| geneid | 57679 |
|---|---|
| ensemblid | ENSG00000003393.16 |
| hgncid | 443 |
| symbol | ALS2 |
| name | alsin Rho guanine nucleotide exchange factor ALS2 |
| refseq_nuc | NM_020919.4 |
| refseq_prot | NP_065970.2 |
| ensembl_nuc | ENST00000264276.11 |
| ensembl_prot | ENSP00000264276.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 201700267 |
| end | 201780933 |
| strand | - |
| ver | v1.2 |
| region | chr2:201700267-201780933 |
| region5000 | chr2:201695267-201785933 |
| regionname0 | ALS2_chr2_201700267_201780933 |
| regionname5000 | ALS2_chr2_201695267_201785933 |
| 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 | 0/1 | 1657 | 311 | 57 | 49 | 155 | 13 | 36 | 121 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002 | 1/0 | 1657 | 19 | 13 | 3 | 0 | 1 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0003 | 0/0 | 1657 | 6 | 4 | 1 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0004 | 0/0 | 1657 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0005 | 0/0 | 1657 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0006 | 0/0 | 1657 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0007 | 0/0 | 1657 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0008 | 0/0 | 1657 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0009 | 0/0 | 1657 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0010 | 0/0 | 1657 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0011 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0012 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0013 | 0/0 | 1657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0014 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0015 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| 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 | 0/0 | 4974 | 131 | 41 | 8 | 65 | 2 | 15 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0002 | 0/1 | 4974 | 94 | 2 | 26 | 46 | 7 | 12 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0003 | 0/0 | 4974 | 60 | 5 | 5 | 42 | 1 | 7 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0004 | 0/0 | 4974 | 19 | 7 | 10 | 1 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0005 | 0/0 | 4974 | 12 | 9 | 2 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0006 | 1/0 | 4974 | 6 | 3 | 1 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0007 | 0/0 | 4974 | 6 | 4 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0008 | 0/0 | 4974 | 4 | 0 | 4 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0009 | 0/0 | 4974 | 4 | 0 | 0 | 0 | 3 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0010 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0011 | 0/0 | 4974 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0012 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0013 | 0/0 | 4974 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0014 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0015 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0016 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0017 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0018 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0019 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0020 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0021 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0022 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| c0023 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1702 | 272 | 59 | 50 | 116 | 14 | 31 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0002 | 0/0 | 1702 | 55 | 2 | 2 | 45 | 1 | 5 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0003 | 0/0 | 1702 | 12 | 10 | 2 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0004 | 0/0 | 1702 | 4 | 0 | 3 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0005 | 0/0 | 1702 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0006 | 0/0 | 1702 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0007 | 0/0 | 1702 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0008 | 0/0 | 1702 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0009 | 0/0 | 1702 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0010 | 0/0 | 1702 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0011 | 0/0 | 1702 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| t0012 | 0/0 | 1702 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| 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 | 4 | 0 | 1 | 2 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| 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 | 0/0 | 4974 | 131 | 41 | 8 | 65 | 2 | 15 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0002 | 0/1 | 4974 | 94 | 2 | 26 | 46 | 7 | 12 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0003 | 0/0 | 4974 | 60 | 5 | 5 | 42 | 1 | 7 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0004 | 0/0 | 4974 | 19 | 7 | 10 | 1 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0009 | 0/0 | 4974 | 4 | 0 | 0 | 0 | 3 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0011 | 0/0 | 4974 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0022 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002c0005 | 0/0 | 4974 | 12 | 9 | 2 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002c0006 | 1/0 | 4974 | 6 | 3 | 1 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002c0020 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0003c0007 | 0/0 | 4974 | 6 | 4 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0004c0008 | 0/0 | 4974 | 4 | 0 | 4 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0005c0012 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0006c0010 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0007c0013 | 0/0 | 4974 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0008c0021 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0009c0015 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0010c0016 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0011c0017 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0012c0019 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0013c0018 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0014c0014 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0015c0023 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6675 | 117 | 30 | 6 | 65 | 2 | 14 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0001t0003 | 0/0 | 6675 | 11 | 9 | 2 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0001t0006 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0001t0008 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0002t0001 | 0/1 | 6675 | 91 | 2 | 25 | 45 | 6 | 12 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0002t0009 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0002t0010 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0002t0011 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0003t0001 | 0/0 | 6675 | 2 | 1 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0003t0002 | 0/0 | 6675 | 52 | 2 | 2 | 42 | 1 | 5 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0003t0004 | 0/0 | 6675 | 4 | 0 | 3 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0003t0007 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0004t0001 | 0/0 | 6675 | 18 | 6 | 10 | 1 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0004t0003 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0009t0001 | 0/0 | 6675 | 4 | 0 | 0 | 0 | 3 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0011t0001 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0001c0022t0001 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002c0005t0001 | 0/0 | 6675 | 12 | 9 | 2 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002c0006t0001 | 1/0 | 6675 | 4 | 1 | 1 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002c0006t0005 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0002c0020t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0003c0007t0001 | 0/0 | 6675 | 6 | 4 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0004c0008t0001 | 0/0 | 6675 | 4 | 0 | 4 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0005c0012t0002 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0006c0010t0001 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0007c0013t0001 | 0/0 | 6675 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0008c0021t0001 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0009c0015t0002 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0010c0016t0001 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0011c0017t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0012c0019t0012 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0013c0018t0001 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0014c0014t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| a0015c0023t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | copy fasta | chr2 | 201695267 | 201785933 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0009g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0010g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0011g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0009t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0009t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0009t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0011t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0011t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0022t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0020t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0005c0012t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0005c0012t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0006c0010t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0006c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0007c0013t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0008c0021t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0009c0015t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0010c0016t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0011c0017t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0012c0019t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0013c0018t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0014c0014t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0015c0023t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0006 | t0001 | g0058 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0220 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00140 | hp2 | a0001 | c0002 | t0011 | g0102 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0052 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00280 | hp2 | a0001 | c0009 | t0001 | g0016 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0104 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00323 | hp2 | a0001 | c0009 | t0001 | g0016 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0192 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0161 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0299 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0075 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00673 | hp2 | a0008 | c0021 | t0001 | g0086 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00741 | hp1 | a0001 | c0003 | t0004 | g0156 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0077 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01074 | hp1 | a0002 | c0005 | t0001 | g0067 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01081 | hp1 | a0002 | c0006 | t0001 | g0057 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0155 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0169 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01175 | hp1 | a0010 | c0016 | t0001 | g0130 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01175 | hp2 | a0001 | c0003 | t0004 | g0154 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01255 | hp2 | a0002 | c0005 | t0001 | g0065 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0048 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0076 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0049 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01496 | hp2 | a0003 | c0007 | t0001 | g0033 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0128 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01515 | hp2 | a0007 | c0013 | t0001 | g0019 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0090 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01517 | hp2 | a0007 | c0013 | t0001 | g0019 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0157 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01884 | hp2 | a0014 | c0014 | t0001 | g0043 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0050 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01943 | hp1 | a0004 | c0008 | t0001 | g0236 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01952 | hp2 | a0004 | c0008 | t0001 | g0241 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0199 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01975 | hp2 | a0001 | c0002 | t0010 | g0112 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01981 | hp1 | a0004 | c0008 | t0001 | g0237 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02004 | hp1 | a0004 | c0008 | t0001 | g0240 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0216 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02055 | hp1 | a0002 | c0006 | t0001 | g0056 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02056 | hp2 | a0001 | c0022 | t0001 | g0124 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0175 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0172 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0176 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02145 | hp1 | a0002 | c0005 | t0001 | g0061 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02145 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0189 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02165 | hp1 | a0009 | c0015 | t0002 | g0188 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0079 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02280 | hp1 | a0002 | c0020 | t0001 | g0062 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02280 | hp2 | a0015 | c0023 | t0001 | g0035 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0073 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02615 | hp1 | a0001 | c0011 | t0001 | g0322 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02622 | hp2 | a0001 | c0003 | t0007 | g0041 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02630 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02647 | hp1 | a0003 | c0007 | t0001 | g0036 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0074 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0200 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02683 | hp2 | a0001 | c0009 | t0001 | g0312 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0122 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02717 | hp2 | a0012 | c0019 | t0012 | g0082 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02738 | hp2 | a0001 | c0003 | t0004 | g0165 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02818 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0184 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02897 | hp1 | a0001 | c0011 | t0001 | g0081 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03017 | hp1 | a0003 | c0007 | t0001 | g0032 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03041 | hp2 | a0002 | c0006 | t0005 | g0060 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0331 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03130 | hp1 | a0001 | c0003 | t0007 | g0040 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03195 | hp1 | a0003 | c0007 | t0001 | g0037 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0002 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0332 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03209 | hp2 | a0011 | c0017 | t0001 | g0228 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0008 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0008 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0194 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03540 | hp1 | a0002 | c0006 | t0005 | g0059 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03579 | hp1 | a0002 | c0005 | t0001 | g0063 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03688 | hp2 | a0002 | c0005 | t0001 | g0055 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0078 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0280 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0135 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0201 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0173 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0315 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0226 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0203 | EAS | CHB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0159 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18944 | hp2 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18945 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18949 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18952 | hp2 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18956 | hp2 | a0001 | c0003 | t0002 | g0186 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18959 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18965 | hp2 | a0013 | c0018 | t0001 | g0218 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18966 | hp2 | a0001 | c0002 | t0009 | g0136 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0197 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18975 | hp1 | a0005 | c0012 | t0002 | g0160 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18978 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0300 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18980 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18981 | hp2 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0181 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18994 | hp2 | a0005 | c0012 | t0002 | g0163 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0087 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0167 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19003 | hp2 | a0001 | c0003 | t0002 | g0164 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19004 | hp1 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19005 | hp1 | a0006 | c0010 | t0001 | g0145 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0162 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19043 | hp1 | a0002 | c0005 | t0001 | g0004 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19057 | hp1 | a0006 | c0010 | t0001 | g0097 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0191 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19065 | hp2 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0174 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19072 | hp2 | a0001 | c0003 | t0002 | g0185 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19079 | hp2 | a0001 | c0003 | t0002 | g0170 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19089 | hp2 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19091 | hp2 | a0001 | c0003 | t0002 | g0198 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0108 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20752 | hp2 | a0001 | c0009 | t0001 | g0229 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02486 | hp2 | a0003 | c0007 | t0001 | g0034 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02559 | hp1 | a0002 | c0005 | t0001 | g0004 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG06807 | hp2 | a0002 | c0005 | t0001 | g0066 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20300 | hp2 | a0002 | c0005 | t0001 | g0064 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0091 | REF | REF | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| homoSapiens_grch38 | hp1 | a0002 | c0006 | t0001 | g0233 | REF | REF | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201706930
|
C | T | 1 | a0012 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.4496G>A | p.Arg1499His | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/34 | 4613/6675 | 4496/4974 | 1499/1657 | chr2 | 201706930 | ||
| chr2:201718204
|
G | T | 1 | a0013 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.3709C>A | p.Leu1237Met | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/34 | 3826/6675 | 3709/4974 | 1237/1657 | chr2 | 201718204 | ||
| chr2:201723437
|
C | T | 2 | a0006a0008 | 3 | HG00673.hp2 NA19005.hp1 NA19057.hp1 |
missense_variant | MODERATE | c.3517G>A | p.Glu1173Lys | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 22/34 | 3634/6675 | 3517/4974 | 1173/1657 | chr2 | 201723437 | ||
| chr2:201726526
|
C | T | 1 | a0011 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.3206G>A | p.Gly1069Glu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/34 | 3323/6675 | 3206/4974 | 1069/1657 | chr2 | 201726526 | ||
| chr2:201726784
|
C | T | 1 | a0010 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.3062G>A | p.Ser1021Asn | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 18/34 | 3179/6675 | 3062/4974 | 1021/1657 | chr2 | 201726784 | ||
| chr2:201726800
|
G | C | 1 | a0015 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.3046C>G | p.Pro1016Ala | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 18/34 | 3163/6675 | 3046/4974 | 1016/1657 | chr2 | 201726800 | ||
| chr2:201727238
|
G | A | 1 | a0005 | 2 | NA18975.hp1 NA18994.hp2 |
missense_variant | MODERATE | c.2953C>T | p.Leu985Phe | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/34 | 3070/6675 | 2953/4974 | 985/1657 | chr2 | 201727238 | ||
| chr2:201746580
|
G | T | 1 | a0009 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1984C>A | p.Leu662Ile | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/34 | 2101/6675 | 1984/4974 | 662/1657 | chr2 | 201746580 | ||
| chr2:201749717
|
C | T | 1 | a0014 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1810G>A | p.Ala604Thr | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/34 | 1927/6675 | 1810/4974 | 604/1657 | chr2 | 201749717 | ||
| chr2:201757758
|
G | C | 1 | a0007 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1115C>G | p.Pro372Arg | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/34 | 1232/6675 | 1115/4974 | 372/1657 | chr2 | 201757758 | ||
| chr2:201760892
|
C | T | 14 | a0001a0003a0004others(11): Show | 335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
missense_variant | MODERATE | c.1102G>A | p.Val368Met | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 1219/6675 | 1102/4974 | 368/1657 | chr2 | 201760892 | ||
| chr2:201761519
|
C | T | 1 | a0004 | 4 | HG01943.hp1 HG01952.hp2 HG01981.hp1 others(1): Show |
missense_variant | MODERATE | c.475G>A | p.Glu159Lys | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 592/6675 | 475/4974 | 159/1657 | chr2 | 201761519 | ||
| chr2:201761599
|
G | A | 1 | a0008 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.395C>T | p.Pro132Leu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 512/6675 | 395/4974 | 132/1657 | chr2 | 201761599 | ||
| chr2:201761714
|
T | C | 2 | a0003a0015 | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.280A>G | p.Ile94Val | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 397/6675 | 280/4974 | 94/1657 | chr2 | 201761714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201704528
|
C | T | 1 | a0001c0011 | 2 | HG02615.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.4764G>A | p.Ala1588Ala | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 32/34 | 4881/6675 | 4764/4974 | 1588/1657 | chr2 | 201704528 | ||
| chr2:201709888
|
G | A | 1 | a0009c0015 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.4273C>T | p.Leu1425Leu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/34 | 4390/6675 | 4273/4974 | 1425/1657 | chr2 | 201709888 | ||
| chr2:201711098
|
G | A | 20 | a0001c0001a0001c0002a0001c0003others(17): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
synonymous_variant | LOW | c.4015C>T | p.Leu1339Leu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/34 | 4132/6675 | 4015/4974 | 1339/1657 | chr2 | 201711098 | ||
| chr2:201715791
|
C | T | 1 | a0001c0009 | 4 | HG00280.hp2 HG00323.hp2 HG02683.hp2 others(1): Show |
synonymous_variant | LOW | c.3885G>A | p.Ala1295Ala | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/34 | 4002/6675 | 3885/4974 | 1295/1657 | chr2 | 201715791 | ||
| chr2:201728557
|
G | A | 3 | a0001c0003a0005c0012a0009c0015 | 63 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
synonymous_variant | LOW | c.2796C>T | p.Ser932Ser | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/34 | 2913/6675 | 2796/4974 | 932/1657 | chr2 | 201728557 | ||
| chr2:201733390
|
C | T | 10 | a0001c0002a0001c0011a0001c0022others(7): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
synonymous_variant | LOW | c.2466G>A | p.Val822Val | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/34 | 2583/6675 | 2466/4974 | 822/1657 | chr2 | 201733390 | ||
| chr2:201761694
|
G | A | 1 | a0001c0022 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.300C>T | p.Ser100Ser | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 417/6675 | 300/4974 | 100/1657 | chr2 | 201761694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201700390
|
C | T | 1 | a0001c0002t0009 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1461G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 1461 | chr2 | 201700390 | |||||
| chr2:201700649
|
G | A | 1 | a0001c0002t0010 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1202C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 1202 | chr2 | 201700649 | |||||
| chr2:201700847
|
C | T | 4 | a0001c0003t0002a0001c0003t0004a0005c0012t0002others(1): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 1004 | chr2 | 201700847 | |||||
| chr2:201700909
|
T | C | 1 | a0001c0002t0011 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 942 | chr2 | 201700909 | |||||
| chr2:201700958
|
G | A | 3 | a0001c0003t0002a0005c0012t0002a0009c0015t0002 | 55 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 893 | chr2 | 201700958 | |||||
| chr2:201701008
|
C | T | 1 | a0001c0001t0006 | 2 | HG03098.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*843G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 843 | chr2 | 201701008 | |||||
| chr2:201701073
|
T | C | 1 | a0012c0019t0012 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 778 | chr2 | 201701073 | |||||
| chr2:201701404
|
C | T | 1 | a0002c0006t0005 | 2 | HG03041.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*447G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 447 | chr2 | 201701404 | |||||
| chr2:201701472
|
A | T | 1 | a0001c0003t0007 | 2 | HG02622.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*379T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 379 | chr2 | 201701472 | |||||
| chr2:201701746
|
T | G | 1 | a0001c0003t0007 | 2 | HG02622.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*105A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 105 | chr2 | 201701746 | |||||
| chr2:201701836
|
A | C | 1 | a0001c0001t0008 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 15 | chr2 | 201701836 | |||||
| chr2:201780911
|
C | G | 2 | a0001c0001t0003a0001c0004t0003 | 12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-95G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/34 | 12026 | chr2 | 201780911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201701972
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4936-83G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201701972 | ||||||
| chr2:201702009
|
C | A | 1 | a0001c0003t0002g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4936-120G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702009 | ||||||
| chr2:201702018
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4936-129A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702018 | ||||||
| chr2:201702041
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(166): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.4936-152G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702041 | ||||||
| chr2:201702122
|
C | T | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4936-233G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702122 | ||||||
| chr2:201702145
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4936-256G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702145 | ||||||
| chr2:201702386
|
C | T | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4936-497G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702386 | ||||||
| chr2:201702400
|
G | GT | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4936-512dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702400 | ||||||
| chr2:201702471
|
T | A | 5 | a0001c0001t0001g0261a0003c0007t0001g0034a0003c0007t0001g0036others(2): Show | 5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4936-582A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702471 | ||||||
| chr2:201702602
|
T | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4936-713A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702602 | ||||||
| chr2:201702682
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4936-793G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702682 | ||||||
| chr2:201702838
|
A | G | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.4936-949T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702838 | ||||||
| chr2:201702868
|
C | A | 1 | a0001c0001t0001g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4936-979G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702868 | ||||||
| chr2:201702887
|
G | A | 8 | a0001c0001t0001g0083a0001c0001t0001g0205a0002c0005t0001g0004others(5): Show | 9 | HG01074.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4936-998C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702887 | ||||||
| chr2:201703169
|
AG | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4935+952delC | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703169 | ||||||
| chr2:201703196
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4935+926T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703196 | ||||||
| chr2:201703466
|
T | C | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4935+656A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703466 | ||||||
| chr2:201703594
|
A | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4935+528T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703594 | ||||||
| chr2:201703841
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4935+281T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703841 | ||||||
| chr2:201703895
|
G | A | 2 | a0001c0004t0001g0216a0001c0004t0003g0029 | 2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.4935+227C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703895 | ||||||
| chr2:201703896
|
G | A | 5 | a0001c0001t0001g0261a0003c0007t0001g0034a0003c0007t0001g0036others(2): Show | 5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4935+226C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703896 | ||||||
| chr2:201704053
|
G | T | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4935+69C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201704053 | ||||||
| chr2:201704931
|
C | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4688+208G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 31/33 | chr2 | 201704931 | ||||||
| chr2:201705124
|
C | T | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4688+15G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 31/33 | chr2 | 201705124 | ||||||
| chr2:201705240
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4627-40A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 30/33 | chr2 | 201705240 | ||||||
| chr2:201705269
|
A | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4627-69T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 30/33 | chr2 | 201705269 | ||||||
| chr2:201705468
|
T | C | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.4581-7A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705468 | ||||||
| chr2:201705509
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4581-48T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705509 | ||||||
| chr2:201705532
|
G | A | 5 | a0001c0001t0001g0261a0003c0007t0001g0034a0003c0007t0001g0036others(2): Show | 5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4581-71C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705532 | ||||||
| chr2:201705641
|
G | A | 2 | a0001c0002t0001g0151a0001c0002t0001g0152 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.4581-180C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705641 | ||||||
| chr2:201705758
|
C | T | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4581-297G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705758 | ||||||
| chr2:201705765
|
T | TA | 18 | a0001c0001t0001g0038a0001c0001t0001g0083a0001c0001t0001g0205others(15): Show | 19 | HG01074.hp1 HG01243.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.4581-305dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705765 | ||||||
| chr2:201705903
|
G | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.4581-442C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705903 | ||||||
| chr2:201705906
|
G | A | 1 | a0001c0003t0002g0010 | 2 | NA18949.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.4581-445C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705906 | ||||||
| chr2:201705943
|
C | T | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4581-482G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705943 | ||||||
| chr2:201705948
|
C | CA | 251 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.4581-488dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705948 | ||||||
| chr2:201705948
|
C | CAA | 52 | a0001c0002t0001g0085a0001c0003t0002g0008a0001c0003t0002g0009others(49): Show | 56 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4581-489_4581-488d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705948 | ||||||
| chr2:201706007
|
G | T | 7 | a0001c0004t0001g0005a0001c0004t0001g0073a0001c0004t0001g0074others(4): Show | 8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4581-546C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706007 | ||||||
| chr2:201706294
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4580+552C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706294 | ||||||
| chr2:201706369
|
G | A | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4580+477C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706369 | ||||||
| chr2:201706393
|
GA | G | 60 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0003t0001g0042others(57): Show | 64 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.4580+452delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706393 | ||||||
| chr2:201706393
|
GAA | G | 135 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0083others(132): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.4580+451_4580+452d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706393 | ||||||
| chr2:201706527
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4580+319G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706527 | ||||||
| chr2:201706535
|
T | TTATATA | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 49 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.4580+305_4580+310d others(8): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | ||||||
| chr2:201706535
|
T | TTATATAT others(1): Show |
44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 50 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.4580+303_4580+310d others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | ||||||
| chr2:201706535
|
T | TTATATAT others(3): Show |
17 | a0001c0001t0001g0012a0001c0001t0001g0235a0001c0001t0001g0258others(14): Show | 18 | HG01069.hp1 HG01496.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.4580+301_4580+310d others(12): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | ||||||
| chr2:201706535
|
T | TTATATAT others(5): Show |
8 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0248others(5): Show | 8 | HG02165.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4580+299_4580+310d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | ||||||
| chr2:201706535
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0313 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4580+297_4580+310d others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | ||||||
| chr2:201706535
|
TTA | T | 191 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0083others(188): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.4580+309_4580+310d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | ||||||
| chr2:201706624
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4580+222A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706624 | ||||||
| chr2:201706824
|
C | T | 1 | a0001c0003t0002g0008 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4580+22G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706824 | ||||||
| chr2:201706825
|
G | A | 1 | a0001c0002t0010g0112 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4580+21C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706825 | ||||||
| chr2:201706839
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(102): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
splice_region_variant&intron_variant | LOW | c.4580+7G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706839 | ||||||
| chr2:201707140
|
G | C | 1 | a0001c0002t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4404-118C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707140 | ||||||
| chr2:201707205
|
T | G | 3 | a0001c0003t0004g0154a0001c0003t0004g0155a0001c0003t0004g0156 | 3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.4404-183A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707205 | ||||||
| chr2:201707431
|
AC | A | 4 | a0001c0002t0001g0128a0001c0002t0001g0310a0001c0002t0001g0325others(1): Show | 4 | HG01515.hp1 NA18978.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.4404-410delG | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707431 | ||||||
| chr2:201707432
|
C | A | 189 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0083others(186): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.4404-410G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707432 | ||||||
| chr2:201707434
|
T | A | 4 | a0001c0002t0001g0128a0001c0002t0001g0310a0001c0002t0001g0325others(1): Show | 4 | HG01515.hp1 NA18978.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.4404-412A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707434 | ||||||
| chr2:201707457
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(100): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.4403+412G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707457 | ||||||
| chr2:201707614
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4403+255C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707614 | ||||||
| chr2:201707623
|
T | C | 55 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(52): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4403+246A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707623 | ||||||
| chr2:201708083
|
C | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4281-92G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708083 | ||||||
| chr2:201708187
|
G | A | 11 | a0001c0004t0001g0003a0001c0004t0001g0044a0001c0004t0001g0045others(8): Show | 12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.4281-196C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708187 | ||||||
| chr2:201708202
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4281-211G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708202 | ||||||
| chr2:201708317
|
C | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4281-326G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708317 | ||||||
| chr2:201708562
|
G | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4281-571C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708562 | ||||||
| chr2:201708662
|
A | G | 1 | a0001c0002t0001g0103 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4281-671T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708662 | ||||||
| chr2:201708753
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0003g0031 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4281-762G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708753 | ||||||
| chr2:201708824
|
T | C | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4281-833A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708824 | ||||||
| chr2:201708879
|
GA | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4281-889delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708879 | ||||||
| chr2:201708892
|
A | G | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4281-901T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708892 | ||||||
| chr2:201708904
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4281-913T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708904 | ||||||
| chr2:201709005
|
A | G | 1 | a0002c0020t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4280+876T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709005 | ||||||
| chr2:201709014
|
C | T | 1 | a0012c0019t0012g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4280+867G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709014 | ||||||
| chr2:201709156
|
C | G | 55 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(52): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4280+725G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709156 | ||||||
| chr2:201709217
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0227 | 2 | HG02004.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.4280+664G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709217 | ||||||
| chr2:201709298
|
T | C | 2 | a0001c0004t0001g0216a0001c0004t0003g0029 | 2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.4280+583A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709298 | ||||||
| chr2:201709368
|
G | A | 1 | a0014c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4280+513C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709368 | ||||||
| chr2:201709490
|
C | T | 1 | a0001c0003t0002g0299 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4280+391G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709490 | ||||||
| chr2:201709524
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4280+357C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709524 | ||||||
| chr2:201709533
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.4280+348G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709533 | ||||||
| chr2:201709711
|
C | T | 1 | a0001c0004t0001g0073 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4280+170G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709711 | ||||||
| chr2:201709779
|
T | C | 1 | a0001c0002t0001g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4280+102A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709779 | ||||||
| chr2:201710091
|
C | A | 1 | a0001c0011t0001g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4123-53G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710091 | ||||||
| chr2:201710102
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.4123-64G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710102 | ||||||
| chr2:201710133
|
G | A | 1 | a0002c0005t0001g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4123-95C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710133 | ||||||
| chr2:201710183
|
A | AT | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4123-146dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710183 | ||||||
| chr2:201710377
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4123-339T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710377 | ||||||
| chr2:201710381
|
G | A | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4123-343C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710381 | ||||||
| chr2:201710423
|
C | G | 1 | a0001c0001t0003g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4123-385G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710423 | ||||||
| chr2:201710433
|
T | TA | 313 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.4123-396dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710433 | ||||||
| chr2:201711183
|
C | T | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4005-75G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711183 | ||||||
| chr2:201711184
|
A | G | 139 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0083others(136): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.4005-76T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711184 | ||||||
| chr2:201711219
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4005-111G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711219 | ||||||
| chr2:201711235
|
A | G | 2 | a0002c0006t0001g0056a0002c0006t0001g0058 | 2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4005-127T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711235 | ||||||
| chr2:201711242
|
C | A | 52 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(49): Show | 56 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4005-134G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711242 | ||||||
| chr2:201711419
|
T | C | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4005-311A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711419 | ||||||
| chr2:201711561
|
A | AG | 103 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(100): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.4005-454dupC | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711561 | ||||||
| chr2:201711853
|
C | T | 11 | a0001c0004t0001g0003a0001c0004t0001g0044a0001c0004t0001g0045others(8): Show | 12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.4005-745G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711853 | ||||||
| chr2:201711861
|
CCTAA | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4005-757_4005-754d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711861 | ||||||
| chr2:201712055
|
A | G | 1 | a0001c0002t0001g0111 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4005-947T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712055 | ||||||
| chr2:201712082
|
GA | G | 5 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0002t0001g0007others(2): Show | 6 | HG01243.hp1 HG02451.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.4005-975delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712082 | ||||||
| chr2:201712202
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4005-1094T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712202 | ||||||
| chr2:201712234
|
C | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4005-1126G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712234 | ||||||
| chr2:201712297
|
T | G | 1 | a0001c0001t0001g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4005-1189A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712297 | ||||||
| chr2:201712413
|
A | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4005-1305T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712413 | ||||||
| chr2:201712578
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 120 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.4005-1470C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712578 | ||||||
| chr2:201712627
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4005-1519G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712627 | ||||||
| chr2:201712718
|
A | G | 3 | a0001c0002t0001g0219a0002c0020t0001g0062a0012c0019t0012g0082 | 3 | HG02280.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4005-1610T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712718 | ||||||
| chr2:201712753
|
GA | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(166): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.4005-1646delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712753 | ||||||
| chr2:201712770
|
G | GAA | 307 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(304): Show | 326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.4005-1664_4005-166 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712770 | ||||||
| chr2:201712849
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4005-1741A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712849 | ||||||
| chr2:201712901
|
T | C | 8 | a0001c0001t0001g0083a0001c0001t0001g0205a0002c0005t0001g0004others(5): Show | 9 | HG01074.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4005-1793A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712901 | ||||||
| chr2:201712915
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4005-1807A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712915 | ||||||
| chr2:201712942
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4005-1834T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712942 | ||||||
| chr2:201713069
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4005-1961T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713069 | ||||||
| chr2:201713122
|
C | CCTTTT | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.4005-2019_4005-201 others(9): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713122 | ||||||
| chr2:201713133
|
C | CT | 124 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0083others(121): Show | 129 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.4005-2026dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | ||||||
| chr2:201713133
|
C | CTT | 7 | a0001c0001t0003g0025a0001c0002t0001g0054a0001c0002t0001g0100others(4): Show | 7 | HG01123.hp1 HG02145.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.4005-2027_4005-202 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | ||||||
| chr2:201713133
|
C | CTTTTCT | 12 | a0001c0003t0007g0040a0001c0004t0001g0003a0001c0004t0001g0044others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4005-2026_4005-202 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | ||||||
| chr2:201713133
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4005-2037_4005-202 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | ||||||
| chr2:201713137
|
T | TC | 54 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(51): Show | 58 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4005-2030_4005-202 others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713137 | ||||||
| chr2:201713138
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 119 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.4005-2030A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713138 | ||||||
| chr2:201713139
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4005-2031A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713139 | ||||||
| chr2:201713208
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4005-2100G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713208 | ||||||
| chr2:201713223
|
A | G | 322 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(319): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.4005-2115T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713223 | ||||||
| chr2:201713310
|
T | C | 55 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(52): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4005-2202A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713310 | ||||||
| chr2:201713397
|
C | A | 3 | a0001c0002t0001g0219a0002c0020t0001g0062a0012c0019t0012g0082 | 3 | HG02280.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4004+2275G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713397 | ||||||
| chr2:201713404
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4004+2268T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713404 | ||||||
| chr2:201713532
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4004+2140C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713532 | ||||||
| chr2:201713602
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4004+2070C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713602 | ||||||
| chr2:201713626
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4004+2046C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713626 | ||||||
| chr2:201713725
|
T | C | 1 | a0001c0003t0002g0183 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4004+1947A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713725 | ||||||
| chr2:201713743
|
GTATTT | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4004+1924_4004+192 others(9): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713743 | ||||||
| chr2:201713791
|
CTA | C | 3 | a0001c0009t0001g0016a0001c0009t0001g0229a0001c0009t0001g0312 | 4 | HG00280.hp2 HG00323.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.4004+1879_4004+188 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713791 | ||||||
| chr2:201714012
|
T | C | 55 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(52): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4004+1660A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714012 | ||||||
| chr2:201714309
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4004+1363C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714309 | ||||||
| chr2:201714419
|
G | T | 1 | a0001c0003t0002g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4004+1253C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714419 | ||||||
| chr2:201714461
|
A | G | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4004+1211T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714461 | ||||||
| chr2:201714711
|
T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4004+961A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714711 | ||||||
| chr2:201714878
|
G | A | 2 | a0001c0002t0001g0221a0001c0002t0001g0232 | 2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.4004+794C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714878 | ||||||
| chr2:201714925
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.4004+747G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714925 | ||||||
| chr2:201714934
|
C | A | 11 | a0001c0004t0001g0003a0001c0004t0001g0044a0001c0004t0001g0045others(8): Show | 12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.4004+738G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714934 | ||||||
| chr2:201715545
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4004+127A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201715545 | ||||||
| chr2:201715605
|
T | G | 7 | a0001c0004t0001g0005a0001c0004t0001g0073a0001c0004t0001g0074others(4): Show | 8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4004+67A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201715605 | ||||||
| chr2:201715647
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.4004+25C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201715647 | ||||||
| chr2:201716466
|
C | T | 2 | a0001c0003t0002g0011a0001c0003t0002g0191 | 3 | NA18970.hp1 NA19054.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3837-627G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716466 | ||||||
| chr2:201716492
|
T | C | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.3837-653A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716492 | ||||||
| chr2:201716542
|
C | CA | 122 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.3837-704dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | ||||||
| chr2:201716542
|
C | CAA | 64 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0267others(61): Show | 70 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.3837-705_3837-704d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | ||||||
| chr2:201716542
|
C | CAAA | 11 | a0001c0003t0001g0042a0001c0003t0002g0161a0001c0003t0002g0162others(8): Show | 11 | HG00597.hp2 HG01175.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.3837-706_3837-704d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | ||||||
| chr2:201716542
|
CA | C | 6 | a0001c0001t0003g0027a0001c0002t0001g0053a0001c0002t0001g0071others(3): Show | 6 | HG01099.hp1 HG02451.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3837-704delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | ||||||
| chr2:201716565
|
A | G | 1 | a0001c0002t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3837-726T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716565 | ||||||
| chr2:201716665
|
A | T | 2 | a0001c0002t0001g0221a0001c0002t0001g0232 | 2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3837-826T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716665 | ||||||
| chr2:201716671
|
C | T | 3 | a0001c0002t0001g0089a0001c0002t0001g0090a0001c0002t0001g0126 | 3 | HG01255.hp1 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.3837-832G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716671 | ||||||
| chr2:201716687
|
C | T | 23 | a0001c0003t0007g0040a0001c0003t0007g0041a0001c0004t0001g0003others(20): Show | 25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3837-848G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716687 | ||||||
| chr2:201716702
|
G | A | 137 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0083others(134): Show | 142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.3837-863C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716702 | ||||||
| chr2:201716706
|
C | A | 11 | a0001c0004t0001g0003a0001c0004t0001g0044a0001c0004t0001g0045others(8): Show | 12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.3837-867G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716706 | ||||||
| chr2:201716714
|
CA | C | 16 | a0001c0002t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070others(13): Show | 16 | HG01952.hp1 NA18941.hp2 NA18942.hp2 others(13): Show |
intron_variant | MODIFIER | c.3837-876delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716714 | ||||||
| chr2:201716737
|
A | T | 1 | a0001c0003t0002g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3837-898T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716737 | ||||||
| chr2:201717004
|
G | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3836+1073C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717004 | ||||||
| chr2:201717045
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3836+1032A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717045 | ||||||
| chr2:201717184
|
G | T | 1 | a0001c0001t0003g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3836+893C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717184 | ||||||
| chr2:201717262
|
C | G | 1 | a0001c0004t0003g0029 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3836+815G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717262 | ||||||
| chr2:201717262
|
C | T | 1 | a0001c0011t0001g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3836+815G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717262 | ||||||
| chr2:201717391
|
G | A | 56 | a0001c0003t0001g0042a0001c0003t0002g0008a0001c0003t0002g0009others(53): Show | 60 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3836+686C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717391 | ||||||
| chr2:201717639
|
GA | G | 66 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0289others(63): Show | 70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.3836+437delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717639 | ||||||
| chr2:201717675
|
G | A | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3836+402C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717675 | ||||||
| chr2:201718345
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3703-135G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718345 | ||||||
| chr2:201718495
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3703-285T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718495 | ||||||
| chr2:201718719
|
C | A | 318 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(315): Show | 339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.3703-509G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718719 | ||||||
| chr2:201718806
|
A | G | 1 | a0001c0002t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3703-596T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718806 | ||||||
| chr2:201718832
|
G | A | 1 | a0001c0002t0001g0308 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3703-622C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718832 | ||||||
| chr2:201719316
|
C | T | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3703-1106G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719316 | ||||||
| chr2:201719370
|
C | T | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3703-1160G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719370 | ||||||
| chr2:201719391
|
C | T | 1 | a0005c0012t0002g0160 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3703-1181G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719391 | ||||||
| chr2:201719481
|
C | T | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3703-1271G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719481 | ||||||
| chr2:201719484
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3703-1274C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719484 | ||||||
| chr2:201719514
|
A | G | 1 | a0001c0003t0002g0300 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3703-1304T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719514 | ||||||
| chr2:201719590
|
A | AAAAAAT | 52 | a0001c0002t0001g0121a0001c0003t0002g0008a0001c0003t0002g0009others(49): Show | 56 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.3703-1386_3703-138 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | ||||||
| chr2:201719590
|
A | AAAAAATA others(5): Show |
1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3703-1392_3703-138 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | ||||||
| chr2:201719590
|
AAAAAAT | A | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3703-1386_3703-138 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | ||||||
| chr2:201719590
|
AAAAAATA others(5): Show |
A | 110 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 121 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3703-1392_3703-138 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | ||||||
| chr2:201719861
|
C | A | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3703-1651G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719861 | ||||||
| chr2:201719943
|
A | G | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3703-1733T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719943 | ||||||
| chr2:201720196
|
T | C | 1 | a0001c0001t0008g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3703-1986A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720196 | ||||||
| chr2:201720224
|
C | G | 23 | a0001c0003t0007g0040a0001c0003t0007g0041a0001c0004t0001g0003others(20): Show | 25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3703-2014G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720224 | ||||||
| chr2:201720267
|
C | A | 1 | a0001c0004t0003g0029 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3703-2057G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720267 | ||||||
| chr2:201720417
|
T | C | 4 | a0001c0004t0001g0003a0001c0004t0001g0048a0001c0004t0001g0049others(1): Show | 5 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3703-2207A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720417 | ||||||
| chr2:201720468
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3703-2258G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720468 | ||||||
| chr2:201720469
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.3703-2259C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720469 | ||||||
| chr2:201720505
|
C | T | 55 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(52): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3703-2295G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720505 | ||||||
| chr2:201720539
|
C | CAA | 42 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(39): Show | 46 | HG00140.hp1 HG00621.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.3703-2331_3703-233 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | ||||||
| chr2:201720539
|
C | CAAA | 13 | a0001c0003t0002g0087a0001c0003t0002g0161a0001c0003t0002g0172others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.3703-2332_3703-233 others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | ||||||
| chr2:201720539
|
CA | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(220): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.3703-2330delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | ||||||
| chr2:201720539
|
CAA | C | 20 | a0001c0001t0003g0027a0001c0002t0001g0128a0001c0004t0001g0003others(17): Show | 22 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.3703-2331_3703-233 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | ||||||
| chr2:201720599
|
A | T | 1 | a0001c0002t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3703-2389T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720599 | ||||||
| chr2:201720608
|
G | C | 1 | a0001c0001t0001g0326 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3703-2398C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720608 | ||||||
| chr2:201720628
|
C | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(100): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.3702+2415G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720628 | ||||||
| chr2:201720714
|
A | AAC | 7 | a0001c0001t0001g0083a0001c0002t0001g0069a0001c0003t0001g0042others(4): Show | 7 | HG01081.hp1 HG02083.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3702+2327_3702+232 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720714 | ||||||
| chr2:201720714
|
AACACAC | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.3702+2323_3702+232 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720714 | ||||||
| chr2:201720918
|
T | C | 7 | a0001c0004t0001g0005a0001c0004t0001g0073a0001c0004t0001g0074others(4): Show | 8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+2125A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720918 | ||||||
| chr2:201720963
|
A | C | 23 | a0001c0003t0007g0040a0001c0003t0007g0041a0001c0004t0001g0003others(20): Show | 25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3702+2080T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720963 | ||||||
| chr2:201721155
|
A | G | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.3702+1888T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721155 | ||||||
| chr2:201721390
|
A | C | 1 | a0001c0004t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3702+1653T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721390 | ||||||
| chr2:201721506
|
T | G | 1 | a0001c0004t0001g0216 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3702+1537A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721506 | ||||||
| chr2:201721572
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3702+1471C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721572 | ||||||
| chr2:201721587
|
T | G | 1 | a0001c0002t0001g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3702+1456A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721587 | ||||||
| chr2:201721620
|
T | C | 1 | a0001c0003t0002g0171 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3702+1423A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721620 | ||||||
| chr2:201721672
|
AT | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(188): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3702+1370delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721672 | ||||||
| chr2:201721764
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0261a0001c0001t0001g0292others(4): Show | 8 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+1279G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721764 | ||||||
| chr2:201721846
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0003g0031 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3702+1197C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721846 | ||||||
| chr2:201722230
|
T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3702+813A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722230 | ||||||
| chr2:201722236
|
T | G | 1 | a0001c0003t0002g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3702+807A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722236 | ||||||
| chr2:201722347
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.3702+696A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722347 | ||||||
| chr2:201722355
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3702+688T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722355 | ||||||
| chr2:201722543
|
T | C | 2 | a0001c0002t0001g0151a0001c0002t0001g0152 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3702+500A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722543 | ||||||
| chr2:201722592
|
T | C | 5 | a0001c0001t0001g0261a0003c0007t0001g0034a0003c0007t0001g0036others(2): Show | 5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3702+451A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722592 | ||||||
| chr2:201722630
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(188): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3702+413G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722630 | ||||||
| chr2:201722727
|
T | G | 7 | a0001c0004t0001g0005a0001c0004t0001g0073a0001c0004t0001g0074others(4): Show | 8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+316A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722727 | ||||||
| chr2:201722860
|
C | A | 23 | a0001c0003t0007g0040a0001c0003t0007g0041a0001c0004t0001g0003others(20): Show | 25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3702+183G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722860 | ||||||
| chr2:201722860
|
C | T | 1 | a0010c0016t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3702+183G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722860 | ||||||
| chr2:201722863
|
T | C | 23 | a0001c0003t0007g0040a0001c0003t0007g0041a0001c0004t0001g0003others(20): Show | 25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3702+180A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722863 | ||||||
| chr2:201722930
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(188): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3702+113G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722930 | ||||||
| chr2:201722936
|
C | A | 7 | a0001c0004t0001g0005a0001c0004t0001g0073a0001c0004t0001g0074others(4): Show | 8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+107G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722936 | ||||||
| chr2:201722979
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3702+64T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722979 | ||||||
| chr2:201722983
|
T | TA | 55 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(52): Show | 59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3702+59dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722983 | ||||||
| chr2:201723019
|
A | G | 2 | a0001c0004t0001g0216a0001c0004t0003g0029 | 2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3702+24T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201723019 | ||||||
| chr2:201723527
|
C | T | 9 | a0001c0004t0001g0003a0001c0004t0001g0044a0001c0004t0001g0045others(6): Show | 10 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.3513-86G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723527 | ||||||
| chr2:201723607
|
T | C | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3513-166A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723607 | ||||||
| chr2:201723809
|
A | G | 1 | a0001c0003t0002g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3513-368T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723809 | ||||||
| chr2:201723857
|
C | T | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3513-416G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723857 | ||||||
| chr2:201723979
|
G | A | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3512+316C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723979 | ||||||
| chr2:201724062
|
G | C | 2 | a0001c0004t0001g0216a0001c0004t0003g0029 | 2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3512+233C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201724062 | ||||||
| chr2:201724534
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.3348-75A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724534 | ||||||
| chr2:201724772
|
T | C | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3348-313A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724772 | ||||||
| chr2:201724794
|
T | C | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3348-335A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724794 | ||||||
| chr2:201724835
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3348-376A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724835 | ||||||
| chr2:201724841
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3348-382G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724841 | ||||||
| chr2:201724909
|
C | G | 2 | a0001c0004t0001g0216a0001c0004t0003g0029 | 2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3347+447G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724909 | ||||||
| chr2:201724968
|
C | A | 1 | a0002c0005t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3347+388G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724968 | ||||||
| chr2:201724972
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3347+384C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724972 | ||||||
| chr2:201725069
|
C | T | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3347+287G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725069 | ||||||
| chr2:201725094
|
C | A | 1 | a0001c0022t0001g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3347+262G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725094 | ||||||
| chr2:201725108
|
A | G | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3347+248T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725108 | ||||||
| chr2:201725112
|
C | CA | 15 | a0001c0002t0001g0089a0001c0002t0001g0114a0001c0002t0001g0134others(12): Show | 17 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.3347+243dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725112 | ||||||
| chr2:201725697
|
CAGA | C | 9 | a0001c0001t0001g0238a0001c0001t0001g0242a0001c0001t0001g0251others(6): Show | 9 | HG00597.hp1 HG00673.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.3249-246_3249-244d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725697 | ||||||
| chr2:201725747
|
C | G | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3249-293G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725747 | ||||||
| chr2:201725847
|
T | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249-393A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725847 | ||||||
| chr2:201725991
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3248+493A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725991 | ||||||
| chr2:201726162
|
A | G | 21 | a0001c0004t0001g0003a0001c0004t0001g0005a0001c0004t0001g0044others(18): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3248+322T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726162 | ||||||
| chr2:201726163
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3248+321A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726163 | ||||||
| chr2:201726277
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0290 | 2 | HG04184.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3248+207G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726277 | ||||||
| chr2:201726434
|
C | G | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3248+50G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726434 | ||||||
| chr2:201726434
|
C | T | 2 | a0001c0003t0002g0169a0001c0003t0002g0199 | 2 | HG01168.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.3248+50G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726434 | ||||||
| chr2:201726892
|
A | T | 3 | a0001c0004t0001g0157a0001c0004t0001g0216a0001c0004t0003g0029 | 3 | HG01884.hp1 HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2980-26T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201726892 | ||||||
| chr2:201726991
|
G | A | 1 | a0001c0003t0002g0176 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2980-125C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201726991 | ||||||
| chr2:201727046
|
T | TA | 158 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(155): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.2979+165dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727046 | ||||||
| chr2:201727058
|
C | A | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2979+154G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727058 | ||||||
| chr2:201727087
|
G | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2979+125C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727087 | ||||||
| chr2:201727098
|
A | G | 2 | a0001c0004t0001g0216a0001c0004t0003g0029 | 2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2979+114T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727098 | ||||||
| chr2:201727131
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2979+81G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727131 | ||||||
| chr2:201727303
|
CCAGGA | C | 3 | a0001c0004t0001g0157a0001c0004t0001g0216a0001c0004t0003g0029 | 3 | HG01884.hp1 HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2913-30_2913-26del others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 16/33 | chr2 | 201727303 | ||||||
| chr2:201727336
|
G | A | 13 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(10): Show | 15 | HG01109.hp2 HG01123.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2913-58C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 16/33 | chr2 | 201727336 | ||||||
| chr2:201727480
|
T | C | 6 | a0001c0001t0001g0261a0003c0007t0001g0034a0003c0007t0001g0036others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2913-202A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 16/33 | chr2 | 201727480 | ||||||
| chr2:201727791
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0206others(6): Show | 11 | HG02451.hp2 HG02976.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842-16G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201727791 | ||||||
| chr2:201727795
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2842-20C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201727795 | ||||||
| chr2:201728251
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0017others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2841+261G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728251 | ||||||
| chr2:201728259
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0288others(1): Show | 6 | HG02976.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2841+253G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728259 | ||||||
| chr2:201728309
|
T | C | 1 | a0002c0020t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2841+203A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728309 | ||||||
| chr2:201728376
|
G | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2841+136C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728376 | ||||||
| chr2:201728463
|
TA | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0227a0001c0001t0001g0281others(3): Show | 7 | HG01515.hp2 HG01517.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2841+48delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728463 | ||||||
| chr2:201728736
|
A | G | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2713-96T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728736 | ||||||
| chr2:201728746
|
C | T | 1 | a0001c0003t0002g0170 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2713-106G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728746 | ||||||
| chr2:201728827
|
GA | G | 14 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0096others(11): Show | 14 | HG04184.hp2 NA18951.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.2713-188delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728827 | ||||||
| chr2:201728834
|
AAAAC | A | 58 | a0001c0003t0001g0173a0001c0003t0002g0008a0001c0003t0002g0009others(55): Show | 62 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2713-198_2713-195d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728834 | ||||||
| chr2:201728950
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2712+102C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728950 | ||||||
| chr2:201729316
|
A | G | 118 | a0001c0001t0001g0080a0001c0001t0003g0020a0001c0001t0003g0021others(115): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2581-133T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729316 | ||||||
| chr2:201729434
|
G | A | 1 | a0002c0006t0005g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2581-251C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729434 | ||||||
| chr2:201729457
|
A | G | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-274T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729457 | ||||||
| chr2:201729474
|
A | G | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-291T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729474 | ||||||
| chr2:201729484
|
C | T | 1 | a0001c0022t0001g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2581-301G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729484 | ||||||
| chr2:201729609
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0003g0023 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2581-426C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729609 | ||||||
| chr2:201729638
|
T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2581-455A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729638 | ||||||
| chr2:201729646
|
C | T | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2581-463G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729646 | ||||||
| chr2:201729737
|
C | T | 115 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0023others(112): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2581-554G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729737 | ||||||
| chr2:201729753
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0286 | 2 | NA18942.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2581-570G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729753 | ||||||
| chr2:201729879
|
CA | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(204): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.2581-697delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729879 | ||||||
| chr2:201729879
|
CAA | C | 71 | a0001c0001t0001g0217a0001c0001t0001g0286a0001c0002t0001g0085others(68): Show | 77 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2581-698_2581-697d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729879 | ||||||
| chr2:201729897
|
A | C | 23 | a0001c0001t0001g0038a0001c0001t0001g0083a0001c0001t0001g0205others(20): Show | 24 | HG01074.hp1 HG01243.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-714T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729897 | ||||||
| chr2:201729898
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2581-715T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729898 | ||||||
| chr2:201729901
|
A | C | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2581-718T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729901 | ||||||
| chr2:201729993
|
A | G | 1 | a0001c0002t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2581-810T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729993 | ||||||
| chr2:201730070
|
A | G | 3 | a0001c0002t0001g0131a0001c0002t0001g0133a0001c0002t0001g0158 | 3 | HG00738.hp1 HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2581-887T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730070 | ||||||
| chr2:201730185
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(100): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2581-1002T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730185 | ||||||
| chr2:201730225
|
G | A | 1 | a0002c0005t0001g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2581-1042C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730225 | ||||||
| chr2:201730325
|
T | C | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-1142A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730325 | ||||||
| chr2:201730579
|
G | A | 1 | a0001c0003t0007g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2581-1396C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730579 | ||||||
| chr2:201730633
|
A | T | 117 | a0001c0001t0001g0235a0001c0001t0003g0020a0001c0001t0003g0021others(114): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2581-1450T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730633 | ||||||
| chr2:201730671
|
TCTCAA | T | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-1493_2581-148 others(9): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730671 | ||||||
| chr2:201730681
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2581-1498T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730681 | ||||||
| chr2:201730693
|
A | G | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-1510T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730693 | ||||||
| chr2:201730840
|
T | A | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2581-1657A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730840 | ||||||
| chr2:201730843
|
T | C | 2 | a0001c0011t0001g0081a0001c0011t0001g0322 | 2 | HG02615.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2581-1660A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730843 | ||||||
| chr2:201730871
|
T | C | 1 | a0005c0012t0002g0160 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2581-1688A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730871 | ||||||
| chr2:201730994
|
G | T | 1 | a0014c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2581-1811C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730994 | ||||||
| chr2:201731063
|
A | C | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2581-1880T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731063 | ||||||
| chr2:201731135
|
T | C | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2581-1952A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731135 | ||||||
| chr2:201731144
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(208): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2581-1961A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731144 | ||||||
| chr2:201731242
|
G | GA | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2580+2033dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731242 | ||||||
| chr2:201731399
|
A | G | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2580+1877T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731399 | ||||||
| chr2:201731412
|
CA | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323 | 3 | NA18966.hp1 NA18973.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2580+1863delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731412 | ||||||
| chr2:201731574
|
T | C | 1 | a0014c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2580+1702A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731574 | ||||||
| chr2:201731677
|
A | G | 9 | a0001c0001t0001g0257a0001c0001t0001g0270a0001c0001t0001g0271others(6): Show | 9 | HG00558.hp1 HG02015.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.2580+1599T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731677 | ||||||
| chr2:201731683
|
AC | A | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2580+1592delG | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731683 | ||||||
| chr2:201731794
|
T | C | 1 | a0001c0002t0001g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2580+1482A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731794 | ||||||
| chr2:201731806
|
G | T | 59 | a0001c0003t0001g0042a0001c0003t0001g0173a0001c0003t0002g0008others(56): Show | 63 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2580+1470C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731806 | ||||||
| chr2:201731862
|
C | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2580+1414G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731862 | ||||||
| chr2:201731867
|
T | C | 9 | a0001c0004t0001g0003a0001c0004t0001g0044a0001c0004t0001g0045others(6): Show | 10 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2580+1409A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731867 | ||||||
| chr2:201731894
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2580+1382A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731894 | ||||||
| chr2:201731930
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2580+1346C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731930 | ||||||
| chr2:201731986
|
A | G | 1 | a0001c0004t0001g0050 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2580+1290T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731986 | ||||||
| chr2:201732033
|
A | G | 9 | a0001c0004t0001g0003a0001c0004t0001g0044a0001c0004t0001g0045others(6): Show | 10 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2580+1243T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732033 | ||||||
| chr2:201732070
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2580+1206T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732070 | ||||||
| chr2:201732184
|
T | A | 1 | a0001c0002t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2580+1092A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732184 | ||||||
| chr2:201732288
|
T | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | HG02922.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2580+988A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732288 | ||||||
| chr2:201732399
|
C | CA | 37 | a0001c0001t0001g0038a0001c0001t0001g0083a0001c0001t0001g0205others(34): Show | 39 | HG00738.hp1 HG01074.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.2580+876dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732399 | ||||||
| chr2:201732399
|
C | CAA | 7 | a0001c0001t0001g0212a0001c0001t0001g0261a0003c0007t0001g0034others(4): Show | 7 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2580+875_2580+876d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732399 | ||||||
| chr2:201732399
|
CA | C | 79 | a0001c0001t0001g0046a0001c0001t0001g0217a0001c0001t0001g0278others(76): Show | 85 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2580+876delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732399 | ||||||
| chr2:201732712
|
T | C | 22 | a0001c0001t0001g0217a0001c0004t0001g0003a0001c0004t0001g0005others(19): Show | 24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2580+564A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732712 | ||||||
| chr2:201732906
|
G | T | 117 | a0001c0001t0001g0080a0001c0001t0003g0020a0001c0001t0003g0022others(114): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2580+370C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732906 | ||||||
| chr2:201732914
|
C | A | 117 | a0001c0001t0001g0080a0001c0001t0003g0020a0001c0001t0003g0022others(114): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2580+362G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732914 | ||||||
| chr2:201732956
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2580+320G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732956 | ||||||
| chr2:201733026
|
A | T | 3 | a0001c0001t0001g0217a0001c0004t0001g0216a0001c0004t0003g0029 | 3 | HG02027.hp2 HG02145.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2580+250T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201733026 | ||||||
| chr2:201733492
|
T | C | 1 | a0001c0003t0002g0198 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2418-54A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201733492 | ||||||
| chr2:201733804
|
T | C | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2418-366A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201733804 | ||||||
| chr2:201733897
|
C | A | 1 | a0001c0002t0001g0114 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2418-459G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201733897 | ||||||
| chr2:201734170
|
T | A | 8 | a0001c0001t0001g0247a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 8 | HG02165.hp2 NA18940.hp2 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.2418-732A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734170 | ||||||
| chr2:201734265
|
G | A | 59 | a0001c0003t0001g0042a0001c0003t0001g0173a0001c0003t0002g0008others(56): Show | 63 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2418-827C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734265 | ||||||
| chr2:201734291
|
A | G | 1 | a0001c0002t0001g0153 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2418-853T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734291 | ||||||
| chr2:201734420
|
A | T | 12 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0096others(9): Show | 12 | HG04184.hp2 NA18951.hp1 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.2418-982T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734420 | ||||||
| chr2:201734428
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(100): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2418-990A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734428 | ||||||
| chr2:201734450
|
G | A | 1 | a0001c0004t0001g0048 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2418-1012C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734450 | ||||||
| chr2:201734467
|
C | CAAAAAAA others(6): Show |
2 | a0001c0004t0001g0047a0014c0014t0001g0043 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2418-1042_2418-103 others(17): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | ||||||
| chr2:201734467
|
C | CAAAAAAA others(7): Show |
14 | a0001c0001t0001g0217a0001c0004t0001g0005a0001c0004t0001g0044others(11): Show | 15 | HG00099.hp1 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2418-1030_2418-102 others(18): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | ||||||
| chr2:201734467
|
C | CAAAAAAA others(8): Show |
4 | a0001c0004t0001g0003a0001c0004t0001g0048a0001c0004t0001g0157others(1): Show | 5 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2418-1030_2418-102 others(19): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | ||||||
| chr2:201734467
|
C | CAAAAAAA others(9): Show |
2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG01361.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2418-1030_2418-102 others(20): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | ||||||
| chr2:201734527
|
A | C | 1 | a0001c0001t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2418-1089T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734527 | ||||||
| chr2:201734550
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0269a0001c0001t0001g0273 | 3 | HG00621.hp2 NA19056.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2418-1112C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734550 | ||||||
| chr2:201734775
|
G | A | 5 | a0003c0007t0001g0034a0003c0007t0001g0036a0003c0007t0001g0037others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2418-1337C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734775 | ||||||
| chr2:201734924
|
T | TA | 12 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2418-1487dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734924 | ||||||
| chr2:201735048
|
G | A | 23 | a0001c0001t0001g0046a0001c0001t0001g0217a0001c0004t0001g0003others(20): Show | 25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.2418-1610C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735048 | ||||||
| chr2:201735154
|
C | T | 139 | a0001c0001t0001g0046a0001c0001t0001g0083a0001c0001t0001g0149others(136): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2418-1716G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735154 | ||||||
| chr2:201735172
|
G | A | 1 | a0014c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2418-1734C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735172 | ||||||
| chr2:201735199
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2418-1761G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735199 | ||||||
| chr2:201735211
|
G | A | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2418-1773C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735211 | ||||||
| chr2:201735341
|
T | G | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2418-1903A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735341 | ||||||
| chr2:201735394
|
G | A | 146 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0080others(143): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2418-1956C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735394 | ||||||
| chr2:201735835
|
C | G | 1 | a0001c0004t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2418-2397G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735835 | ||||||
| chr2:201735851
|
T | C | 10 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0023others(7): Show | 10 | HG01109.hp2 HG01123.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2418-2413A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735851 | ||||||
| chr2:201735978
|
C | G | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2418-2540G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735978 | ||||||
| chr2:201736044
|
A | G | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2418-2606T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736044 | ||||||
| chr2:201736066
|
T | C | 1 | a0014c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2417+2604A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736066 | ||||||
| chr2:201736286
|
A | G | 2 | a0001c0001t0001g0038a0001c0003t0001g0042 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2417+2384T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736286 | ||||||
| chr2:201736431
|
G | A | 1 | a0001c0003t0002g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2417+2239C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736431 | ||||||
| chr2:201736467
|
T | C | 2 | a0001c0003t0002g0169a0001c0003t0002g0199 | 2 | HG01168.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2417+2203A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736467 | ||||||
| chr2:201736550
|
G | A | 1 | a0001c0003t0004g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2417+2120C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736550 | ||||||
| chr2:201736629
|
G | A | 3 | a0001c0003t0004g0154a0001c0003t0004g0155a0001c0003t0004g0156 | 3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2417+2041C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736629 | ||||||
| chr2:201736684
|
C | T | 130 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(127): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2417+1986G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736684 | ||||||
| chr2:201736783
|
T | C | 128 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(125): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.2417+1887A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736783 | ||||||
| chr2:201737014
|
T | C | 128 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(125): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.2417+1656A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737014 | ||||||
| chr2:201737060
|
A | G | 4 | a0002c0005t0001g0055a0002c0005t0001g0064a0002c0005t0001g0065others(1): Show | 4 | HG01074.hp1 HG01255.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2417+1610T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737060 | ||||||
| chr2:201737171
|
T | A | 130 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(127): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2417+1499A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737171 | ||||||
| chr2:201737187
|
G | C | 1 | a0004c0008t0001g0237 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2417+1483C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737187 | ||||||
| chr2:201737662
|
C | T | 109 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(106): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2417+1008G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737662 | ||||||
| chr2:201737672
|
G | A | 1 | a0001c0003t0002g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2417+998C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737672 | ||||||
| chr2:201737900
|
T | C | 127 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(124): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2417+770A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737900 | ||||||
| chr2:201737909
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2417+761C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737909 | ||||||
| chr2:201737916
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2417+754G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737916 | ||||||
| chr2:201737921
|
C | CA | 8 | a0001c0001t0001g0038a0001c0004t0001g0005a0001c0004t0001g0073others(5): Show | 9 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2417+748dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737921 | ||||||
| chr2:201737926
|
A | C | 1 | a0001c0011t0001g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2417+744T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737926 | ||||||
| chr2:201737956
|
A | C | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2417+714T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737956 | ||||||
| chr2:201737970
|
G | C | 1 | a0001c0004t0001g0073 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2417+700C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737970 | ||||||
| chr2:201738066
|
T | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(316): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2417+604A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738066 | ||||||
| chr2:201738091
|
G | C | 128 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(125): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.2417+579C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738091 | ||||||
| chr2:201738163
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2417+507G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738163 | ||||||
| chr2:201738164
|
A | G | 1 | a0014c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2417+506T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738164 | ||||||
| chr2:201738269
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2417+401C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738269 | ||||||
| chr2:201738424
|
A | G | 121 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(118): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.2417+246T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738424 | ||||||
| chr2:201738489
|
T | C | 1 | a0001c0001t0001g0313 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2417+181A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738489 | ||||||
| chr2:201738817
|
T | C | 1 | a0001c0001t0008g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2352-82A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201738817 | ||||||
| chr2:201738867
|
A | T | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2352-132T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201738867 | ||||||
| chr2:201739071
|
T | C | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2352-336A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739071 | ||||||
| chr2:201739114
|
C | T | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2352-379G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739114 | ||||||
| chr2:201739128
|
ACTTGGGA others(1081): Show |
A | 2 | a0001c0001t0001g0038a0001c0003t0001g0042 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2351+1458_2352-394 others(3): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739128 | ||||||
| chr2:201739189
|
T | C | 1 | a0001c0011t0001g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2352-454A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739189 | ||||||
| chr2:201739232
|
T | TC | 106 | a0001c0001t0001g0083a0001c0001t0001g0149a0001c0001t0001g0217others(103): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2352-498dupG | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739232 | ||||||
| chr2:201739235
|
C | CCA | 10 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0002t0001g0114others(7): Show | 10 | HG00099.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2352-501_2352-500i others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739235 | ||||||
| chr2:201739235
|
CA | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(141): Show | 159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2352-501delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739235 | ||||||
| chr2:201739235
|
CAA | C | 11 | a0001c0001t0001g0206a0001c0001t0001g0279a0001c0001t0001g0285others(8): Show | 11 | HG01496.hp2 HG01943.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2352-502_2352-501d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739235 | ||||||
| chr2:201739236
|
A | C | 5 | a0001c0002t0001g0085a0001c0002t0001g0099a0001c0002t0001g0141others(2): Show | 5 | HG03195.hp1 HG03209.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.2352-501T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739236 | ||||||
| chr2:201739237
|
A | C | 4 | a0003c0007t0001g0034a0003c0007t0001g0036a0003c0007t0001g0079others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2352-502T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739237 | ||||||
| chr2:201739357
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(96): Show | 110 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2352-622G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739357 | ||||||
| chr2:201739410
|
A | T | 1 | a0001c0001t0003g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2352-675T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739410 | ||||||
| chr2:201739465
|
G | A | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2352-730C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739465 | ||||||
| chr2:201739508
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2352-773A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739508 | ||||||
| chr2:201739549
|
C | G | 1 | a0001c0002t0001g0089 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2352-814G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739549 | ||||||
| chr2:201739763
|
AAG | A | 12 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2352-1030_2352-102 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739763 | ||||||
| chr2:201739952
|
G | C | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2352-1217C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739952 | ||||||
| chr2:201740031
|
A | G | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2352-1296T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740031 | ||||||
| chr2:201740043
|
C | G | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2352-1308G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740043 | ||||||
| chr2:201740171
|
A | T | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2352-1436T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740171 | ||||||
| chr2:201740324
|
A | C | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2351+1350T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740324 | ||||||
| chr2:201740385
|
C | A | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2351+1289G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740385 | ||||||
| chr2:201740530
|
T | A | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2351+1144A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740530 | ||||||
| chr2:201740536
|
AAAC | A | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2351+1135_2351+113 others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740536 | ||||||
| chr2:201740612
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2351+1062A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740612 | ||||||
| chr2:201740804
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2351+870C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740804 | ||||||
| chr2:201740826
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2351+848G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740826 | ||||||
| chr2:201740939
|
G | A | 11 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0096others(8): Show | 11 | NA18951.hp1 NA18959.hp2 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.2351+735C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740939 | ||||||
| chr2:201741024
|
C | T | 1 | a0010c0016t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2351+650G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741024 | ||||||
| chr2:201741084
|
A | G | 1 | a0001c0003t0002g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2351+590T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741084 | ||||||
| chr2:201741435
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2351+239G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741435 | ||||||
| chr2:201741450
|
T | C | 1 | a0001c0002t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2351+224A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741450 | ||||||
| chr2:201741470
|
C | T | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2351+204G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741470 | ||||||
| chr2:201741867
|
A | G | 1 | a0001c0003t0002g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2171-13T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201741867 | ||||||
| chr2:201741916
|
G | A | 120 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2171-62C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201741916 | ||||||
| chr2:201741935
|
C | T | 1 | a0001c0002t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2171-81G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201741935 | ||||||
| chr2:201742035
|
G | A | 5 | a0003c0007t0001g0034a0003c0007t0001g0036a0003c0007t0001g0037others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2171-181C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742035 | ||||||
| chr2:201742081
|
G | C | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2171-227C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742081 | ||||||
| chr2:201742141
|
G | A | 123 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(120): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.2171-287C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742141 | ||||||
| chr2:201742403
|
T | G | 121 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(118): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.2171-549A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742403 | ||||||
| chr2:201742420
|
T | A | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2171-566A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742420 | ||||||
| chr2:201742641
|
G | C | 1 | a0004c0008t0001g0240 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2171-787C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742641 | ||||||
| chr2:201742794
|
G | A | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2171-940C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742794 | ||||||
| chr2:201742863
|
G | A | 6 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2171-1009C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742863 | ||||||
| chr2:201743010
|
G | T | 1 | a0001c0001t0001g0319 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2171-1156C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743010 | ||||||
| chr2:201743019
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2171-1165G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743019 | ||||||
| chr2:201743070
|
C | CA | 114 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(111): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2170+1187dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743070 | ||||||
| chr2:201743129
|
C | T | 12 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2170+1129G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743129 | ||||||
| chr2:201743133
|
G | A | 2 | a0003c0007t0001g0032a0003c0007t0001g0033 | 2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2170+1125C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743133 | ||||||
| chr2:201743183
|
G | C | 1 | a0004c0008t0001g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2170+1075C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743183 | ||||||
| chr2:201743410
|
G | A | 9 | a0001c0001t0001g0205a0001c0001t0001g0222a0001c0001t0001g0227others(6): Show | 10 | HG01515.hp2 HG01517.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.2170+848C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743410 | ||||||
| chr2:201743486
|
G | A | 12 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2170+772C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743486 | ||||||
| chr2:201743534
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2170+724C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743534 | ||||||
| chr2:201743609
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2170+649G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743609 | ||||||
| chr2:201743610
|
G | A | 9 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0242others(6): Show | 9 | HG00597.hp1 HG00673.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2170+648C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743610 | ||||||
| chr2:201744154
|
C | A | 125 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0080others(122): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.2170+104G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201744154 | ||||||
| chr2:201744600
|
C | G | 5 | a0003c0007t0001g0034a0003c0007t0001g0036a0003c0007t0001g0037others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999-171G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201744600 | ||||||
| chr2:201744642
|
G | A | 107 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1999-213C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201744642 | ||||||
| chr2:201744787
|
C | G | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1999-358G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201744787 | ||||||
| chr2:201745072
|
G | A | 106 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(103): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1999-643C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745072 | ||||||
| chr2:201745127
|
T | C | 3 | a0001c0002t0001g0088a0001c0002t0001g0120a0001c0002t0001g0121 | 3 | HG00733.hp2 HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1999-698A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745127 | ||||||
| chr2:201745273
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1999-844T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745273 | ||||||
| chr2:201745425
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1999-996A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745425 | ||||||
| chr2:201745521
|
T | G | 110 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(107): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1998+1045A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745521 | ||||||
| chr2:201745588
|
A | G | 3 | a0002c0006t0001g0056a0002c0006t0001g0057a0002c0006t0001g0058 | 3 | HG00099.hp1 HG01081.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1998+978T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745588 | ||||||
| chr2:201745664
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1998+902A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745664 | ||||||
| chr2:201745668
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1998+898C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745668 | ||||||
| chr2:201745670
|
C | T | 2 | a0003c0007t0001g0032a0003c0007t0001g0033 | 2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1998+896G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745670 | ||||||
| chr2:201745727
|
T | C | 1 | a0001c0003t0002g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1998+839A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745727 | ||||||
| chr2:201745857
|
G | A | 1 | a0002c0006t0005g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1998+709C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745857 | ||||||
| chr2:201745932
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1998+634C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745932 | ||||||
| chr2:201745945
|
T | C | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1998+621A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745945 | ||||||
| chr2:201745954
|
A | G | 1 | a0001c0002t0001g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1998+612T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745954 | ||||||
| chr2:201745961
|
T | A | 1 | a0001c0002t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1998+605A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745961 | ||||||
| chr2:201746155
|
A | C | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1998+411T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746155 | ||||||
| chr2:201746261
|
T | C | 12 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1998+305A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746261 | ||||||
| chr2:201746372
|
T | C | 10 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(7): Show | 10 | HG01109.hp2 HG01123.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1998+194A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746372 | ||||||
| chr2:201746415
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1998+151C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746415 | ||||||
| chr2:201746440
|
T | G | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1998+126A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746440 | ||||||
| chr2:201746536
|
T | C | 2 | a0001c0001t0003g0022a0001c0004t0003g0029 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1998+30A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746536 | ||||||
| chr2:201746879
|
C | A | 2 | a0001c0003t0002g0162a0001c0003t0002g0187 | 2 | NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1816-131G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201746879 | ||||||
| chr2:201747001
|
A | G | 1 | a0009c0015t0002g0188 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1816-253T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747001 | ||||||
| chr2:201747150
|
C | T | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1816-402G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747150 | ||||||
| chr2:201747253
|
C | T | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | NA18971.hp1 NA19004.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1816-505G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747253 | ||||||
| chr2:201747316
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(306): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1816-568C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747316 | ||||||
| chr2:201747364
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0245a0001c0001t0001g0266others(2): Show | 6 | HG00438.hp1 HG02083.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1816-616G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747364 | ||||||
| chr2:201747456
|
C | T | 9 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0096others(6): Show | 9 | NA18951.hp1 NA18959.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.1816-708G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747456 | ||||||
| chr2:201747462
|
C | CT | 9 | a0001c0001t0001g0210a0001c0001t0001g0253a0001c0001t0001g0266others(6): Show | 9 | HG02055.hp2 HG02486.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1816-715dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747462 | ||||||
| chr2:201747462
|
CT | C | 98 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(95): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1816-715delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747462 | ||||||
| chr2:201747672
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1816-924C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747672 | ||||||
| chr2:201747725
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(239): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1816-977C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747725 | ||||||
| chr2:201747828
|
A | G | 1 | a0001c0001t0001g0313 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1816-1080T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747828 | ||||||
| chr2:201747865
|
G | A | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1816-1117C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747865 | ||||||
| chr2:201748049
|
A | AAC | 13 | a0001c0001t0001g0206a0001c0001t0003g0020a0001c0001t0003g0021others(10): Show | 13 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1816-1303_1816-130 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748049 | ||||||
| chr2:201748057
|
C | T | 1 | a0001c0003t0002g0008 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1816-1309G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748057 | ||||||
| chr2:201748204
|
T | TTGTGTG | 4 | a0001c0003t0002g0175a0001c0003t0002g0176a0001c0003t0002g0177others(1): Show | 4 | HG02071.hp2 HG02083.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-1462_1816-145 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748204 | ||||||
| chr2:201748370
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(326): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1815+1342G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748370 | ||||||
| chr2:201748650
|
CTTTG | C | 121 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0080others(118): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1815+1058_1815+106 others(8): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748650 | ||||||
| chr2:201748694
|
C | T | 2 | a0003c0007t0001g0032a0003c0007t0001g0033 | 2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1815+1018G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748694 | ||||||
| chr2:201748713
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1815+999G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748713 | ||||||
| chr2:201748771
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1815+941A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748771 | ||||||
| chr2:201748912
|
C | T | 9 | a0001c0002t0001g0221a0001c0002t0001g0223a0001c0002t0001g0224others(6): Show | 9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1815+800G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748912 | ||||||
| chr2:201748948
|
G | A | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1815+764C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748948 | ||||||
| chr2:201748957
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1815+755G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748957 | ||||||
| chr2:201749057
|
TGTTCAAG others(6): Show |
T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1815+642_1815+654d others(15): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749057 | ||||||
| chr2:201749218
|
T | TA | 67 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(64): Show | 71 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1815+493dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749218 | ||||||
| chr2:201749218
|
TA | T | 118 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(115): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1815+493delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749218 | ||||||
| chr2:201749400
|
C | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 42 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1815+312G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749400 | ||||||
| chr2:201749496
|
G | C | 108 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(105): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1815+216C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749496 | ||||||
| chr2:201749555
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1815+157C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749555 | ||||||
| chr2:201749605
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1815+107C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749605 | ||||||
| chr2:201749612
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1815+100C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749612 | ||||||
| chr2:201749909
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1738-120A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201749909 | ||||||
| chr2:201749909
|
T | G | 9 | a0001c0002t0001g0221a0001c0002t0001g0223a0001c0002t0001g0224others(6): Show | 9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-120A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201749909 | ||||||
| chr2:201750168
|
C | CA | 88 | a0001c0001t0001g0038a0001c0001t0001g0207a0001c0001t0001g0208others(85): Show | 92 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1738-380dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750168 | ||||||
| chr2:201750190
|
AAAG | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 42 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1738-404_1738-402d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750190 | ||||||
| chr2:201750201
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1738-412G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750201 | ||||||
| chr2:201750585
|
G | A | 1 | a0001c0002t0001g0091 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1738-796C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750585 | ||||||
| chr2:201750591
|
AG | A | 106 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(103): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1738-803delC | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750591 | ||||||
| chr2:201750607
|
T | C | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-818A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750607 | ||||||
| chr2:201750702
|
A | G | 9 | a0001c0001t0001g0257a0001c0001t0001g0270a0001c0001t0001g0271others(6): Show | 9 | HG00558.hp1 HG02015.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-913T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750702 | ||||||
| chr2:201750826
|
G | A | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-1037C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750826 | ||||||
| chr2:201750852
|
C | CT | 8 | a0001c0001t0001g0238a0001c0001t0001g0284a0001c0001t0003g0022others(5): Show | 8 | HG00597.hp1 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-1064dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750852 | ||||||
| chr2:201750883
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1738-1094G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750883 | ||||||
| chr2:201751023
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1738-1234G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751023 | ||||||
| chr2:201751496
|
C | T | 119 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(116): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1737+1650G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751496 | ||||||
| chr2:201751606
|
T | G | 3 | a0001c0003t0002g0164a0001c0003t0002g0181a0001c0003t0002g0182 | 3 | NA18980.hp1 NA18991.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1737+1540A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751606 | ||||||
| chr2:201751648
|
G | A | 106 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(103): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1737+1498C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751648 | ||||||
| chr2:201751756
|
C | T | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+1390G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751756 | ||||||
| chr2:201751785
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1737+1361A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751785 | ||||||
| chr2:201751792
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1737+1354A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751792 | ||||||
| chr2:201751823
|
T | C | 5 | a0003c0007t0001g0034a0003c0007t0001g0036a0003c0007t0001g0037others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+1323A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751823 | ||||||
| chr2:201751973
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1737+1173C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751973 | ||||||
| chr2:201752013
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1737+1133T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752013 | ||||||
| chr2:201752152
|
T | C | 1 | a0002c0005t0001g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1737+994A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752152 | ||||||
| chr2:201752189
|
C | T | 108 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(105): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1737+957G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752189 | ||||||
| chr2:201752528
|
T | A | 11 | a0001c0004t0001g0005a0001c0004t0001g0073a0001c0004t0001g0074others(8): Show | 12 | HG00642.hp2 HG01070.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+618A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752528 | ||||||
| chr2:201752682
|
C | T | 105 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(102): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1737+464G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752682 | ||||||
| chr2:201752788
|
G | A | 1 | a0002c0006t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1737+358C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752788 | ||||||
| chr2:201752975
|
C | T | 2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | NA18971.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1737+171G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752975 | ||||||
| chr2:201753071
|
A | G | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+75T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201753071 | ||||||
| chr2:201753087
|
C | A | 1 | a0001c0001t0001g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1737+59G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201753087 | ||||||
| chr2:201753295
|
G | A | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1641-53C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201753295 | ||||||
| chr2:201753597
|
C | G | 134 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0080others(131): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1641-355G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201753597 | ||||||
| chr2:201753635
|
C | A | 2 | a0001c0003t0002g0180a0001c0003t0002g0183 | 2 | NA18940.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1641-393G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201753635 | ||||||
| chr2:201754020
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1640+483A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754020 | ||||||
| chr2:201754142
|
A | G | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1640+361T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754142 | ||||||
| chr2:201754349
|
G | C | 5 | a0003c0007t0001g0034a0003c0007t0001g0036a0003c0007t0001g0037others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1640+154C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754349 | ||||||
| chr2:201754452
|
G | C | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0298others(1): Show | 5 | HG01515.hp2 HG01517.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1640+51C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754452 | ||||||
| chr2:201754817
|
G | T | 4 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(1): Show | 4 | NA18942.hp1 NA18951.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472-146C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201754817 | ||||||
| chr2:201754859
|
A | C | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1472-188T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201754859 | ||||||
| chr2:201754905
|
G | C | 1 | a0001c0001t0003g0022 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1472-234C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201754905 | ||||||
| chr2:201755115
|
G | A | 1 | a0001c0011t0001g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1472-444C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755115 | ||||||
| chr2:201755162
|
G | A | 8 | a0001c0002t0001g0084a0001c0002t0001g0088a0001c0002t0001g0120others(5): Show | 8 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472-491C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755162 | ||||||
| chr2:201755266
|
C | CT | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472-596dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755266 | ||||||
| chr2:201755365
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1472-694A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755365 | ||||||
| chr2:201755380
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0283 | 2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1472-709T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755380 | ||||||
| chr2:201755396
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1472-725T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755396 | ||||||
| chr2:201755511
|
C | T | 1 | a0001c0002t0001g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1472-840G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755511 | ||||||
| chr2:201755705
|
A | G | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1472-1034T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755705 | ||||||
| chr2:201755733
|
A | C | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1472-1062T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755733 | ||||||
| chr2:201755833
|
T | C | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472-1162A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755833 | ||||||
| chr2:201756051
|
A | C | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1471+1351T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756051 | ||||||
| chr2:201756074
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1471+1328G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756074 | ||||||
| chr2:201756111
|
T | C | 43 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 46 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1471+1291A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756111 | ||||||
| chr2:201756265
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1471+1137A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756265 | ||||||
| chr2:201756279
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1471+1123A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756279 | ||||||
| chr2:201756318
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1471+1084T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756318 | ||||||
| chr2:201756377
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1471+1025T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756377 | ||||||
| chr2:201756430
|
A | C | 1 | a0001c0003t0002g0199 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1471+972T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756430 | ||||||
| chr2:201756467
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1471+935G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756467 | ||||||
| chr2:201756525
|
T | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 16 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1471+877A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756525 | ||||||
| chr2:201756534
|
T | TG | 331 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1471+867dupC | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756534 | ||||||
| chr2:201756593
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1471+809T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756593 | ||||||
| chr2:201756649
|
T | C | 13 | a0001c0001t0001g0257a0001c0001t0001g0270a0001c0001t0001g0271others(10): Show | 13 | HG00558.hp1 HG00621.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1471+753A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756649 | ||||||
| chr2:201756684
|
A | C | 1 | a0001c0001t0008g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1471+718T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756684 | ||||||
| chr2:201756746
|
T | C | 1 | a0001c0002t0001g0128 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1471+656A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756746 | ||||||
| chr2:201756801
|
T | G | 1 | a0001c0001t0001g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1471+601A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756801 | ||||||
| chr2:201756812
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1471+590T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756812 | ||||||
| chr2:201756816
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1471+586G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756816 | ||||||
| chr2:201756901
|
AT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1471+500delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756901 | ||||||
| chr2:201756964
|
T | C | 1 | a0002c0020t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1471+438A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756964 | ||||||
| chr2:201756978
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1471+424A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756978 | ||||||
| chr2:201757017
|
G | A | 1 | a0002c0020t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1471+385C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757017 | ||||||
| chr2:201757053
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1471+349G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757053 | ||||||
| chr2:201757169
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1471+233T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757169 | ||||||
| chr2:201757370
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1471+32T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757370 | ||||||
| chr2:201757396
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19081.hp1 | splice_region_variant&intron_variant | LOW | c.1471+6G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757396 | ||||||
| chr2:201757786
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1114-27A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201757786 | ||||||
| chr2:201758128
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1114-369G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758128 | ||||||
| chr2:201758243
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1114-484A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758243 | ||||||
| chr2:201758285
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1114-526C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758285 | ||||||
| chr2:201758342
|
C | T | 203 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0083others(200): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1114-583G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758342 | ||||||
| chr2:201758588
|
A | C | 1 | a0014c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1114-829T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758588 | ||||||
| chr2:201758643
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114-884G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758643 | ||||||
| chr2:201758653
|
C | T | 1 | a0001c0003t0002g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1114-894G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758653 | ||||||
| chr2:201758681
|
C | T | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1114-922G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758681 | ||||||
| chr2:201758732
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1114-973T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758732 | ||||||
| chr2:201758740
|
TATA | T | 13 | a0002c0005t0001g0002a0002c0005t0001g0004a0002c0005t0001g0055others(10): Show | 16 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1114-984_1114-982d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758740 | ||||||
| chr2:201758755
|
T | TGC | 6 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0141others(3): Show | 6 | HG03209.hp2 HG04115.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-998_1114-997d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758755 | ||||||
| chr2:201758755
|
T | TGCGC | 4 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0123others(1): Show | 4 | HG01517.hp1 HG01884.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-1000_1114-997 others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758755 | ||||||
| chr2:201758759
|
C | CGCGT | 98 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(95): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1114-1001_1114-100 others(8): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758759 | ||||||
| chr2:201758760
|
A | ATG | 22 | a0001c0001t0001g0038a0001c0001t0001g0206a0001c0001t0003g0020others(19): Show | 23 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1114-1003_1114-100 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758760
|
A | ATGTGTG | 3 | a0001c0001t0003g0023a0001c0001t0006g0331a0001c0001t0006g0332 | 3 | HG03098.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1114-1007_1114-100 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758760
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0245a0001c0001t0001g0255 | 4 | NA18949.hp2 NA18968.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-1009_1114-100 others(12): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758760
|
A | ATGTGTGT others(3): Show |
95 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(92): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1114-1011_1114-100 others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758760
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1114-1013_1114-100 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758760
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0303a0001c0001t0001g0314 | 2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1114-1015_1114-100 others(18): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758760
|
A | ATTGTGTG others(4): Show |
1 | a0001c0001t0001g0321 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1114-1002_1114-100 others(15): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758760
|
A | G | 177 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(174): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1114-1001T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | ||||||
| chr2:201758761
|
T | C | 63 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0209others(60): Show | 68 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1114-1002A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758761 | ||||||
| chr2:201758763
|
T | C | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-1004A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758763 | ||||||
| chr2:201758785
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0248 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1114-1027_1114-102 others(15): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758785 | ||||||
| chr2:201758786
|
T | G | 9 | a0001c0001t0001g0038a0001c0003t0002g0159a0003c0007t0001g0032others(6): Show | 9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-1027A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758786 | ||||||
| chr2:201758862
|
G | T | 2 | a0001c0001t0001g0235a0001c0002t0001g0091 | 2 | HG04204.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1114-1103C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758862 | ||||||
| chr2:201758919
|
T | A | 9 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(6): Show | 10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1114-1160A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758919 | ||||||
| chr2:201758923
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1114-1164T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758923 | ||||||
| chr2:201758971
|
A | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1114-1212T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758971 | ||||||
| chr2:201758977
|
T | C | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1114-1218A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758977 | ||||||
| chr2:201759221
|
T | C | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1114-1462A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759221 | ||||||
| chr2:201759296
|
A | C | 2 | a0001c0009t0001g0016a0001c0009t0001g0312 | 3 | HG00280.hp2 HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1114-1537T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759296 | ||||||
| chr2:201759344
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+1537G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759344 | ||||||
| chr2:201759413
|
T | C | 1 | a0002c0006t0005g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1113+1468A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759413 | ||||||
| chr2:201759415
|
T | C | 1 | a0002c0005t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1113+1466A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759415 | ||||||
| chr2:201759587
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1113+1294T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759587 | ||||||
| chr2:201759604
|
A | G | 1 | a0002c0020t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1113+1277T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759604 | ||||||
| chr2:201759649
|
T | C | 1 | a0001c0002t0001g0091 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1113+1232A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759649 | ||||||
| chr2:201760043
|
C | T | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1113+838G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760043 | ||||||
| chr2:201760244
|
G | A | 1 | a0001c0004t0001g0050 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1113+637C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760244 | ||||||
| chr2:201760250
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1113+631C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760250 | ||||||
| chr2:201760295
|
A | G | 1 | a0001c0004t0001g0216 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1113+586T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760295 | ||||||
| chr2:201760380
|
A | G | 1 | a0001c0003t0004g0154 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1113+501T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760380 | ||||||
| chr2:201760395
|
T | G | 3 | a0001c0001t0003g0021a0001c0001t0003g0024a0001c0001t0003g0025 | 3 | HG01123.hp1 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1113+486A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760395 | ||||||
| chr2:201760574
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1113+307G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760574 | ||||||
| chr2:201760659
|
T | C | 1 | a0001c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1113+222A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760659 | ||||||
| chr2:201760679
|
A | C | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+202T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760679 | ||||||
| chr2:201760796
|
G | A | 1 | a0004c0008t0001g0241 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1113+85C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760796 | ||||||
| chr2:201761897
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-79G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201761897 | ||||||
| chr2:201761902
|
A | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-84T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201761902 | ||||||
| chr2:201762057
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.176-239C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762057 | ||||||
| chr2:201762124
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.176-306G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762124 | ||||||
| chr2:201762296
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-478C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762296 | ||||||
| chr2:201762500
|
G | T | 1 | a0001c0002t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.176-682C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762500 | ||||||
| chr2:201762636
|
G | A | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.176-818C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762636 | ||||||
| chr2:201762781
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-963T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762781 | ||||||
| chr2:201762854
|
C | T | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.176-1036G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762854 | ||||||
| chr2:201762940
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.176-1122C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762940 | ||||||
| chr2:201762992
|
T | C | 1 | a0001c0002t0001g0125 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.176-1174A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762992 | ||||||
| chr2:201763066
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.176-1248C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763066 | ||||||
| chr2:201763068
|
C | G | 2 | a0001c0004t0001g0044a0001c0004t0001g0045 | 2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.176-1250G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763068 | ||||||
| chr2:201763120
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.176-1302A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763120 | ||||||
| chr2:201763142
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.176-1324C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763142 | ||||||
| chr2:201763194
|
G | A | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-1376C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763194 | ||||||
| chr2:201763207
|
G | A | 9 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(6): Show | 10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-1389C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763207 | ||||||
| chr2:201763237
|
T | C | 49 | a0001c0001t0001g0207a0001c0003t0001g0173a0001c0003t0002g0008others(46): Show | 53 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.176-1419A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763237 | ||||||
| chr2:201763285
|
T | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0314 | 2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.176-1467A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763285 | ||||||
| chr2:201763351
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.176-1533G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763351 | ||||||
| chr2:201763508
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.176-1690G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763508 | ||||||
| chr2:201763557
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(313): Show | 335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.176-1739A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763557 | ||||||
| chr2:201763742
|
C | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(313): Show | 335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.176-1924G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763742 | ||||||
| chr2:201763871
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.176-2053T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763871 | ||||||
| chr2:201763924
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-2106A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763924 | ||||||
| chr2:201764026
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.176-2208T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764026 | ||||||
| chr2:201764044
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.176-2226G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764044 | ||||||
| chr2:201764098
|
C | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(313): Show | 335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.176-2280G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764098 | ||||||
| chr2:201764266
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | HG02922.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.176-2448G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764266 | ||||||
| chr2:201764413
|
C | A | 1 | a0011c0017t0001g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.176-2595G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764413 | ||||||
| chr2:201764475
|
C | CAA | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-2659_176-2658d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764475 | ||||||
| chr2:201764529
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+2700C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764529 | ||||||
| chr2:201764629
|
G | A | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.175+2600C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764629 | ||||||
| chr2:201764634
|
A | AAAAT | 41 | a0001c0001t0001g0046a0001c0001t0001g0080a0001c0001t0001g0208others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.175+2591_175+2594d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | ||||||
| chr2:201764634
|
A | AAAATAAA others(1): Show |
8 | a0001c0001t0001g0149a0001c0002t0001g0131a0001c0003t0002g0220others(5): Show | 8 | HG00140.hp1 HG01175.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+2587_175+2594d others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | ||||||
| chr2:201764634
|
A | AAAATAAA others(5): Show |
1 | a0001c0011t0001g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.175+2583_175+2594d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | ||||||
| chr2:201764634
|
AAAAT | A | 92 | a0001c0001t0001g0015a0001c0001t0001g0205a0001c0001t0001g0207others(89): Show | 101 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.175+2591_175+2594d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | ||||||
| chr2:201764634
|
AAAATAAA others(1): Show |
A | 83 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0017others(80): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.175+2587_175+2594d others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | ||||||
| chr2:201764634
|
AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0304 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.175+2583_175+2594d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | ||||||
| chr2:201764686
|
A | T | 7 | a0001c0004t0001g0003a0001c0004t0001g0048a0001c0004t0001g0049others(4): Show | 8 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+2543T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764686 | ||||||
| chr2:201764705
|
T | G | 1 | a0001c0001t0001g0316 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.175+2524A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764705 | ||||||
| chr2:201764709
|
T | C | 4 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(1): Show | 4 | NA18956.hp1 NA18994.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+2520A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764709 | ||||||
| chr2:201764764
|
T | C | 1 | a0001c0002t0001g0308 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.175+2465A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764764 | ||||||
| chr2:201764864
|
G | A | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | NA18971.hp1 NA19004.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.175+2365C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764864 | ||||||
| chr2:201764906
|
T | C | 5 | a0001c0003t0002g0164a0001c0003t0002g0180a0001c0003t0002g0181others(2): Show | 5 | NA18940.hp1 NA18980.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+2323A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764906 | ||||||
| chr2:201764997
|
C | CT | 9 | a0001c0001t0001g0205a0001c0003t0004g0154a0001c0004t0001g0005others(6): Show | 10 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.175+2231dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764997 | ||||||
| chr2:201765102
|
A | C | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.175+2127T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765102 | ||||||
| chr2:201765276
|
C | T | 2 | a0006c0010t0001g0097a0006c0010t0001g0145 | 2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.175+1953G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765276 | ||||||
| chr2:201765645
|
A | ATACTT | 17 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0222others(14): Show | 17 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+1579_175+1583d others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765645 | ||||||
| chr2:201765701
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+1528C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765701 | ||||||
| chr2:201765753
|
T | G | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.175+1476A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765753 | ||||||
| chr2:201765790
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+1439A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765790 | ||||||
| chr2:201765915
|
G | A | 15 | a0002c0005t0001g0002a0002c0005t0001g0004a0002c0005t0001g0055others(12): Show | 18 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+1314C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765915 | ||||||
| chr2:201766102
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+1127A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766102 | ||||||
| chr2:201766108
|
T | G | 1 | a0001c0002t0001g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.175+1121A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766108 | ||||||
| chr2:201766235
|
A | C | 3 | a0001c0003t0004g0154a0001c0003t0004g0155a0001c0003t0004g0156 | 3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.175+994T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766235 | ||||||
| chr2:201766694
|
C | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.175+535G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766694 | ||||||
| chr2:201766722
|
G | GAAAATGT others(314): Show |
1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(321): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766722
|
G | GAAAATGT others(302): Show |
1 | a0001c0002t0001g0223 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(309): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766722
|
G | GAAAATGT others(312): Show |
1 | a0001c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(319): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766722
|
G | GAAAATGT others(313): Show |
41 | a0001c0001t0001g0207a0001c0002t0001g0096a0001c0002t0001g0224others(38): Show | 44 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.175+506_175+507ins others(320): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766722
|
G | GAAAATGT others(314): Show |
93 | a0001c0001t0001g0083a0001c0001t0001g0149a0001c0001t0001g0205others(90): Show | 96 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.175+506_175+507ins others(321): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766722
|
G | GAAAATGT others(315): Show |
37 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(34): Show | 38 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.175+506_175+507ins others(322): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766722
|
G | GAAAATGT others(316): Show |
3 | a0001c0002t0001g0142a0001c0002t0001g0143a0001c0003t0001g0042 | 3 | HG00741.hp2 HG02486.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.175+506_175+507ins others(323): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766722
|
G | GAAAATGT others(315): Show |
1 | a0001c0001t0001g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(322): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | ||||||
| chr2:201766727
|
T | TGTGGCAC others(315): Show |
1 | a0001c0002t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.175+501_175+502ins others(322): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766727 | ||||||
| chr2:201766751
|
A | G | 1 | a0001c0001t0001g0327 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.175+478T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766751 | ||||||
| chr2:201766768
|
A | G | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+461T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766768 | ||||||
| chr2:201766854
|
ACACCGCA others(6): Show |
A | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+362_175+374del others(13): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766854 | ||||||
| chr2:201766874
|
T | C | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.175+355A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766874 | ||||||
| chr2:201766889
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+340T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766889 | ||||||
| chr2:201766892
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(319): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.175+337G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766892 | ||||||
| chr2:201766956
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.175+273G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766956 | ||||||
| chr2:201766978
|
A | G | 49 | a0001c0001t0001g0207a0001c0003t0001g0173a0001c0003t0002g0008others(46): Show | 53 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.175+251T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766978 | ||||||
| chr2:201766990
|
C | T | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+239G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766990 | ||||||
| chr2:201767034
|
T | A | 1 | a0001c0004t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.175+195A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767034 | ||||||
| chr2:201767058
|
G | A | 2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.175+171C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767058 | ||||||
| chr2:201767106
|
A | T | 1 | a0001c0011t0001g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.175+123T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767106 | ||||||
| chr2:201767201
|
G | A | 3 | a0001c0001t0001g0217a0001c0001t0001g0309a0001c0004t0001g0216 | 3 | HG02027.hp2 NA19060.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175+28C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767201 | ||||||
| chr2:201767559
|
A | G | 9 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(6): Show | 10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-176T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767559 | ||||||
| chr2:201767572
|
A | T | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.21-189T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767572 | ||||||
| chr2:201767588
|
C | T | 14 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(11): Show | 14 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.21-205G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767588 | ||||||
| chr2:201767611
|
C | T | 2 | a0001c0003t0002g0166a0001c0003t0002g0198 | 2 | NA18981.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.21-228G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767611 | ||||||
| chr2:201767629
|
G | A | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.21-246C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767629 | ||||||
| chr2:201767639
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.21-256C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767639 | ||||||
| chr2:201767677
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(319): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.21-294G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767677 | ||||||
| chr2:201767705
|
C | CAA | 100 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(97): Show | 111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.21-324_21-323dupTT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767705 | ||||||
| chr2:201767705
|
CA | C | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-323delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767705 | ||||||
| chr2:201767707
|
A | C | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.21-324T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767707 | ||||||
| chr2:201767782
|
C | T | 14 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(11): Show | 14 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.21-399G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767782 | ||||||
| chr2:201767866
|
T | A | 2 | a0001c0004t0001g0073a0001c0004t0001g0074 | 2 | HG02293.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.21-483A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | ||||||
| chr2:201767866
|
T | TA | 93 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(90): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.21-484dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | ||||||
| chr2:201767866
|
T | TAA | 11 | a0001c0001t0001g0242a0001c0001t0001g0249a0001c0001t0001g0254others(8): Show | 11 | HG00438.hp1 HG00673.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-485_21-484dupTT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | ||||||
| chr2:201767866
|
TA | T | 138 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0080others(135): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.21-484delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | ||||||
| chr2:201767866
|
TAA | T | 50 | a0001c0001t0001g0207a0001c0002t0001g0092a0001c0002t0001g0093others(47): Show | 53 | HG00423.hp1 HG00597.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.21-485_21-484delTT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | ||||||
| chr2:201768057
|
A | C | 68 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(65): Show | 73 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.21-674T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768057 | ||||||
| chr2:201768158
|
A | G | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.20+708T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768158 | ||||||
| chr2:201768215
|
T | C | 179 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(176): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.20+651A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768215 | ||||||
| chr2:201768249
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.20+617G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768249 | ||||||
| chr2:201768638
|
A | T | 1 | a0001c0001t0001g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.20+228T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768638 | ||||||
| chr2:201768744
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.20+122A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768744 | ||||||
| chr2:201768859
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
splice_region_variant&intron_variant | LOW | c.20+7T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768859 | ||||||
| chr2:201768963
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-18C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201768963 | ||||||
| chr2:201769002
|
T | TA | 110 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 121 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-60-58dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769002 | ||||||
| chr2:201769263
|
G | A | 7 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-318C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769263 | ||||||
| chr2:201769273
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-60-328G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769273 | ||||||
| chr2:201769325
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-380T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769325 | ||||||
| chr2:201769335
|
A | T | 1 | a0001c0002t0001g0091 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-60-390T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769335 | ||||||
| chr2:201769613
|
T | C | 6 | a0001c0003t0002g0011a0001c0003t0002g0189a0001c0003t0002g0190others(3): Show | 7 | HG00544.hp1 HG02155.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.-60-668A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769613 | ||||||
| chr2:201769661
|
T | C | 1 | a0002c0005t0001g0067 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-60-716A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769661 | ||||||
| chr2:201770095
|
C | A | 6 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(3): Show | 6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-1150G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770095 | ||||||
| chr2:201770120
|
G | T | 2 | a0001c0004t0001g0073a0001c0004t0001g0074 | 2 | HG02293.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-60-1175C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770120 | ||||||
| chr2:201770309
|
CCTA | C | 9 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(6): Show | 10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-60-1367_-60-1365d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770309 | ||||||
| chr2:201770450
|
A | AT | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-1506dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770450 | ||||||
| chr2:201770450
|
AT | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(236): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.-60-1506delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770450 | ||||||
| chr2:201770466
|
TA | T | 3 | a0001c0003t0001g0042a0001c0003t0007g0040a0001c0003t0007g0041 | 3 | HG02486.hp1 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-60-1522delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770466 | ||||||
| chr2:201770551
|
G | C | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | NA18971.hp1 NA19004.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-60-1606C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770551 | ||||||
| chr2:201770686
|
G | A | 1 | a0001c0002t0001g0315 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-60-1741C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770686 | ||||||
| chr2:201770881
|
T | C | 105 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(102): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-60-1936A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770881 | ||||||
| chr2:201770926
|
A | C | 106 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(103): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-60-1981T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770926 | ||||||
| chr2:201771027
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(319): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-60-2082G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771027 | ||||||
| chr2:201771042
|
A | AT | 13 | a0001c0001t0001g0238a0001c0001t0001g0243a0001c0001t0001g0244others(10): Show | 13 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.-60-2098dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | ||||||
| chr2:201771042
|
AT | A | 67 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0222others(64): Show | 71 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-60-2098delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | ||||||
| chr2:201771042
|
ATT | A | 152 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0080others(149): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-60-2099_-60-2098d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | ||||||
| chr2:201771042
|
ATTT | A | 7 | a0001c0001t0003g0023a0001c0001t0003g0031a0003c0007t0001g0032others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-2100_-60-2098d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | ||||||
| chr2:201771116
|
G | A | 6 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(3): Show | 6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-2171C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771116 | ||||||
| chr2:201771203
|
C | T | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-60-2258G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771203 | ||||||
| chr2:201771259
|
C | T | 2 | a0003c0007t0001g0032a0003c0007t0001g0033 | 2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-60-2314G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771259 | ||||||
| chr2:201771298
|
C | T | 2 | a0001c0003t0002g0087a0008c0021t0001g0086 | 2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-60-2353G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771298 | ||||||
| chr2:201771344
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2399T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771344 | ||||||
| chr2:201771348
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2403G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771348 | ||||||
| chr2:201771414
|
G | A | 61 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(58): Show | 65 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.-60-2469C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771414 | ||||||
| chr2:201771429
|
C | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2484G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771429 | ||||||
| chr2:201771450
|
T | C | 6 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(3): Show | 6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-2505A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771450 | ||||||
| chr2:201771453
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2508A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771453 | ||||||
| chr2:201771483
|
T | C | 1 | a0001c0002t0001g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-60-2538A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771483 | ||||||
| chr2:201771693
|
A | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(1): Show | 4 | NA18967.hp2 NA18968.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-60-2748T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771693 | ||||||
| chr2:201771722
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2777T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771722 | ||||||
| chr2:201771921
|
G | T | 1 | a0004c0008t0001g0237 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-60-2976C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771921 | ||||||
| chr2:201771929
|
A | T | 2 | a0001c0003t0007g0040a0001c0003t0007g0041 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-60-2984T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771929 | ||||||
| chr2:201772123
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-60-3178C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772123 | ||||||
| chr2:201772188
|
T | C | 88 | a0001c0001t0001g0149a0001c0002t0001g0006a0001c0002t0001g0007others(85): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-60-3243A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772188 | ||||||
| chr2:201772278
|
T | TAAC | 179 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(176): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-60-3336_-60-3334d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772278 | ||||||
| chr2:201772278
|
TAAC | T | 12 | a0001c0001t0001g0217a0001c0001t0003g0020a0001c0001t0003g0021others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-3336_-60-3334d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772278 | ||||||
| chr2:201772318
|
C | T | 70 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(67): Show | 75 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-60-3373G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772318 | ||||||
| chr2:201772359
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-3414G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772359 | ||||||
| chr2:201772499
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-3554T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772499 | ||||||
| chr2:201772503
|
C | T | 6 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(3): Show | 6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-3558G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772503 | ||||||
| chr2:201772530
|
T | C | 1 | a0001c0002t0001g0150 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-60-3585A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772530 | ||||||
| chr2:201772649
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-60-3704G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772649 | ||||||
| chr2:201772706
|
G | T | 9 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0242others(6): Show | 9 | HG00597.hp1 HG00673.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-60-3761C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772706 | ||||||
| chr2:201772850
|
A | AT | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-60-3906dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | ||||||
| chr2:201772850
|
A | ATT | 21 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(18): Show | 22 | HG00597.hp1 HG00673.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-60-3907_-60-3906d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | ||||||
| chr2:201772850
|
AT | A | 27 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0222others(24): Show | 27 | HG00280.hp1 HG00423.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-60-3906delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | ||||||
| chr2:201772850
|
ATT | A | 82 | a0001c0001t0001g0149a0001c0002t0001g0006a0001c0002t0001g0007others(79): Show | 84 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-60-3907_-60-3906d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | ||||||
| chr2:201772850
|
ATTT | A | 27 | a0001c0001t0001g0205a0001c0001t0003g0031a0001c0002t0001g0071others(24): Show | 31 | HG00099.hp1 HG00642.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.-60-3908_-60-3906d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | ||||||
| chr2:201772872
|
T | TTC | 6 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0036others(3): Show | 6 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-3928_-60-3927i others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772872 | ||||||
| chr2:201772901
|
G | A | 105 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(102): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-60-3956C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772901 | ||||||
| chr2:201773008
|
C | T | 3 | a0002c0006t0001g0056a0002c0006t0001g0057a0002c0006t0001g0058 | 3 | HG00099.hp1 HG01081.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-60-4063G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773008 | ||||||
| chr2:201773142
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-4197C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773142 | ||||||
| chr2:201773151
|
C | A | 1 | a0001c0002t0001g0153 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-60-4206G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773151 | ||||||
| chr2:201773166
|
T | A | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-60-4221A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773166 | ||||||
| chr2:201773167
|
T | G | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-60-4222A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773167 | ||||||
| chr2:201773179
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-4234C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773179 | ||||||
| chr2:201773282
|
C | T | 1 | a0003c0007t0001g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-60-4337G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773282 | ||||||
| chr2:201773341
|
C | T | 1 | a0001c0003t0002g0159 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-60-4396G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773341 | ||||||
| chr2:201773358
|
G | A | 3 | a0001c0003t0004g0154a0001c0003t0004g0155a0001c0003t0004g0156 | 3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-60-4413C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773358 | ||||||
| chr2:201773449
|
A | G | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-60-4504T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773449 | ||||||
| chr2:201773525
|
C | T | 5 | a0001c0002t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070others(2): Show | 5 | NA18942.hp2 NA18968.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-4580G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773525 | ||||||
| chr2:201773620
|
G | A | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-60-4675C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773620 | ||||||
| chr2:201773621
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(102): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-60-4676G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773621 | ||||||
| chr2:201773722
|
T | C | 1 | a0001c0002t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-60-4777A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773722 | ||||||
| chr2:201773773
|
C | G | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-60-4828G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773773 | ||||||
| chr2:201773804
|
C | T | 15 | a0002c0005t0001g0002a0002c0005t0001g0004a0002c0005t0001g0055others(12): Show | 18 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-60-4859G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773804 | ||||||
| chr2:201773805
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-4860C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773805 | ||||||
| chr2:201773832
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-60-4887C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773832 | ||||||
| chr2:201774001
|
A | G | 1 | a0003c0007t0001g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-60-5056T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774001 | ||||||
| chr2:201774004
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-60-5059A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774004 | ||||||
| chr2:201774147
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 119 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-60-5202A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774147 | ||||||
| chr2:201774266
|
G | A | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-60-5321C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774266 | ||||||
| chr2:201774318
|
A | G | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-60-5373T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774318 | ||||||
| chr2:201774326
|
G | A | 1 | a0001c0002t0001g0325 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-60-5381C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774326 | ||||||
| chr2:201774475
|
A | G | 191 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0149others(188): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-60-5530T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774475 | ||||||
| chr2:201774556
|
G | A | 49 | a0001c0001t0001g0207a0001c0003t0001g0173a0001c0003t0002g0008others(46): Show | 53 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-60-5611C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774556 | ||||||
| chr2:201774629
|
CTACTCAA others(5): Show |
C | 1 | a0001c0001t0001g0326 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-60-5696_-60-5685d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774629 | ||||||
| chr2:201774649
|
TAA | T | 13 | a0001c0001t0001g0222a0001c0001t0001g0227a0001c0002t0001g0221others(10): Show | 13 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.-60-5706_-60-5705d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774649 | ||||||
| chr2:201774797
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-60-5852A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774797 | ||||||
| chr2:201774880
|
T | G | 4 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329others(1): Show | 4 | NA18945.hp2 NA18971.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-60-5935A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774880 | ||||||
| chr2:201775049
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-61+5828C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775049 | ||||||
| chr2:201775423
|
A | G | 1 | a0004c0008t0001g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-61+5454T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775423 | ||||||
| chr2:201775532
|
T | C | 1 | a0001c0002t0001g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-61+5345A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775532 | ||||||
| chr2:201775639
|
T | C | 14 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(11): Show | 14 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-61+5238A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775639 | ||||||
| chr2:201775718
|
T | C | 1 | a0001c0002t0001g0051 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-61+5159A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775718 | ||||||
| chr2:201775740
|
C | A | 1 | a0001c0003t0002g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-61+5137G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775740 | ||||||
| chr2:201775741
|
C | A | 1 | a0001c0003t0002g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-61+5136G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775741 | ||||||
| chr2:201775763
|
T | C | 1 | a0001c0002t0001g0204 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-61+5114A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775763 | ||||||
| chr2:201775792
|
C | G | 1 | a0002c0005t0001g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-61+5085G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775792 | ||||||
| chr2:201775823
|
A | C | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-61+5054T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775823 | ||||||
| chr2:201776039
|
C | G | 1 | a0001c0002t0001g0054 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-61+4838G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776039 | ||||||
| chr2:201776171
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-61+4706A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776171 | ||||||
| chr2:201776272
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-61+4605A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776272 | ||||||
| chr2:201776374
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-61+4503C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776374 | ||||||
| chr2:201776534
|
C | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+4343G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776534 | ||||||
| chr2:201776558
|
T | C | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-61+4319A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776558 | ||||||
| chr2:201776720
|
T | C | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61+4157A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776720 | ||||||
| chr2:201776795
|
G | A | 1 | a0001c0002t0001g0215 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-61+4082C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776795 | ||||||
| chr2:201777036
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-61+3841A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777036 | ||||||
| chr2:201777060
|
C | G | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-61+3817G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777060 | ||||||
| chr2:201777185
|
C | T | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-61+3692G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777185 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(322): Show |
2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-61+3615_-61+3616i others(331): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(323): Show |
5 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(2): Show | 5 | HG01109.hp2 HG01123.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61+3615_-61+3616i others(332): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(324): Show |
1 | a0001c0001t0003g0027 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(333): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(325): Show |
2 | a0001c0001t0003g0030a0001c0004t0003g0029 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-61+3615_-61+3616i others(334): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(326): Show |
1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(335): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(328): Show |
1 | a0001c0001t0006g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(337): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(329): Show |
1 | a0001c0001t0006g0332 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(338): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777261
|
T | TAAAGAAA others(325): Show |
1 | a0001c0001t0003g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(334): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | ||||||
| chr2:201777336
|
G | A | 6 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(3): Show | 6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61+3541C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777336 | ||||||
| chr2:201777364
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-61+3513C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777364 | ||||||
| chr2:201777491
|
T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-61+3386A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777491 | ||||||
| chr2:201777736
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-61+3141A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777736 | ||||||
| chr2:201777963
|
T | C | 2 | a0001c0001t0001g0217a0001c0004t0001g0216 | 2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-61+2914A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777963 | ||||||
| chr2:201778028
|
T | C | 1 | a0013c0018t0001g0218 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-61+2849A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778028 | ||||||
| chr2:201778386
|
G | C | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61+2491C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778386 | ||||||
| chr2:201778500
|
C | A | 1 | a0001c0002t0001g0219 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-61+2377G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778500 | ||||||
| chr2:201778720
|
G | A | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-61+2157C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778720 | ||||||
| chr2:201779194
|
G | C | 13 | a0001c0001t0001g0222a0001c0001t0001g0227a0001c0002t0001g0221others(10): Show | 13 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.-61+1683C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779194 | ||||||
| chr2:201779600
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-61+1277G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779600 | ||||||
| chr2:201779669
|
C | T | 331 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-61+1208G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779669 | ||||||
| chr2:201779832
|
T | C | 1 | a0001c0002t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-61+1045A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779832 | ||||||
| chr2:201779942
|
A | G | 9 | a0001c0001t0001g0046a0001c0004t0001g0003a0001c0004t0001g0044others(6): Show | 10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-61+935T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779942 | ||||||
| chr2:201780215
|
A | G | 3 | a0001c0003t0001g0042a0001c0003t0007g0040a0001c0003t0007g0041 | 3 | HG02486.hp1 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-61+662T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780215 | ||||||
| chr2:201780490
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-61+387C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780490 | ||||||
| chr2:201780628
|
C | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-61+249G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780628 | ||||||
| chr2:201780674
|
C | A | 2 | a0001c0001t0006g0331a0001c0001t0006g0332 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61+203G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780674 | ||||||
| chr2:201780744
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-61+133G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780744 | ||||||
| chr2:201780781
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-61+96G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780781 | ||||||
| chr2:201780819
|
G | T | 6 | a0003c0007t0001g0032a0003c0007t0001g0033a0003c0007t0001g0034others(3): Show | 6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61+58C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780819 |