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774344 | ||||||
| chr8:21774349
|
A | G | 140 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(137): Show | 140 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.439+623T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774349 | ||||||
| chr8:21774417
|
C | CAAG | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+552_439+554dup others(3): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774417 | ||||||
| chr8:21774430
|
CAA | C | 22 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0008g0302others(19): Show | 22 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.439+540_439+541del others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774430 | ||||||
| chr8:21774439
|
G | A | 5 | a0001c0001t0007g0164a0001c0001t0035g0113a0002c0002t0002g0111others(2): Show | 5 | HG02004.hp1 HG02602.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+533C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774439 | ||||||
| chr8:21774512
|
G | A | 1 | a0001c0003t0032g0148 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.439+460C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774512 | ||||||
| chr8:21774528
|
C | A | 5 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+444G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774528 | ||||||
| chr8:21774580
|
C | T | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+392G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774580 | ||||||
| chr8:21774636
|
G | C | 52 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0006g0036others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.439+336C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774636 | ||||||
| chr8:21774688
|
G | C | 147 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(144): Show | 147 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.439+284C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774688 | ||||||
| chr8:21774736
|
G | A | 50 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0001t0020g0307others(47): Show | 50 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.439+236C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774736 | ||||||
| chr8:21774811
|
T | G | 1 | a0001c0006t0009g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.439+161A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774811 | ||||||
| chr8:21774832
|
C | A | 2 | a0001c0001t0007g0112a0001c0004t0008g0224 | 2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.439+140G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 3/8 | chr8 | 21774832 | ||||||
| chr8:21775059
|
G | A | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.356-4C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775059 | ||||||
| chr8:21775085
|
G | C | 37 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0004g0221others(34): Show | 37 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-30C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775085 | ||||||
| chr8:21775109
|
G | A | 2 | a0001c0003t0001g0171a0002c0005t0026g0175 | 2 | HG01993.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.356-54C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775109 | ||||||
| chr8:21775199
|
G | A | 1 | a0001c0001t0035g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356-144C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775199 | ||||||
| chr8:21775222
|
C | T | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-167G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775222 | ||||||
| chr8:21775521
|
C | T | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-466G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775521 | ||||||
| chr8:21775794
|
G | C | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-739C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775794 | ||||||
| chr8:21775795
|
A | T | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-740T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775795 | ||||||
| chr8:21775896
|
T | A | 1 | a0001c0001t0005g0254 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.356-841A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775896 | ||||||
| chr8:21775923
|
C | T | 4 | a0001c0006t0009g0304a0002c0002t0015g0004a0002c0002t0015g0006others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-868G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775923 | ||||||
| chr8:21775967
|
T | C | 53 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0001t0020g0307others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.356-912A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775967 | ||||||
| chr8:21775981
|
C | A | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-926G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775981 | ||||||
| chr8:21775989
|
C | CTG | 8 | a0001c0001t0001g0132a0001c0001t0007g0087a0001c0001t0009g0202others(5): Show | 8 | HG01515.hp1 HG02257.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.356-936_356-935dup others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
C | CTGTGTGT others(5): Show |
1 | a0002c0002t0015g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.356-935_356-934ins others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
C | CTGTGTGT others(9): Show |
1 | a0002c0002t0015g0007 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.356-935_356-934ins others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
C | CTGTGTGT others(11): Show |
1 | a0002c0002t0015g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.356-935_356-934ins others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTG | C | 57 | a0001c0001t0001g0024a0001c0001t0001g0096a0001c0001t0001g0097others(54): Show | 57 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.356-936_356-935del others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTG | C | 41 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0114others(38): Show | 41 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.356-938_356-935del others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTG | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0023others(39): Show | 42 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.356-940_356-935del others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(1): Show |
C | 18 | a0001c0001t0001g0060a0001c0001t0001g0149a0001c0001t0003g0226others(15): Show | 18 | HG00642.hp2 HG01168.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.356-942_356-935del others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(3): Show |
C | 10 | a0001c0001t0001g0160a0002c0002t0002g0081a0002c0002t0002g0129others(7): Show | 10 | HG00438.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.356-944_356-935del others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(5): Show |
C | 5 | a0001c0001t0005g0284a0001c0001t0020g0309a0001c0003t0001g0053others(2): Show | 5 | HG02622.hp1 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-946_356-935del others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0011a0002c0002t0002g0131 | 2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.356-948_356-935del others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(9): Show |
C | 2 | a0001c0006t0009g0243a0002c0002t0005g0242 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.356-950_356-935del others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0004g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.356-952_356-935del others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(15): Show |
C | 12 | a0001c0006t0002g0028a0004c0009t0005g0200a0004c0009t0013g0190others(9): Show | 12 | HG01243.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.356-956_356-935del others(22): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21775989
|
CTGTGTGT others(17): Show |
C | 1 | a0004c0018t0040g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.356-958_356-935del others(24): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21775989 | ||||||
| chr8:21776037
|
G | A | 96 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0080others(93): Show | 96 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.356-982C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTA | 14 | a0001c0001t0001g0141a0001c0001t0004g0273a0001c0001t0005g0192others(11): Show | 14 | HG00597.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.356-983_356-982ins others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTA | 10 | a0001c0001t0004g0213a0001c0001t0004g0219a0001c0001t0006g0027others(7): Show | 10 | HG02074.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.356-986_356-983dup others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTA | 14 | a0001c0001t0004g0277a0001c0001t0004g0278a0001c0001t0005g0264others(11): Show | 14 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.356-983_356-982ins others(6): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(1): Show |
8 | a0001c0001t0001g0068a0001c0001t0007g0067a0001c0006t0007g0033others(5): Show | 8 | HG01433.hp2 HG01891.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.356-983_356-982ins others(8): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(3): Show |
8 | a0001c0001t0001g0145a0001c0001t0005g0223a0001c0001t0006g0018others(5): Show | 8 | HG01255.hp1 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.356-983_356-982ins others(10): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(5): Show |
4 | a0001c0001t0001g0064a0001c0001t0007g0063a0001c0006t0016g0031others(1): Show | 4 | HG00738.hp2 HG01255.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-983_356-982ins others(12): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(7): Show |
2 | a0002c0002t0002g0030a0007c0024t0019g0062 | 2 | HG01099.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.356-983_356-982ins others(14): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(9): Show |
3 | a0001c0001t0006g0146a0001c0006t0023g0208a0002c0002t0003g0193 | 3 | HG02615.hp1 HG02717.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.356-983_356-982ins others(16): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.356-983_356-982ins others(18): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0025g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.356-983_356-982ins others(20): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776037
|
G | GTGTGTGT others(10): Show |
1 | a0002c0002t0015g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.356-983_356-982ins others(17): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776037 | ||||||
| chr8:21776351
|
A | C | 4 | a0001c0001t0005g0231a0001c0004t0013g0232a0001c0006t0009g0243others(1): Show | 4 | HG03516.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-1296T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776351 | ||||||
| chr8:21776385
|
A | G | 49 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0003t0001g0014others(46): Show | 49 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.356-1330T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776385 | ||||||
| chr8:21776413
|
G | A | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.356-1358C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776413 | ||||||
| chr8:21776460
|
G | A | 26 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(23): Show | 26 | HG01243.hp2 HG02056.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.356-1405C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776460 | ||||||
| chr8:21776469
|
CT | C | 12 | a0001c0001t0001g0039a0001c0001t0001g0132a0001c0001t0004g0214others(9): Show | 12 | HG00099.hp1 HG01515.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.356-1415delA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776469 | ||||||
| chr8:21776469
|
CTT | C | 151 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(148): Show | 151 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.356-1416_356-1415d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776469 | ||||||
| chr8:21776469
|
CTTT | C | 10 | a0001c0001t0001g0145a0001c0001t0004g0218a0001c0001t0004g0219others(7): Show | 10 | HG01515.hp2 HG02074.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.356-1417_356-1415d others(5): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776469 | ||||||
| chr8:21776562
|
C | T | 2 | a0001c0001t0001g0161a0002c0002t0002g0156 | 2 | HG02523.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.356-1507G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776562 | ||||||
| chr8:21776584
|
C | T | 9 | a0001c0001t0025g0001a0001c0006t0007g0033a0001c0006t0016g0031others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.356-1529G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776584 | ||||||
| chr8:21776633
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.356-1578C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776633 | ||||||
| chr8:21776692
|
A | G | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-1637T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776692 | ||||||
| chr8:21776848
|
C | G | 182 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(179): Show | 182 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.356-1793G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776848 | ||||||
| chr8:21776995
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.356-1940C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21776995 | ||||||
| chr8:21777256
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.356-2201A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777256 | ||||||
| chr8:21777327
|
T | G | 225 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(222): Show | 225 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.356-2272A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777327 | ||||||
| chr8:21777504
|
A | G | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.356-2449T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777504 | ||||||
| chr8:21777517
|
G | A | 1 | a0002c0002t0003g0255 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.356-2462C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777517 | ||||||
| chr8:21777551
|
G | C | 203 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(200): Show | 203 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.356-2496C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777551 | ||||||
| chr8:21777603
|
C | A | 83 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(80): Show | 83 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.356-2548G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777603 | ||||||
| chr8:21777603
|
C | G | 1 | a0001c0001t0013g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.356-2548G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777603 | ||||||
| chr8:21777610
|
T | C | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.356-2555A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777610 | ||||||
| chr8:21777616
|
G | A | 22 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0008g0302others(19): Show | 22 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.356-2561C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777616 | ||||||
| chr8:21777690
|
A | T | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.356-2635T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777690 | ||||||
| chr8:21777769
|
A | G | 66 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0003t0001g0014others(63): Show | 66 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.356-2714T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777769 | ||||||
| chr8:21777778
|
C | T | 22 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0008g0302others(19): Show | 22 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.356-2723G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777778 | ||||||
| chr8:21777817
|
G | T | 5 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-2762C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777817 | ||||||
| chr8:21777844
|
C | A | 84 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.356-2789G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21777844 | ||||||
| chr8:21778017
|
G | A | 2 | a0001c0003t0001g0056a0002c0005t0002g0055 | 2 | NA18979.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.356-2962C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778017 | ||||||
| chr8:21778143
|
G | A | 42 | a0001c0003t0001g0014a0001c0003t0001g0040a0001c0003t0001g0041others(39): Show | 42 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.356-3088C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778143 | ||||||
| chr8:21778172
|
C | A | 18 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0004g0221others(15): Show | 18 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.356-3117G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778172 | ||||||
| chr8:21778213
|
A | G | 22 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0008g0302others(19): Show | 22 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.356-3158T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778213 | ||||||
| chr8:21778218
|
G | GA | 88 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0006g0036others(85): Show | 88 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.356-3164dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778218 | ||||||
| chr8:21778391
|
T | A | 1 | a0001c0001t0005g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.356-3336A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778391 | ||||||
| chr8:21778527
|
C | A | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.356-3472G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778527 | ||||||
| chr8:21778547
|
G | T | 84 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.356-3492C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778547 | ||||||
| chr8:21778581
|
A | G | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-3526T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778581 | ||||||
| chr8:21778619
|
C | T | 2 | a0001c0001t0013g0182a0001c0020t0005g0186 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.356-3564G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778619 | ||||||
| chr8:21778631
|
A | G | 10 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.356-3576T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778631 | ||||||
| chr8:21778748
|
G | T | 1 | a0005c0013t0010g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.356-3693C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778748 | ||||||
| chr8:21778764
|
G | A | 5 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-3709C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778764 | ||||||
| chr8:21778779
|
C | T | 4 | a0001c0001t0004g0214a0001c0001t0004g0217a0002c0002t0003g0215others(1): Show | 4 | NA18747.hp1 NA18990.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-3724G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778779 | ||||||
| chr8:21778806
|
C | G | 213 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(210): Show | 213 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.356-3751G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778806 | ||||||
| chr8:21778908
|
A | AT | 5 | a0004c0011t0005g0197a0004c0011t0009g0195a0004c0015t0008g0196others(2): Show | 5 | HG01243.hp2 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+3676_355+3677i others(3): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21778908 | ||||||
| chr8:21779037
|
C | CT | 8 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0004t0009g0228others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.355+3547dupA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779037 | ||||||
| chr8:21779040
|
A | T | 206 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(203): Show | 206 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.355+3545T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779040 | ||||||
| chr8:21779041
|
A | T | 1 | a0001c0001t0005g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.355+3544T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779041 | ||||||
| chr8:21779154
|
C | G | 84 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.355+3431G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779154 | ||||||
| chr8:21779187
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+3398C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779187 | ||||||
| chr8:21779191
|
C | A | 14 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0001t0025g0001others(11): Show | 14 | HG00738.hp2 HG01099.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.355+3394G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779191 | ||||||
| chr8:21779206
|
C | T | 86 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(83): Show | 86 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.355+3379G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779206 | ||||||
| chr8:21779207
|
G | A | 1 | a0001c0001t0006g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355+3378C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779207 | ||||||
| chr8:21779252
|
C | G | 5 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+3333G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779252 | ||||||
| chr8:21779280
|
A | G | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.355+3305T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779280 | ||||||
| chr8:21779413
|
GC | G | 17 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0004g0221others(14): Show | 17 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.355+3171delG | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779413 | ||||||
| chr8:21779416
|
C | G | 10 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+3169G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779416 | ||||||
| chr8:21779563
|
T | C | 183 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0064others(180): Show | 183 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.355+3022A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779563 | ||||||
| chr8:21779616
|
G | A | 89 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0068others(86): Show | 89 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.355+2969C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779616 | ||||||
| chr8:21779628
|
G | A | 10 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+2957C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779628 | ||||||
| chr8:21779716
|
G | A | 4 | a0001c0006t0009g0304a0002c0002t0015g0004a0002c0002t0015g0006others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+2869C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779716 | ||||||
| chr8:21779742
|
A | G | 10 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+2843T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779742 | ||||||
| chr8:21779825
|
C | T | 97 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0064others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.355+2760G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779825 | ||||||
| chr8:21779915
|
C | T | 5 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+2670G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779915 | ||||||
| chr8:21779916
|
T | G | 5 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+2669A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779916 | ||||||
| chr8:21779960
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.355+2625C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779960 | ||||||
| chr8:21779968
|
C | T | 5 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+2617G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21779968 | ||||||
| chr8:21780056
|
C | CT | 10 | a0001c0001t0005g0192a0001c0001t0020g0307a0001c0001t0020g0309others(7): Show | 10 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+2528dupA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780056 | ||||||
| chr8:21780056
|
CT | C | 111 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(108): Show | 111 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.355+2528delA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780056 | ||||||
| chr8:21780056
|
CTT | C | 8 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(5): Show | 8 | HG00323.hp1 HG02056.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.355+2527_355+2528d others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780056 | ||||||
| chr8:21780182
|
C | T | 43 | a0001c0001t0001g0084a0001c0003t0001g0014a0001c0003t0001g0040others(40): Show | 43 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.355+2403G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780182 | ||||||
| chr8:21780188
|
T | G | 1 | a0003c0008t0014g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.355+2397A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780188 | ||||||
| chr8:21780211
|
G | A | 11 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(8): Show | 11 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.355+2374C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780211 | ||||||
| chr8:21780249
|
G | A | 1 | a0001c0001t0005g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.355+2336C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780249 | ||||||
| chr8:21780255
|
G | A | 1 | a0002c0002t0002g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.355+2330C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780255 | ||||||
| chr8:21780334
|
T | C | 12 | a0001c0001t0001g0141a0001c0001t0008g0302a0001c0001t0008g0303others(9): Show | 12 | HG00597.hp1 HG02109.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.355+2251A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780334 | ||||||
| chr8:21780336
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.355+2249G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780336 | ||||||
| chr8:21780423
|
C | G | 13 | a0001c0006t0002g0028a0004c0009t0005g0200a0004c0009t0013g0190others(10): Show | 13 | HG01243.hp2 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.355+2162G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780423 | ||||||
| chr8:21780438
|
C | G | 1 | a0001c0001t0009g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.355+2147G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780438 | ||||||
| chr8:21780480
|
G | A | 3 | a0002c0002t0002g0081a0002c0002t0003g0193a0002c0002t0008g0220 | 3 | HG00438.hp1 HG01884.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.355+2105C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780480 | ||||||
| chr8:21780514
|
T | C | 1 | a0001c0001t0007g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.355+2071A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780514 | ||||||
| chr8:21780588
|
C | T | 1 | a0001c0001t0019g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.355+1997G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780588 | ||||||
| chr8:21780593
|
G | A | 26 | a0001c0001t0001g0039a0001c0001t0001g0149a0001c0001t0004g0213others(23): Show | 26 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.355+1992C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780593 | ||||||
| chr8:21780606
|
C | T | 9 | a0001c0001t0004g0222a0001c0001t0005g0241a0001c0001t0005g0251others(6): Show | 9 | HG02135.hp1 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.355+1979G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780606 | ||||||
| chr8:21780669
|
C | T | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.355+1916G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780669 | ||||||
| chr8:21780912
|
G | A | 31 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0003g0226others(28): Show | 31 | HG00438.hp1 HG00639.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.355+1673C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780912 | ||||||
| chr8:21780968
|
A | T | 74 | a0001c0001t0001g0084a0001c0001t0006g0036a0001c0001t0019g0025others(71): Show | 74 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.355+1617T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780968 | ||||||
| chr8:21780999
|
T | G | 1 | a0002c0002t0002g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.355+1586A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21780999 | ||||||
| chr8:21781015
|
C | T | 1 | a0001c0020t0005g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.355+1570G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781015 | ||||||
| chr8:21781051
|
A | G | 48 | a0001c0001t0001g0084a0001c0003t0001g0014a0001c0003t0001g0040others(45): Show | 48 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.355+1534T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781051 | ||||||
| chr8:21781079
|
A | C | 2 | a0001c0001t0013g0182a0001c0020t0005g0186 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.355+1506T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781079 | ||||||
| chr8:21781092
|
T | TA | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+1492dupT | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781092 | ||||||
| chr8:21781113
|
T | A | 60 | a0001c0001t0001g0084a0001c0003t0001g0014a0001c0003t0001g0040others(57): Show | 60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.355+1472A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781113 | ||||||
| chr8:21781238
|
C | T | 1 | a0002c0005t0017g0009 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.355+1347G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781238 | ||||||
| chr8:21781266
|
G | C | 1 | a0005c0013t0010g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.355+1319C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781266 | ||||||
| chr8:21781415
|
G | C | 13 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(10): Show | 13 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+1170C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781415 | ||||||
| chr8:21781620
|
A | G | 225 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(222): Show | 225 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.355+965T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781620 | ||||||
| chr8:21781632
|
C | T | 10 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(7): Show | 10 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+953G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781632 | ||||||
| chr8:21781655
|
A | AC | 18 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0001t0025g0001others(15): Show | 18 | HG00738.hp2 HG01099.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.355+929dupG | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781655 | ||||||
| chr8:21781655
|
A | ACC | 55 | a0001c0001t0001g0084a0001c0003t0001g0014a0001c0003t0001g0040others(52): Show | 55 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.355+928_355+929dup others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781655 | ||||||
| chr8:21781658
|
T | C | 221 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(218): Show | 221 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.355+927A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781658 | ||||||
| chr8:21781662
|
C | A | 5 | a0001c0001t0001g0039a0001c0001t0004g0214a0001c0001t0004g0217others(2): Show | 5 | HG02056.hp1 NA18747.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+923G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781662 | ||||||
| chr8:21781807
|
A | G | 5 | a0001c0001t0005g0192a0001c0004t0009g0228a0002c0002t0003g0193others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+778T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781807 | ||||||
| chr8:21781839
|
G | T | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.355+746C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781839 | ||||||
| chr8:21781869
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.355+716G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781869 | ||||||
| chr8:21781870
|
G | A | 1 | a0002c0002t0003g0275 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.355+715C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781870 | ||||||
| chr8:21781980
|
TG | T | 75 | a0001c0001t0001g0084a0001c0001t0006g0036a0001c0001t0019g0025others(72): Show | 75 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.355+604delC | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21781980 | ||||||
| chr8:21782049
|
AG | A | 5 | a0001c0006t0009g0304a0002c0002t0002g0163a0002c0002t0015g0004others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+535delC | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782049 | ||||||
| chr8:21782057
|
C | A | 1 | a0002c0002t0002g0082 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.355+528G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782057 | ||||||
| chr8:21782095
|
T | C | 74 | a0001c0001t0001g0084a0001c0001t0006g0036a0001c0001t0019g0025others(71): Show | 74 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.355+490A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782095 | ||||||
| chr8:21782263
|
T | C | 1 | a0001c0001t0013g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.355+322A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782263 | ||||||
| chr8:21782264
|
A | T | 44 | a0001c0001t0001g0084a0001c0003t0001g0014a0001c0003t0001g0040others(41): Show | 44 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.355+321T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782264 | ||||||
| chr8:21782313
|
C | A | 74 | a0001c0001t0001g0084a0001c0001t0006g0036a0001c0001t0019g0025others(71): Show | 74 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.355+272G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782313 | ||||||
| chr8:21782313
|
C | T | 17 | a0001c0001t0001g0060a0001c0001t0003g0226a0001c0001t0004g0221others(14): Show | 17 | HG00639.hp2 HG01168.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.355+272G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782313 | ||||||
| chr8:21782320
|
TCTC | T | 74 | a0001c0001t0001g0084a0001c0001t0006g0036a0001c0001t0019g0025others(71): Show | 74 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.355+262_355+264del others(3): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782320 | ||||||
| chr8:21782369
|
C | T | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.355+216G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782369 | ||||||
| chr8:21782486
|
G | C | 11 | a0001c0001t0001g0039a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02056.hp1 HG02074.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.355+99C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 2/8 | chr8 | 21782486 | ||||||
| chr8:21782984
|
G | T | 1 | a0002c0002t0010g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41-85C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21782984 | ||||||
| chr8:21783083
|
G | A | 1 | a0002c0005t0003g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.41-184C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783083 | ||||||
| chr8:21783113
|
C | T | 4 | a0001c0001t0006g0018a0001c0001t0006g0027a0001c0004t0006g0010others(1): Show | 4 | HG00733.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-214G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783113 | ||||||
| chr8:21783132
|
C | T | 2 | a0001c0001t0013g0182a0001c0020t0005g0186 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.41-233G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783132 | ||||||
| chr8:21783140
|
G | A | 4 | a0001c0001t0004g0214a0001c0001t0004g0217a0002c0002t0003g0215others(1): Show | 4 | NA18747.hp1 NA18990.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-241C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783140 | ||||||
| chr8:21783159
|
A | G | 114 | a0001c0001t0001g0039a0001c0001t0001g0080a0001c0001t0001g0149others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.41-260T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783159 | ||||||
| chr8:21783177
|
C | T | 13 | a0001c0001t0006g0036a0001c0001t0019g0025a0001c0001t0025g0001others(10): Show | 13 | HG00738.hp2 HG01099.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.41-278G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783177 | ||||||
| chr8:21783249
|
C | T | 3 | a0001c0001t0006g0027a0001c0004t0006g0010a0001c0006t0016g0026 | 3 | HG00733.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.41-350G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783249 | ||||||
| chr8:21783295
|
G | T | 130 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0061others(127): Show | 130 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.41-396C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783295 | ||||||
| chr8:21783375
|
G | A | 9 | a0001c0001t0001g0149a0001c0001t0011g0316a0001c0001t0011g0318others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-476C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783375 | ||||||
| chr8:21783500
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.41-601C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783500 | ||||||
| chr8:21783559
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-660C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783559 | ||||||
| chr8:21783624
|
CT | C | 8 | a0001c0001t0011g0316a0001c0001t0011g0318a0001c0001t0011g0319others(5): Show | 8 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.41-726delA | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783624 | ||||||
| chr8:21783689
|
C | T | 26 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0217others(23): Show | 26 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.41-790G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783689 | ||||||
| chr8:21783769
|
C | T | 5 | a0001c0001t0005g0231a0001c0001t0019g0025a0001c0004t0013g0232others(2): Show | 5 | HG02280.hp2 HG03516.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-870G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783769 | ||||||
| chr8:21783810
|
A | G | 65 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0168others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.41-911T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21783810 | ||||||
| chr8:21784057
|
T | C | 14 | a0001c0001t0009g0202a0001c0004t0009g0228a0002c0021t0010g0225others(11): Show | 14 | HG01243.hp2 HG02109.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-1158A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784057 | ||||||
| chr8:21784175
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.41-1276T>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784175 | ||||||
| chr8:21784307
|
G | A | 2 | a0001c0006t0009g0233a0001c0006t0023g0234 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.41-1408C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784307 | ||||||
| chr8:21784474
|
A | G | 2 | a0001c0001t0005g0231a0001c0004t0013g0232 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.41-1575T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784474 | ||||||
| chr8:21784490
|
T | G | 4 | a0001c0001t0007g0005a0002c0002t0015g0004a0002c0002t0015g0006others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-1591A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784490 | ||||||
| chr8:21784500
|
A | G | 10 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0217others(7): Show | 10 | HG02074.hp2 NA18747.hp1 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-1601T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784500 | ||||||
| chr8:21784503
|
G | A | 1 | a0001c0006t0009g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-1604C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784503 | ||||||
| chr8:21784550
|
G | A | 1 | a0001c0001t0011g0322 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.41-1651C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784550 | ||||||
| chr8:21784670
|
G | T | 1 | a0001c0023t0018g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.41-1771C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784670 | ||||||
| chr8:21784714
|
A | G | 11 | a0001c0001t0006g0013a0001c0001t0006g0018a0001c0004t0008g0224others(8): Show | 11 | HG00438.hp1 HG00639.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-1815T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784714 | ||||||
| chr8:21784734
|
A | G | 1 | a0002c0005t0003g0183 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.41-1835T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784734 | ||||||
| chr8:21784738
|
C | A | 2 | a0001c0023t0018g0150a0002c0002t0002g0151 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.41-1839G>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784738 | ||||||
| chr8:21784738
|
C | T | 8 | a0001c0001t0005g0192a0001c0006t0009g0233a0001c0006t0023g0234others(5): Show | 8 | HG02258.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.41-1839G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784738 | ||||||
| chr8:21784862
|
C | T | 13 | a0001c0001t0005g0241a0001c0001t0005g0251a0001c0001t0005g0254others(10): Show | 13 | HG00408.hp2 HG00597.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.41-1963G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784862 | ||||||
| chr8:21784863
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-1964C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784863 | ||||||
| chr8:21784863
|
G | T | 1 | a0002c0016t0006g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41-1964C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784863 | ||||||
| chr8:21784879
|
T | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0036g0155 | 3 | HG02132.hp1 HG02165.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.41-1980A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784879 | ||||||
| chr8:21784938
|
G | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0006g0158others(3): Show | 6 | HG02027.hp2 HG02083.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-2039C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784938 | ||||||
| chr8:21784955
|
C | T | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.41-2056G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784955 | ||||||
| chr8:21784995
|
A | G | 6 | a0001c0001t0004g0214a0001c0001t0004g0217a0001c0003t0004g0209others(3): Show | 6 | NA18747.hp1 NA18990.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-2096T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21784995 | ||||||
| chr8:21785056
|
T | C | 62 | a0001c0001t0001g0016a0001c0001t0001g0168a0001c0001t0004g0184others(59): Show | 62 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.41-2157A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21785056 | ||||||
| chr8:21785102
|
T | A | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-2203A>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21785102 | ||||||
| chr8:21785158
|
G | C | 1 | a0001c0001t0008g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41-2259C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21785158 | ||||||
| chr8:21785307
|
G | A | 2 | a0001c0001t0004g0296a0001c0001t0008g0285 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.41-2408C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21785307 | ||||||
| chr8:21785594
|
G | C | 18 | a0001c0001t0004g0184a0001c0001t0004g0244a0001c0001t0004g0245others(15): Show | 18 | HG00408.hp2 HG00597.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.40+2526C>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21785594 | ||||||
| chr8:21785664
|
G | A | 1 | a0005c0013t0010g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.40+2456C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21785664 | ||||||
| chr8:21785784
|
G | T | 3 | a0001c0006t0009g0233a0001c0006t0023g0234a0002c0002t0003g0181 | 3 | HG02258.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.40+2336C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21785784 | ||||||
| chr8:21786139
|
T | C | 6 | a0001c0001t0004g0214a0001c0001t0004g0217a0001c0001t0004g0218others(3): Show | 6 | HG02074.hp2 NA18747.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+1981A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786139 | ||||||
| chr8:21786249
|
G | T | 5 | a0001c0001t0008g0302a0001c0001t0008g0303a0001c0006t0009g0304others(2): Show | 5 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+1871C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786249 | ||||||
| chr8:21786308
|
G | GGCCC | 30 | a0001c0001t0001g0003a0001c0001t0001g0176a0001c0001t0004g0263others(27): Show | 30 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.40+1808_40+1811dup others(4): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786308 | ||||||
| chr8:21786313
|
A | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0168others(104): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.40+1807T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786313 | ||||||
| chr8:21786430
|
T | G | 1 | a0001c0006t0009g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.40+1690A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786430 | ||||||
| chr8:21786436
|
C | T | 5 | a0001c0001t0005g0231a0001c0004t0013g0230a0001c0004t0013g0232others(2): Show | 5 | HG02615.hp2 HG03516.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+1684G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786436 | ||||||
| chr8:21786469
|
G | T | 1 | a0001c0001t0005g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40+1651C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786469 | ||||||
| chr8:21786530
|
T | C | 5 | a0001c0001t0005g0306a0001c0001t0008g0302a0001c0001t0008g0303others(2): Show | 5 | HG02572.hp2 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+1590A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786530 | ||||||
| chr8:21786566
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40+1554G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786566 | ||||||
| chr8:21786704
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.40+1416G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786704 | ||||||
| chr8:21786771
|
G | A | 9 | a0001c0001t0004g0184a0001c0001t0005g0254a0001c0003t0005g0253others(6): Show | 9 | HG00408.hp2 HG00597.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+1349C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786771 | ||||||
| chr8:21786912
|
G | T | 1 | a0001c0004t0006g0010 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.40+1208C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786912 | ||||||
| chr8:21786920
|
A | G | 4 | a0001c0001t0007g0005a0002c0002t0015g0004a0002c0002t0015g0006others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+1200T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786920 | ||||||
| chr8:21786932
|
G | A | 4 | a0001c0001t0020g0307a0001c0001t0020g0309a0001c0019t0020g0310others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+1188C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786932 | ||||||
| chr8:21786948
|
G | A | 1 | a0002c0002t0002g0162 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.40+1172C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786948 | ||||||
| chr8:21786972
|
C | T | 1 | a0002c0002t0003g0271 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.40+1148G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786972 | ||||||
| chr8:21786993
|
C | G | 1 | a0002c0005t0017g0009 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.40+1127G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21786993 | ||||||
| chr8:21787009
|
CAT | C | 3 | a0001c0004t0013g0230a0001c0006t0009g0243a0002c0002t0005g0242 | 3 | HG02615.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.40+1109_40+1110del others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787009 | ||||||
| chr8:21787132
|
T | C | 17 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0217others(14): Show | 17 | HG02074.hp2 HG02109.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.40+988A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787132 | ||||||
| chr8:21787207
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.40+913T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787207 | ||||||
| chr8:21787257
|
AGGC | A | 12 | a0001c0001t0004g0184a0001c0001t0005g0251a0001c0001t0005g0254others(9): Show | 12 | HG00597.hp1 HG01952.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.40+860_40+862delGC others(1): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787257 | ||||||
| chr8:21787260
|
C | CG | 21 | a0001c0001t0001g0003a0001c0001t0001g0168a0001c0001t0001g0176others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.40+859dupC | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787260 | ||||||
| chr8:21787260
|
C | CGG | 37 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0217others(34): Show | 37 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(34): Show |
intron_variant | MODIFIER | c.40+858_40+859dupCC | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787260 | ||||||
| chr8:21787260
|
C | CGGG | 12 | a0001c0001t0004g0267a0001c0001t0004g0269a0001c0001t0004g0270others(9): Show | 12 | HG02132.hp2 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.40+859_40+860insCC others(1): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787260 | ||||||
| chr8:21787260
|
C | CGGGG | 6 | a0001c0001t0004g0263a0002c0002t0003g0260a0002c0002t0003g0261others(3): Show | 6 | HG00735.hp2 HG01433.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+859_40+860insCC others(2): Show |
GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787260 | ||||||
| chr8:21787261
|
GGC | G | 35 | a0001c0001t0005g0192a0001c0001t0005g0231a0001c0001t0005g0238others(32): Show | 35 | HG00408.hp2 HG00639.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.40+857_40+858delGC | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787261 | ||||||
| chr8:21787262
|
GC | G | 12 | a0001c0001t0003g0226a0001c0001t0005g0306a0001c0004t0009g0228others(9): Show | 12 | HG02055.hp2 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.40+857delG | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787262 | ||||||
| chr8:21787263
|
C | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0168a0001c0001t0001g0176others(82): Show | 85 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.40+857G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787263 | ||||||
| chr8:21787271
|
G | A | 1 | a0002c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.40+849C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787271 | ||||||
| chr8:21787272
|
C | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0168a0001c0001t0001g0176others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.40+848G>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787272 | ||||||
| chr8:21787273
|
A | T | 1 | a0002c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.40+847T>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787273 | ||||||
| chr8:21787275
|
T | G | 1 | a0002c0002t0003g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.40+845A>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787275 | ||||||
| chr8:21787275
|
T | TG | 18 | a0001c0001t0004g0184a0001c0001t0005g0251a0001c0001t0005g0254others(15): Show | 18 | HG00408.hp2 HG00597.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.40+844dupC | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787275 | ||||||
| chr8:21787350
|
C | T | 6 | a0001c0006t0023g0208a0002c0002t0003g0203a0002c0002t0003g0205others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+770G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787350 | ||||||
| chr8:21787394
|
C | T | 15 | a0001c0001t0005g0192a0001c0001t0009g0202a0002c0002t0003g0193others(12): Show | 15 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+726G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787394 | ||||||
| chr8:21787416
|
G | A | 1 | a0002c0007t0002g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.40+704C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787416 | ||||||
| chr8:21787647
|
C | T | 4 | a0001c0001t0013g0182a0001c0020t0005g0186a0002c0002t0010g0185others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+473G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787647 | ||||||
| chr8:21787673
|
G | A | 57 | a0001c0001t0001g0168a0001c0001t0001g0176a0001c0001t0004g0263others(54): Show | 57 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.40+447C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787673 | ||||||
| chr8:21787690
|
A | G | 2 | a0001c0001t0004g0184a0002c0005t0003g0183 | 2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.40+430T>C | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787690 | ||||||
| chr8:21787777
|
T | C | 6 | a0001c0001t0005g0306a0001c0001t0008g0302a0001c0001t0008g0303others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+343A>G | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787777 | ||||||
| chr8:21787849
|
G | A | 1 | a0002c0002t0002g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.40+271C>T | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787849 | ||||||
| chr8:21787852
|
G | T | 1 | a0002c0002t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.40+268C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787852 | ||||||
| chr8:21787977
|
C | T | 1 | a0001c0001t0013g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+143G>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21787977 | ||||||
| chr8:21788035
|
G | T | 1 | a0002c0002t0003g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40+85C>A | GFRA2 | ENSG00000168546.11 | transcript | ENST00000524240.6 | protein_coding | 1/8 | chr8 | 21788035 |