| geneid | 10003 |
|---|---|
| ensemblid | ENSG00000077616.11 |
| hgncid | 14526 |
| symbol | NAALAD2 |
| name | N-acetylated alpha-linked acidic dipeptidase 2 |
| refseq_nuc | NM_005467.4 |
| refseq_prot | NP_005458.1 |
| ensembl_nuc | ENST00000534061.6 |
| ensembl_prot | ENSP00000432481.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 90134663 |
| end | 90192894 |
| strand | + |
| ver | v1.2 |
| region | chr11:90134663-90192894 |
| region5000 | chr11:90129663-90197894 |
| regionname0 | NAALAD2_chr11_90134663_90192894 |
| regionname5000 | NAALAD2_chr11_90129663_90197894 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 740 | 274 | 47 | 48 | 138 | 11 | 28 | 112 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002 | 0/0 | 740 | 42 | 17 | 7 | 2 | 1 | 15 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0003 | 0/0 | 740 | 14 | 1 | 3 | 9 | 0 | 1 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004 | 0/0 | 740 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0005 | 0/0 | 740 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0006 | 0/0 | 740 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0007 | 0/0 | 740 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0008 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0009 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0010 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0011 | 0/0 | 399 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0012 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0013 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0014 | 0/0 | 740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2223 | 148 | 25 | 29 | 70 | 6 | 16 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0002 | 0/0 | 2223 | 117 | 16 | 17 | 67 | 5 | 12 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0003 | 0/0 | 2223 | 40 | 17 | 7 | 2 | 1 | 13 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0004 | 0/0 | 2223 | 14 | 1 | 3 | 9 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0005 | 0/0 | 2223 | 13 | 13 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0006 | 0/0 | 2223 | 6 | 5 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0007 | 0/0 | 2223 | 6 | 5 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0008 | 0/0 | 2223 | 3 | 3 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0009 | 0/0 | 2223 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0010 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0011 | 0/0 | 2223 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0012 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0013 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0014 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0015 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0016 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0017 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0018 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0019 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0020 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0021 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| c0022 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1244 | 114 | 21 | 20 | 51 | 3 | 19 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0002 | 1/1 | 1244 | 74 | 21 | 18 | 24 | 3 | 6 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0003 | 0/0 | 1244 | 45 | 2 | 3 | 34 | 0 | 6 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0004 | 0/0 | 1244 | 41 | 27 | 2 | 10 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0005 | 0/0 | 1244 | 38 | 13 | 5 | 12 | 3 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0006 | 0/0 | 1244 | 21 | 0 | 9 | 3 | 3 | 6 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0007 | 0/0 | 1244 | 9 | 1 | 0 | 6 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0008 | 0/0 | 1244 | 7 | 1 | 1 | 4 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0009 | 0/0 | 1244 | 5 | 0 | 0 | 5 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0010 | 0/0 | 1244 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0011 | 0/0 | 1244 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0012 | 0/0 | 1244 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0013 | 0/0 | 1244 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0014 | 0/0 | 1244 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0015 | 0/0 | 1244 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0016 | 0/0 | 1244 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0017 | 0/0 | 1216 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| t0018 | 0/0 | 1244 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2223 | 148 | 25 | 29 | 70 | 6 | 16 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0002 | 0/0 | 2223 | 117 | 16 | 17 | 67 | 5 | 12 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0006 | 0/0 | 2223 | 6 | 5 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0015 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0016 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0020 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0003 | 0/0 | 2223 | 40 | 17 | 7 | 2 | 1 | 13 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0009 | 0/0 | 2223 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0003c0004 | 0/0 | 2223 | 14 | 1 | 3 | 9 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004c0005 | 0/0 | 2223 | 13 | 13 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004c0021 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0005c0007 | 0/0 | 2223 | 6 | 5 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0005c0014 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0006c0008 | 0/0 | 2223 | 3 | 3 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0007c0011 | 0/0 | 2223 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0008c0010 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0009c0022 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0010c0017 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0011c0019 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0012c0012 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0013c0013 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0014c0018 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 3466 | 69 | 20 | 17 | 22 | 3 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0001t0003 | 0/0 | 3466 | 44 | 2 | 3 | 34 | 0 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0001t0006 | 0/0 | 3466 | 19 | 0 | 8 | 3 | 3 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0001t0008 | 0/0 | 3466 | 7 | 1 | 1 | 4 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0001t0009 | 0/0 | 3466 | 5 | 0 | 0 | 5 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0001t0010 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0001t0012 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0001t0013 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0002t0001 | 0/0 | 3466 | 73 | 5 | 12 | 47 | 2 | 7 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0002t0004 | 0/0 | 3466 | 20 | 9 | 2 | 9 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0002t0005 | 0/0 | 3466 | 16 | 2 | 2 | 4 | 3 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0002t0007 | 0/0 | 3466 | 6 | 0 | 0 | 6 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0002t0015 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0002t0016 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0006t0001 | 0/0 | 3466 | 3 | 2 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0006t0004 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0006t0005 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0015t0001 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0016t0002 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0001c0020t0002 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0003t0001 | 0/0 | 3466 | 29 | 10 | 6 | 2 | 1 | 10 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0003t0004 | 0/0 | 3466 | 5 | 4 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0003t0005 | 0/0 | 3466 | 3 | 3 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0003t0007 | 0/0 | 3466 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0003t0017 | 0/0 | 3438 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0002c0009t0001 | 0/0 | 3466 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0003c0004t0001 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0003c0004t0004 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0003c0004t0005 | 0/0 | 3466 | 11 | 1 | 2 | 8 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0003c0004t0018 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004c0005t0001 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004c0005t0004 | 0/0 | 3466 | 8 | 8 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004c0005t0005 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004c0005t0014 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0004c0021t0011 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0005c0007t0001 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0005c0007t0005 | 0/0 | 3466 | 4 | 3 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0005c0007t0007 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0005c0014t0001 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0006c0008t0004 | 0/0 | 3466 | 3 | 3 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0007c0011t0002 | 0/0 | 3466 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0008c0010t0004 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0009c0022t0002 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0010c0017t0003 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0011c0019t0006 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0012c0012t0001 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0013c0013t0004 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| a0014c0018t0006 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | copy fasta | chr11 | 90129663 | 90197894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0008g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0001t0013g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0015g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0002t0016g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0006t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0006t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0006t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0006t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0006t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0006t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0015t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0016t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0001c0020t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0004g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0007g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0007g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0003t0017g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0009t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0002c0009t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0003c0004t0018g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0005t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0004c0021t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0005c0007t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0005c0007t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0005c0007t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0005c0007t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0005c0007t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0005c0007t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0005c0014t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0006c0008t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0006c0008t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0006c0008t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0007c0011t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0007c0011t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0008c0010t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0008c0010t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0009c0022t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0010c0017t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0011c0019t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0012c0012t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0013c0013t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| a0014c0018t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0052 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0210 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0172 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0342 | EUR | FIN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0219 | EUR | FIN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00438 | hp2 | a0003 | c0004 | t0005 | g0249 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0310 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00558 | hp2 | a0001 | c0001 | t0012 | g0108 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00609 | hp1 | a0007 | c0011 | t0002 | g0127 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00642 | hp2 | a0001 | c0002 | t0016 | g0345 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0178 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0180 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00741 | hp1 | a0014 | c0018 | t0006 | g0179 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0173 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0174 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01074 | hp1 | a0001 | c0002 | t0004 | g0273 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0351 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01081 | hp1 | a0005 | c0007 | t0005 | g0324 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0286 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01106 | hp2 | a0001 | c0002 | t0005 | g0344 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0334 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01168 | hp1 | a0002 | c0003 | t0017 | g0010 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0182 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01175 | hp2 | a0003 | c0004 | t0001 | g0255 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0301 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0337 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01255 | hp1 | a0001 | c0002 | t0005 | g0012 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0183 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0065 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01261 | hp1 | a0001 | c0002 | t0004 | g0024 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01346 | hp1 | a0001 | c0001 | t0008 | g0136 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01346 | hp2 | a0003 | c0004 | t0005 | g0248 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0295 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01516 | hp1 | a0001 | c0002 | t0005 | g0343 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0176 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01517 | hp1 | a0001 | c0002 | t0005 | g0341 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0292 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01934 | hp2 | a0003 | c0004 | t0005 | g0244 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0298 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0305 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02015 | hp2 | a0001 | c0001 | t0009 | g0005 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02027 | hp2 | a0003 | c0004 | t0005 | g0259 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02055 | hp1 | a0006 | c0008 | t0004 | g0308 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0270 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02056 | hp1 | a0001 | c0002 | t0004 | g0204 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02083 | hp2 | a0003 | c0004 | t0005 | g0250 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02129 | hp1 | a0003 | c0004 | t0004 | g0256 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02132 | hp2 | a0001 | c0001 | t0009 | g0169 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02145 | hp2 | a0002 | c0003 | t0004 | g0274 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02155 | hp2 | a0001 | c0002 | t0004 | g0350 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02165 | hp2 | a0001 | c0002 | t0004 | g0209 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02258 | hp2 | a0003 | c0004 | t0005 | g0254 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02280 | hp1 | a0004 | c0005 | t0004 | g0280 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02300 | hp2 | a0001 | c0016 | t0002 | g0096 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0294 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02451 | hp2 | a0004 | c0005 | t0004 | g0281 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0006 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02615 | hp2 | a0004 | c0005 | t0001 | g0266 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0314 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0282 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0039 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0312 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02723 | hp1 | a0004 | c0005 | t0004 | g0262 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0306 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0315 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02809 | hp1 | a0001 | c0006 | t0001 | g0313 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0291 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02818 | hp2 | a0002 | c0003 | t0005 | g0275 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0289 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02886 | hp2 | a0004 | c0005 | t0001 | g0261 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02895 | hp2 | a0004 | c0005 | t0014 | g0265 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02896 | hp1 | a0004 | c0005 | t0004 | g0279 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02896 | hp2 | a0001 | c0006 | t0004 | g0335 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0269 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02922 | hp2 | a0008 | c0010 | t0004 | g0329 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02965 | hp1 | a0004 | c0005 | t0005 | g0260 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0162 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02970 | hp2 | a0002 | c0003 | t0004 | g0317 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02976 | hp1 | a0004 | c0005 | t0004 | g0277 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0319 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0307 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03041 | hp1 | a0004 | c0005 | t0004 | g0278 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03041 | hp2 | a0005 | c0007 | t0005 | g0326 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0271 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0333 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03130 | hp1 | a0004 | c0021 | t0011 | g0185 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03139 | hp2 | a0005 | c0014 | t0001 | g0328 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0268 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03195 | hp2 | a0002 | c0003 | t0005 | g0009 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03209 | hp1 | a0002 | c0003 | t0004 | g0287 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0163 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0332 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03239 | hp1 | a0001 | c0002 | t0005 | g0340 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03239 | hp2 | a0002 | c0003 | t0007 | g0311 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03453 | hp1 | a0004 | c0005 | t0004 | g0263 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03453 | hp2 | a0001 | c0006 | t0005 | g0336 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03486 | hp1 | a0005 | c0007 | t0001 | g0330 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0322 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0170 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03491 | hp1 | a0002 | c0009 | t0001 | g0283 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0046 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0177 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0171 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0288 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03516 | hp2 | a0005 | c0007 | t0005 | g0323 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03540 | hp1 | a0004 | c0005 | t0004 | g0264 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03579 | hp1 | a0005 | c0007 | t0007 | g0325 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0272 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0010 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0316 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03688 | hp1 | a0010 | c0017 | t0003 | g0079 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0300 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03704 | hp2 | a0001 | c0002 | t0005 | g0339 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0318 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03831 | hp1 | a0002 | c0003 | t0004 | g0320 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03834 | hp1 | a0001 | c0002 | t0005 | g0012 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03834 | hp2 | a0003 | c0004 | t0018 | g0247 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03927 | hp2 | a0009 | c0022 | t0002 | g0126 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0285 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04115 | hp1 | a0011 | c0019 | t0006 | g0042 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04115 | hp2 | a0001 | c0002 | t0005 | g0202 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0230 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04184 | hp2 | a0013 | c0013 | t0004 | g0309 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0297 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0199 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04228 | hp1 | a0001 | c0001 | t0008 | g0049 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG04228 | hp2 | a0002 | c0003 | t0007 | g0304 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0040 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18522 | hp2 | a0005 | c0007 | t0005 | g0327 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CHB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18747 | hp2 | a0012 | c0012 | t0001 | g0242 | EAS | CHB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18940 | hp1 | a0001 | c0001 | t0008 | g0113 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18941 | hp1 | a0001 | c0002 | t0007 | g0205 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18941 | hp2 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0066 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18946 | hp2 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18951 | hp1 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18956 | hp2 | a0001 | c0002 | t0007 | g0013 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18957 | hp2 | a0003 | c0004 | t0005 | g0252 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18967 | hp2 | a0003 | c0004 | t0005 | g0257 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18973 | hp2 | a0003 | c0004 | t0005 | g0258 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18975 | hp2 | a0001 | c0002 | t0004 | g0239 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18977 | hp2 | a0007 | c0011 | t0002 | g0081 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18979 | hp2 | a0001 | c0002 | t0007 | g0022 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18985 | hp1 | a0001 | c0002 | t0005 | g0347 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18987 | hp2 | a0001 | c0015 | t0001 | g0223 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18992 | hp1 | a0001 | c0002 | t0015 | g0020 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18994 | hp2 | a0001 | c0001 | t0013 | g0004 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18995 | hp1 | a0001 | c0001 | t0008 | g0122 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18998 | hp2 | a0003 | c0004 | t0005 | g0251 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18999 | hp1 | a0001 | c0002 | t0007 | g0031 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19000 | hp2 | a0001 | c0002 | t0004 | g0189 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19009 | hp2 | a0001 | c0002 | t0005 | g0348 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19043 | hp1 | a0001 | c0020 | t0002 | g0095 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0016 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19060 | hp1 | a0001 | c0002 | t0005 | g0193 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0109 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19062 | hp2 | a0003 | c0004 | t0005 | g0253 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19063 | hp1 | a0001 | c0002 | t0007 | g0015 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19068 | hp2 | a0001 | c0002 | t0005 | g0349 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19079 | hp2 | a0001 | c0002 | t0004 | g0195 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0188 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0102 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19084 | hp1 | a0001 | c0002 | t0007 | g0216 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19085 | hp1 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19240 | hp1 | a0006 | c0008 | t0004 | g0302 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | ASW | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20129 | hp2 | a0002 | c0003 | t0004 | g0296 | AFR | ASW | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0303 | EUR | TSI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0165 | EUR | TSI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20905 | hp1 | a0002 | c0009 | t0001 | g0321 | SAS | GIH | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20905 | hp2 | a0001 | c0002 | t0005 | g0346 | SAS | GIH | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02109 | hp1 | a0001 | c0006 | t0005 | g0338 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02486 | hp1 | a0004 | c0005 | t0005 | g0276 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0290 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0299 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG02559 | hp2 | a0006 | c0008 | t0004 | g0243 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| HG03471 | hp2 | a0002 | c0003 | t0005 | g0009 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20300 | hp1 | a0002 | c0003 | t0001 | g0293 | AFR | USA | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA20300 | hp2 | a0008 | c0010 | t0004 | g0331 | AFR | USA | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0003 | REF | REF | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0111 | REF | REF | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:90147362
|
C | T | 1 | a0009 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.227C>T | p.Thr76Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/19 | 323/3466 | 227/2223 | 76/740 | chr11 | 90147362 | ||
| chr11:90147436
|
G | A | 1 | a0003 | 14 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(11): Show |
missense_variant | MODERATE | c.301G>A | p.Val101Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/19 | 397/3466 | 301/2223 | 101/740 | chr11 | 90147436 | ||
| chr11:90150540
|
A | G | 2 | a0005a0008 | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
missense_variant | MODERATE | c.542A>G | p.Glu181Gly | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/19 | 638/3466 | 542/2223 | 181/740 | chr11 | 90150540 | ||
| chr11:90150558
|
C | T | 1 | a0004 | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
missense_variant | MODERATE | c.560C>T | p.Thr187Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/19 | 656/3466 | 560/2223 | 187/740 | chr11 | 90150558 | ||
| chr11:90152299
|
T | C | 1 | a0006 | 3 | HG02055.hp1 HG02559.hp2 NA19240.hp1 |
missense_variant&splice_region_variant | MODERATE | c.611T>C | p.Val204Ala | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/19 | 707/3466 | 611/2223 | 204/740 | chr11 | 90152299 | ||
| chr11:90159272
|
T | G | 1 | a0010 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.924T>G | p.Ser308Arg | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/19 | 1020/3466 | 924/2223 | 308/740 | chr11 | 90159272 | ||
| chr11:90163031
|
C | A | 1 | a0007 | 2 | HG00609.hp1 NA18977.hp2 |
missense_variant | MODERATE | c.1072C>A | p.Pro358Thr | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/19 | 1168/3466 | 1072/2223 | 358/740 | chr11 | 90163031 | ||
| chr11:90163351
|
T | A | 1 | a0014 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1117T>A | p.Phe373Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/19 | 1213/3466 | 1117/2223 | 373/740 | chr11 | 90163351 | ||
| chr11:90163539
|
G | A | 1 | a0011 | 1 | HG04115.hp1 | stop_gained | HIGH | c.1200G>A | p.Trp400* | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/19 | 1296/3466 | 1200/2223 | 400/740 | chr11 | 90163539 | ||
| chr11:90168986
|
A | G | 4 | a0002a0006a0008others(1): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
missense_variant | MODERATE | c.1336A>G | p.Ile446Val | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/19 | 1432/3466 | 1336/2223 | 446/740 | chr11 | 90168986 | ||
| chr11:90170086
|
G | A | 1 | a0013 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1360G>A | p.Val454Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/19 | 1456/3466 | 1360/2223 | 454/740 | chr11 | 90170086 | ||
| chr11:90178091
|
A | T | 1 | a0012 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1832A>T | p.Gln611Leu | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/19 | 1928/3466 | 1832/2223 | 611/740 | chr11 | 90178091 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:90135587
|
G | A | 13 | a0001c0002a0001c0006a0001c0015others(10): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
synonymous_variant | LOW | c.111G>A | p.Thr37Thr | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/19 | 207/3466 | 111/2223 | 37/740 | chr11 | 90135587 | ||
| chr11:90150493
|
A | G | 1 | a0001c0015 | 1 | NA18987.hp2 | synonymous_variant | LOW | c.495A>G | p.Val165Val | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/19 | 591/3466 | 495/2223 | 165/740 | chr11 | 90150493 | ||
| chr11:90152369
|
T | G | 1 | a0001c0016 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.681T>G | p.Pro227Pro | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/19 | 777/3466 | 681/2223 | 227/740 | chr11 | 90152369 | ||
| chr11:90163000
|
T | C | 1 | a0001c0006 | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.1041T>C | p.Asn347Asn | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/19 | 1137/3466 | 1041/2223 | 347/740 | chr11 | 90163000 | ||
| chr11:90163596
|
G | A | 1 | a0004c0005 | 13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
synonymous_variant | LOW | c.1257G>A | p.Leu419Leu | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/19 | 1353/3466 | 1257/2223 | 419/740 | chr11 | 90163596 | ||
| chr11:90168988
|
A | C | 1 | a0002c0009 | 2 | HG03491.hp1 NA20905.hp1 |
synonymous_variant | LOW | c.1338A>C | p.Ile446Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/19 | 1434/3466 | 1338/2223 | 446/740 | chr11 | 90168988 | ||
| chr11:90173875
|
T | C | 1 | a0001c0020 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1462T>C | p.Leu488Leu | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/19 | 1558/3466 | 1462/2223 | 488/740 | chr11 | 90173875 | ||
| chr11:90182973
|
C | T | 1 | a0005c0014 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1998C>T | p.Ile666Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/19 | 2094/3466 | 1998/2223 | 666/740 | chr11 | 90182973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:90134664
|
G | A | 1 | a0004c0021t0011 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-95G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/19 | 95 | chr11 | 90134664 | |||||
| chr11:90134704
|
C | T | 32 | a0001c0002t0001a0001c0002t0004a0001c0002t0005others(29): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
5_prime_UTR_variant | MODIFIER | c.-55C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/19 | 55 | chr11 | 90134704 | |||||
| chr11:90191813
|
A | C | 1 | a0003c0004t0018 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 66 | chr11 | 90191813 | |||||
| chr11:90191821
|
T | A | 1 | a0001c0001t0012 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 74 | chr11 | 90191821 | |||||
| chr11:90192011
|
C | G | 6 | a0001c0001t0003a0001c0001t0013a0001c0002t0007others(3): Show | 55 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*264C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 264 | chr11 | 90192011 | |||||
| chr11:90192066
|
AAAACAGT others(21): Show |
A | 1 | a0002c0003t0017 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325_*352delGTTTGG others(22): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 325 | INFO_REALIGN_3_PRIME | chr11 | 90192066 | ||||
| chr11:90192141
|
T | C | 1 | a0001c0001t0009 | 5 | HG02015.hp2 HG02132.hp2 NA18941.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*394T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 394 | chr11 | 90192141 | |||||
| chr11:90192175
|
A | T | 1 | a0001c0002t0016 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 428 | chr11 | 90192175 | |||||
| chr11:90192185
|
T | C | 1 | a0004c0005t0014 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 438 | chr11 | 90192185 | |||||
| chr11:90192239
|
G | A | 1 | a0001c0001t0010 | 2 | HG02965.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 492 | chr11 | 90192239 | |||||
| chr11:90192244
|
T | G | 33 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(30): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 497 | chr11 | 90192244 | |||||
| chr11:90192594
|
C | T | 20 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(17): Show | 179 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 847 | chr11 | 90192594 | |||||
| chr11:90192665
|
G | A | 1 | a0001c0001t0013 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*918G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 918 | chr11 | 90192665 | |||||
| chr11:90192827
|
C | A | 1 | a0001c0002t0015 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1080C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 1080 | chr11 | 90192827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:90135107
|
C | T | 1 | a0001c0001t0002g0351 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.82+267C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135107 | ||||||
| chr11:90135260
|
G | A | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.83-299G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135260 | ||||||
| chr11:90135305
|
T | A | 1 | a0001c0001t0002g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.83-254T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135305 | ||||||
| chr11:90135414
|
A | G | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.83-145A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135414 | ||||||
| chr11:90135426
|
T | G | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.83-133T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135426 | ||||||
| chr11:90135446
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.83-113C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135446 | ||||||
| chr11:90135524
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.83-35G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135524 | ||||||
| chr11:90135783
|
T | C | 1 | a0011c0019t0006g0042 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.194+113T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90135783 | ||||||
| chr11:90135796
|
CT | C | 85 | a0001c0001t0002g0045a0001c0001t0003g0043a0001c0001t0003g0044others(82): Show | 87 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(84): Show |
intron_variant | MODIFIER | c.194+141delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90135796 | |||||
| chr11:90135796
|
CTT | C | 105 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(102): Show | 108 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.194+140_194+141del others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90135796 | |||||
| chr11:90135870
|
G | C | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+200G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90135870 | ||||||
| chr11:90136293
|
T | C | 7 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(4): Show | 7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+623T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136293 | ||||||
| chr11:90136298
|
A | G | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.194+628A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136298 | ||||||
| chr11:90136446
|
C | T | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+776C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136446 | ||||||
| chr11:90136648
|
C | T | 1 | a0001c0006t0001g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194+978C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136648 | ||||||
| chr11:90136659
|
A | C | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+989A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136659 | ||||||
| chr11:90136836
|
A | G | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+1166A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136836 | ||||||
| chr11:90137174
|
CAG | C | 65 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(62): Show | 67 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.194+1508_194+1509d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90137174 | |||||
| chr11:90137186
|
T | C | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.194+1516T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137186 | ||||||
| chr11:90137223
|
C | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+1553C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137223 | ||||||
| chr11:90137242
|
G | C | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+1572G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137242 | ||||||
| chr11:90137411
|
AT | A | 10 | a0001c0006t0001g0334a0005c0007t0001g0330a0005c0007t0005g0323others(7): Show | 10 | HG01081.hp1 HG01109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.194+1742delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137411 | ||||||
| chr11:90137422
|
T | A | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+1752T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137422 | ||||||
| chr11:90137499
|
A | T | 1 | a0001c0006t0001g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194+1829A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137499 | ||||||
| chr11:90137582
|
C | T | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.194+1912C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137582 | ||||||
| chr11:90137670
|
C | T | 4 | a0001c0002t0004g0350a0001c0002t0005g0347a0001c0002t0005g0348others(1): Show | 4 | HG02155.hp2 NA18985.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+2000C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137670 | ||||||
| chr11:90137671
|
T | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+2001T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137671 | ||||||
| chr11:90137862
|
C | T | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+2192C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137862 | ||||||
| chr11:90137891
|
C | T | 2 | a0001c0001t0006g0183a0001c0001t0006g0184 | 2 | HG00621.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.194+2221C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137891 | ||||||
| chr11:90137943
|
C | T | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.194+2273C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137943 | ||||||
| chr11:90137948
|
A | C | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+2278A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137948 | ||||||
| chr11:90137954
|
A | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+2284A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137954 | ||||||
| chr11:90137971
|
A | G | 1 | a0012c0012t0001g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.194+2301A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137971 | ||||||
| chr11:90138010
|
A | T | 16 | a0001c0001t0002g0175a0001c0001t0003g0181a0001c0001t0006g0006others(13): Show | 17 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.194+2340A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138010 | ||||||
| chr11:90138059
|
C | G | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+2389C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138059 | ||||||
| chr11:90138241
|
T | G | 93 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(90): Show | 95 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.194+2571T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138241 | ||||||
| chr11:90138315
|
T | C | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+2645T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138315 | ||||||
| chr11:90138410
|
T | A | 4 | a0001c0002t0001g0322a0002c0003t0004g0274a0002c0003t0005g0009others(1): Show | 5 | HG02145.hp2 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.194+2740T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138410 | ||||||
| chr11:90138500
|
T | C | 27 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(24): Show | 28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.194+2830T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138500 | ||||||
| chr11:90138585
|
C | T | 2 | a0001c0001t0006g0170a0001c0001t0006g0171 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.194+2915C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138585 | ||||||
| chr11:90138725
|
C | CT | 38 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0135others(35): Show | 38 | HG00621.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.194+3089dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
C | CTT | 8 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(5): Show | 8 | HG00544.hp1 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.194+3088_194+3089d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
C | CTTTTTTT others(5): Show |
1 | a0001c0002t0004g0350 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.194+3078_194+3089d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
C | CTTTTTTT others(8): Show |
2 | a0001c0002t0005g0339a0001c0002t0005g0340 | 2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.194+3075_194+3089d others(17): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
C | CTTTTTTT others(9): Show |
4 | a0001c0002t0005g0012a0001c0002t0005g0341a0001c0002t0005g0342others(1): Show | 5 | HG00323.hp1 HG01255.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+3074_194+3089d others(18): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
C | CTTTTTTT others(10): Show |
2 | a0001c0002t0005g0344a0001c0002t0016g0345 | 2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.194+3073_194+3089d others(19): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
C | CTTTTTTT others(11): Show |
1 | a0001c0002t0005g0346 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.194+3072_194+3089d others(20): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTT | C | 10 | a0001c0002t0001g0322a0001c0002t0004g0319a0001c0006t0004g0335others(7): Show | 11 | HG00639.hp1 HG01069.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.194+3087_194+3089d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTT | C | 42 | a0001c0002t0001g0337a0001c0002t0004g0269a0001c0002t0004g0270others(39): Show | 43 | HG00544.hp2 HG01099.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.194+3086_194+3089d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTT | C | 6 | a0001c0002t0001g0267a0001c0002t0004g0268a0002c0003t0001g0282others(3): Show | 6 | HG02698.hp1 HG02895.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+3085_194+3089d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTTTT | C | 12 | a0004c0005t0001g0261a0004c0005t0004g0262a0004c0005t0004g0263others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.194+3083_194+3089d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTTTT others(3): Show |
C | 25 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(22): Show | 26 | HG00597.hp1 HG01261.hp1 HG02683.hp2 others(23): Show |
intron_variant | MODIFIER | c.194+3080_194+3089d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0002g0047a0001c0002t0001g0014a0001c0002t0007g0013others(3): Show | 6 | HG02027.hp2 HG02615.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+3079_194+3089d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0002t0001g0240a0001c0002t0001g0241a0001c0002t0001g0245others(12): Show | 15 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+3078_194+3089d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTTTT others(6): Show |
C | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.194+3077_194+3089d others(15): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0006t0001g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194+3074_194+3089d others(18): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138725
|
CTTTTTTT others(12): Show |
C | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+3071_194+3089d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | |||||
| chr11:90138772
|
A | G | 75 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(72): Show | 77 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.194+3102A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138772 | ||||||
| chr11:90138800
|
C | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+3130C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138800 | ||||||
| chr11:90138920
|
A | G | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+3250A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138920 | ||||||
| chr11:90139058
|
G | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+3388G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139058 | ||||||
| chr11:90139075
|
C | T | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.194+3405C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139075 | ||||||
| chr11:90139146
|
C | T | 1 | a0004c0005t0004g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.194+3476C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139146 | ||||||
| chr11:90139226
|
C | A | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+3556C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139226 | ||||||
| chr11:90139249
|
A | G | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+3579A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139249 | ||||||
| chr11:90139253
|
A | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+3583A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139253 | ||||||
| chr11:90139294
|
A | G | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+3624A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139294 | ||||||
| chr11:90139321
|
A | G | 7 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(4): Show | 7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+3651A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139321 | ||||||
| chr11:90139388
|
G | C | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194+3718G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139388 | ||||||
| chr11:90139489
|
A | G | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+3819A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139489 | ||||||
| chr11:90139518
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.194+3848T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139518 | ||||||
| chr11:90139579
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.194+3909G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139579 | ||||||
| chr11:90139586
|
T | C | 1 | a0001c0002t0004g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+3916T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139586 | ||||||
| chr11:90139813
|
C | A | 1 | a0002c0003t0001g0282 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.194+4143C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139813 | ||||||
| chr11:90139855
|
CT | C | 8 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0003g0134others(5): Show | 8 | HG00099.hp2 HG01255.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.194+4202delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | |||||
| chr11:90139855
|
CTT | C | 14 | a0001c0002t0004g0268a0004c0005t0001g0261a0004c0005t0001g0266others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.194+4201_194+4202d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | |||||
| chr11:90139855
|
CTTT | C | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.194+4200_194+4202d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | |||||
| chr11:90139855
|
CTTTT | C | 6 | a0001c0002t0001g0037a0001c0002t0001g0186a0001c0002t0001g0187others(3): Show | 6 | HG02055.hp2 HG03491.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+4199_194+4202d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | |||||
| chr11:90139902
|
G | A | 17 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(14): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.194+4232G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139902 | ||||||
| chr11:90139940
|
C | T | 20 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(17): Show | 21 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.194+4270C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139940 | ||||||
| chr11:90139987
|
C | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+4317C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139987 | ||||||
| chr11:90139995
|
A | G | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194+4325A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139995 | ||||||
| chr11:90140005
|
C | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+4335C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140005 | ||||||
| chr11:90140041
|
T | C | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+4371T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140041 | ||||||
| chr11:90140127
|
A | G | 1 | a0001c0001t0006g0184 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.194+4457A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140127 | ||||||
| chr11:90140137
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.194+4467A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140137 | ||||||
| chr11:90140181
|
C | T | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+4511C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140181 | ||||||
| chr11:90140189
|
C | A | 1 | a0001c0001t0002g0048 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.194+4519C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140189 | ||||||
| chr11:90140221
|
A | G | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+4551A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140221 | ||||||
| chr11:90140305
|
A | G | 5 | a0001c0001t0003g0129a0001c0001t0003g0131a0001c0001t0003g0132others(2): Show | 5 | HG02129.hp2 HG02132.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+4635A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140305 | ||||||
| chr11:90140418
|
C | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+4748C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140418 | ||||||
| chr11:90140447
|
C | T | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194+4777C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140447 | ||||||
| chr11:90140450
|
CT | C | 194 | a0001c0001t0002g0135a0001c0002t0001g0002a0001c0002t0001g0007others(191): Show | 200 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.194+4790delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90140450 | |||||
| chr11:90140450
|
CTT | C | 7 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(4): Show | 7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+4789_194+4790d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90140450 | |||||
| chr11:90140492
|
GT | G | 10 | a0002c0003t0001g0284a0002c0003t0001g0286a0002c0003t0001g0288others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.194+4830delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90140492 | |||||
| chr11:90140532
|
A | G | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+4862A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140532 | ||||||
| chr11:90140558
|
A | G | 183 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(180): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.194+4888A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140558 | ||||||
| chr11:90140694
|
G | T | 200 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(197): Show | 206 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.194+5024G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140694 | ||||||
| chr11:90140791
|
T | C | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.194+5121T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140791 | ||||||
| chr11:90140826
|
A | G | 1 | a0001c0002t0005g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.194+5156A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140826 | ||||||
| chr11:90140865
|
C | T | 1 | a0002c0003t0001g0011 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.194+5195C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140865 | ||||||
| chr11:90141298
|
T | G | 3 | a0001c0001t0006g0052a0001c0001t0008g0053a0001c0001t0008g0136 | 3 | HG00099.hp1 HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.194+5628T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141298 | ||||||
| chr11:90141345
|
C | G | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.194+5675C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141345 | ||||||
| chr11:90141385
|
A | T | 1 | a0001c0002t0001g0036 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.194+5715A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141385 | ||||||
| chr11:90141434
|
A | G | 1 | a0001c0002t0004g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+5764A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141434 | ||||||
| chr11:90141447
|
T | G | 1 | a0001c0001t0002g0351 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.194+5777T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141447 | ||||||
| chr11:90141585
|
C | G | 2 | a0001c0002t0001g0034a0001c0002t0001g0035 | 2 | NA19001.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.195-5745C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141585 | ||||||
| chr11:90141594
|
T | TTCTGTTT others(1): Show |
13 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(10): Show | 13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-5735_195-5734i others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90141594 | |||||
| chr11:90141594
|
T | TTTTG | 258 | a0001c0001t0002g0041a0001c0001t0002g0047a0001c0001t0002g0057others(255): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.195-5720_195-5717d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90141594 | |||||
| chr11:90141594
|
T | TTTTGTTT others(1): Show |
8 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(5): Show | 8 | HG01074.hp1 HG01243.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.195-5724_195-5717d others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90141594 | |||||
| chr11:90141636
|
G | C | 1 | a0001c0001t0003g0043 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.195-5694G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141636 | ||||||
| chr11:90141688
|
G | A | 8 | a0002c0003t0001g0010a0002c0003t0001g0011a0002c0003t0001g0315others(5): Show | 9 | HG00639.hp1 HG01069.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-5642G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141688 | ||||||
| chr11:90141703
|
G | T | 10 | a0001c0006t0001g0334a0005c0007t0001g0330a0005c0007t0005g0323others(7): Show | 10 | HG01081.hp1 HG01109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-5627G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141703 | ||||||
| chr11:90141713
|
G | A | 1 | a0002c0003t0001g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.195-5617G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141713 | ||||||
| chr11:90141722
|
T | C | 7 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(4): Show | 7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-5608T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141722 | ||||||
| chr11:90141755
|
G | A | 5 | a0001c0002t0001g0190a0001c0002t0001g0191a0001c0002t0001g0192others(2): Show | 5 | HG00558.hp1 NA18982.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-5575G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141755 | ||||||
| chr11:90141783
|
T | G | 183 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(180): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.195-5547T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141783 | ||||||
| chr11:90141884
|
T | G | 1 | a0001c0001t0002g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195-5446T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141884 | ||||||
| chr11:90141953
|
G | A | 1 | a0001c0002t0005g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.195-5377G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141953 | ||||||
| chr11:90142037
|
G | A | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195-5293G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142037 | ||||||
| chr11:90142136
|
G | A | 1 | a0002c0003t0001g0285 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.195-5194G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142136 | ||||||
| chr11:90142162
|
C | T | 5 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0004g0335others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-5168C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142162 | ||||||
| chr11:90142185
|
G | C | 46 | a0001c0002t0001g0322a0001c0002t0004g0319a0002c0003t0001g0010others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.195-5145G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142185 | ||||||
| chr11:90142268
|
C | T | 2 | a0001c0001t0002g0161a0001c0002t0001g0033 | 2 | HG02155.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.195-5062C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142268 | ||||||
| chr11:90142269
|
G | A | 59 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.195-5061G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142269 | ||||||
| chr11:90142330
|
G | C | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.195-5000G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142330 | ||||||
| chr11:90142363
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-4967C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142363 | ||||||
| chr11:90142496
|
C | T | 78 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(75): Show | 80 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.195-4834C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142496 | ||||||
| chr11:90142923
|
C | T | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.195-4407C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142923 | ||||||
| chr11:90142960
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-4370C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142960 | ||||||
| chr11:90142966
|
G | A | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-4364G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142966 | ||||||
| chr11:90142968
|
A | G | 46 | a0001c0002t0001g0267a0001c0002t0004g0319a0002c0003t0001g0010others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.195-4362A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142968 | ||||||
| chr11:90143143
|
G | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-4187G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143143 | ||||||
| chr11:90143170
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-4160G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143170 | ||||||
| chr11:90143188
|
T | C | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.195-4142T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143188 | ||||||
| chr11:90143291
|
T | C | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-4039T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143291 | ||||||
| chr11:90143471
|
G | A | 13 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(10): Show | 13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-3859G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143471 | ||||||
| chr11:90143522
|
G | T | 1 | a0001c0006t0001g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.195-3808G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143522 | ||||||
| chr11:90143578
|
A | G | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195-3752A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143578 | ||||||
| chr11:90143648
|
C | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-3682C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143648 | ||||||
| chr11:90143653
|
C | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-3677C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143653 | ||||||
| chr11:90143775
|
A | C | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.195-3555A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143775 | ||||||
| chr11:90143818
|
T | C | 6 | a0001c0002t0004g0268a0001c0002t0004g0269a0001c0002t0004g0270others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-3512T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143818 | ||||||
| chr11:90143860
|
T | A | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195-3470T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143860 | ||||||
| chr11:90143911
|
G | A | 1 | a0003c0004t0018g0247 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.195-3419G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143911 | ||||||
| chr11:90144012
|
G | A | 1 | a0001c0002t0001g0194 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.195-3318G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144012 | ||||||
| chr11:90144067
|
A | G | 13 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(10): Show | 13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-3263A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144067 | ||||||
| chr11:90144071
|
T | C | 1 | a0001c0006t0001g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.195-3259T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144071 | ||||||
| chr11:90144123
|
C | G | 5 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0004g0335others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-3207C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144123 | ||||||
| chr11:90144383
|
A | T | 14 | a0003c0004t0001g0255a0003c0004t0004g0256a0003c0004t0005g0244others(11): Show | 14 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.195-2947A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144383 | ||||||
| chr11:90144412
|
G | A | 1 | a0001c0001t0003g0054 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.195-2918G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144412 | ||||||
| chr11:90144460
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.195-2870G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144460 | ||||||
| chr11:90144570
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.195-2760A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144570 | ||||||
| chr11:90144619
|
G | A | 2 | a0001c0001t0002g0135a0001c0016t0002g0096 | 2 | HG02300.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.195-2711G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144619 | ||||||
| chr11:90144690
|
C | T | 1 | a0007c0011t0002g0127 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.195-2640C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144690 | ||||||
| chr11:90144704
|
T | C | 1 | a0001c0002t0001g0322 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.195-2626T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144704 | ||||||
| chr11:90144740
|
T | TA | 7 | a0001c0001t0002g0098a0001c0001t0002g0138a0001c0001t0002g0146others(4): Show | 7 | HG01243.hp2 HG02083.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-2575dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAA | 23 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(20): Show | 24 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.195-2580_195-2575d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(1): Show |
17 | a0001c0002t0004g0039a0001c0002t0004g0040a0002c0003t0001g0294others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-2582_195-2575d others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(2): Show |
36 | a0001c0002t0004g0319a0001c0006t0001g0313a0001c0006t0001g0314others(33): Show | 38 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.195-2583_195-2575d others(11): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(3): Show |
24 | a0001c0002t0001g0246a0001c0002t0001g0322a0001c0002t0004g0350others(21): Show | 25 | HG00323.hp1 HG00642.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.195-2584_195-2575d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(4): Show |
9 | a0001c0002t0001g0337a0001c0002t0005g0333a0001c0002t0005g0339others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-2585_195-2575d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(5): Show |
8 | a0001c0002t0001g0245a0001c0002t0004g0269a0001c0002t0004g0271others(5): Show | 8 | HG01074.hp1 HG01081.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.195-2586_195-2575d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(6): Show |
14 | a0001c0002t0001g0192a0001c0002t0001g0234a0001c0002t0001g0235others(11): Show | 14 | HG00558.hp1 HG01109.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.195-2587_195-2575d others(15): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(7): Show |
44 | a0001c0002t0001g0007a0001c0002t0001g0187a0001c0002t0001g0190others(41): Show | 46 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.195-2588_195-2575d others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(8): Show |
18 | a0001c0002t0001g0186a0001c0002t0001g0194a0001c0002t0001g0196others(15): Show | 18 | HG00621.hp1 HG00642.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-2589_195-2575d others(17): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144740
|
T | TAAAAAAA others(9): Show |
4 | a0003c0004t0005g0248a0003c0004t0005g0249a0003c0004t0005g0257others(1): Show | 4 | HG00438.hp2 HG01346.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-2575_195-2574i others(18): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | |||||
| chr11:90144741
|
A | T | 1 | a0001c0020t0002g0095 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195-2589A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144741 | ||||||
| chr11:90144757
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2573G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144757 | ||||||
| chr11:90144846
|
G | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-2484G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144846 | ||||||
| chr11:90144911
|
G | A | 2 | a0001c0001t0002g0099a0001c0001t0002g0148 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.195-2419G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144911 | ||||||
| chr11:90145041
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2289T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145041 | ||||||
| chr11:90145076
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2254G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145076 | ||||||
| chr11:90145243
|
C | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2087C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145243 | ||||||
| chr11:90145260
|
T | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-2070T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145260 | ||||||
| chr11:90145558
|
T | C | 1 | a0001c0002t0001g0194 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.195-1772T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145558 | ||||||
| chr11:90145636
|
T | A | 1 | a0001c0002t0001g0194 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.195-1694T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145636 | ||||||
| chr11:90145720
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-1610G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145720 | ||||||
| chr11:90145910
|
A | G | 7 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(4): Show | 7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-1420A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145910 | ||||||
| chr11:90145981
|
T | G | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.195-1349T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145981 | ||||||
| chr11:90146028
|
A | G | 1 | a0004c0005t0014g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.195-1302A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146028 | ||||||
| chr11:90146282
|
T | TA | 8 | a0001c0001t0003g0055a0001c0001t0003g0139a0001c0006t0001g0313others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.195-1033dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146282 | |||||
| chr11:90146294
|
A | G | 1 | a0001c0001t0003g0094 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.195-1036A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146294 | ||||||
| chr11:90146343
|
A | AT | 23 | a0001c0001t0002g0125a0001c0001t0002g0144a0001c0001t0002g0146others(20): Show | 23 | HG00673.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.195-954dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146343
|
AT | A | 54 | a0001c0001t0002g0005a0001c0001t0002g0048a0001c0001t0002g0057others(51): Show | 54 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.195-954delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146343
|
ATTTTT | A | 32 | a0001c0002t0001g0322a0001c0002t0001g0337a0001c0002t0004g0270others(29): Show | 32 | HG00544.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.195-958_195-954del others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146343
|
ATTTTTT | A | 54 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(51): Show | 57 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.195-959_195-954del others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146343
|
ATTTTTTT | A | 22 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(19): Show | 23 | HG02280.hp1 HG02486.hp1 HG02683.hp2 others(20): Show |
intron_variant | MODIFIER | c.195-960_195-954del others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146343
|
ATTTTTTT others(1): Show |
A | 29 | a0001c0002t0001g0187a0001c0002t0001g0201a0001c0002t0001g0226others(26): Show | 29 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.195-961_195-954del others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146343
|
ATTTTTTT others(2): Show |
A | 58 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0190others(55): Show | 60 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.195-962_195-954del others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146343
|
ATTTTTTT others(9): Show |
A | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195-969_195-954del others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | |||||
| chr11:90146513
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-817G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146513 | ||||||
| chr11:90146707
|
C | T | 1 | a0011c0019t0006g0042 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.195-623C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146707 | ||||||
| chr11:90146936
|
A | G | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-394A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146936 | ||||||
| chr11:90146948
|
A | G | 9 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(6): Show | 10 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-382A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146948 | ||||||
| chr11:90147065
|
A | T | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.195-265A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147065 | ||||||
| chr11:90147094
|
T | G | 1 | a0003c0004t0005g0257 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.195-236T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147094 | ||||||
| chr11:90147281
|
C | A | 1 | a0002c0003t0001g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.195-49C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147281 | ||||||
| chr11:90147301
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-29T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147301 | ||||||
| chr11:90147537
|
T | A | 1 | a0005c0007t0005g0324 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.381+21T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147537 | ||||||
| chr11:90147663
|
C | T | 3 | a0002c0003t0004g0274a0002c0003t0005g0009a0002c0003t0005g0275 | 4 | HG02145.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+147C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147663 | ||||||
| chr11:90147677
|
A | G | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+161A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147677 | ||||||
| chr11:90147685
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+169T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147685 | ||||||
| chr11:90147687
|
C | G | 2 | a0001c0002t0004g0039a0001c0002t0004g0040 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.381+171C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147687 | ||||||
| chr11:90147706
|
A | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.381+190A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147706 | ||||||
| chr11:90147794
|
G | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.381+278G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147794 | ||||||
| chr11:90147808
|
G | A | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.381+292G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147808 | ||||||
| chr11:90147929
|
T | G | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+413T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147929 | ||||||
| chr11:90148003
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+487T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148003 | ||||||
| chr11:90148098
|
C | T | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.381+582C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148098 | ||||||
| chr11:90148113
|
G | A | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+597G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148113 | ||||||
| chr11:90148118
|
T | C | 2 | a0001c0001t0002g0057a0001c0001t0002g0140 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.381+602T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148118 | ||||||
| chr11:90148205
|
C | T | 45 | a0001c0002t0004g0319a0002c0003t0001g0010a0002c0003t0001g0011others(42): Show | 47 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.381+689C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148205 | ||||||
| chr11:90148348
|
T | C | 1 | a0001c0002t0004g0272 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382-658T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148348 | ||||||
| chr11:90148380
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382-626G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148380 | ||||||
| chr11:90148463
|
G | A | 1 | a0001c0001t0008g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.382-543G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148463 | ||||||
| chr11:90148472
|
G | A | 1 | a0003c0004t0005g0250 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.382-534G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148472 | ||||||
| chr11:90148610
|
C | T | 1 | a0002c0003t0004g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-396C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148610 | ||||||
| chr11:90148637
|
A | T | 3 | a0004c0005t0004g0279a0004c0005t0004g0280a0004c0005t0004g0281 | 3 | HG02280.hp1 HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.382-369A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148637 | ||||||
| chr11:90148647
|
G | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-359G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148647 | ||||||
| chr11:90148723
|
CA | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.382-275delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 90148723 | |||||
| chr11:90148738
|
C | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.382-268C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148738 | ||||||
| chr11:90148857
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.382-149C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148857 | ||||||
| chr11:90148887
|
C | G | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.382-119C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148887 | ||||||
| chr11:90149253
|
C | T | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.483+146C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149253 | ||||||
| chr11:90149291
|
G | A | 2 | a0001c0002t0004g0016a0001c0002t0004g0024 | 2 | HG01261.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.483+184G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149291 | ||||||
| chr11:90149299
|
G | C | 1 | a0002c0003t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+192G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149299 | ||||||
| chr11:90149404
|
G | T | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+297G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149404 | ||||||
| chr11:90149464
|
C | T | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.483+357C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149464 | ||||||
| chr11:90149465
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.483+358G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149465 | ||||||
| chr11:90149487
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.483+380T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149487 | ||||||
| chr11:90149488
|
G | C | 1 | a0001c0002t0001g0038 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.483+381G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149488 | ||||||
| chr11:90149509
|
C | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.483+402C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149509 | ||||||
| chr11:90149587
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.483+480G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149587 | ||||||
| chr11:90149638
|
A | G | 4 | a0003c0004t0005g0244a0003c0004t0005g0248a0003c0004t0005g0252others(1): Show | 4 | HG01346.hp2 HG01934.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+531A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149638 | ||||||
| chr11:90149728
|
G | A | 6 | a0001c0001t0006g0046a0001c0001t0006g0174a0001c0001t0006g0177others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+621G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149728 | ||||||
| chr11:90149734
|
G | A | 1 | a0002c0003t0004g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.483+627G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149734 | ||||||
| chr11:90150203
|
C | T | 2 | a0001c0002t0001g0337a0001c0002t0004g0350 | 2 | HG01243.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.484-279C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90150203 | ||||||
| chr11:90150236
|
C | CAG | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.484-245_484-244dup others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 90150236 | |||||
| chr11:90150387
|
A | C | 1 | a0001c0001t0002g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.484-95A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90150387 | ||||||
| chr11:90150427
|
GTT | G | 199 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(196): Show | 205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.484-45_484-44delTT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 90150427 | |||||
| chr11:90150622
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0013g0004 | 2 | NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.609+15G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150622 | ||||||
| chr11:90150632
|
A | G | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.609+25A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150632 | ||||||
| chr11:90150717
|
C | CT | 166 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(163): Show | 171 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.609+117dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 90150717 | |||||
| chr11:90150717
|
C | CTT | 36 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(33): Show | 37 | HG00597.hp1 HG01074.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.609+116_609+117dup others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 90150717 | |||||
| chr11:90150725
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+118C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150725 | ||||||
| chr11:90150773
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+166T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150773 | ||||||
| chr11:90151090
|
T | A | 186 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(183): Show | 192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.609+483T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151090 | ||||||
| chr11:90151144
|
C | G | 1 | a0003c0004t0005g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.609+537C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151144 | ||||||
| chr11:90151238
|
C | T | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+631C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151238 | ||||||
| chr11:90151246
|
C | T | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.609+639C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151246 | ||||||
| chr11:90151249
|
A | G | 4 | a0001c0001t0003g0110a0001c0001t0003g0123a0001c0001t0003g0124others(1): Show | 4 | HG00597.hp2 NA18747.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+642A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151249 | ||||||
| chr11:90151272
|
G | A | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+665G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151272 | ||||||
| chr11:90151328
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+721T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151328 | ||||||
| chr11:90151341
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+734C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151341 | ||||||
| chr11:90151414
|
C | T | 1 | a0001c0001t0003g0110 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.609+807C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151414 | ||||||
| chr11:90151760
|
G | A | 3 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334 | 3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.610-538G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151760 | ||||||
| chr11:90151785
|
A | T | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.610-513A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151785 | ||||||
| chr11:90152198
|
G | A | 27 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(24): Show | 28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.610-100G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90152198 | ||||||
| chr11:90152250
|
C | G | 1 | a0001c0001t0002g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.610-48C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90152250 | ||||||
| chr11:90152602
|
A | C | 1 | a0001c0001t0002g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.796+118A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152602 | ||||||
| chr11:90152618
|
G | A | 1 | a0002c0003t0001g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.796+134G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152618 | ||||||
| chr11:90152632
|
A | T | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+148A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152632 | ||||||
| chr11:90152635
|
A | G | 7 | a0001c0002t0001g0267a0001c0006t0001g0313a0001c0006t0001g0314others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+151A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152635 | ||||||
| chr11:90152783
|
A | G | 46 | a0001c0002t0001g0322a0001c0002t0004g0319a0002c0003t0001g0010others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.796+299A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152783 | ||||||
| chr11:90152798
|
A | G | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+314A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152798 | ||||||
| chr11:90152802
|
C | T | 1 | a0002c0003t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.796+318C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152802 | ||||||
| chr11:90152854
|
T | G | 2 | a0001c0002t0005g0341a0001c0002t0005g0343 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.796+370T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152854 | ||||||
| chr11:90152870
|
C | CCGATAGA others(4): Show |
202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.796+386_796+387ins others(11): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152870 | ||||||
| chr11:90152878
|
A | T | 1 | a0001c0001t0006g0183 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.796+394A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152878 | ||||||
| chr11:90152927
|
A | G | 1 | a0001c0002t0004g0319 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.796+443A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152927 | ||||||
| chr11:90152983
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.796+499G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152983 | ||||||
| chr11:90153116
|
G | A | 104 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(101): Show | 107 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.796+632G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153116 | ||||||
| chr11:90153151
|
C | G | 4 | a0001c0002t0004g0269a0001c0002t0004g0270a0001c0002t0004g0271others(1): Show | 4 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+667C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153151 | ||||||
| chr11:90153229
|
C | T | 104 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(101): Show | 107 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.796+745C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153229 | ||||||
| chr11:90153430
|
A | G | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796+946A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153430 | ||||||
| chr11:90153525
|
G | A | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.796+1041G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153525 | ||||||
| chr11:90153637
|
G | A | 1 | a0005c0007t0001g0330 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.796+1153G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153637 | ||||||
| chr11:90153642
|
G | C | 1 | a0004c0005t0004g0262 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.796+1158G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153642 | ||||||
| chr11:90153786
|
T | G | 46 | a0001c0002t0001g0322a0001c0002t0004g0319a0002c0003t0001g0010others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.796+1302T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153786 | ||||||
| chr11:90154030
|
CCT | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.796+1569_796+1570d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154030 | |||||
| chr11:90154030
|
CCTCT | C | 125 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(122): Show | 128 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.796+1567_796+1570d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154030 | |||||
| chr11:90154030
|
CCTCTCT | C | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+1565_796+1570d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154030 | |||||
| chr11:90154051
|
C | G | 2 | a0001c0002t0001g0245a0001c0002t0001g0246 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.796+1567C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154051 | ||||||
| chr11:90154065
|
CTCTT | C | 73 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(70): Show | 75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.796+1593_796+1596d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154065 | |||||
| chr11:90154073
|
T | G | 31 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(28): Show | 32 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.796+1589T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154073 | ||||||
| chr11:90154126
|
C | T | 1 | a0001c0020t0002g0095 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.796+1642C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154126 | ||||||
| chr11:90154154
|
C | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.796+1670C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154154 | ||||||
| chr11:90154192
|
G | A | 1 | a0005c0007t0005g0323 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.796+1708G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154192 | ||||||
| chr11:90154280
|
G | C | 16 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.796+1796G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154280 | ||||||
| chr11:90154316
|
T | G | 53 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(50): Show | 56 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.796+1832T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154316 | ||||||
| chr11:90154324
|
T | C | 46 | a0001c0002t0001g0322a0001c0002t0004g0319a0002c0003t0001g0010others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.796+1840T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154324 | ||||||
| chr11:90154478
|
A | G | 1 | a0001c0001t0003g0094 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.796+1994A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154478 | ||||||
| chr11:90154676
|
T | G | 27 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(24): Show | 28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+2192T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154676 | ||||||
| chr11:90154773
|
G | C | 2 | a0001c0002t0001g0203a0001c0002t0001g0234 | 2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.796+2289G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154773 | ||||||
| chr11:90154830
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.796+2346G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154830 | ||||||
| chr11:90154842
|
A | C | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2358A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154842 | ||||||
| chr11:90154854
|
AATATGTA others(73): Show |
A | 2 | a0004c0005t0001g0261a0004c0005t0005g0260 | 2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.796+2403_796+2482d others(82): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154854 | |||||
| chr11:90154859
|
G | A | 2 | a0001c0002t0004g0268a0001c0002t0004g0272 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.796+2375G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154859 | ||||||
| chr11:90154866
|
T | G | 61 | a0001c0002t0001g0322a0001c0002t0004g0319a0001c0002t0004g0350others(58): Show | 64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.796+2382T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154866 | ||||||
| chr11:90154873
|
C | T | 1 | a0001c0001t0006g0176 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.796+2389C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154873 | ||||||
| chr11:90154874
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.796+2390G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154874 | ||||||
| chr11:90154879
|
C | A | 1 | a0004c0005t0005g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.796+2395C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154879 | ||||||
| chr11:90154882
|
AAT | A | 173 | a0001c0001t0003g0074a0001c0002t0001g0002a0001c0002t0001g0007others(170): Show | 178 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.796+2403_796+2404d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154882 | |||||
| chr11:90154882
|
AATAT | A | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.796+2401_796+2404d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154882 | |||||
| chr11:90154882
|
AATATATG others(45): Show |
A | 13 | a0002c0003t0004g0274a0002c0003t0005g0275a0004c0005t0001g0266others(10): Show | 13 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.796+2403_796+2454d others(54): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154882 | |||||
| chr11:90154884
|
T | TATATGTA others(18): Show |
2 | a0001c0001t0002g0068a0001c0001t0003g0067 | 2 | NA18944.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.796+2454_796+2478d others(27): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154884 | |||||
| chr11:90154884
|
TATATGTA others(18): Show |
T | 2 | a0001c0001t0003g0075a0001c0001t0003g0076 | 2 | NA18977.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.796+2454_796+2478d others(27): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154884 | |||||
| chr11:90154896
|
T | G | 1 | a0002c0003t0001g0318 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.796+2412T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154896 | ||||||
| chr11:90154903
|
C | T | 1 | a0001c0002t0004g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.796+2419C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154903 | ||||||
| chr11:90154909
|
C | CATA | 113 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(110): Show | 116 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.796+2426_796+2428d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154909 | |||||
| chr11:90154909
|
C | CATAAT | 13 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(10): Show | 13 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.796+2428_796+2429i others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154909 | |||||
| chr11:90154912
|
ATGTATAT others(13): Show |
A | 14 | a0001c0002t0001g0030a0001c0002t0001g0337a0001c0002t0004g0268others(11): Show | 14 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2429_796+2448d others(22): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154912 | ||||||
| chr11:90154912
|
ATGTATAT others(15): Show |
A | 56 | a0001c0002t0004g0319a0001c0002t0004g0350a0001c0002t0005g0012others(53): Show | 59 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.796+2429_796+2450d others(24): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154912 | ||||||
| chr11:90154934
|
C | CATA | 108 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(105): Show | 111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.796+2451_796+2453d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154934 | |||||
| chr11:90154934
|
C | CATAAT | 10 | a0001c0001t0003g0074a0001c0002t0001g0021a0001c0002t0001g0034others(7): Show | 10 | HG01192.hp2 HG02922.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.796+2453_796+2454i others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154934 | |||||
| chr11:90154934
|
C | CATATGTA others(21): Show |
1 | a0001c0001t0003g0089 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.796+2487_796+2514d others(30): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154934 | |||||
| chr11:90154934
|
C | T | 14 | a0001c0002t0001g0030a0001c0002t0001g0337a0001c0002t0004g0268others(11): Show | 14 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2450C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154934 | ||||||
| chr11:90154959
|
CATA | C | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2479_796+2481d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154959 | |||||
| chr11:90154962
|
A | AAT | 120 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(117): Show | 124 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.796+2481_796+2482d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154962 | |||||
| chr11:90154993
|
ATGTATG | A | 121 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0018others(118): Show | 125 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.796+2513_796+2518d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154993 | |||||
| chr11:90154993
|
ATGTATGT others(1): Show |
A | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2515_796+2522d others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154993 | |||||
| chr11:90154995
|
G | A | 4 | a0001c0002t0001g0017a0001c0002t0001g0029a0001c0002t0007g0013others(1): Show | 4 | HG02451.hp2 NA18956.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+2511G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154995 | ||||||
| chr11:90154996
|
T | TATATATT others(15): Show |
1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(24): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(71): Show |
1 | a0001c0002t0007g0205 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.796+2514_796+2515i others(80): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(99): Show |
7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG00438.hp1 HG02165.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(108): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(129): Show |
1 | a0003c0004t0005g0251 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(138): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(127): Show |
41 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(38): Show | 43 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(136): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(157): Show |
8 | a0001c0002t0001g0194a0003c0004t0005g0244a0003c0004t0005g0249others(5): Show | 8 | HG00438.hp2 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(166): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(187): Show |
2 | a0001c0002t0001g0245a0003c0004t0005g0258 | 2 | HG03139.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.796+2514_796+2515i others(196): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(155): Show |
6 | a0001c0002t0001g0200a0001c0002t0001g0222a0001c0002t0001g0224others(3): Show | 6 | HG00642.hp1 HG01943.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(164): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(185): Show |
3 | a0001c0002t0001g0246a0001c0002t0001g0322a0003c0004t0005g0248 | 3 | HG01346.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.796+2514_796+2515i others(194): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(183): Show |
3 | a0001c0002t0001g0225a0003c0004t0001g0255a0003c0004t0005g0254 | 3 | HG01175.hp2 HG01256.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.796+2514_796+2515i others(192): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TATATATT others(211): Show |
1 | a0001c0002t0005g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(220): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | |||||
| chr11:90154996
|
T | TGTATATA others(17): Show |
3 | a0001c0002t0001g0017a0001c0002t0001g0029a0001c0002t0007g0013 | 3 | NA18956.hp2 NA18968.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.796+2512_796+2513i others(26): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154996 | ||||||
| chr11:90154998
|
T | TATATTAT others(13): Show |
1 | a0001c0002t0004g0204 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.796+2514_796+2515i others(22): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154998 | ||||||
| chr11:90154998
|
T | TATATTAT others(97): Show |
1 | a0001c0002t0001g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(106): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154998 | ||||||
| chr11:90154998
|
T | TATATTAT others(125): Show |
1 | a0001c0002t0001g0240 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.796+2514_796+2515i others(134): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154998 | ||||||
| chr11:90154999
|
G | A | 80 | a0001c0002t0001g0007a0001c0002t0001g0017a0001c0002t0001g0029others(77): Show | 82 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.796+2515G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154999 | ||||||
| chr11:90155001
|
G | A | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.796+2517G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155001 | ||||||
| chr11:90155018
|
A | G | 211 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(208): Show | 217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.796+2534A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155018 | ||||||
| chr11:90155026
|
A | AAT | 13 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(10): Show | 13 | HG02280.hp1 HG02486.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.796+2545_796+2546d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155026 | |||||
| chr11:90155026
|
AATATGTA others(69): Show |
A | 6 | a0001c0001t0002g0041a0001c0001t0002g0047a0001c0001t0002g0137others(3): Show | 6 | HG02615.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.796+2567_796+2642d others(78): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155026 | |||||
| chr11:90155029
|
A | G | 1 | a0004c0005t0004g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2545A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155029 | ||||||
| chr11:90155031
|
G | A | 1 | a0004c0005t0004g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2547G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155031 | ||||||
| chr11:90155031
|
GTATA | G | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2551_796+2554d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155031 | |||||
| chr11:90155037
|
A | G | 1 | a0004c0005t0004g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2553A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155037 | ||||||
| chr11:90155043
|
GTATATAT others(32): Show |
G | 1 | a0004c0005t0004g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2574_796+2612d others(41): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155043 | |||||
| chr11:90155058
|
A | G | 14 | a0001c0002t0001g0233a0004c0005t0001g0261a0004c0005t0001g0266others(11): Show | 14 | HG02280.hp1 HG02300.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2574A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155058 | ||||||
| chr11:90155059
|
T | TATACATA others(16): Show |
1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.796+2591_796+2592i others(25): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155059 | |||||
| chr11:90155061
|
T | C | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.796+2577T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155061 | ||||||
| chr11:90155066
|
ATGTATAT others(4): Show |
A | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2583_796+2593d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155066 | ||||||
| chr11:90155074
|
ATG | A | 11 | a0001c0002t0004g0039a0001c0002t0004g0040a0005c0007t0001g0330others(8): Show | 11 | HG01081.hp1 HG02717.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.796+2596_796+2597d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155074 | |||||
| chr11:90155082
|
A | G | 12 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.796+2598A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155082 | ||||||
| chr11:90155088
|
ATT | A | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.796+2605_796+2606d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155088 | ||||||
| chr11:90155097
|
G | A | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2613G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155097 | ||||||
| chr11:90155102
|
C | CATA | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2619_796+2621d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155102 | |||||
| chr11:90155134
|
G | A | 1 | a0005c0007t0001g0330 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.796+2650G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155134 | ||||||
| chr11:90155186
|
GTA | G | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+2708_796+2709d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155186 | |||||
| chr11:90155200
|
A | G | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+2716A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155200 | ||||||
| chr11:90155230
|
G | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0140 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.796+2746G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155230 | ||||||
| chr11:90155256
|
A | C | 1 | a0001c0002t0001g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.796+2772A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155256 | ||||||
| chr11:90155283
|
TATGCATA others(4): Show |
T | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.796+2800_796+2810d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155283 | ||||||
| chr11:90155305
|
G | GTATATAT others(24): Show |
2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796+2829_797-2802d others(33): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155305 | |||||
| chr11:90155316
|
A | G | 1 | a0011c0019t0006g0042 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.797-2829A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155316 | ||||||
| chr11:90155336
|
TTATA | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.797-2803_797-2800d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155336 | |||||
| chr11:90155352
|
TTA | T | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2792_797-2791d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155352 | ||||||
| chr11:90155353
|
T | A | 2 | a0001c0002t0001g0206a0001c0002t0001g0210 | 2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2792T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155353 | ||||||
| chr11:90155355
|
C | A | 59 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.797-2790C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155355 | ||||||
| chr11:90155358
|
G | A | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2787G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155358 | ||||||
| chr11:90155364
|
T | TATGTAAT others(35): Show |
1 | a0001c0001t0002g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.797-2740_797-2699d others(44): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155364 | |||||
| chr11:90155364
|
TATGTAAT others(35): Show |
T | 30 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(27): Show | 30 | HG00438.hp2 HG01074.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.797-2740_797-2699d others(44): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155364 | |||||
| chr11:90155365
|
A | G | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2780A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155365 | ||||||
| chr11:90155367
|
G | A | 59 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.797-2778G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155367 | ||||||
| chr11:90155372
|
A | T | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2773A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155372 | ||||||
| chr11:90155373
|
T | A | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2772T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155373 | ||||||
| chr11:90155376
|
C | T | 59 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.797-2769C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155376 | ||||||
| chr11:90155381
|
T | A | 2 | a0001c0002t0001g0206a0001c0002t0001g0210 | 2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2764T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155381 | ||||||
| chr11:90155385
|
C | A | 2 | a0001c0002t0001g0206a0001c0002t0001g0210 | 2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2760C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155385 | ||||||
| chr11:90155385
|
C | T | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2760C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155385 | ||||||
| chr11:90155388
|
G | T | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2757G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155388 | ||||||
| chr11:90155389
|
T | A | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2756T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155389 | ||||||
| chr11:90155390
|
A | C | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2755A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155390 | ||||||
| chr11:90155393
|
A | G | 57 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(54): Show | 59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2752A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155393 | ||||||
| chr11:90155395
|
A | G | 3 | a0001c0001t0002g0059a0001c0001t0002g0073a0001c0001t0002g0138 | 3 | HG01243.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.797-2750A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155395 | ||||||
| chr11:90155398
|
A | T | 2 | a0001c0002t0001g0206a0001c0002t0001g0210 | 2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2747A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155398 | ||||||
| chr11:90155399
|
TATATATA | T | 60 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(57): Show | 62 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.797-2743_797-2737d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155399 | |||||
| chr11:90155402
|
A | G | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.797-2743A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155402 | ||||||
| chr11:90155405
|
T | A | 110 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(107): Show | 114 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.797-2740T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155405 | ||||||
| chr11:90155405
|
T | TTACATGT others(4): Show |
2 | a0001c0002t0001g0206a0001c0002t0001g0210 | 2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2740_797-2739i others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155405 | ||||||
| chr11:90155406
|
A | T | 112 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(109): Show | 116 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.797-2739A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155406 | ||||||
| chr11:90155430
|
GTAATATA | G | 7 | a0004c0005t0004g0277a0004c0005t0004g0278a0004c0005t0004g0279others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.797-2701_797-2695d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155430 | |||||
| chr11:90155437
|
A | ATAATATG others(21): Show |
7 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(4): Show | 7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2702_797-2701i others(30): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155437 | |||||
| chr11:90155443
|
TATA | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.797-2698_797-2696d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155443 | |||||
| chr11:90155444
|
A | G | 1 | a0001c0001t0009g0109 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.797-2701A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155444 | ||||||
| chr11:90155459
|
T | A | 16 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-2686T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155459 | ||||||
| chr11:90155471
|
T | C | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.797-2674T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155471 | ||||||
| chr11:90155472
|
A | G | 1 | a0001c0001t0012g0108 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.797-2673A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155472 | ||||||
| chr11:90155473
|
C | A | 7 | a0002c0003t0001g0282a0002c0003t0001g0301a0002c0003t0001g0303others(4): Show | 7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2672C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155473 | ||||||
| chr11:90155477
|
TATATATT others(7): Show |
T | 1 | a0001c0002t0007g0031 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.797-2651_797-2638d others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155477 | |||||
| chr11:90155492
|
ATATAT | A | 3 | a0001c0002t0001g0267a0004c0005t0004g0279a0004c0005t0004g0280 | 3 | HG02280.hp1 HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.797-2647_797-2643d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155492 | |||||
| chr11:90155538
|
T | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2607T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155538 | ||||||
| chr11:90155547
|
A | C | 2 | a0001c0001t0008g0122a0001c0001t0012g0108 | 2 | HG00558.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.797-2598A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155547 | ||||||
| chr11:90155566
|
TA | T | 6 | a0004c0005t0004g0277a0004c0005t0004g0278a0004c0005t0004g0279others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.797-2577delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155566 | |||||
| chr11:90155573
|
TAA | T | 19 | a0001c0001t0002g0175a0001c0001t0003g0181a0001c0001t0006g0006others(16): Show | 20 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.797-2571_797-2570d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155573 | ||||||
| chr11:90155574
|
AAT | A | 17 | a0001c0001t0003g0150a0001c0002t0001g0337a0001c0002t0004g0268others(14): Show | 17 | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.797-2564_797-2563d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155574 | |||||
| chr11:90155590
|
ATATG | A | 16 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-2552_797-2549d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155590 | |||||
| chr11:90155592
|
ATG | A | 185 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(182): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.797-2551_797-2550d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155592 | |||||
| chr11:90155594
|
G | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2551G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155594 | ||||||
| chr11:90155600
|
A | G | 73 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(70): Show | 75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.797-2545A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155600 | ||||||
| chr11:90155610
|
CATATAAA others(14): Show |
C | 38 | a0001c0002t0004g0319a0002c0003t0001g0010a0002c0003t0001g0011others(35): Show | 40 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.797-2529_797-2509d others(23): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155610 | |||||
| chr11:90155610
|
CATATAAA others(16): Show |
C | 7 | a0002c0003t0001g0282a0002c0003t0001g0301a0002c0003t0001g0303others(4): Show | 7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2529_797-2507d others(25): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155610 | |||||
| chr11:90155621
|
CATATATA others(3): Show |
C | 136 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(133): Show | 139 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.797-2515_797-2506d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155621 | |||||
| chr11:90155621
|
CATATATA others(5): Show |
C | 20 | a0001c0002t0001g0267a0001c0002t0004g0268a0001c0002t0004g0269others(17): Show | 21 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.797-2515_797-2504d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155621 | |||||
| chr11:90155630
|
T | G | 1 | a0003c0004t0005g0257 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.797-2515T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155630 | ||||||
| chr11:90155631
|
A | T | 1 | a0003c0004t0005g0257 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.797-2514A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155631 | ||||||
| chr11:90155655
|
GTATGTAT others(42): Show |
G | 1 | a0004c0005t0004g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.797-2486_797-2438d others(51): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155655 | |||||
| chr11:90155659
|
GTAT | G | 8 | a0001c0002t0001g0232a0001c0006t0001g0313a0001c0006t0001g0314others(5): Show | 8 | HG00609.hp2 HG01109.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.797-2478_797-2476d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155659 | |||||
| chr11:90155659
|
GTATTATT others(38): Show |
G | 186 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(183): Show | 192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.797-2478_797-2434d others(47): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155659 | |||||
| chr11:90155665
|
TTATTGTA others(42): Show |
T | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2478_797-2430d others(51): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155665 | |||||
| chr11:90155674
|
GTATGTAA others(54): Show |
G | 1 | a0001c0002t0001g0232 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.797-2464_797-2404d others(63): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155674 | |||||
| chr11:90155691
|
ACATATGT others(12): Show |
A | 1 | a0002c0003t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.797-2453_797-2435d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155691 | ||||||
| chr11:90155704
|
TTATTATT others(12): Show |
T | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.797-2438_797-2420d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155704 | |||||
| chr11:90155733
|
A | T | 5 | a0001c0002t0001g0190a0001c0002t0001g0191a0001c0002t0001g0192others(2): Show | 5 | HG00558.hp1 NA18982.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-2412A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155733 | ||||||
| chr11:90155734
|
C | T | 178 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(175): Show | 184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.797-2411C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155734 | ||||||
| chr11:90155735
|
A | G | 178 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(175): Show | 184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.797-2410A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155735 | ||||||
| chr11:90155753
|
A | T | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.797-2392A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155753 | ||||||
| chr11:90155758
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-2387T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155758 | ||||||
| chr11:90155842
|
A | G | 5 | a0001c0002t0001g0221a0001c0006t0001g0313a0001c0006t0001g0314others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-2303A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155842 | ||||||
| chr11:90155843
|
TGTTA | T | 5 | a0001c0002t0001g0221a0001c0006t0001g0313a0001c0006t0001g0314others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-2301_797-2298d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155843 | ||||||
| chr11:90155845
|
TTA | T | 196 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(193): Show | 202 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.797-2292_797-2291d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155845 | |||||
| chr11:90155847
|
A | ATATATTA others(37): Show |
1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2293_797-2292i others(46): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155847 | |||||
| chr11:90155854
|
T | TTATATTA others(27): Show |
2 | a0001c0001t0003g0077a0001c0001t0003g0089 | 2 | HG02698.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.797-2278_797-2245d others(36): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155854 | |||||
| chr11:90155877
|
G | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2268G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155877 | ||||||
| chr11:90155877
|
GTATATGT others(32): Show |
G | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.797-2257_797-2219d others(41): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155877 | |||||
| chr11:90155885
|
A | T | 46 | a0001c0002t0001g0322a0001c0002t0004g0319a0002c0003t0001g0010others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.797-2260A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155885 | ||||||
| chr11:90155929
|
A | G | 16 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-2216A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155929 | ||||||
| chr11:90155933
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-2212G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155933 | ||||||
| chr11:90156030
|
G | T | 1 | a0001c0001t0002g0068 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.797-2115G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156030 | ||||||
| chr11:90156044
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-2101T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156044 | ||||||
| chr11:90156048
|
C | G | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.797-2097C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156048 | ||||||
| chr11:90156188
|
T | A | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.797-1957T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156188 | ||||||
| chr11:90156205
|
A | C | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.797-1940A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156205 | ||||||
| chr11:90156270
|
C | T | 16 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-1875C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156270 | ||||||
| chr11:90156301
|
A | G | 2 | a0001c0001t0008g0122a0001c0001t0012g0108 | 2 | HG00558.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.797-1844A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156301 | ||||||
| chr11:90156501
|
G | A | 1 | a0001c0001t0008g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.797-1644G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156501 | ||||||
| chr11:90156693
|
C | G | 6 | a0001c0002t0004g0268a0001c0002t0004g0269a0001c0002t0004g0270others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.797-1452C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156693 | ||||||
| chr11:90156737
|
A | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-1408A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156737 | ||||||
| chr11:90156876
|
A | C | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.797-1269A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156876 | ||||||
| chr11:90156924
|
T | G | 3 | a0001c0001t0002g0048a0001c0001t0002g0050a0001c0001t0002g0154 | 3 | HG00099.hp2 HG01106.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.797-1221T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156924 | ||||||
| chr11:90156966
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.797-1179G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156966 | ||||||
| chr11:90157049
|
A | C | 1 | a0001c0002t0001g0220 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.797-1096A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157049 | ||||||
| chr11:90157075
|
G | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-1070G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157075 | ||||||
| chr11:90157365
|
C | A | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.797-780C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157365 | ||||||
| chr11:90157367
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.797-778A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157367 | ||||||
| chr11:90157367
|
A | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-778A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157367 | ||||||
| chr11:90157506
|
C | G | 1 | a0001c0002t0004g0272 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.797-639C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157506 | ||||||
| chr11:90157560
|
A | G | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.797-585A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157560 | ||||||
| chr11:90157691
|
A | G | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-454A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157691 | ||||||
| chr11:90157728
|
C | CT | 199 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(196): Show | 205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.797-406dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90157728 | |||||
| chr11:90157878
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-267G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157878 | ||||||
| chr11:90157996
|
G | T | 1 | a0001c0006t0001g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.797-149G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157996 | ||||||
| chr11:90158010
|
C | T | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.797-135C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90158010 | ||||||
| chr11:90158023
|
A | G | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.797-122A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90158023 | ||||||
| chr11:90158333
|
A | G | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.890+95A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158333 | ||||||
| chr11:90158371
|
C | T | 1 | a0006c0008t0004g0308 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.890+133C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158371 | ||||||
| chr11:90158558
|
G | A | 6 | a0001c0002t0004g0268a0001c0002t0004g0269a0001c0002t0004g0270others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.890+320G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158558 | ||||||
| chr11:90158599
|
G | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.890+361G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158599 | ||||||
| chr11:90159041
|
A | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.891-198A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159041 | ||||||
| chr11:90159082
|
T | G | 185 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(182): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.891-157T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159082 | ||||||
| chr11:90159098
|
C | T | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.891-141C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159098 | ||||||
| chr11:90159113
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.891-126T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159113 | ||||||
| chr11:90159123
|
T | G | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.891-116T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159123 | ||||||
| chr11:90159131
|
T | C | 2 | a0001c0001t0002g0057a0001c0001t0002g0140 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.891-108T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159131 | ||||||
| chr11:90159141
|
T | C | 1 | a0001c0006t0001g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.891-98T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159141 | ||||||
| chr11:90159359
|
A | C | 3 | a0001c0001t0006g0006a0001c0001t0006g0172a0001c0001t0006g0173 | 4 | HG00140.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.989+22A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159359 | ||||||
| chr11:90159391
|
C | T | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.989+54C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159391 | ||||||
| chr11:90159407
|
TTCTGCCA | T | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.989+71_989+77delTC others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159407 | ||||||
| chr11:90159413
|
C | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.989+76C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159413 | ||||||
| chr11:90159452
|
A | G | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.989+115A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159452 | ||||||
| chr11:90159552
|
A | G | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.989+215A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159552 | ||||||
| chr11:90159635
|
A | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.989+298A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159635 | ||||||
| chr11:90159679
|
T | C | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.989+342T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159679 | ||||||
| chr11:90159680
|
G | A | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.989+343G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159680 | ||||||
| chr11:90159725
|
C | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.989+388C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159725 | ||||||
| chr11:90159776
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.989+439C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159776 | ||||||
| chr11:90159916
|
T | TGCACTTG others(65): Show |
2 | a0003c0004t0001g0255a0003c0004t0005g0257 | 2 | HG01175.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.989+637_989+638ins others(72): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159916 | |||||
| chr11:90159936
|
A | G | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.989+599A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159936 | ||||||
| chr11:90159953
|
T | TA | 10 | a0001c0001t0002g0057a0001c0001t0002g0141a0001c0001t0002g0155others(7): Show | 10 | HG00673.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.989+639dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | |||||
| chr11:90159953
|
TA | T | 24 | a0001c0001t0002g0133a0001c0001t0003g0044a0001c0001t0003g0064others(21): Show | 24 | HG01069.hp2 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.989+639delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | |||||
| chr11:90159953
|
TAA | T | 84 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(81): Show | 87 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.989+638_989+639del others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | |||||
| chr11:90159953
|
TAAA | T | 15 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(12): Show | 16 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.989+637_989+639del others(3): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | |||||
| chr11:90159954
|
A | AAAAAAAA others(65): Show |
1 | a0001c0002t0001g0221 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.989+638_989+639ins others(72): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159954 | |||||
| chr11:90159954
|
A | AAAAAAAA others(64): Show |
5 | a0001c0002t0001g0212a0001c0002t0001g0226a0001c0002t0001g0227others(2): Show | 5 | HG00673.hp2 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.989+637_989+638ins others(71): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159954 | |||||
| chr11:90159955
|
A | AAAAAAAA others(64): Show |
3 | a0001c0002t0001g0211a0001c0002t0001g0232a0001c0002t0001g0235 | 3 | HG00609.hp2 HG01257.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.989+638_989+639ins others(71): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | |||||
| chr11:90159955
|
A | AAAAAAAA others(63): Show |
59 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(56): Show | 61 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.989+637_989+638ins others(70): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | |||||
| chr11:90159955
|
A | AAAAAAAA others(62): Show |
1 | a0001c0002t0001g0225 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.989+636_989+637ins others(69): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | |||||
| chr11:90159955
|
A | AAAAAAAA others(63): Show |
2 | a0001c0002t0001g0203a0001c0002t0001g0234 | 2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.989+627_989+628ins others(70): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | |||||
| chr11:90159956
|
A | AAAAAAAA others(62): Show |
3 | a0001c0002t0001g0191a0001c0002t0001g0219a0003c0004t0005g0252 | 3 | HG00323.hp2 NA18957.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.989+637_989+638ins others(69): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159956 | |||||
| chr11:90160057
|
G | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.989+720G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160057 | ||||||
| chr11:90160087
|
A | G | 1 | a0001c0001t0003g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.989+750A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160087 | ||||||
| chr11:90160352
|
A | C | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.989+1015A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160352 | ||||||
| chr11:90160441
|
C | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.989+1104C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160441 | ||||||
| chr11:90160796
|
A | T | 1 | a0014c0018t0006g0179 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.989+1459A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160796 | ||||||
| chr11:90160836
|
A | G | 186 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(183): Show | 192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.989+1499A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160836 | ||||||
| chr11:90160926
|
C | A | 1 | a0001c0002t0001g0241 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.989+1589C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160926 | ||||||
| chr11:90160927
|
A | C | 1 | a0001c0002t0001g0241 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.989+1590A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160927 | ||||||
| chr11:90160928
|
T | A | 1 | a0001c0002t0001g0241 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.989+1591T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160928 | ||||||
| chr11:90160971
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.989+1634C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160971 | ||||||
| chr11:90161013
|
T | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0025 | 2 | NA18968.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.989+1676T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161013 | ||||||
| chr11:90161052
|
T | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.989+1715T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161052 | ||||||
| chr11:90161126
|
G | C | 73 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(70): Show | 75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.989+1789G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161126 | ||||||
| chr11:90161165
|
C | G | 1 | a0001c0001t0002g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.990-1784C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161165 | ||||||
| chr11:90161171
|
C | T | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.990-1778C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161171 | ||||||
| chr11:90161351
|
G | A | 2 | a0001c0002t0004g0016a0001c0002t0004g0024 | 2 | HG01261.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.990-1598G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161351 | ||||||
| chr11:90161416
|
T | C | 1 | a0008c0010t0004g0329 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.990-1533T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161416 | ||||||
| chr11:90161435
|
A | G | 6 | a0001c0002t0004g0268a0001c0002t0004g0269a0001c0002t0004g0270others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.990-1514A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161435 | ||||||
| chr11:90161504
|
G | A | 1 | a0001c0002t0001g0014 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.990-1445G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161504 | ||||||
| chr11:90161523
|
C | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.990-1426C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161523 | ||||||
| chr11:90161642
|
C | T | 9 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(6): Show | 9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.990-1307C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161642 | ||||||
| chr11:90161833
|
A | G | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.990-1116A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161833 | ||||||
| chr11:90161857
|
C | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.990-1092C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161857 | ||||||
| chr11:90161925
|
GA | G | 204 | a0001c0001t0002g0041a0001c0001t0002g0047a0001c0001t0002g0072others(201): Show | 210 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.990-1011delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90161925 | |||||
| chr11:90161941
|
T | A | 1 | a0001c0002t0001g0241 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.990-1008T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161941 | ||||||
| chr11:90161978
|
T | C | 1 | a0005c0007t0005g0324 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.990-971T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161978 | ||||||
| chr11:90162086
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.990-863A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162086 | ||||||
| chr11:90162359
|
G | A | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.990-590G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162359 | ||||||
| chr11:90162401
|
G | T | 1 | a0002c0003t0001g0300 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.990-548G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162401 | ||||||
| chr11:90162466
|
T | C | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.990-483T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162466 | ||||||
| chr11:90162475
|
A | C | 3 | a0001c0001t0002g0059a0001c0001t0002g0073a0001c0001t0002g0138 | 3 | HG01243.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.990-474A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162475 | ||||||
| chr11:90162682
|
A | T | 14 | a0004c0005t0001g0261a0004c0005t0001g0266a0004c0005t0004g0262others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.990-267A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162682 | ||||||
| chr11:90162772
|
A | G | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.990-177A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162772 | ||||||
| chr11:90162780
|
C | T | 1 | a0004c0005t0004g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.990-169C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162780 | ||||||
| chr11:90162851
|
C | CATAATAA others(25): Show |
2 | a0001c0001t0006g0176a0001c0001t0006g0180 | 2 | HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.990-84_990-53dupAT others(30): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90162851 | |||||
| chr11:90162873
|
A | G | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.990-76A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162873 | ||||||
| chr11:90163249
|
A | G | 73 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(70): Show | 75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1076-61A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/18 | chr11 | 90163249 | ||||||
| chr11:90163289
|
C | T | 239 | a0001c0001t0002g0041a0001c0001t0002g0047a0001c0001t0002g0058others(236): Show | 246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1076-21C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/18 | chr11 | 90163289 | ||||||
| chr11:90163448
|
C | A | 1 | a0001c0001t0002g0112 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1195+19C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163448 | ||||||
| chr11:90163449
|
T | A | 1 | a0001c0001t0002g0112 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1195+20T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163449 | ||||||
| chr11:90163472
|
A | C | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1195+43A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163472 | ||||||
| chr11:90163514
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1196-21G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163514 | ||||||
| chr11:90164026
|
T | A | 2 | a0001c0001t0008g0102a0001c0001t0008g0113 | 2 | NA18940.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1278+409T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164026 | ||||||
| chr11:90164092
|
C | A | 1 | a0001c0001t0003g0129 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1278+475C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164092 | ||||||
| chr11:90164403
|
G | A | 2 | a0001c0002t0001g0207a0001c0002t0001g0228 | 2 | NA18990.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1278+786G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164403 | ||||||
| chr11:90164590
|
TTAATAA | T | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1278+981_1278+986d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90164590 | |||||
| chr11:90164793
|
T | C | 4 | a0001c0002t0004g0269a0001c0002t0004g0270a0001c0002t0004g0271others(1): Show | 4 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+1176T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164793 | ||||||
| chr11:90164821
|
G | T | 2 | a0001c0006t0001g0313a0001c0006t0001g0334 | 2 | HG01109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1278+1204G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164821 | ||||||
| chr11:90165062
|
C | T | 1 | a0006c0008t0004g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1278+1445C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165062 | ||||||
| chr11:90165163
|
C | T | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1278+1546C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165163 | ||||||
| chr11:90165246
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1278+1629G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165246 | ||||||
| chr11:90165299
|
A | G | 1 | a0001c0001t0003g0054 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1278+1682A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165299 | ||||||
| chr11:90165300
|
T | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1278+1683T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165300 | ||||||
| chr11:90165318
|
C | A | 1 | a0001c0001t0008g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1278+1701C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165318 | ||||||
| chr11:90165322
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1278+1705G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165322 | ||||||
| chr11:90165414
|
G | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1278+1797G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165414 | ||||||
| chr11:90165417
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1278+1800A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165417 | ||||||
| chr11:90165419
|
C | T | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1278+1802C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165419 | ||||||
| chr11:90165514
|
G | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1278+1897G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165514 | ||||||
| chr11:90165635
|
C | T | 24 | a0002c0003t0001g0010a0002c0003t0001g0011a0002c0003t0001g0285others(21): Show | 25 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1278+2018C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165635 | ||||||
| chr11:90165673
|
G | T | 156 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(153): Show | 161 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1278+2056G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165673 | ||||||
| chr11:90165798
|
A | G | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1278+2181A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165798 | ||||||
| chr11:90165874
|
A | C | 1 | a0005c0007t0001g0330 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1278+2257A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165874 | ||||||
| chr11:90165905
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0002g0137a0001c0001t0010g0162others(1): Show | 4 | HG02965.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+2288G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165905 | ||||||
| chr11:90166104
|
C | CTGGCCTA others(33): Show |
1 | a0001c0002t0001g0241 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1278+2489_1278+252 others(44): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90166104 | |||||
| chr11:90166247
|
CTCTG | C | 44 | a0002c0003t0001g0010a0002c0003t0001g0011a0002c0003t0001g0282others(41): Show | 46 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1278+2636_1278+263 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90166247 | |||||
| chr11:90166253
|
CTGTG | C | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1278+2640_1278+264 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90166253 | |||||
| chr11:90166293
|
C | G | 2 | a0008c0010t0004g0329a0008c0010t0004g0331 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1279-2636C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166293 | ||||||
| chr11:90166319
|
A | G | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1279-2610A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166319 | ||||||
| chr11:90166324
|
A | T | 1 | a0001c0002t0004g0024 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1279-2605A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166324 | ||||||
| chr11:90166334
|
C | T | 18 | a0001c0001t0002g0141a0001c0001t0002g0144a0001c0002t0001g0337others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1279-2595C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166334 | ||||||
| chr11:90166523
|
T | C | 5 | a0002c0003t0001g0300a0002c0003t0001g0310a0002c0003t0007g0304others(2): Show | 5 | HG00544.hp2 HG03239.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-2406T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166523 | ||||||
| chr11:90166561
|
C | T | 16 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1279-2368C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166561 | ||||||
| chr11:90166571
|
C | T | 1 | a0002c0003t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1279-2358C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166571 | ||||||
| chr11:90166588
|
C | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1279-2341C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166588 | ||||||
| chr11:90166695
|
C | T | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-2234C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166695 | ||||||
| chr11:90166727
|
C | T | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-2202C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166727 | ||||||
| chr11:90166743
|
G | A | 7 | a0001c0002t0001g0337a0001c0002t0004g0268a0001c0002t0004g0269others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-2186G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166743 | ||||||
| chr11:90166743
|
G | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-2186G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166743 | ||||||
| chr11:90166849
|
A | AG | 185 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(182): Show | 191 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.1279-2080_1279-207 others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166849 | ||||||
| chr11:90166942
|
G | A | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1279-1987G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166942 | ||||||
| chr11:90167024
|
G | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-1905G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167024 | ||||||
| chr11:90167061
|
C | T | 5 | a0001c0001t0002g0041a0001c0001t0002g0137a0001c0001t0002g0145others(2): Show | 5 | HG02965.hp2 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-1868C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167061 | ||||||
| chr11:90167115
|
C | A | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279-1814C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167115 | ||||||
| chr11:90167128
|
G | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-1801G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167128 | ||||||
| chr11:90167132
|
C | A | 6 | a0001c0002t0004g0268a0001c0002t0004g0269a0001c0002t0004g0270others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279-1797C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167132 | ||||||
| chr11:90167133
|
C | G | 1 | a0001c0020t0002g0095 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1279-1796C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167133 | ||||||
| chr11:90167138
|
C | T | 12 | a0002c0003t0001g0282a0002c0003t0001g0301a0002c0003t0001g0303others(9): Show | 13 | HG01192.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1279-1791C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167138 | ||||||
| chr11:90167160
|
C | T | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1279-1769C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167160 | ||||||
| chr11:90167161
|
G | A | 14 | a0003c0004t0001g0255a0003c0004t0004g0256a0003c0004t0005g0244others(11): Show | 14 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279-1768G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167161 | ||||||
| chr11:90167177
|
T | G | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-1752T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167177 | ||||||
| chr11:90167208
|
ACCGGGGC others(8): Show |
A | 1 | a0001c0002t0007g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1279-1719_1279-170 others(19): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90167208 | |||||
| chr11:90167230
|
C | T | 1 | a0001c0001t0003g0063 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1279-1699C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167230 | ||||||
| chr11:90167308
|
G | A | 59 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1279-1621G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167308 | ||||||
| chr11:90167309
|
C | T | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-1620C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167309 | ||||||
| chr11:90167316
|
G | A | 2 | a0001c0006t0004g0335a0001c0006t0005g0336 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279-1613G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167316 | ||||||
| chr11:90167379
|
C | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1279-1550C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167379 | ||||||
| chr11:90167393
|
T | G | 1 | a0001c0001t0002g0045 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1279-1536T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167393 | ||||||
| chr11:90167405
|
C | T | 159 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(156): Show | 164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1279-1524C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167405 | ||||||
| chr11:90167461
|
G | C | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279-1468G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167461 | ||||||
| chr11:90167462
|
A | C | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1279-1467A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167462 | ||||||
| chr11:90167481
|
C | T | 6 | a0001c0002t0004g0268a0001c0002t0004g0269a0001c0002t0004g0270others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279-1448C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167481 | ||||||
| chr11:90167528
|
C | T | 1 | a0001c0006t0001g0313 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1279-1401C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167528 | ||||||
| chr11:90167568
|
C | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(198): Show | 207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1279-1361C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167568 | ||||||
| chr11:90167569
|
G | A | 1 | a0009c0022t0002g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1279-1360G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167569 | ||||||
| chr11:90167614
|
T | C | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1279-1315T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167614 | ||||||
| chr11:90167763
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1279-1166A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167763 | ||||||
| chr11:90167776
|
G | T | 44 | a0002c0003t0001g0010a0002c0003t0001g0011a0002c0003t0001g0282others(41): Show | 46 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1279-1153G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167776 | ||||||
| chr11:90167800
|
G | T | 1 | a0001c0002t0001g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1279-1129G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167800 | ||||||
| chr11:90167821
|
C | G | 1 | a0001c0002t0001g0207 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1279-1108C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167821 | ||||||
| chr11:90167827
|
T | A | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1279-1102T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167827 | ||||||
| chr11:90167850
|
GCAATCGG others(17): Show |
G | 4 | a0001c0002t0001g0267a0001c0002t0004g0268a0001c0002t0004g0272others(1): Show | 4 | HG02109.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-1059_1279-103 others(28): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90167850 | |||||
| chr11:90167879
|
C | T | 2 | a0001c0002t0004g0195a0001c0002t0004g0239 | 2 | NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1279-1050C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167879 | ||||||
| chr11:90167913
|
T | G | 15 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(12): Show | 15 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1279-1016T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167913 | ||||||
| chr11:90167949
|
C | T | 202 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(199): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1279-980C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167949 | ||||||
| chr11:90167960
|
T | G | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-969T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167960 | ||||||
| chr11:90167969
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279-960T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167969 | ||||||
| chr11:90167990
|
G | A | 61 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0332others(58): Show | 64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1279-939G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167990 | ||||||
| chr11:90168083
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1279-846G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168083 | ||||||
| chr11:90168120
|
A | AC | 61 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0332others(58): Show | 64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1279-806dupC | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90168120 | |||||
| chr11:90168176
|
G | A | 1 | a0003c0004t0004g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1279-753G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168176 | ||||||
| chr11:90168214
|
A | C | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1279-715A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168214 | ||||||
| chr11:90168306
|
C | G | 1 | a0001c0002t0004g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1279-623C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168306 | ||||||
| chr11:90168329
|
C | G | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279-600C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168329 | ||||||
| chr11:90168352
|
C | T | 3 | a0004c0005t0001g0266a0004c0005t0004g0262a0004c0005t0004g0263 | 3 | HG02615.hp2 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1279-577C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168352 | ||||||
| chr11:90168390
|
C | T | 15 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(12): Show | 15 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1279-539C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168390 | ||||||
| chr11:90168404
|
G | A | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-525G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168404 | ||||||
| chr11:90168458
|
G | A | 1 | a0001c0001t0003g0075 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1279-471G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168458 | ||||||
| chr11:90168517
|
TAAAA | T | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-411_1279-408d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168517 | ||||||
| chr11:90168600
|
G | C | 1 | a0001c0001t0002g0114 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1279-329G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168600 | ||||||
| chr11:90168634
|
C | T | 2 | a0002c0003t0001g0295a0002c0003t0001g0299 | 2 | HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1279-295C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168634 | ||||||
| chr11:90168654
|
C | T | 7 | a0002c0003t0001g0282a0002c0003t0001g0301a0002c0003t0001g0303others(4): Show | 7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-275C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168654 | ||||||
| chr11:90168665
|
T | C | 1 | a0001c0002t0001g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1279-264T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168665 | ||||||
| chr11:90168679
|
G | A | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-250G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168679 | ||||||
| chr11:90168711
|
T | C | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-218T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168711 | ||||||
| chr11:90168857
|
A | G | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-72A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168857 | ||||||
| chr11:90168866
|
A | G | 5 | a0001c0002t0004g0319a0004c0005t0001g0266a0004c0005t0004g0262others(2): Show | 5 | HG02615.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-63A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168866 | ||||||
| chr11:90169108
|
A | G | 195 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(192): Show | 201 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1342+116A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169108 | ||||||
| chr11:90169143
|
A | G | 1 | a0008c0010t0004g0329 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1342+151A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169143 | ||||||
| chr11:90169181
|
T | A | 5 | a0001c0001t0002g0068a0001c0001t0002g0100a0001c0001t0002g0155others(2): Show | 5 | NA18940.hp1 NA18944.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342+189T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169181 | ||||||
| chr11:90169300
|
A | AT | 187 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(184): Show | 193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1342+309dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169300 | |||||
| chr11:90169363
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1342+371G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169363 | ||||||
| chr11:90169390
|
A | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1342+398A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169390 | ||||||
| chr11:90169448
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1342+456G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169448 | ||||||
| chr11:90169454
|
A | T | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1342+462A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169454 | ||||||
| chr11:90169507
|
C | CA | 6 | a0001c0001t0006g0065a0001c0002t0001g0023a0001c0002t0001g0032others(3): Show | 6 | HG00621.hp1 HG01257.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1342+528dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169507 | |||||
| chr11:90169507
|
C | CAA | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1342+527_1342+528d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169507 | |||||
| chr11:90169507
|
CAAAAA | C | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1342+524_1342+528d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169507 | |||||
| chr11:90169527
|
G | T | 2 | a0002c0003t0001g0298a0002c0003t0001g0306 | 2 | HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1342+535G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169527 | ||||||
| chr11:90169590
|
C | A | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-479C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169590 | ||||||
| chr11:90169601
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1343-468G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169601 | ||||||
| chr11:90169633
|
C | G | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343-436C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169633 | ||||||
| chr11:90169675
|
G | A | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1343-394G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169675 | ||||||
| chr11:90169814
|
G | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343-255G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169814 | ||||||
| chr11:90169882
|
G | C | 8 | a0001c0001t0002g0003a0001c0001t0002g0048a0001c0001t0002g0050others(5): Show | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1343-187G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169882 | ||||||
| chr11:90169888
|
T | G | 2 | a0001c0001t0006g0170a0001c0001t0006g0171 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1343-181T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169888 | ||||||
| chr11:90169916
|
A | T | 1 | a0001c0002t0001g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1343-153A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169916 | ||||||
| chr11:90169926
|
C | A | 1 | a0001c0001t0003g0134 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1343-143C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169926 | ||||||
| chr11:90170166
|
C | T | 196 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(193): Show | 202 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1410+30C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170166 | ||||||
| chr11:90170237
|
G | A | 152 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(149): Show | 157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1410+101G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170237 | ||||||
| chr11:90170717
|
G | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+581G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170717 | ||||||
| chr11:90170836
|
C | T | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+700C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170836 | ||||||
| chr11:90170877
|
A | G | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1410+741A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170877 | ||||||
| chr11:90170905
|
A | G | 8 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(5): Show | 8 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1410+769A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170905 | ||||||
| chr11:90170977
|
G | T | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1410+841G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170977 | ||||||
| chr11:90171070
|
C | A | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1410+934C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171070 | ||||||
| chr11:90171126
|
A | C | 1 | a0001c0002t0001g0237 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1410+990A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171126 | ||||||
| chr11:90171168
|
A | G | 61 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0332others(58): Show | 64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1410+1032A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171168 | ||||||
| chr11:90171369
|
C | T | 2 | a0001c0002t0001g0194a0001c0002t0001g0222 | 2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1410+1233C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171369 | ||||||
| chr11:90171383
|
C | G | 2 | a0002c0003t0001g0282a0002c0003t0001g0303 | 2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1410+1247C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171383 | ||||||
| chr11:90171421
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1410+1285T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171421 | ||||||
| chr11:90171461
|
G | A | 2 | a0001c0001t0003g0061a0001c0001t0003g0064 | 2 | NA19074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1410+1325G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171461 | ||||||
| chr11:90171494
|
G | T | 1 | a0001c0001t0002g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1410+1358G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171494 | ||||||
| chr11:90171518
|
T | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+1382T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171518 | ||||||
| chr11:90171538
|
T | C | 163 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(160): Show | 168 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1410+1402T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171538 | ||||||
| chr11:90171548
|
G | T | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1410+1412G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171548 | ||||||
| chr11:90171578
|
A | G | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1410+1442A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171578 | ||||||
| chr11:90171809
|
A | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1410+1673A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171809 | ||||||
| chr11:90171891
|
C | T | 73 | a0001c0002t0004g0319a0001c0002t0004g0350a0001c0002t0005g0012others(70): Show | 76 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1410+1755C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171891 | ||||||
| chr11:90171937
|
A | G | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1410+1801A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171937 | ||||||
| chr11:90171983
|
AAAAAAAG others(9): Show |
A | 49 | a0002c0003t0001g0010a0002c0003t0001g0011a0002c0003t0001g0282others(46): Show | 51 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.1411-1826_1411-181 others(20): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 90171983 | |||||
| chr11:90172042
|
C | T | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1782C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172042 | ||||||
| chr11:90172043
|
G | A | 73 | a0001c0002t0004g0319a0001c0002t0004g0350a0001c0002t0005g0012others(70): Show | 76 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1411-1781G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172043 | ||||||
| chr11:90172068
|
T | C | 345 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(342): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1411-1756T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172068 | ||||||
| chr11:90172068
|
T | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0015g0020 | 3 | NA18974.hp2 NA18992.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1411-1756T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172068 | ||||||
| chr11:90172071
|
T | G | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1411-1753T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172071 | ||||||
| chr11:90172142
|
G | A | 2 | a0001c0002t0004g0016a0001c0002t0004g0024 | 2 | HG01261.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1411-1682G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172142 | ||||||
| chr11:90172226
|
C | T | 2 | a0001c0001t0006g0170a0001c0001t0006g0171 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1411-1598C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172226 | ||||||
| chr11:90172257
|
AG | A | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1564delG | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 90172257 | |||||
| chr11:90172262
|
G | A | 2 | a0001c0002t0004g0039a0001c0002t0004g0040 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1411-1562G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172262 | ||||||
| chr11:90172350
|
C | T | 3 | a0001c0002t0005g0347a0001c0002t0005g0348a0001c0002t0005g0349 | 3 | NA18985.hp1 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1411-1474C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172350 | ||||||
| chr11:90172421
|
G | A | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1411-1403G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172421 | ||||||
| chr11:90172431
|
G | C | 1 | a0001c0001t0002g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1411-1393G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172431 | ||||||
| chr11:90172442
|
A | G | 6 | a0001c0001t0003g0181a0001c0001t0006g0006a0001c0001t0006g0172others(3): Show | 7 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-1382A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172442 | ||||||
| chr11:90172455
|
G | C | 156 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(153): Show | 161 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1411-1369G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172455 | ||||||
| chr11:90172518
|
C | G | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1306C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172518 | ||||||
| chr11:90172643
|
T | G | 1 | a0001c0002t0005g0346 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1411-1181T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172643 | ||||||
| chr11:90172716
|
G | A | 12 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(9): Show | 12 | HG02486.hp1 HG02615.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1411-1108G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172716 | ||||||
| chr11:90172838
|
A | G | 1 | a0002c0003t0001g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1411-986A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172838 | ||||||
| chr11:90172979
|
A | G | 1 | a0001c0001t0003g0091 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1411-845A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172979 | ||||||
| chr11:90172996
|
T | G | 348 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(345): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1411-828T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172996 | ||||||
| chr11:90173083
|
A | G | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-741A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173083 | ||||||
| chr11:90173137
|
A | G | 3 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334 | 3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1411-687A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173137 | ||||||
| chr11:90173186
|
T | C | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-638T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173186 | ||||||
| chr11:90173188
|
C | T | 1 | a0002c0003t0001g0284 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1411-636C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173188 | ||||||
| chr11:90173247
|
T | C | 1 | a0002c0003t0001g0310 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1411-577T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173247 | ||||||
| chr11:90173248
|
T | C | 2 | a0001c0002t0004g0268a0001c0002t0004g0272 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1411-576T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173248 | ||||||
| chr11:90173337
|
G | A | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411-487G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173337 | ||||||
| chr11:90173348
|
A | G | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1411-476A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173348 | ||||||
| chr11:90173430
|
T | C | 3 | a0001c0001t0003g0004a0001c0001t0003g0143a0001c0001t0013g0004 | 3 | NA18967.hp1 NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1411-394T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173430 | ||||||
| chr11:90173543
|
A | G | 1 | a0001c0006t0001g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1411-281A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173543 | ||||||
| chr11:90173716
|
C | T | 3 | a0001c0002t0001g0267a0003c0004t0001g0255a0003c0004t0005g0254 | 3 | HG01175.hp2 HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1411-108C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173716 | ||||||
| chr11:90173928
|
T | TA | 3 | a0001c0001t0006g0052a0001c0001t0008g0053a0001c0001t0008g0136 | 3 | HG00099.hp1 HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1502+14dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90173928 | |||||
| chr11:90174149
|
C | T | 27 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(24): Show | 28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.1502+234C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174149 | ||||||
| chr11:90174150
|
G | A | 1 | a0002c0003t0001g0286 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1502+235G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174150 | ||||||
| chr11:90174188
|
G | A | 46 | a0002c0003t0001g0010a0002c0003t0001g0011a0002c0003t0001g0282others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1502+273G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174188 | ||||||
| chr11:90174199
|
C | T | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502+284C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174199 | ||||||
| chr11:90174219
|
T | C | 185 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(182): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1502+304T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174219 | ||||||
| chr11:90174496
|
A | C | 12 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(9): Show | 12 | HG02486.hp1 HG02615.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1502+581A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174496 | ||||||
| chr11:90174527
|
A | T | 1 | a0001c0002t0004g0270 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1502+612A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174527 | ||||||
| chr11:90174608
|
T | A | 2 | a0001c0002t0001g0194a0001c0002t0001g0222 | 2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1502+693T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174608 | ||||||
| chr11:90174729
|
TTTTTA | T | 3 | a0001c0002t0001g0245a0001c0002t0001g0246a0001c0002t0001g0322 | 3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1502+819_1502+823d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90174729 | |||||
| chr11:90174746
|
C | A | 178 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(175): Show | 184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1502+831C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174746 | ||||||
| chr11:90174866
|
T | G | 1 | a0001c0002t0004g0319 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1502+951T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174866 | ||||||
| chr11:90175044
|
G | GATGGGGT others(5): Show |
1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-926_1503-925i others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175044 | |||||
| chr11:90175049
|
C | G | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-923C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175049 | ||||||
| chr11:90175051
|
C | A | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-921C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175051 | ||||||
| chr11:90175053
|
C | A | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-919C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175053 | ||||||
| chr11:90175056
|
C | T | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-916C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175056 | ||||||
| chr11:90175058
|
T | A | 1 | a0001c0006t0005g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-914T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175058 | ||||||
| chr11:90175284
|
A | T | 1 | a0002c0003t0001g0306 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1503-688A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175284 | ||||||
| chr11:90175408
|
T | C | 1 | a0001c0002t0004g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1503-564T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175408 | ||||||
| chr11:90175554
|
G | T | 46 | a0002c0003t0001g0010a0002c0003t0001g0011a0002c0003t0001g0282others(43): Show | 48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1503-418G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175554 | ||||||
| chr11:90175600
|
T | C | 185 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(182): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1503-372T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175600 | ||||||
| chr11:90175619
|
GT | G | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1503-349delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175619 | |||||
| chr11:90175836
|
T | A | 2 | a0001c0002t0004g0039a0001c0002t0004g0040 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1503-136T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175836 | ||||||
| chr11:90175928
|
A | ATG | 13 | a0001c0001t0002g0072a0001c0001t0002g0137a0001c0001t0003g0044others(10): Show | 13 | HG01099.hp2 HG01256.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1503-21_1503-20dup others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | |||||
| chr11:90175928
|
A | ATGTGTG | 80 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0018others(77): Show | 83 | HG00597.hp1 HG00639.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.1503-25_1503-20dup others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | |||||
| chr11:90175928
|
A | ATGTGTGT others(1): Show |
82 | a0001c0002t0001g0007a0001c0002t0001g0017a0001c0002t0001g0186others(79): Show | 84 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1503-27_1503-20dup others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | |||||
| chr11:90175928
|
A | ATGTGTGT others(3): Show |
21 | a0001c0002t0001g0236a0001c0002t0004g0350a0001c0002t0005g0012others(18): Show | 22 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1503-29_1503-20dup others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | |||||
| chr11:90175928
|
A | ATGTGTGT others(7): Show |
1 | a0001c0002t0001g0218 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1503-33_1503-20dup others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | |||||
| chr11:90175928
|
A | G | 10 | a0001c0001t0002g0175a0001c0001t0006g0046a0001c0001t0006g0052others(7): Show | 10 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1503-44A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175928 | ||||||
| chr11:90175929
|
T | TGTGC | 3 | a0005c0007t0005g0323a0005c0007t0005g0326a0005c0007t0005g0327 | 3 | HG03041.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1503-40_1503-39ins others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175929 | |||||
| chr11:90175931
|
T | TGC | 4 | a0005c0007t0001g0330a0005c0007t0005g0324a0005c0007t0007g0325others(1): Show | 4 | HG01081.hp1 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503-40_1503-39ins others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175931 | |||||
| chr11:90176196
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1593+134G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176196 | ||||||
| chr11:90176221
|
G | A | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1593+159G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176221 | ||||||
| chr11:90176306
|
T | C | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1593+244T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176306 | ||||||
| chr11:90176451
|
A | G | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1593+389A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176451 | ||||||
| chr11:90176700
|
G | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1593+638G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176700 | ||||||
| chr11:90176740
|
A | T | 1 | a0001c0001t0002g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1593+678A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176740 | ||||||
| chr11:90176800
|
T | C | 1 | a0008c0010t0004g0329 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1593+738T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176800 | ||||||
| chr11:90176853
|
C | G | 1 | a0001c0002t0007g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1593+791C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176853 | ||||||
| chr11:90176890
|
C | T | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1593+828C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176890 | ||||||
| chr11:90176937
|
A | C | 5 | a0001c0001t0003g0063a0001c0001t0003g0084a0001c0001t0003g0085others(2): Show | 5 | HG02040.hp2 NA18968.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1593+875A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176937 | ||||||
| chr11:90176957
|
T | G | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1593+895T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176957 | ||||||
| chr11:90176966
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1594-887T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176966 | ||||||
| chr11:90176968
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1594-885T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176968 | ||||||
| chr11:90177057
|
C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0032a0001c0002t0001g0037 | 3 | NA18943.hp2 NA19076.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1594-796C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177057 | ||||||
| chr11:90177164
|
C | T | 3 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334 | 3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1594-689C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177164 | ||||||
| chr11:90177313
|
C | CT | 15 | a0001c0001t0002g0107a0001c0001t0002g0149a0001c0001t0006g0093others(12): Show | 15 | HG01099.hp1 HG01891.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.1594-526dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177313 | |||||
| chr11:90177313
|
CT | C | 32 | a0001c0001t0002g0051a0001c0001t0002g0155a0001c0001t0003g0078others(29): Show | 33 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(30): Show |
intron_variant | MODIFIER | c.1594-526delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177313 | |||||
| chr11:90177401
|
C | T | 7 | a0002c0003t0001g0282a0002c0003t0001g0301a0002c0003t0001g0303others(4): Show | 7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-452C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177401 | ||||||
| chr11:90177526
|
C | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1594-327C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177526 | ||||||
| chr11:90177527
|
G | A | 1 | a0001c0001t0003g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1594-326G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177527 | ||||||
| chr11:90177560
|
A | G | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1594-293A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177560 | ||||||
| chr11:90177586
|
G | GT | 37 | a0001c0001t0002g0003a0001c0001t0002g0041a0001c0001t0002g0045others(34): Show | 38 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1594-229dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GT | G | 41 | a0001c0001t0002g0057a0001c0001t0002g0059a0001c0001t0002g0068others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.1594-229delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTT | G | 17 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0047others(14): Show | 19 | HG00544.hp1 HG01081.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1594-230_1594-229d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTT | G | 7 | a0002c0003t0001g0011a0002c0003t0001g0315a0002c0009t0001g0283others(4): Show | 8 | HG00639.hp1 HG01069.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1594-232_1594-229d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTT | G | 23 | a0001c0001t0002g0156a0001c0002t0004g0319a0002c0003t0001g0010others(20): Show | 23 | HG01168.hp1 HG01261.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1594-233_1594-229d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTT | G | 22 | a0002c0003t0001g0282a0002c0003t0001g0285a0002c0003t0001g0289others(19): Show | 22 | HG00544.hp2 HG01192.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1594-234_1594-229d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(3): Show |
G | 11 | a0001c0002t0001g0014a0001c0002t0001g0028a0001c0002t0001g0029others(8): Show | 11 | HG00597.hp1 HG03130.hp1 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.1594-238_1594-229d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(4): Show |
G | 32 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(29): Show | 33 | HG01109.hp1 HG01261.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1594-239_1594-229d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(5): Show |
G | 42 | a0001c0001t0006g0006a0001c0001t0006g0172a0001c0001t0006g0173others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1594-240_1594-229d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(6): Show |
G | 40 | a0001c0002t0001g0199a0001c0002t0001g0200a0001c0002t0001g0210others(37): Show | 41 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1594-241_1594-229d others(15): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0002t0001g0225 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1594-242_1594-229d others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1594-245_1594-229d others(19): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(11): Show |
G | 1 | a0005c0007t0005g0323 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1594-246_1594-229d others(20): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(12): Show |
G | 6 | a0005c0007t0001g0330a0005c0007t0005g0324a0005c0007t0005g0326others(3): Show | 6 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1594-247_1594-229d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(14): Show |
G | 1 | a0002c0003t0001g0286 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1594-249_1594-229d others(23): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177586
|
GTTTTTTT others(17): Show |
G | 3 | a0003c0004t0005g0250a0003c0004t0005g0251a0003c0004t0005g0258 | 3 | HG02083.hp2 NA18973.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1594-252_1594-229d others(26): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | |||||
| chr11:90177677
|
TC | T | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1594-174delC | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177677 | |||||
| chr11:90177683
|
G | A | 7 | a0005c0007t0001g0330a0005c0007t0005g0323a0005c0007t0005g0324others(4): Show | 7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-170G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177683 | ||||||
| chr11:90178242
|
C | A | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+125C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178242 | ||||||
| chr11:90178255
|
TAAAAC | T | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+142_1858+146d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90178255 | |||||
| chr11:90178312
|
T | A | 1 | a0001c0002t0001g0025 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1858+195T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178312 | ||||||
| chr11:90178425
|
A | G | 1 | a0005c0007t0007g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1858+308A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178425 | ||||||
| chr11:90178453
|
T | C | 194 | a0001c0001t0002g0041a0001c0001t0002g0137a0001c0001t0010g0162others(191): Show | 200 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1858+336T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178453 | ||||||
| chr11:90178454
|
G | A | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+337G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178454 | ||||||
| chr11:90178467
|
C | T | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1858+350C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178467 | ||||||
| chr11:90178485
|
T | C | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1858+368T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178485 | ||||||
| chr11:90178498
|
C | T | 3 | a0001c0001t0002g0041a0001c0001t0010g0162a0001c0001t0010g0163 | 3 | HG02965.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1858+381C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178498 | ||||||
| chr11:90178534
|
G | A | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1858+417G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178534 | ||||||
| chr11:90178661
|
G | T | 1 | a0001c0006t0001g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1858+544G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178661 | ||||||
| chr11:90178670
|
C | CA | 6 | a0001c0001t0002g0116a0001c0001t0002g0147a0001c0001t0002g0159others(3): Show | 6 | HG00597.hp2 HG00741.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+568dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90178670 | |||||
| chr11:90178670
|
CA | C | 79 | a0001c0001t0003g0076a0001c0001t0003g0088a0001c0001t0006g0093others(76): Show | 81 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1858+568delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90178670 | |||||
| chr11:90178699
|
A | G | 1 | a0001c0002t0001g0211 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1858+582A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178699 | ||||||
| chr11:90178766
|
G | A | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1858+649G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178766 | ||||||
| chr11:90179087
|
C | T | 1 | a0003c0004t0004g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1858+970C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179087 | ||||||
| chr11:90179151
|
A | G | 192 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(189): Show | 198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1858+1034A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179151 | ||||||
| chr11:90179280
|
C | G | 5 | a0001c0001t0003g0103a0001c0001t0003g0110a0001c0001t0003g0129others(2): Show | 5 | HG02129.hp2 HG02132.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858+1163C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179280 | ||||||
| chr11:90179308
|
T | C | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+1191T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179308 | ||||||
| chr11:90179333
|
G | A | 1 | a0001c0001t0006g0093 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1858+1216G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179333 | ||||||
| chr11:90179449
|
T | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1858+1332T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179449 | ||||||
| chr11:90179484
|
T | C | 76 | a0001c0002t0001g0007a0001c0002t0001g0186a0001c0002t0001g0187others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1858+1367T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179484 | ||||||
| chr11:90179567
|
T | A | 8 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(5): Show | 8 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1858+1450T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179567 | ||||||
| chr11:90179619
|
T | G | 1 | a0004c0005t0004g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1858+1502T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179619 | ||||||
| chr11:90179705
|
C | G | 1 | a0001c0002t0007g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1858+1588C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179705 | ||||||
| chr11:90179784
|
T | TA | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1858+1668dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90179784 | |||||
| chr11:90179864
|
T | G | 185 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(182): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1858+1747T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179864 | ||||||
| chr11:90180066
|
G | GATGA | 3 | a0001c0001t0003g0134a0001c0002t0004g0268a0001c0002t0004g0272 | 3 | HG03195.hp1 HG03579.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1859-1527_1859-152 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90180066 | |||||
| chr11:90180066
|
GATGA | G | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1859-1527_1859-152 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90180066 | |||||
| chr11:90180088
|
T | C | 4 | a0001c0001t0002g0116a0001c0001t0002g0147a0001c0001t0002g0159others(1): Show | 4 | HG00741.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1859-1532T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180088 | ||||||
| chr11:90180138
|
T | A | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1859-1482T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180138 | ||||||
| chr11:90180200
|
C | T | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1859-1420C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180200 | ||||||
| chr11:90180301
|
C | T | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1859-1319C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180301 | ||||||
| chr11:90180359
|
A | G | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1859-1261A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180359 | ||||||
| chr11:90180561
|
A | G | 171 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(168): Show | 176 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1859-1059A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180561 | ||||||
| chr11:90180816
|
A | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1859-804A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180816 | ||||||
| chr11:90181060
|
T | C | 7 | a0002c0003t0001g0284a0002c0003t0001g0286a0002c0003t0001g0289others(4): Show | 7 | HG01099.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1859-560T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181060 | ||||||
| chr11:90181236
|
AT | A | 11 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(8): Show | 11 | HG02486.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1859-375delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90181236 | |||||
| chr11:90181250
|
T | A | 1 | a0001c0001t0002g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1859-370T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181250 | ||||||
| chr11:90181588
|
A | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1859-32A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181588 | ||||||
| chr11:90181618
|
A | T | 1 | a0007c0011t0002g0127 | 1 | HG00609.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1859-2A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181618 | ||||||
| chr11:90181719
|
T | C | 29 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(26): Show | 30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1940+18T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181719 | ||||||
| chr11:90181725
|
TTAAA | T | 6 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940+25_1940+28del others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181725 | ||||||
| chr11:90181725
|
TTAAAAA | T | 42 | a0002c0003t0001g0010a0002c0003t0001g0282a0002c0003t0001g0284others(39): Show | 43 | HG00544.hp2 HG01099.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1940+25_1940+30del others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181725 | ||||||
| chr11:90181726
|
TA | T | 30 | a0001c0001t0002g0059a0001c0001t0002g0098a0001c0001t0002g0128others(27): Show | 30 | HG00597.hp2 HG01081.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1940+41delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181726 | |||||
| chr11:90181726
|
TAA | T | 14 | a0001c0001t0003g0064a0001c0002t0004g0268a0001c0002t0004g0272others(11): Show | 14 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1940+40_1940+41del others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181726 | |||||
| chr11:90181726
|
TAAAAA | T | 115 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(112): Show | 120 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1940+37_1940+41del others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181726 | |||||
| chr11:90181727
|
A | T | 1 | a0001c0001t0008g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1940+26A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181727 | ||||||
| chr11:90181728
|
A | T | 3 | a0004c0005t0004g0279a0004c0005t0004g0280a0004c0005t0004g0281 | 3 | HG02280.hp1 HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1940+27A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181728 | ||||||
| chr11:90181732
|
A | T | 27 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0018others(24): Show | 28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.1940+31A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181732 | ||||||
| chr11:90181733
|
A | T | 4 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0026others(1): Show | 4 | NA18943.hp1 NA18956.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1940+32A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181733 | ||||||
| chr11:90181772
|
A | C | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1940+71A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181772 | ||||||
| chr11:90181779
|
T | C | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1940+78T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181779 | ||||||
| chr11:90181837
|
A | G | 4 | a0001c0002t0001g0200a0001c0002t0001g0224a0001c0002t0001g0225others(1): Show | 4 | HG00642.hp1 HG01256.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940+136A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181837 | ||||||
| chr11:90181844
|
C | A | 1 | a0001c0001t0002g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1940+143C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181844 | ||||||
| chr11:90181878
|
A | C | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1940+177A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181878 | ||||||
| chr11:90181965
|
T | TG | 9 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0069others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1940+268dupG | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181965 | |||||
| chr11:90181974
|
C | T | 1 | a0003c0004t0005g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1940+273C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181974 | ||||||
| chr11:90182009
|
G | A | 2 | a0001c0002t0004g0268a0001c0002t0004g0272 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1940+308G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182009 | ||||||
| chr11:90182082
|
G | A | 7 | a0002c0003t0001g0286a0002c0003t0001g0289a0002c0003t0001g0290others(4): Show | 7 | HG01099.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1940+381G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182082 | ||||||
| chr11:90182112
|
A | G | 1 | a0001c0002t0005g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1940+411A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182112 | ||||||
| chr11:90182141
|
G | C | 1 | a0002c0003t0001g0312 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1940+440G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182141 | ||||||
| chr11:90182222
|
T | C | 13 | a0001c0002t0004g0350a0001c0002t0005g0012a0001c0002t0005g0339others(10): Show | 14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1940+521T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182222 | ||||||
| chr11:90182249
|
A | C | 1 | a0001c0001t0003g0080 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1940+548A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182249 | ||||||
| chr11:90182271
|
A | T | 3 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334 | 3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1940+570A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182271 | ||||||
| chr11:90182279
|
ATG | A | 3 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334 | 3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1940+582_1940+583d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90182279 | |||||
| chr11:90182287
|
A | G | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1940+586A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182287 | ||||||
| chr11:90182340
|
A | G | 4 | a0001c0002t0001g0200a0001c0002t0001g0224a0001c0002t0001g0225others(1): Show | 4 | HG00642.hp1 HG01256.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1941-576A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182340 | ||||||
| chr11:90182398
|
G | C | 2 | a0001c0002t0005g0332a0001c0002t0005g0333 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1941-518G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182398 | ||||||
| chr11:90182474
|
A | G | 5 | a0001c0001t0002g0041a0001c0001t0002g0137a0001c0001t0002g0145others(2): Show | 5 | HG02965.hp2 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1941-442A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182474 | ||||||
| chr11:90182476
|
C | G | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-440C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182476 | ||||||
| chr11:90182499
|
C | T | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-417C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182499 | ||||||
| chr11:90182510
|
T | A | 1 | a0001c0006t0001g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1941-406T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182510 | ||||||
| chr11:90182523
|
T | C | 47 | a0001c0006t0004g0335a0002c0003t0001g0010a0002c0003t0001g0011others(44): Show | 49 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1941-393T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182523 | ||||||
| chr11:90182577
|
T | C | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1941-339T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182577 | ||||||
| chr11:90182635
|
T | TAGAA | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-280_1941-277d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90182635 | |||||
| chr11:90182708
|
A | T | 184 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(181): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1941-208A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182708 | ||||||
| chr11:90182849
|
T | G | 1 | a0004c0021t0011g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1941-67T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182849 | ||||||
| chr11:90182885
|
C | G | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-31C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182885 | ||||||
| chr11:90182912
|
G | C | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
splice_region_variant&intron_variant | LOW | c.1941-4G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182912 | ||||||
| chr11:90183026
|
G | A | 1 | a0001c0001t0003g0054 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2033+18G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183026 | ||||||
| chr11:90183058
|
A | G | 3 | a0001c0001t0006g0052a0001c0001t0008g0053a0001c0001t0008g0136 | 3 | HG00099.hp1 HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2033+50A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183058 | ||||||
| chr11:90183179
|
T | G | 2 | a0001c0002t0001g0029a0001c0002t0007g0031 | 2 | NA18991.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2033+171T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183179 | ||||||
| chr11:90183189
|
T | G | 4 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2033+181T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183189 | ||||||
| chr11:90183227
|
T | G | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2033+219T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183227 | ||||||
| chr11:90183316
|
C | T | 180 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(177): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2033+308C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183316 | ||||||
| chr11:90183328
|
TC | T | 9 | a0001c0002t0004g0319a0004c0005t0001g0261a0004c0005t0001g0266others(6): Show | 9 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2033+321delC | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183328 | ||||||
| chr11:90183394
|
G | A | 192 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(189): Show | 198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.2033+386G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183394 | ||||||
| chr11:90183477
|
C | A | 8 | a0001c0002t0001g0196a0001c0002t0001g0207a0001c0002t0001g0212others(5): Show | 8 | NA18939.hp2 NA18956.hp1 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2033+469C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183477 | ||||||
| chr11:90183494
|
G | A | 181 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0014others(178): Show | 187 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.2033+486G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183494 | ||||||
| chr11:90183502
|
C | T | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+494C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183502 | ||||||
| chr11:90183585
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2033+577C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183585 | ||||||
| chr11:90183700
|
T | C | 183 | a0001c0001t0002g0057a0001c0002t0001g0002a0001c0002t0001g0007others(180): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.2033+692T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183700 | ||||||
| chr11:90183740
|
T | G | 1 | a0004c0005t0004g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2033+732T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183740 | ||||||
| chr11:90183857
|
G | C | 1 | a0001c0001t0003g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2033+849G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183857 | ||||||
| chr11:90183940
|
C | G | 2 | a0001c0002t0001g0245a0001c0002t0001g0246 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2033+932C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183940 | ||||||
| chr11:90184094
|
A | G | 152 | a0001c0001t0002g0057a0001c0002t0001g0007a0001c0002t0001g0186others(149): Show | 157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2033+1086A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184094 | ||||||
| chr11:90184162
|
T | C | 1 | a0001c0002t0005g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2033+1154T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184162 | ||||||
| chr11:90184417
|
A | G | 22 | a0001c0002t0001g0337a0001c0002t0004g0319a0001c0002t0005g0332others(19): Show | 22 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2033+1409A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184417 | ||||||
| chr11:90184475
|
G | A | 15 | a0001c0001t0003g0074a0001c0002t0001g0337a0001c0002t0005g0332others(12): Show | 15 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2033+1467G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184475 | ||||||
| chr11:90184487
|
G | A | 8 | a0001c0001t0003g0074a0001c0020t0002g0095a0005c0007t0001g0330others(5): Show | 8 | HG01081.hp1 HG03041.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.2033+1479G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184487 | ||||||
| chr11:90184524
|
G | A | 1 | a0002c0003t0001g0306 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2033+1516G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184524 | ||||||
| chr11:90184531
|
G | A | 236 | a0001c0001t0002g0041a0001c0001t0002g0047a0001c0001t0002g0057others(233): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2033+1523G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184531 | ||||||
| chr11:90184595
|
CT | C | 10 | a0001c0001t0003g0074a0001c0006t0001g0313a0001c0006t0001g0334others(7): Show | 10 | HG01081.hp1 HG01109.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2033+1588delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184595 | ||||||
| chr11:90184691
|
T | A | 2 | a0001c0006t0001g0334a0004c0005t0001g0261 | 2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2033+1683T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184691 | ||||||
| chr11:90184701
|
G | A | 43 | a0001c0001t0002g0125a0001c0001t0002g0160a0001c0001t0008g0049others(40): Show | 43 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.2033+1693G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184701 | ||||||
| chr11:90184702
|
C | A | 1 | a0001c0002t0001g0197 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2033+1694C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184702 | ||||||
| chr11:90184715
|
G | A | 23 | a0001c0001t0002g0098a0001c0001t0002g0161a0001c0001t0006g0006others(20): Show | 24 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2033+1707G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184715 | ||||||
| chr11:90184723
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2033+1715T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184723 | ||||||
| chr11:90184739
|
T | C | 30 | a0001c0001t0002g0158a0001c0001t0002g0175a0001c0001t0003g0056others(27): Show | 31 | HG00099.hp1 HG00597.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.2033+1731T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184739 | ||||||
| chr11:90184760
|
G | A | 57 | a0001c0001t0006g0097a0001c0001t0008g0049a0001c0002t0001g0007others(54): Show | 58 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2033+1752G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184760 | ||||||
| chr11:90184792
|
G | A | 9 | a0001c0002t0004g0269a0001c0002t0004g0270a0001c0002t0004g0271others(6): Show | 9 | HG01074.hp1 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2033+1784G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184792 | ||||||
| chr11:90184800
|
T | A | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+1792T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184800 | ||||||
| chr11:90184882
|
G | C | 1 | a0004c0005t0004g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2033+1874G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184882 | ||||||
| chr11:90184898
|
A | G | 58 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(55): Show | 58 | HG00673.hp1 HG01099.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.2033+1890A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184898 | ||||||
| chr11:90185072
|
A | T | 2 | a0004c0005t0005g0276a0004c0021t0011g0185 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2033+2064A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185072 | ||||||
| chr11:90185205
|
G | A | 241 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(238): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2033+2197G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185205 | ||||||
| chr11:90185241
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2033+2233A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185241 | ||||||
| chr11:90185451
|
G | A | 12 | a0001c0001t0006g0097a0003c0004t0005g0244a0003c0004t0005g0248others(9): Show | 12 | HG00438.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2033+2443G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185451 | ||||||
| chr11:90185515
|
T | G | 39 | a0001c0001t0008g0053a0001c0002t0001g0033a0001c0002t0001g0200others(36): Show | 40 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2033+2507T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185515 | ||||||
| chr11:90185555
|
T | A | 1 | a0001c0002t0004g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2033+2547T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185555 | ||||||
| chr11:90185644
|
G | A | 2 | a0001c0002t0004g0039a0001c0002t0004g0040 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2033+2636G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185644 | ||||||
| chr11:90185648
|
A | G | 1 | a0001c0002t0004g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2033+2640A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185648 | ||||||
| chr11:90185766
|
A | T | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+2758A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185766 | ||||||
| chr11:90185850
|
G | C | 52 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(49): Show | 52 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2033+2842G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185850 | ||||||
| chr11:90185858
|
C | CT | 51 | a0001c0001t0002g0047a0001c0001t0002g0057a0001c0001t0002g0058others(48): Show | 51 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.2033+2866dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | |||||
| chr11:90185858
|
C | CTT | 10 | a0001c0002t0004g0271a0001c0002t0005g0342a0001c0006t0001g0313others(7): Show | 11 | HG00323.hp1 HG01109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2033+2865_2033+286 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | |||||
| chr11:90185858
|
C | CTTT | 13 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(10): Show | 14 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2033+2864_2033+286 others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | |||||
| chr11:90185858
|
C | CTTTT | 6 | a0002c0003t0001g0290a0002c0003t0001g0291a0002c0003t0001g0292others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2033+2863_2033+286 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | |||||
| chr11:90185858
|
C | CTTTTT | 31 | a0001c0001t0008g0053a0001c0002t0001g0033a0001c0002t0001g0200others(28): Show | 32 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2033+2862_2033+286 others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | |||||
| chr11:90185858
|
CT | C | 17 | a0001c0001t0002g0112a0001c0001t0002g0155a0001c0001t0006g0097others(14): Show | 17 | HG00438.hp2 HG01934.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2033+2866delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | |||||
| chr11:90185873
|
T | A | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+2865T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185873 | ||||||
| chr11:90185873
|
TTA | T | 49 | a0001c0001t0003g0004a0001c0001t0003g0044a0001c0001t0003g0054others(46): Show | 49 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2033+2870_2033+287 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185873 | |||||
| chr11:90185874
|
T | A | 2 | a0001c0001t0002g0101a0001c0002t0001g0230 | 2 | HG02148.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2033+2866T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185874 | ||||||
| chr11:90185911
|
G | T | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+2903G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185911 | ||||||
| chr11:90185949
|
T | C | 48 | a0001c0001t0008g0049a0001c0001t0008g0066a0001c0001t0008g0122others(45): Show | 49 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.2033+2941T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185949 | ||||||
| chr11:90185979
|
G | C | 147 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(144): Show | 150 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.2033+2971G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185979 | ||||||
| chr11:90186028
|
T | A | 3 | a0001c0002t0004g0269a0001c0002t0004g0270a0001c0002t0004g0273 | 3 | HG01074.hp1 HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2033+3020T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186028 | ||||||
| chr11:90186029
|
A | T | 1 | a0004c0005t0004g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2033+3021A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186029 | ||||||
| chr11:90186184
|
C | G | 1 | a0001c0002t0005g0342 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2033+3176C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186184 | ||||||
| chr11:90186454
|
G | C | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+3446G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186454 | ||||||
| chr11:90186502
|
T | C | 1 | a0005c0007t0001g0330 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2033+3494T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186502 | ||||||
| chr11:90186505
|
A | C | 1 | a0001c0001t0002g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2033+3497A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186505 | ||||||
| chr11:90186515
|
GATTTATA others(14): Show |
G | 2 | a0001c0002t0001g0245a0001c0002t0001g0322 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2033+3508_2033+352 others(25): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186515 | ||||||
| chr11:90186635
|
G | A | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+3627G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186635 | ||||||
| chr11:90186729
|
G | T | 9 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(6): Show | 10 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2033+3721G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186729 | ||||||
| chr11:90186730
|
T | A | 244 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(241): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.2033+3722T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186730 | ||||||
| chr11:90186811
|
A | C | 5 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(2): Show | 5 | HG01109.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2033+3803A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186811 | ||||||
| chr11:90186829
|
A | T | 1 | a0005c0007t0005g0327 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2033+3821A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186829 | ||||||
| chr11:90186897
|
A | G | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+3889A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186897 | ||||||
| chr11:90186915
|
G | A | 128 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(125): Show | 130 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.2033+3907G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186915 | ||||||
| chr11:90186941
|
A | G | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+3933A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186941 | ||||||
| chr11:90186942
|
A | C | 1 | a0001c0001t0002g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2033+3934A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186942 | ||||||
| chr11:90186952
|
T | G | 2 | a0002c0003t0004g0287a0008c0010t0004g0329 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2033+3944T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186952 | ||||||
| chr11:90186969
|
C | G | 3 | a0001c0002t0005g0347a0001c0002t0005g0348a0001c0002t0005g0349 | 3 | NA18985.hp1 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2033+3961C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186969 | ||||||
| chr11:90187009
|
G | A | 2 | a0001c0001t0006g0046a0001c0001t0006g0177 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2033+4001G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187009 | ||||||
| chr11:90187010
|
A | G | 1 | a0003c0004t0018g0247 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2033+4002A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187010 | ||||||
| chr11:90187017
|
T | C | 9 | a0001c0001t0002g0003a0001c0001t0002g0048a0001c0001t0002g0050others(6): Show | 10 | HG00099.hp2 HG00735.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2033+4009T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187017 | ||||||
| chr11:90187022
|
A | G | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+4014A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187022 | ||||||
| chr11:90187063
|
T | A | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+4055T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187063 | ||||||
| chr11:90187150
|
A | G | 4 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(1): Show | 4 | HG01109.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2033+4142A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187150 | ||||||
| chr11:90187199
|
T | C | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+4191T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187199 | ||||||
| chr11:90187304
|
C | T | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2034-4254C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187304 | ||||||
| chr11:90187313
|
C | CACATTTT others(92): Show |
1 | a0001c0002t0005g0332 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2034-4148_2034-414 others(103): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90187313 | |||||
| chr11:90187348
|
G | T | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2034-4210G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187348 | ||||||
| chr11:90187426
|
T | C | 90 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(87): Show | 91 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.2034-4132T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187426 | ||||||
| chr11:90187532
|
CTT | C | 35 | a0001c0001t0003g0086a0001c0001t0006g0006a0001c0001t0006g0046others(32): Show | 36 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2034-4022_2034-402 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90187532 | |||||
| chr11:90187537
|
T | C | 96 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(93): Show | 97 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.2034-4021T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187537 | ||||||
| chr11:90187570
|
A | G | 3 | a0001c0002t0004g0195a0001c0002t0004g0209a0001c0002t0004g0239 | 3 | HG02165.hp2 NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2034-3988A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187570 | ||||||
| chr11:90187757
|
C | G | 91 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(88): Show | 92 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.2034-3801C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187757 | ||||||
| chr11:90187888
|
A | G | 1 | a0001c0006t0005g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2034-3670A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187888 | ||||||
| chr11:90187986
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0140 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2034-3572C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187986 | ||||||
| chr11:90188064
|
C | T | 95 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(92): Show | 96 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.2034-3494C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188064 | ||||||
| chr11:90188367
|
C | G | 1 | a0004c0005t0004g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2034-3191C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188367 | ||||||
| chr11:90188444
|
T | C | 1 | a0001c0002t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2034-3114T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188444 | ||||||
| chr11:90188496
|
G | T | 143 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(140): Show | 146 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2034-3062G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188496 | ||||||
| chr11:90188518
|
G | A | 2 | a0002c0003t0001g0298a0002c0003t0001g0306 | 2 | HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2034-3040G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188518 | ||||||
| chr11:90188551
|
T | A | 1 | a0001c0002t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2034-3007T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188551 | ||||||
| chr11:90188574
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2034-2984A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188574 | ||||||
| chr11:90188825
|
T | A | 1 | a0004c0005t0004g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2034-2733T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188825 | ||||||
| chr11:90188859
|
C | G | 14 | a0001c0002t0005g0012a0001c0002t0005g0333a0001c0002t0005g0339others(11): Show | 15 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2034-2699C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188859 | ||||||
| chr11:90188986
|
G | T | 146 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(143): Show | 148 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.2034-2572G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188986 | ||||||
| chr11:90189034
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2034-2524T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189034 | ||||||
| chr11:90189062
|
A | G | 28 | a0001c0001t0003g0086a0001c0001t0006g0006a0001c0001t0006g0046others(25): Show | 29 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2034-2496A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189062 | ||||||
| chr11:90189125
|
G | A | 2 | a0001c0002t0001g0245a0001c0002t0001g0322 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2034-2433G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189125 | ||||||
| chr11:90189135
|
A | AT | 43 | a0001c0002t0001g0033a0001c0002t0001g0200a0001c0002t0001g0224others(40): Show | 44 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.2034-2422dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90189135 | |||||
| chr11:90189147
|
G | A | 1 | a0003c0004t0005g0248 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2034-2411G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189147 | ||||||
| chr11:90189249
|
A | G | 48 | a0001c0001t0006g0006a0001c0001t0006g0046a0001c0001t0006g0065others(45): Show | 50 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2034-2309A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189249 | ||||||
| chr11:90189255
|
C | G | 57 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(54): Show | 57 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.2034-2303C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189255 | ||||||
| chr11:90189280
|
AT | A | 36 | a0001c0001t0008g0053a0001c0002t0001g0033a0001c0002t0001g0200others(33): Show | 36 | HG00544.hp2 HG00642.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.2034-2277delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189280 | ||||||
| chr11:90189498
|
G | A | 1 | a0002c0003t0005g0275 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2034-2060G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189498 | ||||||
| chr11:90189531
|
G | A | 1 | a0001c0002t0001g0337 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2034-2027G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189531 | ||||||
| chr11:90189561
|
G | A | 3 | a0002c0003t0005g0009a0002c0003t0005g0275a0003c0004t0005g0254 | 4 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034-1997G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189561 | ||||||
| chr11:90189718
|
G | A | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-1840G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189718 | ||||||
| chr11:90189737
|
C | G | 39 | a0001c0001t0008g0053a0001c0002t0001g0033a0001c0002t0001g0200others(36): Show | 39 | HG00544.hp2 HG00642.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.2034-1821C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189737 | ||||||
| chr11:90189748
|
C | T | 2 | a0001c0001t0003g0078a0001c0001t0003g0092 | 2 | NA18970.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2034-1810C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189748 | ||||||
| chr11:90189769
|
C | CA | 41 | a0001c0001t0008g0053a0001c0002t0001g0023a0001c0002t0001g0033others(38): Show | 41 | HG00544.hp2 HG00642.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.2034-1777dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90189769 | |||||
| chr11:90189769
|
C | CAA | 75 | a0001c0001t0006g0052a0001c0001t0008g0049a0001c0001t0008g0066others(72): Show | 78 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.2034-1778_2034-177 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90189769 | |||||
| chr11:90189778
|
A | AG | 3 | a0002c0003t0001g0282a0002c0003t0001g0301a0002c0003t0001g0303 | 3 | HG01192.hp2 HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2034-1780_2034-177 others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189778 | ||||||
| chr11:90189805
|
A | G | 1 | a0004c0005t0014g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2034-1753A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189805 | ||||||
| chr11:90189857
|
G | T | 2 | a0001c0002t0001g0245a0001c0002t0001g0322 | 2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2034-1701G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189857 | ||||||
| chr11:90190049
|
T | G | 1 | a0002c0003t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2034-1509T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190049 | ||||||
| chr11:90190082
|
G | A | 1 | a0002c0003t0001g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2034-1476G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190082 | ||||||
| chr11:90190114
|
G | T | 172 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(169): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2034-1444G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190114 | ||||||
| chr11:90190200
|
C | CACA | 223 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(220): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2034-1356_2034-135 others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90190200 | |||||
| chr11:90190317
|
T | C | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-1241T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190317 | ||||||
| chr11:90190349
|
A | C | 2 | a0004c0005t0005g0276a0004c0021t0011g0185 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2034-1209A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190349 | ||||||
| chr11:90190437
|
G | C | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-1121G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190437 | ||||||
| chr11:90190712
|
C | G | 176 | a0001c0001t0003g0004a0001c0001t0003g0043a0001c0001t0003g0044others(173): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.2034-846C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190712 | ||||||
| chr11:90190731
|
G | A | 2 | a0001c0001t0006g0176a0001c0001t0006g0180 | 2 | HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2034-827G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190731 | ||||||
| chr11:90190769
|
GTCATTAA | G | 6 | a0001c0002t0001g0245a0001c0002t0001g0322a0001c0006t0001g0313others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2034-773_2034-767d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90190769 | |||||
| chr11:90190833
|
C | T | 12 | a0001c0002t0005g0012a0001c0002t0005g0339a0001c0002t0005g0340others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-725C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190833 | ||||||
| chr11:90190964
|
T | C | 4 | a0001c0002t0005g0332a0001c0006t0005g0338a0004c0005t0005g0260others(1): Show | 4 | HG02109.hp1 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034-594T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190964 | ||||||
| chr11:90191100
|
A | G | 2 | a0001c0002t0005g0333a0001c0006t0005g0336 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2034-458A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191100 | ||||||
| chr11:90191151
|
T | C | 1 | a0002c0003t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2034-407T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191151 | ||||||
| chr11:90191270
|
C | T | 1 | a0002c0003t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2034-288C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191270 | ||||||
| chr11:90191288
|
T | A | 1 | a0003c0004t0005g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2034-270T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191288 | ||||||
| chr11:90191300
|
T | TAAAAGAA others(314): Show |
4 | a0001c0006t0001g0313a0001c0006t0001g0314a0001c0006t0001g0334others(1): Show | 4 | HG01109.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034-244_2034-243i others(323): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90191300 | |||||
| chr11:90191300
|
T | TAAAAGAA others(333): Show |
1 | a0001c0002t0001g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2034-244_2034-243i others(342): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90191300 | |||||
| chr11:90191300
|
T | TAAAAGAA others(339): Show |
1 | a0001c0002t0001g0322 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2034-244_2034-243i others(348): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90191300 | |||||
| chr11:90191461
|
G | A | 3 | a0002c0003t0005g0009a0002c0003t0005g0275a0003c0004t0005g0254 | 4 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034-97G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191461 | ||||||
| chr11:90191479
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2034-79C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191479 |